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. 1995 Aug;187(Pt 1):1–26.

The effects of ageing on cutaneous wound healing in mammals.

G S Ashcroft 1, M A Horan 1, M W Ferguson 1
PMCID: PMC1167345  PMID: 7591970

Abstract

The dogma that cutaneous wound healing is impaired as a function of age is largely unsubstantiated. This can be attributed to poor experimental design of human studies, the lack of subject characterisation with the exclusion of disease processes, and the study of inappropriate animal models. Structural and functional changes in skin with age have been reported, such as a decrease in dermal thickness, decline in collagen content, a subtle alteration in the glycosaminoglycan profile, and a loss of elasticity, but these reports are subject to the above criticisms in addition to the often-neglected requirement for site specificity. Wound repair can be thought of as a culmination of three major overlapping phases: inflammation, proliferation and remodelling. The inflammatory process has not been studied systematically with respect to age, and despite a reported decline in cellular function and number, there is a confounding increase in the production of specific cytokines involved in the process of repair. The proliferative phase is associated with a loss of cellular responsiveness to specific cytokines with a decline in motility and proliferation; however caution in interpreting these findings is important as, for example, the definition of 'ageing' is used rather loosely with the result that neonatal versus young adult cells are compared instead of young versus old adults. During remodelling, fibronectin and collagen production may increase with age, as may wound contraction; the deposition of elastin has not been assessed and the resulting mechanical properties of the scar are controversial, not least because human in vivo studies have been ignored. The absence of a critical review on the effects of advancing age on wound healing has conspired to permit the perpetuation of the belief that well defined tenets exist. This review aims to redress this imbalance and to highlight the need for well designed research into an increasingly important field.

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Selected References

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  1. ABT A. F., VON SCHUCHING S. Aging as a factor in wound healing. L-ascorbic-1-C14 acid catabolism and tissue retention following wounding in young and older guinea pigs. Arch Surg. 1963 Apr;86:627–632. doi: 10.1001/archsurg.1963.01310100111017. [DOI] [PubMed] [Google Scholar]
  2. Adams J. C., Watt F. M. Fibronectin inhibits the terminal differentiation of human keratinocytes. Nature. 1989 Jul 27;340(6231):307–309. doi: 10.1038/340307a0. [DOI] [PubMed] [Google Scholar]
  3. Agrez M. V., Bates R. C., Boyd A. W., Burns G. F. Arg-Gly-Asp-containing peptides expose novel collagen receptors on fibroblasts: implications for wound healing. Cell Regul. 1991 Dec;2(12):1035–1044. doi: 10.1091/mbc.2.12.1035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Albini A., Pontz B., Pulz M., Allavena G., Mensing H., Müller P. K. Decline of fibroblast chemotaxis with age of donor and cell passage number. Coll Relat Res. 1988 Jan;8(1):23–37. doi: 10.1016/s0174-173x(88)80033-5. [DOI] [PubMed] [Google Scholar]
  5. Ando Y., Jensen P. J. Epidermal growth factor and insulin-like growth factor I enhance keratinocyte migration. J Invest Dermatol. 1993 May;100(5):633–639. doi: 10.1111/1523-1747.ep12472297. [DOI] [PubMed] [Google Scholar]
  6. Ansel J. C., Tiesman J. P., Olerud J. E., Krueger J. G., Krane J. F., Tara D. C., Shipley G. D., Gilbertson D., Usui M. L., Hart C. E. Human keratinocytes are a major source of cutaneous platelet-derived growth factor. J Clin Invest. 1993 Aug;92(2):671–678. doi: 10.1172/JCI116636. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Antoniades H. N., Galanopoulos T., Neville-Golden J., Kiritsy C. P., Lynch S. E. Expression of growth factor and receptor mRNAs in skin epithelial cells following acute cutaneous injury. Am J Pathol. 1993 Apr;142(4):1099–1110. [PMC free article] [PubMed] [Google Scholar]
  8. Antoniades H. N., Galanopoulos T., Neville-Golden J., Kiritsy C. P., Lynch S. E. Injury induces in vivo expression of platelet-derived growth factor (PDGF) and PDGF receptor mRNAs in skin epithelial cells and PDGF mRNA in connective tissue fibroblasts. Proc Natl Acad Sci U S A. 1991 Jan 15;88(2):565–569. doi: 10.1073/pnas.88.2.565. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Arakawa M., Hatamochi A., Takeda K., Ueki H. Increased collagen synthesis accompanying elevated m-RNA levels in cultured Werner's syndrome fibroblasts. J Invest Dermatol. 1990 Feb;94(2):187–190. doi: 10.1111/1523-1747.ep12874489. [DOI] [PubMed] [Google Scholar]
  10. Arbogast B. W., Berry D. L., Newell C. L. Injury of arterial endothelial cells in diabetic, sucrose-fed and aged rats. Atherosclerosis. 1984 Apr;51(1):31–45. doi: 10.1016/0021-9150(84)90142-4. [DOI] [PubMed] [Google Scholar]
  11. Assouline M., Chew S. J., Thompson H. W., Beuerman R. Effect of growth factors on collagen lattice contraction by human keratocytes. Invest Ophthalmol Vis Sci. 1992 Apr;33(5):1742–1755. [PubMed] [Google Scholar]
  12. Azizkhan R. G., Azizkhan J. C., Zetter B. R., Folkman J. Mast cell heparin stimulates migration of capillary endothelial cells in vitro. J Exp Med. 1980 Oct 1;152(4):931–944. doi: 10.1084/jem.152.4.931. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Bailey A. J., Bazin S., Delaunay A. Changes in the nature of the collagen during development and resorption of granulatin tissue. Biochim Biophys Acta. 1973 Dec 6;328(2):383–390. doi: 10.1016/0005-2795(73)90272-9. [DOI] [PubMed] [Google Scholar]
  14. Baker H., Blair C. P. Cell replacement in the human stratum corneum in old age. Br J Dermatol. 1968 Jun;80(6):367–372. doi: 10.1111/j.1365-2133.1968.tb12322.x. [DOI] [PubMed] [Google Scholar]
  15. Ballard F. J., Read L. C. Changes in protein synthesis and breakdown rates and responsiveness to growth factors with ageing in human lung fibroblasts. Mech Ageing Dev. 1985 Apr;30(1):11–22. doi: 10.1016/0047-6374(85)90055-7. [DOI] [PubMed] [Google Scholar]
  16. Barbul A., Knud-Hansen J., Wasserkrug H. L., Efron G. Interleukin 2 enhances wound healing in rats. J Surg Res. 1986 Apr;40(4):315–319. doi: 10.1016/0022-4804(86)90193-9. [DOI] [PubMed] [Google Scholar]
  17. Barbul A. Role of T-cell-dependent immune system in wound healing. Prog Clin Biol Res. 1988;266:161–175. [PubMed] [Google Scholar]
  18. Barnes M. J., Bailey A. J., Gordon J. L., MacIntyre D. E. Platelet aggregaton by basement membrane-associated collagens. Thromb Res. 1980 May 1;18(3-4):375–388. doi: 10.1016/0049-3848(80)90333-3. [DOI] [PubMed] [Google Scholar]
  19. Baroody R. A., Bito L. Z., DeRousseau C. J., Kaufman P. L. Ocular development and aging. 1. Corneal endothelial changes in cats and in free-ranging and caged rhesus monkeys. Exp Eye Res. 1987 Oct;45(4):607–622. doi: 10.1016/s0014-4835(87)80070-2. [DOI] [PubMed] [Google Scholar]
  20. Barrandon Y., Green H. Cell migration is essential for sustained growth of keratinocyte colonies: the roles of transforming growth factor-alpha and epidermal growth factor. Cell. 1987 Sep 25;50(7):1131–1137. doi: 10.1016/0092-8674(87)90179-6. [DOI] [PubMed] [Google Scholar]
  21. Bauer E. A., Silverman N., Busiek D. F., Kronberger A., Deuel T. F. Diminished response of Werner's syndrome fibroblasts to growth factors PDGF and FGF. Science. 1986 Dec 5;234(4781):1240–1243. doi: 10.1126/science.3022382. [DOI] [PubMed] [Google Scholar]
  22. Beavan L. A., Quentin-Hoffmann E., Schönherr E., Snigula F., Leroy J. G., Kresse H. Deficient expression of decorin in infantile progeroid patients. J Biol Chem. 1993 May 5;268(13):9856–9862. [PubMed] [Google Scholar]
  23. Beck L. S., DeGuzman L., Lee W. P., Xu Y., Siegel M. W., Amento E. P. One systemic administration of transforming growth factor-beta 1 reverses age- or glucocorticoid-impaired wound healing. J Clin Invest. 1993 Dec;92(6):2841–2849. doi: 10.1172/JCI116904. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Bellas R. E., Bendori R., Farmer S. R. Epidermal growth factor activation of vinculin and beta 1-integrin gene transcription in quiescent Swiss 3T3 cells. Regulation through a protein kinase C-independent pathway. J Biol Chem. 1991 Jun 25;266(18):12008–12014. [PubMed] [Google Scholar]
  25. Bhangoo K. S., Quinlivan J. K., Connelly J. R. Elastin fibers in scar tissue. Plast Reconstr Surg. 1976 Mar;57(3):308–313. doi: 10.1097/00006534-197603000-00005. [DOI] [PubMed] [Google Scholar]
  26. Bloom E. T. Functional importance of CD4+ and CD8+ cells in cytotoxic lymphocytes activity and associated gene expression. Impact on the age-related decline in lytic activity. Eur J Immunol. 1991 Apr;21(4):1013–1017. doi: 10.1002/eji.1830210423. [DOI] [PubMed] [Google Scholar]
  27. Border W. A., Noble N. A., Yamamoto T., Harper J. R., Yamaguchi Y. u., Pierschbacher M. D., Ruoslahti E. Natural inhibitor of transforming growth factor-beta protects against scarring in experimental kidney disease. Nature. 1992 Nov 26;360(6402):361–364. doi: 10.1038/360361a0. [DOI] [PubMed] [Google Scholar]
  28. Braverman I. M. Elastic fiber and microvascular abnormalities in aging skin. Clin Geriatr Med. 1989 Feb;5(1):69–90. [PubMed] [Google Scholar]
  29. Braverman I. M., Fonferko E. Studies in cutaneous aging: II. The microvasculature. J Invest Dermatol. 1982 May;78(5):444–448. doi: 10.1111/1523-1747.ep12508027. [DOI] [PubMed] [Google Scholar]
  30. Broadley K. N., Aquino A. M., Woodward S. C., Buckley-Sturrock A., Sato Y., Rifkin D. B., Davidson J. M. Monospecific antibodies implicate basic fibroblast growth factor in normal wound repair. Lab Invest. 1989 Nov;61(5):571–575. [PubMed] [Google Scholar]
  31. Brown L. F., Yeo K. T., Berse B., Yeo T. K., Senger D. R., Dvorak H. F., van de Water L. Expression of vascular permeability factor (vascular endothelial growth factor) by epidermal keratinocytes during wound healing. J Exp Med. 1992 Nov 1;176(5):1375–1379. doi: 10.1084/jem.176.5.1375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Bruce S. A., Deamond S. F. Longitudinal study of in vivo wound repair and in vitro cellular senescence of dermal fibroblasts. Exp Gerontol. 1991;26(1):17–27. doi: 10.1016/0531-5565(91)90058-t. [DOI] [PubMed] [Google Scholar]
  33. Buntrock P., Jentzsch K. D., Heder G. Stimulation of wound healing, using brain extract with fibroblast growth factor (FGF) activity. I. Quantitative and biochemical studies into formation of granulation tissue. Exp Pathol. 1982;21(1):46–53. doi: 10.1016/s0232-1513(82)80051-0. [DOI] [PubMed] [Google Scholar]
  34. CLAUSEN B. Influence of age on connective tissue. Hexosamine and hydroxyproline in human aorta, myocardium, and skin. Lab Invest. 1962 Mar;11:229–234. [PubMed] [Google Scholar]
  35. Cannon J. G., Dinarello C. A. Increased plasma interleukin-1 activity in women after ovulation. Science. 1985 Mar 8;227(4691):1247–1249. doi: 10.1126/science.3871966. [DOI] [PubMed] [Google Scholar]
  36. Chandrasekhar S., Millis A. J. Fibronectin from aged fibroblasts is defective in promoting cellular adhesion. J Cell Physiol. 1980 Apr;103(1):47–54. doi: 10.1002/jcp.1041030108. [DOI] [PubMed] [Google Scholar]
  37. Chen W. Y., Grant M. E., Schor A. M., Schor S. L. Differences between adult and foetal fibroblasts in the regulation of hyaluronate synthesis: correlation with migratory activity. J Cell Sci. 1989 Nov;94(Pt 3):577–584. doi: 10.1242/jcs.94.3.577. [DOI] [PubMed] [Google Scholar]
  38. Chen Y. Q., Mauviel A., Ryynänen J., Sollberg S., Uitto J. Type VII collagen gene expression by human skin fibroblasts and keratinocytes in culture: influence of donor age and cytokine responses. J Invest Dermatol. 1994 Feb;102(2):205–209. doi: 10.1111/1523-1747.ep12371763. [DOI] [PubMed] [Google Scholar]
  39. Chiarugi V. P., Vannucchi S. Surface heparan sulphate as a control element in eukariotic cells: a working model. J Theor Biol. 1976 Sep 21;61(2):459–475. doi: 10.1016/0022-5193(76)90030-8. [DOI] [PubMed] [Google Scholar]
  40. Clark R. A., Lanigan J. M., DellaPelle P., Manseau E., Dvorak H. F., Colvin R. B. Fibronectin and fibrin provide a provisional matrix for epidermal cell migration during wound reepithelialization. J Invest Dermatol. 1982 Nov;79(5):264–269. doi: 10.1111/1523-1747.ep12500075. [DOI] [PubMed] [Google Scholar]
  41. Coffey R. J., Jr, Derynck R., Wilcox J. N., Bringman T. S., Goustin A. S., Moses H. L., Pittelkow M. R. Production and auto-induction of transforming growth factor-alpha in human keratinocytes. 1987 Aug 27-Sep 2Nature. 328(6133):817–820. doi: 10.1038/328817a0. [DOI] [PubMed] [Google Scholar]
  42. Cohen B. J., Cutler R. G., Roth G. S. Accelerated wound repair in old deer mice (Peromyscus maniculatus) and white-footed mice (Peromyscus leucopus). J Gerontol. 1987 May;42(3):302–307. doi: 10.1093/geronj/42.3.302. [DOI] [PubMed] [Google Scholar]
  43. Cohen B. J., Danon D., Roth G. S. Wound repair in mice as influenced by age and antimacrophage serum. J Gerontol. 1987 May;42(3):295–301. doi: 10.1093/geronj/42.3.295. [DOI] [PubMed] [Google Scholar]
  44. Colige A., Nusgens B., Lapiere C. M. Altered response of progeria fibroblasts to epidermal growth factor. J Cell Sci. 1991 Nov;100(Pt 3):649–655. doi: 10.1242/jcs.100.3.649. [DOI] [PubMed] [Google Scholar]
  45. Colige A., Nusgens B., Lapiere C. M. Response to epidermal growth factor of skin fibroblasts from donors of varying age is modulated by the extracellular matrix. J Cell Physiol. 1990 Dec;145(3):450–457. doi: 10.1002/jcp.1041450309. [DOI] [PubMed] [Google Scholar]
  46. Cossarizza A., Monti D., Bersani F., Paganelli R., Montagnani G., Cadossi R., Cantini M., Franceschi C. Extremely low frequency pulsed electromagnetic fields increase interleukin-2 (IL-2) utilization and IL-2 receptor expression in mitogen-stimulated human lymphocytes from old subjects. FEBS Lett. 1989 May 8;248(1-2):141–144. doi: 10.1016/0014-5793(89)80449-1. [DOI] [PubMed] [Google Scholar]
  47. Cox D. A., Kunz S., Cerletti N., McMaster G. K., Burk R. R. Wound healing in aged animals--effects of locally applied transforming growth factor beta 2 in different model systems. EXS. 1992;61:287–295. doi: 10.1007/978-3-0348-7001-6_46. [DOI] [PubMed] [Google Scholar]
  48. Dahlbäck K., Löfberg H., Alumets J., Dahlbäck B. Immunohistochemical demonstration of age-related deposition of vitronectin (S-protein of complement) and terminal complement complex on dermal elastic fibers. J Invest Dermatol. 1989 May;92(5):727–733. doi: 10.1111/1523-1747.ep12721619. [DOI] [PubMed] [Google Scholar]
  49. Danon D., Kowatch M. A., Roth G. S. Promotion of wound repair in old mice by local injection of macrophages. Proc Natl Acad Sci U S A. 1989 Mar;86(6):2018–2020. doi: 10.1073/pnas.86.6.2018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Darby I., Skalli O., Gabbiani G. Alpha-smooth muscle actin is transiently expressed by myofibroblasts during experimental wound healing. Lab Invest. 1990 Jul;63(1):21–29. [PubMed] [Google Scholar]
  51. Davidson J. M., Zoia O., Liu J. M. Modulation of transforming growth factor-beta 1 stimulated elastin and collagen production and proliferation in porcine vascular smooth muscle cells and skin fibroblasts by basic fibroblast growth factor, transforming growth factor-alpha, and insulin-like growth factor-I. J Cell Physiol. 1993 Apr;155(1):149–156. doi: 10.1002/jcp.1041550119. [DOI] [PubMed] [Google Scholar]
  52. DeLapp N. W., Dieckman D. K. Effect of basic fibroblast growth factor (bFGF) and insulin-like growth factors type I (IGF-I) and type II (IGF-II) on adult human keratinocyte growth and fibronectin secretion. J Invest Dermatol. 1990 Jun;94(6):777–780. doi: 10.1111/1523-1747.ep12874637. [DOI] [PubMed] [Google Scholar]
  53. Derynck R. Transforming growth factor alpha. Cell. 1988 Aug 26;54(5):593–595. doi: 10.1016/s0092-8674(88)80001-1. [DOI] [PubMed] [Google Scholar]
  54. Doillon C. J., Dunn M. G., Bender E., Silver F. H. Collagen fiber formation in repair tissue: development of strength and toughness. Coll Relat Res. 1985 Dec;5(6):481–492. doi: 10.1016/s0174-173x(85)80002-9. [DOI] [PubMed] [Google Scholar]
  55. Dyer D. G., Dunn J. A., Thorpe S. R., Bailie K. E., Lyons T. J., McCance D. R., Baynes J. W. Accumulation of Maillard reaction products in skin collagen in diabetes and aging. J Clin Invest. 1993 Jun;91(6):2463–2469. doi: 10.1172/JCI116481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Edwards D. R., Heath J. K., Hogan B. L., Nomura S., Wills A. J. Expression of TIMP in fetal and adult mouse tissues studied by in situ hybridization. Matrix Suppl. 1992;1:286–293. [PubMed] [Google Scholar]
  57. Ershler W. B., Gamelli R. L., Moore A. L., Hacker M. P., Blow A. J. Experimental tumors and aging: local factors that may account for the observed age advantage in the B16 murine melanoma model. Exp Gerontol. 1984;19(6):367–376. doi: 10.1016/0531-5565(84)90046-9. [DOI] [PubMed] [Google Scholar]
  58. Escoffier C., de Rigal J., Rochefort A., Vasselet R., Lévêque J. L., Agache P. G. Age-related mechanical properties of human skin: an in vivo study. J Invest Dermatol. 1989 Sep;93(3):353–357. [PubMed] [Google Scholar]
  59. FORSCHER B. K., CECIL H. C. Some effects of age on the biochemistry of acute inflammation. Gerontologia. 1958;2(3):174–182. doi: 10.1159/000210736. [DOI] [PubMed] [Google Scholar]
  60. Fagiolo U., Cossarizza A., Santacaterina S., Ortolani C., Monti D., Paganelli R., Franceschi C. Increased cytokine production by peripheral blood mononuclear cells from healthy elderly people. Ann N Y Acad Sci. 1992 Nov 21;663:490–493. doi: 10.1111/j.1749-6632.1992.tb38712.x. [DOI] [PubMed] [Google Scholar]
  61. Fargnoli J., Kunisada T., Fornace A. J., Jr, Schneider E. L., Holbrook N. J. Decreased expression of heat shock protein 70 mRNA and protein after heat treatment in cells of aged rats. Proc Natl Acad Sci U S A. 1990 Jan;87(2):846–850. doi: 10.1073/pnas.87.2.846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Fenske N. A., Lober C. W. Structural and functional changes of normal aging skin. J Am Acad Dermatol. 1986 Oct;15(4 Pt 1):571–585. doi: 10.1016/s0190-9622(86)70208-9. [DOI] [PubMed] [Google Scholar]
  63. Fine J. D., Couchman J. R. Chondroitin 6-sulfate proteoglycan but not heparan sulfate proteoglycan is abnormally expressed in skin basement membrane from patients with dominant and recessive dystrophic epidermolysis bullosa. J Invest Dermatol. 1989 Apr;92(4):611–616. doi: 10.1111/1523-1747.ep12712151. [DOI] [PubMed] [Google Scholar]
  64. Finesmith T. H., Broadley K. N., Davidson J. M. Fibroblasts from wounds of different stages of repair vary in their ability to contract a collagen gel in response to growth factors. J Cell Physiol. 1990 Jul;144(1):99–107. doi: 10.1002/jcp.1041440113. [DOI] [PubMed] [Google Scholar]
  65. Fleischmajer R., Nedwich A. Werner's syndrome. Am J Med. 1973 Jan;54(1):111–118. doi: 10.1016/0002-9343(73)90089-2. [DOI] [PubMed] [Google Scholar]
  66. Fleischmajer R., Perlish J. S., Bashey R. I. Human dermal glycosaminoglycans and aging. Biochim Biophys Acta. 1972 Sep 15;279(2):265–275. doi: 10.1016/0304-4165(72)90142-0. [DOI] [PubMed] [Google Scholar]
  67. Furth J. J. The steady-state levels of type I collagen mRNA are reduced in senescent fibroblasts. J Gerontol. 1991 May;46(3):B122–B124. doi: 10.1093/geronj/46.3.b122. [DOI] [PubMed] [Google Scholar]
  68. Gabbiani G., Ryan G. B., Majne G. Presence of modified fibroblasts in granulation tissue and their possible role in wound contraction. Experientia. 1971 May 15;27(5):549–550. doi: 10.1007/BF02147594. [DOI] [PubMed] [Google Scholar]
  69. Gamble J. R., Harlan J. M., Klebanoff S. J., Vadas M. A. Stimulation of the adherence of neutrophils to umbilical vein endothelium by human recombinant tumor necrosis factor. Proc Natl Acad Sci U S A. 1985 Dec;82(24):8667–8671. doi: 10.1073/pnas.82.24.8667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  70. Gamble J. R., Vadas M. A. Endothelial adhesiveness for blood neutrophils is inhibited by transforming growth factor-beta. Science. 1988 Oct 7;242(4875):97–99. doi: 10.1126/science.3175638. [DOI] [PubMed] [Google Scholar]
  71. Garmyn M., Yaar M., Boileau N., Backendorf C., Gilchrest B. A. Effect of aging and habitual sun exposure on the genetic response of cultured human keratinocytes to solar-simulated irradiation. J Invest Dermatol. 1992 Dec;99(6):743–748. doi: 10.1111/1523-1747.ep12614470. [DOI] [PubMed] [Google Scholar]
  72. Gerhard G. S., Phillips P. D., Cristofalo V. J. EGF- and PDGF-stimulated phosphorylation in young and senescent WI-38 cells. Exp Cell Res. 1991 Mar;193(1):87–92. doi: 10.1016/0014-4827(91)90541-2. [DOI] [PubMed] [Google Scholar]
  73. Gessin J. C., Brown L. J., Gordon J. S., Berg R. A. Regulation of collagen synthesis in human dermal fibroblasts in contracted collagen gels by ascorbic acid, growth factors, and inhibitors of lipid peroxidation. Exp Cell Res. 1993 Jun;206(2):283–290. doi: 10.1006/excr.1993.1148. [DOI] [PubMed] [Google Scholar]
  74. Gibson J. M., Milam S. B., Klebe R. J. Late passage cells display an increase in contractile behavior. Mech Ageing Dev. 1989 May;48(2):101–110. doi: 10.1016/0047-6374(89)90042-0. [DOI] [PubMed] [Google Scholar]
  75. Gilchrest B. A., Blog F. B., Szabo G. Effects of aging and chronic sun exposure on melanocytes in human skin. J Invest Dermatol. 1979 Aug;73(2):141–143. doi: 10.1111/1523-1747.ep12581580. [DOI] [PubMed] [Google Scholar]
  76. Gilchrest B. A. In vitro assessment of keratinocyte aging. J Invest Dermatol. 1983 Jul;81(1 Suppl):184s–189s. doi: 10.1111/1523-1747.ep12541084. [DOI] [PubMed] [Google Scholar]
  77. Gilchrest B. A., Murphy G. F., Soter N. A. Effect of chronologic aging and ultraviolet irradiation on Langerhans cells in human epidermis. J Invest Dermatol. 1982 Aug;79(2):85–88. doi: 10.1111/1523-1747.ep12500031. [DOI] [PubMed] [Google Scholar]
  78. Gilhar A., Aizen E., Pillar T., Eidelman S. Response of aged versus young skin to intradermal administration of interferon gamma. J Am Acad Dermatol. 1992 Nov;27(5 Pt 1):710–716. doi: 10.1016/0190-9622(92)70243-9. [DOI] [PubMed] [Google Scholar]
  79. Giro M., Davidson J. M. Familial co-segregation of the elastin phenotype in skin fibroblasts from Hutchinson-Gilford progeria. Mech Ageing Dev. 1993 Aug 15;70(3):163–136. doi: 10.1016/0047-6374(93)90046-t. [DOI] [PubMed] [Google Scholar]
  80. Goodson W. H., 3rd, Hunt T. K. Wound healing and aging. J Invest Dermatol. 1979 Jul;73(1):88–91. doi: 10.1111/1523-1747.ep12532775. [DOI] [PubMed] [Google Scholar]
  81. Gospodarowicz D., Bialecki H., Thakral T. K. The angiogenic activity of the fibroblast and epidermal growth factor. Exp Eye Res. 1979 May;28(5):501–514. doi: 10.1016/0014-4835(79)90038-1. [DOI] [PubMed] [Google Scholar]
  82. Granstein R. D., Deak M. R., Jacques S. L., Margolis R. J., Flotte T. J., Whitaker D., Long F. H., Amento E. P. The systemic administration of gamma interferon inhibits collagen synthesis and acute inflammation in a murine skin wounding model. J Invest Dermatol. 1989 Jul;93(1):18–27. doi: 10.1111/1523-1747.ep12277336. [DOI] [PubMed] [Google Scholar]
  83. Grey A. M., Schor A. M., Rushton G., Ellis I., Schor S. L. Purification of the migration stimulating factor produced by fetal and breast cancer patient fibroblasts. Proc Natl Acad Sci U S A. 1989 Apr;86(7):2438–2442. doi: 10.1073/pnas.86.7.2438. [DOI] [PMC free article] [PubMed] [Google Scholar]
  84. Grigorova-Borsos A. M., Bara L., Aberer E., Grochulski A., André J., Mozère G., Peyroux J., Sternberg M. Aging and diabetes increase the aggregating potency of rat skin collagen towards normal platelets. Thromb Haemost. 1988 Aug 30;60(1):75–78. [PubMed] [Google Scholar]
  85. Grinnell F., Billingham R. E., Burgess L. Distribution of fibronectin during wound healing in vivo. J Invest Dermatol. 1981 Mar;76(3):181–189. doi: 10.1111/1523-1747.ep12525694. [DOI] [PubMed] [Google Scholar]
  86. Gross J. L., Moscatelli D., Jaffe E. A., Rifkin D. B. Plasminogen activator and collagenase production by cultured capillary endothelial cells. J Cell Biol. 1982 Dec;95(3):974–981. doi: 10.1083/jcb.95.3.974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  87. Grove G. L. Age-related differences in healing of superficial skin wounds in humans. Arch Dermatol Res. 1982;272(3-4):381–385. doi: 10.1007/BF00509069. [DOI] [PubMed] [Google Scholar]
  88. Grove G. L., Duncan S., Kligman A. M. Effect of ageing on the blistering of human skin with ammonium hydroxide. Br J Dermatol. 1982 Oct;107(4):393–400. doi: 10.1111/j.1365-2133.1982.tb00382.x. [DOI] [PubMed] [Google Scholar]
  89. Grove G. L., Kligman A. M. Age-associated changes in human epidermal cell renewal. J Gerontol. 1983 Mar;38(2):137–142. doi: 10.1093/geronj/38.2.137. [DOI] [PubMed] [Google Scholar]
  90. Gutman R. L., Cohen M. R., McAmis W., Ramchand C. N., Sailer V. Free radical scavenging systems and the effect of peroxide damage in aged human skin fibroblasts. Exp Gerontol. 1987;22(6):373–378. doi: 10.1016/0531-5565(87)90018-0. [DOI] [PubMed] [Google Scholar]
  91. HAYFLICK L. THE LIMITED IN VITRO LIFETIME OF HUMAN DIPLOID CELL STRAINS. Exp Cell Res. 1965 Mar;37:614–636. doi: 10.1016/0014-4827(65)90211-9. [DOI] [PubMed] [Google Scholar]
  92. Hagisawa S., Barbenel J. C., Kenedi R. M. Influence of age on postischaemic reactive hyperaemia. Clin Phys Physiol Meas. 1991 Aug;12(3):227–237. doi: 10.1088/0143-0815/12/3/003. [DOI] [PubMed] [Google Scholar]
  93. Halasz N. A. Dehiscence of laparotomy wounds. Am J Surg. 1968 Aug;116(2):210–214. doi: 10.1016/0002-9610(68)90495-9. [DOI] [PubMed] [Google Scholar]
  94. Harley C. B., Goldstein S., Posner B. I., Guyda H. Decreased sensitivity of old and progeric human fibroblasts to a preparation of factors with insulinlike activity. J Clin Invest. 1981 Oct;68(4):988–994. doi: 10.1172/JCI110353. [DOI] [PMC free article] [PubMed] [Google Scholar]
  95. Hata R. Age-dependent changes in collagen metabolism and response to hypertonic culture conditions of rat aortic smooth muscle cells and skin fibroblasts. Cell Biol Int Rep. 1990 Jan;14(1):25–33. doi: 10.1016/0309-1651(90)90068-a. [DOI] [PubMed] [Google Scholar]
  96. Heikkinen E., Aalto M., Vihersaari T., Kulonen E. Age factor in the formation and metabolism of experimental granulation tissue. J Gerontol. 1971 Jul;26(3):294–298. doi: 10.1093/geronj/26.3.294. [DOI] [PubMed] [Google Scholar]
  97. Heino J., Ignotz R. A., Hemler M. E., Crouse C., Massagué J. Regulation of cell adhesion receptors by transforming growth factor-beta. Concomitant regulation of integrins that share a common beta 1 subunit. J Biol Chem. 1989 Jan 5;264(1):380–388. [PubMed] [Google Scholar]
  98. Hennessey P. J., Nirgiotis J. G., Andrassy R. J. The effects of age and various fat/carbohydrate caloric ratios on nitrogen retention and wound healing in rats. J Pediatr Surg. 1991 Apr;26(4):367–373. doi: 10.1016/0022-3468(91)90981-x. [DOI] [PubMed] [Google Scholar]
  99. Herzberg A. J., Dinehart S. M. Chronologic aging in black skin. Am J Dermatopathol. 1989 Aug;11(4):319–328. doi: 10.1097/00000372-198908000-00005. [DOI] [PubMed] [Google Scholar]
  100. Higashimoto Y., Fukuchi Y., Shimada Y., Ishida K., Ohata M., Furuse T., Shu C., Teramoto S., Matsuse T., Sudo E. The effects of aging on the function of alveolar macrophages in mice. Mech Ageing Dev. 1993 Jul;69(3):207–217. doi: 10.1016/0047-6374(93)90024-l. [DOI] [PubMed] [Google Scholar]
  101. Hobbs M. V., Weigle W. O., Noonan D. J., Torbett B. E., McEvilly R. J., Koch R. J., Cardenas G. J., Ernst D. N. Patterns of cytokine gene expression by CD4+ T cells from young and old mice. J Immunol. 1993 Apr 15;150(8 Pt 1):3602–3614. [PubMed] [Google Scholar]
  102. Hollenberg M. D., Schneider E. L. Receptors for insulin and epidermal growth factor-urogastrone in adult human fibroblasts do not change with donor age. Mech Ageing Dev. 1979 Aug;11(1):37–43. doi: 10.1016/0047-6374(79)90062-9. [DOI] [PubMed] [Google Scholar]
  103. Holliday R., Rattan S. I. Evidence that paromomycin induces premature ageing in human fibroblasts. Monogr Dev Biol. 1984;17:221–233. [PubMed] [Google Scholar]
  104. Holm-Pedersen P., Fenstad A. M., Folke L. E. DNA, RNA and protein synthesis in healing wounds in young and old mice. Mech Ageing Dev. 1974 Sep-Oct;3(3-4):173–185. doi: 10.1016/0047-6374(74)90014-1. [DOI] [PubMed] [Google Scholar]
  105. Holm-Pedersen P., Viidik A. Maturation of collagen in healing wounds in young and old rats. Scand J Plast Reconstr Surg. 1972;6(1):16–23. doi: 10.3109/02844317209103454. [DOI] [PubMed] [Google Scholar]
  106. Holm-Pedersen P., Zederfeldt B. Granulation tissue formation in subcutaneously implanted cellulose sponges in young and old rats. Scand J Plast Reconstr Surg. 1971;5(1):13–16. doi: 10.3109/02844317109042931. [DOI] [PubMed] [Google Scholar]
  107. Holm-Pedersen P., Zederfeldt B. Respiratory gas tensions and blood flow in wounds in young and old rats. Scand J Plast Reconstr Surg. 1973;7(2):91–96. doi: 10.3109/02844317309056415. [DOI] [PubMed] [Google Scholar]
  108. Holm-Pedersen P., Zederfeldt B. Strength development of skin incisions in young and old rats. Scand J Plast Reconstr Surg. 1971;5(1):7–12. doi: 10.3109/02844317109042930. [DOI] [PubMed] [Google Scholar]
  109. Holt D. R., Kirk S. J., Regan M. C., Hurson M., Lindblad W. J., Barbul A. Effect of age on wound healing in healthy human beings. Surgery. 1992 Aug;112(2):293–298. [PubMed] [Google Scholar]
  110. Homsy R., Pelletier-Lebon P., Tixier J. M., Godeau G., Robert L., Hornebeck W. Characterization of human skin fibroblasts elastase activity. J Invest Dermatol. 1988 Nov;91(5):472–477. doi: 10.1111/1523-1747.ep12476608. [DOI] [PubMed] [Google Scholar]
  111. Hsieh P., Chen L. B. Behavior of cells seeded in isolated fibronectin matrices. J Cell Biol. 1983 May;96(5):1208–1217. doi: 10.1083/jcb.96.5.1208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  112. Iiyama M., Shimada Y., Kita T., Ito H. Effect of aging on macrophage adherence to extracellular matrix proteins. Mech Ageing Dev. 1992 Nov;66(2):149–158. doi: 10.1016/0047-6374(92)90132-w. [DOI] [PubMed] [Google Scholar]
  113. Imayama S., Braverman I. M. A hypothetical explanation for the aging of skin. Chronologic alteration of the three-dimensional arrangement of collagen and elastic fibers in connective tissue. Am J Pathol. 1989 May;134(5):1019–1025. [PMC free article] [PubMed] [Google Scholar]
  114. JANSEN L. H., ROTTIER P. B. Elasticity of human skin related to age. Dermatologica. 1957 Aug;115(2):106–111. doi: 10.1159/000255991. [DOI] [PubMed] [Google Scholar]
  115. Jongkind J. F., Verkerk A., Poot M. Glucose flux through the hexose monophosphate shunt and NADP(H) levels during in vitro ageing of human skin fibroblasts. Gerontology. 1987;33(5):281–286. doi: 10.1159/000212891. [DOI] [PubMed] [Google Scholar]
  116. Ju W. D., Schiller J. T., Kazempour M. K., Lowy D. R. TGF alpha enhances locomotion of cultured human keratinocytes. J Invest Dermatol. 1993 May;100(5):628–632. [PubMed] [Google Scholar]
  117. Kadish J. L., Butterfield C. E., Folkman J. The effect of fibrin on cultured vascular endothelial cells. Tissue Cell. 1979;11(1):99–108. doi: 10.1016/0040-8166(79)90010-7. [DOI] [PubMed] [Google Scholar]
  118. Karlsson C., Paulsson Y. Age related induction of platelet-derived growth factor A-chain mRNA in normal human fibroblasts. J Cell Physiol. 1994 Feb;158(2):256–262. doi: 10.1002/jcp.1041580207. [DOI] [PubMed] [Google Scholar]
  119. Keast D., Nguyen T., Newsholme E. A. Maximal activities of glutaminase, citrate synthase, hexokinase, phosphofructokinase and lactate dehydrogenase in skin of rats and mice at different ages. FEBS Lett. 1989 Apr 10;247(1):132–134. doi: 10.1016/0014-5793(89)81255-4. [DOI] [PubMed] [Google Scholar]
  120. Kirkwood T. B., Rose M. R. Evolution of senescence: late survival sacrificed for reproduction. Philos Trans R Soc Lond B Biol Sci. 1991 Apr 29;332(1262):15–24. doi: 10.1098/rstb.1991.0028. [DOI] [PubMed] [Google Scholar]
  121. Kirstein M., Aston C., Hintz R., Vlassara H. Receptor-specific induction of insulin-like growth factor I in human monocytes by advanced glycosylation end product-modified proteins. J Clin Invest. 1992 Aug;90(2):439–446. doi: 10.1172/JCI115879. [DOI] [PMC free article] [PubMed] [Google Scholar]
  122. Kligman A. M. Perspectives and problems in cutaneous gerontology. J Invest Dermatol. 1979 Jul;73(1):39–46. doi: 10.1111/1523-1747.ep12532758. [DOI] [PubMed] [Google Scholar]
  123. Kohase M., Henriksen-DeStefano D., May L. T., Vilcek J., Sehgal P. B. Induction of beta 2-interferon by tumor necrosis factor: a homeostatic mechanism in the control of cell proliferation. Cell. 1986 Jun 6;45(5):659–666. doi: 10.1016/0092-8674(86)90780-4. [DOI] [PubMed] [Google Scholar]
  124. Kondo H., Nomaguchi T. A. Effects of serum from rabbits of various ages on cell proliferation. Mech Ageing Dev. 1985 Oct 14;32(1):1–10. doi: 10.1016/0047-6374(85)90030-2. [DOI] [PubMed] [Google Scholar]
  125. Kondo H., Nomaguchi T. A., Sakurai Y., Yonezawa Y., Kaji K., Matsuo M., Okabe H. Effects of serum from human subjects of various ages on proliferation of human lung and skin fibroblasts. Exp Cell Res. 1988 Oct;178(2):287–295. doi: 10.1016/0014-4827(88)90399-0. [DOI] [PubMed] [Google Scholar]
  126. Kondo H., Nomaguchi T. A., Yonezawa Y. Effects of serum from human subjects of different ages on migration in vitro of human fibroblasts. Mech Ageing Dev. 1989 Jan;47(1):25–37. doi: 10.1016/0047-6374(89)90004-3. [DOI] [PubMed] [Google Scholar]
  127. Kono T., Tanii T., Furukawa M., Mizuno N., Kitajima J., Ishii M., Hamada T. Correlation between ageing and collagen gel contractility of human fibroblasts. Acta Derm Venereol. 1990;70(3):241–244. [PubMed] [Google Scholar]
  128. Kramer R. H., Fuh G. M., Bensch K. G., Karasek M. A. Synthesis of extracellular matrix glycoproteins by cultured microvascular endothelial cells isolated from the dermis of neonatal and adult skin. J Cell Physiol. 1985 Apr;123(1):1–9. doi: 10.1002/jcp.1041230102. [DOI] [PubMed] [Google Scholar]
  129. Kumar S., Vinci J. M., Millis A. J., Baglioni C. Expression of interleukin-1 alpha and beta in early passage fibroblasts from aging individuals. Exp Gerontol. 1993 Nov-Dec;28(6):505–513. doi: 10.1016/0531-5565(93)90039-g. [DOI] [PubMed] [Google Scholar]
  130. Kurban R. S., Bhawan J. Histologic changes in skin associated with aging. J Dermatol Surg Oncol. 1990 Oct;16(10):908–914. doi: 10.1111/j.1524-4725.1990.tb01554.x. [DOI] [PubMed] [Google Scholar]
  131. Kurkinen M., Vaheri A., Roberts P. J., Stenman S. Sequential appearance of fibronectin and collagen in experimental granulation tissue. Lab Invest. 1980 Jul;43(1):47–51. [PubMed] [Google Scholar]
  132. Kähäri V. M., Olsen D. R., Rhudy R. W., Carrillo P., Chen Y. Q., Uitto J. Transforming growth factor-beta up-regulates elastin gene expression in human skin fibroblasts. Evidence for post-transcriptional modulation. Lab Invest. 1992 May;66(5):580–588. [PubMed] [Google Scholar]
  133. LAGIER R., EXER B. [Study of the chemical composition of human tissues of connective nature in relation to age: dermis and aponeurosis of the abdominal wall, Achilles tendon (glucuronie acid, aldoses, arginine, tyrosine and hydroxyproline)]. Gerontologia. 1960;4:39–59. [PubMed] [Google Scholar]
  134. La Belle M., Linn S. DNA repair in cultured mouse cells of increasing population doubling level. Mutat Res. 1984 Jul-Aug;132(1-2):51–61. doi: 10.1016/0167-8817(84)90066-x. [DOI] [PubMed] [Google Scholar]
  135. Lavker R. M., Kwong F., Kligman A. M. Changes in skin surface patterns with age. J Gerontol. 1980 May;35(3):348–354. doi: 10.1093/geronj/35.3.348. [DOI] [PubMed] [Google Scholar]
  136. Lavker R. M. Structural alterations in exposed and unexposed aged skin. J Invest Dermatol. 1979 Jul;73(1):59–66. doi: 10.1111/1523-1747.ep12532763. [DOI] [PubMed] [Google Scholar]
  137. Lavker R. M., Zheng P. S., Dong G. Aged skin: a study by light, transmission electron, and scanning electron microscopy. J Invest Dermatol. 1987 Mar;88(3 Suppl):44s–51s. doi: 10.1111/1523-1747.ep12468934. [DOI] [PubMed] [Google Scholar]
  138. Lavker R. M., Zheng P. S., Dong G. Morphology of aged skin. Clin Geriatr Med. 1989 Feb;5(1):53–67. [PubMed] [Google Scholar]
  139. Leyden J. J. Clinical features of ageing skin. Br J Dermatol. 1990 Apr;122 (Suppl 35):1–3. doi: 10.1111/j.1365-2133.1990.tb16118.x. [DOI] [PubMed] [Google Scholar]
  140. Lipschitz D. A., Udupa K. B. Influence of aging and protein deficiency on neutrophil function. J Gerontol. 1986 Nov;41(6):690–694. doi: 10.1093/geronj/41.6.690. [DOI] [PubMed] [Google Scholar]
  141. Lombard N., Masse R. Influence du vieillissement in vivo sur la croissance des cellules fibroblastiques de rat issues d'explants cutanés. C R Seances Soc Biol Fil. 1987;181(3):267–273. [PubMed] [Google Scholar]
  142. Longas M. O., Russell C. S., He X. Y. Evidence for structural changes in dermatan sulfate and hyaluronic acid with aging. Carbohydr Res. 1987 Jan 15;159(1):127–136. doi: 10.1016/s0008-6215(00)90010-7. [DOI] [PubMed] [Google Scholar]
  143. Lovell C. R., Smolenski K. A., Duance V. C., Light N. D., Young S., Dyson M. Type I and III collagen content and fibre distribution in normal human skin during ageing. Br J Dermatol. 1987 Oct;117(4):419–428. doi: 10.1111/j.1365-2133.1987.tb04921.x. [DOI] [PubMed] [Google Scholar]
  144. Luce M. C., Bunn C. L. Altered sensitivity of protein synthesis to paromomycin in extracts from aging human diploid fibroblasts. Exp Gerontol. 1987;22(3):165–177. doi: 10.1016/0531-5565(87)90037-4. [DOI] [PubMed] [Google Scholar]
  145. Lumpkin C. K., Jr, McClung J. K., Pereira-Smith O. M., Smith J. R. Existence of high abundance antiproliferative mRNA's in senescent human diploid fibroblasts. Science. 1986 Apr 18;232(4748):393–395. doi: 10.1126/science.2421407. [DOI] [PubMed] [Google Scholar]
  146. Mackay I. R. Ageing and immunological function in man. Gerontologia. 1972;18(5-6):285–304. doi: 10.1159/000211941. [DOI] [PubMed] [Google Scholar]
  147. Madri J. A., Williams S. K. Capillary endothelial cell cultures: phenotypic modulation by matrix components. J Cell Biol. 1983 Jul;97(1):153–165. doi: 10.1083/jcb.97.1.153. [DOI] [PMC free article] [PubMed] [Google Scholar]
  148. Maekawa T., Rathinasamy T. K., Altman K. I., Forbes W. F. Changes in collagen with age. I. The extraction of acid soluble collagens from the skin of mice. Exp Gerontol. 1970 Jul;5(2):177–186. doi: 10.1016/0531-5565(70)90007-0. [DOI] [PubMed] [Google Scholar]
  149. Maier J. A., Voulalas P., Roeder D., Maciag T. Extension of the life-span of human endothelial cells by an interleukin-1 alpha antisense oligomer. Science. 1990 Sep 28;249(4976):1570–1574. doi: 10.1126/science.2218499. [DOI] [PubMed] [Google Scholar]
  150. Marinkovich M. P. The molecular genetics of basement membrane diseases. Arch Dermatol. 1993 Dec;129(12):1557–1565. [PubMed] [Google Scholar]
  151. Marks M. W., Morykwas M. J., Wheatley M. J. Fibroblast-mediated contraction in actinically exposed and actinically protected aging skin. Plast Reconstr Surg. 1990 Aug;86(2):255–259. doi: 10.1097/00006534-199008000-00008. [DOI] [PubMed] [Google Scholar]
  152. Martin M., el Nabout R., Lafuma C., Crechet F., Remy J. Fibronectin and collagen gene expression during in vitro ageing of pig skin fibroblasts. Exp Cell Res. 1990 Nov;191(1):8–13. doi: 10.1016/0014-4827(90)90028-9. [DOI] [PubMed] [Google Scholar]
  153. Matrisian L. M., Davis D., Magun B. E. Internalization and processing of epidermal growth factor in aging human fibroblasts in culture. Exp Gerontol. 1987;22(2):81–89. doi: 10.1016/0531-5565(87)90043-x. [DOI] [PubMed] [Google Scholar]
  154. Mays P. K., McAnulty R. J., Campa J. S., Laurent G. J. Age-related changes in collagen synthesis and degradation in rat tissues. Importance of degradation of newly synthesized collagen in regulating collagen production. Biochem J. 1991 Jun 1;276(Pt 2):307–313. doi: 10.1042/bj2760307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  155. McCaffrey T. A., Falcone D. J. Evidence for an age-related dysfunction in the antiproliferative response to transforming growth factor-beta in vascular smooth muscle cells. Mol Biol Cell. 1993 Mar;4(3):315–322. doi: 10.1091/mbc.4.3.315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  156. McGurk M., Hanford L., Justice S., Metcalfe R. A. The secretory characteristics of epidermal growth factor in human saliva. Arch Oral Biol. 1990;35(8):653–659. doi: 10.1016/0003-9969(90)90032-6. [DOI] [PubMed] [Google Scholar]
  157. Mendoza C. B., Jr, Postlethwait R. W., Johnson W. D. Veterans Administration cooperative study of surgery for duodenal ulcer. II. Incidence of wound disruption following operation. Arch Surg. 1970 Sep;101(3):396–398. doi: 10.1001/archsurg.1970.01340270044012. [DOI] [PubMed] [Google Scholar]
  158. Meyer L. J., Stern R. Age-dependent changes of hyaluronan in human skin. J Invest Dermatol. 1994 Mar;102(3):385–389. doi: 10.1111/1523-1747.ep12371800. [DOI] [PubMed] [Google Scholar]
  159. Miller R. A. Age-associated decline in precursor frequency for different T cell-mediated reactions, with preservation of helper or cytotoxic effect per precursor cell. J Immunol. 1984 Jan;132(1):63–68. [PubMed] [Google Scholar]
  160. Moerman E. J., Thweatt R., Moerman A. M., Jones R. A., Goldstein S. Insulin-like growth factor binding protein-3 is overexpressed in senescent and quiescent human fibroblasts. Exp Gerontol. 1993 Jul-Oct;28(4-5):361–370. doi: 10.1016/0531-5565(93)90063-j. [DOI] [PubMed] [Google Scholar]
  161. Mollenhauer J., Bayreuther K. Donor-age-related changes in the morphology, growth potential, and collagen biosynthesis in rat fibroblast subpopulations in vitro. Differentiation. 1986;32(2):165–172. doi: 10.1111/j.1432-0436.1986.tb00569.x. [DOI] [PubMed] [Google Scholar]
  162. Montagna W., Carlisle K. Structural changes in ageing skin. Br J Dermatol. 1990 Apr;122 (Suppl 35):61–70. doi: 10.1111/j.1365-2133.1990.tb16127.x. [DOI] [PubMed] [Google Scholar]
  163. Montagna W., Carlisle K. Structural changes in aging human skin. J Invest Dermatol. 1979 Jul;73(1):47–53. doi: 10.1111/1523-1747.ep12532761. [DOI] [PubMed] [Google Scholar]
  164. Montagna W., Carlisle K. The architecture of black and white facial skin. J Am Acad Dermatol. 1991 Jun;24(6 Pt 1):929–937. doi: 10.1016/0190-9622(91)70148-u. [DOI] [PubMed] [Google Scholar]
  165. Monticone R. E., Nick R. J., Eichhorn G. L. The effect of cellular age on zinc levels in untreated and zinc-treated human diploid fibroblasts. J Inorg Biochem. 1987 Aug;30(4):291–298. doi: 10.1016/0162-0134(87)80072-7. [DOI] [PubMed] [Google Scholar]
  166. Morris G. M., Hamlet R., Hopewell J. W. The cell kinetics of the epidermis and follicular epithelium of the rat: variations with age and body site. Cell Tissue Kinet. 1989 May;22(3):213–222. doi: 10.1111/j.1365-2184.1989.tb00207.x. [DOI] [PubMed] [Google Scholar]
  167. Muggleton-Harris A. L., Reisert P. S., Burghoff R. L. In vitro characterization of response to stimulus (wounding) with regard to ageing in human skin fibroblasts. Mech Ageing Dev. 1982 May;19(1):37–43. doi: 10.1016/0047-6374(82)90048-3. [DOI] [PubMed] [Google Scholar]
  168. Mullaart E., Roza L., Lohman P. H., Vijg J. The removal of UV-induced pyrimidine dimers from DNA of rat skin cells in vitro and in vivo in relation to aging. Mech Ageing Dev. 1989 Mar;47(3):253–264. doi: 10.1016/0047-6374(89)90037-7. [DOI] [PubMed] [Google Scholar]
  169. Mustoe T. A., Pierce G. F., Thomason A., Gramates P., Sporn M. B., Deuel T. F. Accelerated healing of incisional wounds in rats induced by transforming growth factor-beta. Science. 1987 Sep 11;237(4820):1333–1336. doi: 10.1126/science.2442813. [DOI] [PubMed] [Google Scholar]
  170. Nagelkerken L., Hertogh-Huijbregts A., Dobber R., Dräger A. Age-related changes in lymphokine production related to a decreased number of CD45RBhi CD4+ T cells. Eur J Immunol. 1991 Feb;21(2):273–281. doi: 10.1002/eji.1830210206. [DOI] [PubMed] [Google Scholar]
  171. Ning Y., Pereira-Smith O. M. Molecular genetic approaches to the study of cellular senescence. Mutat Res. 1991 Mar-Nov;256(2-6):303–310. doi: 10.1016/0921-8734(91)90021-3. [DOI] [PubMed] [Google Scholar]
  172. Olerud J. E., Gown A. M., Bickenbach J., Dale B., Odland G. F. An assessment of human epidermal repair in elderly normal subjects using immunohistochemical methods. J Invest Dermatol. 1988 Jun;90(6):845–850. doi: 10.1111/1523-1747.ep12462083. [DOI] [PubMed] [Google Scholar]
  173. Olsen D. R., Uitto J. Differential expression of type IV procollagen and laminin genes by fetal vs adult skin fibroblasts in culture: determination of subunit mRNA steady-state levels. J Invest Dermatol. 1989 Jul;93(1):127–131. doi: 10.1111/1523-1747.ep12277381. [DOI] [PubMed] [Google Scholar]
  174. Olson J. A., Hodges R. E. Recommended dietary intakes (RDI) of vitamin C in humans. Am J Clin Nutr. 1987 Apr;45(4):693–703. doi: 10.1093/ajcn/45.4.693. [DOI] [PubMed] [Google Scholar]
  175. Orson F. M., Saadeh C. K., Lewis D. E., Nelson D. L. Interleukin 2 receptor expression by T cells in human aging. Cell Immunol. 1989 Dec;124(2):278–291. doi: 10.1016/0008-8749(89)90131-7. [DOI] [PubMed] [Google Scholar]
  176. Overall C. M., Wrana J. L., Sodek J. Independent regulation of collagenase, 72-kDa progelatinase, and metalloendoproteinase inhibitor expression in human fibroblasts by transforming growth factor-beta. J Biol Chem. 1989 Jan 25;264(3):1860–1869. [PubMed] [Google Scholar]
  177. Parry D. A., Barnes G. R., Craig A. S. A comparison of the size distribution of collagen fibrils in connective tissues as a function of age and a possible relation between fibril size distribution and mechanical properties. Proc R Soc Lond B Biol Sci. 1978 Dec 18;203(1152):305–321. doi: 10.1098/rspb.1978.0107. [DOI] [PubMed] [Google Scholar]
  178. Peacocke M., Yaar M., Gilchrest B. A. Interferon and the epidermis: implications for cellular senescence. Exp Gerontol. 1989;24(5-6):415–421. doi: 10.1016/0531-5565(89)90048-x. [DOI] [PubMed] [Google Scholar]
  179. Pepper M. S., Sappino A. P., Montesano R., Orci L., Vassalli J. D. Plasminogen activator inhibitor-1 is induced in migrating endothelial cells. J Cell Physiol. 1992 Oct;153(1):129–139. doi: 10.1002/jcp.1041530117. [DOI] [PubMed] [Google Scholar]
  180. Pepper M. S., Vassalli J. D., Montesano R., Orci L. Urokinase-type plasminogen activator is induced in migrating capillary endothelial cells. J Cell Biol. 1987 Dec;105(6 Pt 1):2535–2541. doi: 10.1083/jcb.105.6.2535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  181. Phillips P. D., Kaji K., Cristofalo V. J. Progressive loss of the proliferative response of senescing WI-38 cells to platelet-derived growth factor, epidermal growth factor, insulin, transferrin, and dexamethasone. J Gerontol. 1984 Jan;39(1):11–17. doi: 10.1093/geronj/39.1.11. [DOI] [PubMed] [Google Scholar]
  182. Pienta K. J., Coffey D. S. Characterization of the subtypes of cell motility in ageing human skin fibroblasts. Mech Ageing Dev. 1990 Nov;56(2):99–105. doi: 10.1016/0047-6374(90)90001-v. [DOI] [PubMed] [Google Scholar]
  183. Pieraggi M. T., Bouissou H., Angelier C., Uhart D., Magnol J. P., Kokolo J. Le fibroblaste. Ann Pathol. 1985;5(2):65–76. [PubMed] [Google Scholar]
  184. Pierce G. F., Mustoe T. A., Lingelbach J., Masakowski V. R., Griffin G. L., Senior R. M., Deuel T. F. Platelet-derived growth factor and transforming growth factor-beta enhance tissue repair activities by unique mechanisms. J Cell Biol. 1989 Jul;109(1):429–440. doi: 10.1083/jcb.109.1.429. [DOI] [PMC free article] [PubMed] [Google Scholar]
  185. Pigeolet E., Raes M., Houbion A., Remacle J. Effect of procaine on cultivated human WI-38 fibroblasts. Exp Gerontol. 1988;23(2):87–96. doi: 10.1016/0531-5565(88)90073-3. [DOI] [PubMed] [Google Scholar]
  186. Pochi P. E., Strauss J. S., Downing D. T. Age-related changes in sebaceous gland activity. J Invest Dermatol. 1979 Jul;73(1):108–111. doi: 10.1111/1523-1747.ep12532792. [DOI] [PubMed] [Google Scholar]
  187. Quaglino D., Jr, Nanney L. B., Ditesheim J. A., Davidson J. M. Transforming growth factor-beta stimulates wound healing and modulates extracellular matrix gene expression in pig skin: incisional wound model. J Invest Dermatol. 1991 Jul;97(1):34–42. [PubMed] [Google Scholar]
  188. Quevedo W. C., Szabó G., Virks J. Influence of age and UV on the populations of dopa-positive melanocytes in human skin. J Invest Dermatol. 1969 Mar;52(3):287–290. [PubMed] [Google Scholar]
  189. Quirinia A., Viidik A. The influence of age on the healing of normal and ischemic incisional skin wounds. Mech Ageing Dev. 1991 May;58(2-3):221–232. doi: 10.1016/0047-6374(91)90094-g. [DOI] [PubMed] [Google Scholar]
  190. Rappolee D. A., Mark D., Banda M. J., Werb Z. Wound macrophages express TGF-alpha and other growth factors in vivo: analysis by mRNA phenotyping. Science. 1988 Aug 5;241(4866):708–712. doi: 10.1126/science.3041594. [DOI] [PubMed] [Google Scholar]
  191. Rattan S. I., Derventzi A. Altered cellular responsiveness during ageing. Bioessays. 1991 Nov;13(11):601–606. doi: 10.1002/bies.950131111. [DOI] [PubMed] [Google Scholar]
  192. Reed B. R., Clark R. A. Cutaneous tissue repair: practical implications of current knowledge. II. J Am Acad Dermatol. 1985 Dec;13(6):919–941. doi: 10.1016/s0190-9622(85)70242-3. [DOI] [PubMed] [Google Scholar]
  193. Reed M. J., Vernon R. B., Abrass I. B., Sage E. H. TGF-beta 1 induces the expression of type I collagen and SPARC, and enhances contraction of collagen gels, by fibroblasts from young and aged donors. J Cell Physiol. 1994 Jan;158(1):169–179. doi: 10.1002/jcp.1041580121. [DOI] [PubMed] [Google Scholar]
  194. Reenstra W. R., Yaar M., Gilchrest B. A. Effect of donor age on epidermal growth factor processing in man. Exp Cell Res. 1993 Nov;209(1):118–122. doi: 10.1006/excr.1993.1291. [DOI] [PubMed] [Google Scholar]
  195. Reiser K. M., Hennessy S. M., Last J. A. Analysis of age-associated changes in collagen crosslinking in the skin and lung in monkeys and rats. Biochim Biophys Acta. 1987 Dec 7;926(3):339–348. doi: 10.1016/0304-4165(87)90220-0. [DOI] [PubMed] [Google Scholar]
  196. Reiser K., McCormick R. J., Rucker R. B. Enzymatic and nonenzymatic cross-linking of collagen and elastin. FASEB J. 1992 Apr;6(7):2439–2449. doi: 10.1096/fasebj.6.7.1348714. [DOI] [PubMed] [Google Scholar]
  197. Richard S., Querleux B., Bittoun J., Jolivet O., Idy-Peretti I., de Lacharriere O., Leveque J. L. Characterization of the skin in vivo by high resolution magnetic resonance imaging: water behavior and age-related effects. J Invest Dermatol. 1993 May;100(5):705–709. doi: 10.1111/1523-1747.ep12472356. [DOI] [PubMed] [Google Scholar]
  198. Ridge M. D., Wright V. The ageing of skin. A bio-engineering approach. Gerontologia. 1966;12(3):174–192. doi: 10.1159/000211548. [DOI] [PubMed] [Google Scholar]
  199. Robert C., Blanc M., Lesty C., Dikstein S., Robert L. Study of skin ageing as a function of social and professional conditions: modification of the rheological parameters measured with a noninvasive method--indentometry. Gerontology. 1988;34(5-6):284–290. doi: 10.1159/000212967. [DOI] [PubMed] [Google Scholar]
  200. Robert C., Lesty C., Robert A. M. Ageing of the skin: study of elastic fiber network modifications by computerized image analysis. Gerontology. 1988;34(5-6):291–296. doi: 10.1159/000212969. [DOI] [PubMed] [Google Scholar]
  201. Roberts A. B., Sporn M. B., Assoian R. K., Smith J. M., Roche N. S., Wakefield L. M., Heine U. I., Liotta L. A., Falanga V., Kehrl J. H. Transforming growth factor type beta: rapid induction of fibrosis and angiogenesis in vivo and stimulation of collagen formation in vitro. Proc Natl Acad Sci U S A. 1986 Jun;83(12):4167–4171. doi: 10.1073/pnas.83.12.4167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  202. Rosa L. F., De Almeida A. F., Safi D. A., Curi R. Metabolic and functional changes in lymphocytes and macrophages as induced by ageing. Physiol Behav. 1993 Apr;53(4):651–656. doi: 10.1016/0031-9384(93)90169-g. [DOI] [PubMed] [Google Scholar]
  203. Rosen E. M., Grant D., Kleinman H., Jaken S., Donovan M. A., Setter E., Luckett P. M., Carley W., Bhargava M., Goldberg I. D. Scatter factor stimulates migration of vascular endothelium and capillary-like tube formation. EXS. 1991;59:76–88. doi: 10.1007/978-3-0348-7494-6_6. [DOI] [PubMed] [Google Scholar]
  204. Rosenbloom A. L., Goldstein S., Yip C. C. Insulin binding to cultured human fibroblasts increases with normal and precocious aging. Science. 1976 Jul 30;193(4251):412–415. doi: 10.1126/science.180604. [DOI] [PubMed] [Google Scholar]
  205. Ross R., Raines E. W., Bowen-Pope D. F. The biology of platelet-derived growth factor. Cell. 1986 Jul 18;46(2):155–169. doi: 10.1016/0092-8674(86)90733-6. [DOI] [PubMed] [Google Scholar]
  206. Ruberg R. L. Role of nutrition in wound healing. Surg Clin North Am. 1984 Aug;64(4):705–714. doi: 10.1016/s0039-6109(16)43386-4. [DOI] [PubMed] [Google Scholar]
  207. SANDBLOM P., PETERSEN P., MUREN A. Determination of the tensile strength of the healing wound as a clinical test. Acta Chir Scand. 1953;105(1-4):252–257. [PubMed] [Google Scholar]
  208. SCHILLER S., DORFMAN A. Effect of age on the heparin content of rat skin. Nature. 1960 Jan 9;185:111–112. doi: 10.1038/185111a0. [DOI] [PubMed] [Google Scholar]
  209. SMITH J. G., Jr, DAVIDSON E. A., SAMS W. M., Jr, CLARK R. D. Alterations in human dermal connective tissue with age and chronic sun damage. J Invest Dermatol. 1962 Oct;39:347–350. doi: 10.1038/jid.1962.122. [DOI] [PubMed] [Google Scholar]
  210. Sauder D. N. Effect of age on epidermal immune function. Clin Geriatr Med. 1989 Feb;5(1):149–160. [PubMed] [Google Scholar]
  211. Sauder D. N., Stanulis-Praeger B. M., Gilchrest B. A. Autocrine growth stimulation of human keratinocytes by epidermal cell-derived thymocyte-activating factor: implications for skin aging. Arch Dermatol Res. 1988;280(2):71–76. doi: 10.1007/BF00417707. [DOI] [PubMed] [Google Scholar]
  212. Schneider E. L. Aging and cultured human skin fibroblasts. J Invest Dermatol. 1979 Jul;73(1):15–18. doi: 10.1111/1523-1747.ep12532753. [DOI] [PubMed] [Google Scholar]
  213. Schroeder F., Goetz I., Roberts E. Age-related alterations in cultured human fibroblast membrane structure and function. Mech Ageing Dev. 1984 Jun;25(3):365–389. doi: 10.1016/0047-6374(84)90010-1. [DOI] [PubMed] [Google Scholar]
  214. Schwartz D. The proliferation of elastic fibres after skin incisions in albino mice and rats: a light and electron microscopic study. J Anat. 1977 Nov;124(Pt 2):401–411. [PMC free article] [PubMed] [Google Scholar]
  215. Sephel G. C., Davidson J. M. Elastin production in human skin fibroblast cultures and its decline with age. J Invest Dermatol. 1986 Mar;86(3):279–285. doi: 10.1111/1523-1747.ep12285424. [DOI] [PubMed] [Google Scholar]
  216. Shevitz J., Jenkins C. S., Hatcher V. B. Fibronectin synthesis and degradation in human fibroblasts with aging. Mech Ageing Dev. 1986 Aug;35(3):221–232. doi: 10.1016/0047-6374(86)90125-9. [DOI] [PubMed] [Google Scholar]
  217. Shigeoka H., Yang H. C. Early kinase C dependent events in aging human diploid fibroblasts. Mech Ageing Dev. 1990 Jul;55(1):49–59. doi: 10.1016/0047-6374(90)90105-o. [DOI] [PubMed] [Google Scholar]
  218. Shimada Y., Ito H., Kaji K., Fukuda M. Tumor necrosis factor reduces lifespan of human endothelial cells in vitro. Mech Ageing Dev. 1990 Sep;55(3):245–254. doi: 10.1016/0047-6374(90)90152-6. [DOI] [PubMed] [Google Scholar]
  219. Shindo Y., Akiyama J., Yamazaki Y., Saito K., Takase Y. Changes in enzyme activities in skin fibroblasts derived from persons of various ages. Exp Gerontol. 1991;26(1):29–35. doi: 10.1016/0531-5565(91)90059-u. [DOI] [PubMed] [Google Scholar]
  220. Sholley M. M., Gimbrone M. A., Jr, Cotran R. S. The effects of leukocyte depletion on corneal neovascularization. Lab Invest. 1978 Jan;38(1):32–40. [PubMed] [Google Scholar]
  221. Shuster S., Black M. M., McVitie E. The influence of age and sex on skin thickness, skin collagen and density. Br J Dermatol. 1975 Dec;93(6):639–643. doi: 10.1111/j.1365-2133.1975.tb05113.x. [DOI] [PubMed] [Google Scholar]
  222. Sibbitt W. L., Jr, Mills R. G., Bigler C. F., Eaton R. P., Griffey R. H., Vander Jagt D. L. Glucose inhibition of human fibroblast proliferation and response to growth factors is prevented by inhibitors of aldose reductase. Mech Ageing Dev. 1989 Mar;47(3):265–279. doi: 10.1016/0047-6374(89)90038-9. [DOI] [PubMed] [Google Scholar]
  223. Silverman E. M., Silverman A. G. Granulocyte adherence in the elderly. Am J Clin Pathol. 1977 Jan;67(1):49–52. doi: 10.1093/ajcp/67.1.49. [DOI] [PubMed] [Google Scholar]
  224. Sluke G., Schachtschabel D. O., Wever J. Age-related changes in the distribution pattern of glycosaminoglycans synthesized by cultured human diploid fibroblasts (WI-38). Mech Ageing Dev. 1981 May;16(1):19–27. doi: 10.1016/0047-6374(81)90028-2. [DOI] [PubMed] [Google Scholar]
  225. Sobin S. S., Bernick S., Ballard K. W. Acute wound repair in an aged animal: a model for accelerated aging of the microvasculature? J Gerontol. 1992 Jul;47(4):B121–B125. doi: 10.1093/geronj/47.4.b121. [DOI] [PubMed] [Google Scholar]
  226. Sohal R. S. The free radical hypothesis of aging: an appraisal of the current status. Aging (Milano) 1993 Feb;5(1):3–17. doi: 10.1007/BF03324120. [DOI] [PubMed] [Google Scholar]
  227. Song L., Kim Y. H., Chopra R. K., Proust J. J., Nagel J. E., Nordin A. A., Adler W. H. Age-related effects in T cell activation and proliferation. Exp Gerontol. 1993 Jul-Oct;28(4-5):313–321. doi: 10.1016/0531-5565(93)90058-l. [DOI] [PubMed] [Google Scholar]
  228. Sorrentino J. A., Millis A. J. Structural comparisons of fibronectins isolated from early and late passage cells. Mech Ageing Dev. 1984 Nov;28(1):83–97. doi: 10.1016/0047-6374(84)90155-6. [DOI] [PubMed] [Google Scholar]
  229. Spagnoli L. G., Sambuy Y., Palmieri G., Mauriello A. Age-related modulation of vascular smooth muscle cells proliferation following arterial wall damage. Artery. 1985;13(3):187–198. [PubMed] [Google Scholar]
  230. Sporn M. B., Roberts A. B. Transforming growth factor-beta: recent progress and new challenges. J Cell Biol. 1992 Dec;119(5):1017–1021. doi: 10.1083/jcb.119.5.1017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  231. Stanulis-Praeger B. M., Gilchrest B. A. Growth factor responsiveness declines during adulthood for human skin-derived cells. Mech Ageing Dev. 1986 Jul;35(2):185–198. doi: 10.1016/0047-6374(86)90009-6. [DOI] [PubMed] [Google Scholar]
  232. Stolpen A. H., Guinan E. C., Fiers W., Pober J. S. Recombinant tumor necrosis factor and immune interferon act singly and in combination to reorganize human vascular endothelial cell monolayers. Am J Pathol. 1986 Apr;123(1):16–24. [PMC free article] [PubMed] [Google Scholar]
  233. Strain A. J. Hepatocyte growth factor: another ubiquitous cytokine. J Endocrinol. 1993 Apr;137(1):1–5. doi: 10.1677/joe.0.1370001. [DOI] [PubMed] [Google Scholar]
  234. Sussman M. D. Aging of connective tissue: physical properties of healing wounds in young and old rats. Am J Physiol. 1973 May;224(5):1167–1171. doi: 10.1152/ajplegacy.1973.224.5.1167. [DOI] [PubMed] [Google Scholar]
  235. Takeda K., Gosiewska A., Peterkofsky B. Similar, but not identical, modulation of expression of extracellular matrix components during in vitro and in vivo aging of human skin fibroblasts. J Cell Physiol. 1992 Dec;153(3):450–459. doi: 10.1002/jcp.1041530303. [DOI] [PubMed] [Google Scholar]
  236. Tamm I., Kikuchi T., Wang E., Pfeffer L. M. Growth rate of control and beta-interferon-treated human fibroblast populations over the course of their in vitro life span. Cancer Res. 1984 Jun;44(6):2291–2296. [PubMed] [Google Scholar]
  237. Tan C. Y., Statham B., Marks R., Payne P. A. Skin thickness measurement by pulsed ultrasound: its reproducibility, validation and variability. Br J Dermatol. 1982 Jun;106(6):657–667. doi: 10.1111/j.1365-2133.1982.tb14702.x. [DOI] [PubMed] [Google Scholar]
  238. Thiers B. H., Maize J. C., Spicer S. S., Cantor A. B. The effect of aging and chronic sun exposure on human Langerhans cell populations. J Invest Dermatol. 1984 Mar;82(3):223–226. doi: 10.1111/1523-1747.ep12260055. [DOI] [PubMed] [Google Scholar]
  239. Thivolet J., Faure M., Thomas L., Gaucherand M., de Grouchy J., Malpuech G. NM1 keratinocytes display biochemical markers of keratinization. J Invest Dermatol. 1989 Oct;93(4):535–535. doi: 10.1111/1523-1747.ep12284278. [DOI] [PubMed] [Google Scholar]
  240. Tsuboi R., Sato C., Kurita Y., Ron D., Rubin J. S., Ogawa H. Keratinocyte growth factor (FGF-7) stimulates migration and plasminogen activator activity of normal human keratinocytes. J Invest Dermatol. 1993 Jul;101(1):49–53. doi: 10.1111/1523-1747.ep12358892. [DOI] [PubMed] [Google Scholar]
  241. Tzeng D. Y., Deuel T. F., Huang J. S., Baehner R. L. Platelet-derived growth factor promotes human peripheral monocyte activation. Blood. 1985 Jul;66(1):179–183. [PubMed] [Google Scholar]
  242. Vitellaro-Zuccarello L., Garbelli R., Rossi V. D. Immunocytochemical localization of collagen types I, III, IV, and fibronectin in the human dermis. Modifications with ageing. Cell Tissue Res. 1992 Jun;268(3):505–511. doi: 10.1007/BF00319157. [DOI] [PubMed] [Google Scholar]
  243. WINTER G. D. Formation of the scab and the rate of epithelization of superficial wounds in the skin of the young domestic pig. Nature. 1962 Jan 20;193:293–294. doi: 10.1038/193293a0. [DOI] [PubMed] [Google Scholar]
  244. Wang S. Y., Merrill C., Bell E. Effects of ageing and long-term subcultivation on collagen lattice contraction and intra-lattice proliferation in three rat cell types. Mech Ageing Dev. 1988 Aug;44(2):127–141. doi: 10.1016/0047-6374(88)90085-1. [DOI] [PubMed] [Google Scholar]
  245. Werner S., Peters K. G., Longaker M. T., Fuller-Pace F., Banda M. J., Williams L. T. Large induction of keratinocyte growth factor expression in the dermis during wound healing. Proc Natl Acad Sci U S A. 1992 Aug 1;89(15):6896–6900. doi: 10.1073/pnas.89.15.6896. [DOI] [PMC free article] [PubMed] [Google Scholar]
  246. Whitton J. T., Everall J. D. The thickness of the epidermis. Br J Dermatol. 1973 Nov;89(5):467–476. doi: 10.1111/j.1365-2133.1973.tb03007.x. [DOI] [PubMed] [Google Scholar]
  247. Willen M. D., Sorrell J. M., Lekan C. C., Davis B. R., Caplan A. I. Patterns of glycosaminoglycan/proteoglycan immunostaining in human skin during aging. J Invest Dermatol. 1991 Jun;96(6):968–974. doi: 10.1111/1523-1747.ep12476335. [DOI] [PubMed] [Google Scholar]
  248. Winkles J. A., O'Connor M. L., Friesel R. Altered regulation of platelet-derived growth factor A-chain and c-fos gene expression in senescent progeria fibroblasts. J Cell Physiol. 1990 Aug;144(2):313–325. doi: 10.1002/jcp.1041440218. [DOI] [PubMed] [Google Scholar]
  249. Wistrom C., Feng J. L., Villeponteau B. Proliferative capacity of human fibroblasts when cultured in serum from young or old cows. J Gerontol. 1989 Nov;44(6):B160–B163. doi: 10.1093/geronj/44.6.b160. [DOI] [PubMed] [Google Scholar]
  250. Yamaura H., Matsuzawa T. Decrease in capillary growth during aging. Exp Gerontol. 1980;15(2):145–150. doi: 10.1016/0531-5565(80)90086-8. [DOI] [PubMed] [Google Scholar]
  251. Yonezawa Y., Kondo H., Nomaguchi T. A. Age-related changes in serotonin content and its release reaction of rat platelets. Mech Ageing Dev. 1989 Jan;47(1):65–75. doi: 10.1016/0047-6374(89)90008-0. [DOI] [PubMed] [Google Scholar]
  252. de Rigal J., Escoffier C., Querleux B., Faivre B., Agache P., Lévêque J. L. Assessment of aging of the human skin by in vivo ultrasonic imaging. J Invest Dermatol. 1989 Nov;93(5):621–625. doi: 10.1111/1523-1747.ep12319741. [DOI] [PubMed] [Google Scholar]

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