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. 1962 Oct 1;15(1):99–108. doi: 10.1083/jcb.15.1.99

WOUND HEALING AND COLLAGEN FORMATION

III. A Quantitative Radioautographic Study of the Utilization of Proline-H3 in Wounds from Normal and Scorbutic Guinea Pigs

Russell Ross 1, Earl P Benditt 1
PMCID: PMC2106131  PMID: 13975120

Abstract

The sequence of incorporation and utilization of tritium-labeled proline has been examined in healing wounds from normal and scorbutic guinea pigs. Linear incisions in the skin of the animals were allowed to heal for 7 days. Each animal was given proline-H3, and the wounds were excised 30 minutes, 1 and 4 hours, 1, 3 and 7 days after proline administration. The tissues were fixed in osmium tetroxide, fixed again in neutral buffered formalin, embedded in epoxy resin, and sectioned at 1 micron thickness. The sections were coated with nuclear track emulsion, exposed, developed, and stained. The results of grain counts were quantitated as the number of counts per unit area overlying cells, fibers, etc. In both groups the proline reaches a maximum over the fibroblasts within 4 hours and subsequently disappears from the cells. Concomitantly, the proline reaches a maximum over the collagen (in normal animals) and extracellular fibrillar material (in scorbutic animals) by 4 hours, where it remains. The modified technique of radioautography used in this study allows not only resolution of approximately 1 micron, but also minimal background, decreased artifact, and a clear separation of the randomly situated elements within the wounds so that grain counting is facilitated. The results correlated with previous electron microscopic studies are consistent with the utilization of proline by the fibroblasts and its incorporation into collagen (in normal animals) and into the extracellular, fibrillar, non-collagenous material seen in scorbutic animals.

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Selected References

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  1. CHEN R. W., POSTLETHWAIT R. W. Ascorbic acid in the biosynthesis and maintenance of collagen. Surg Gynecol Obstet. 1961 Jun;112:667–674. [PubMed] [Google Scholar]
  2. EASTOE J. E. The composition of collagen from subcellular fractions of guinea-pig granuloma tissue. Biochem J. 1961 Jun;79:648–652. doi: 10.1042/bj0790648. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. KELLER E. B., ZAMECNIK P. C., LOFTFIELD R. B. The role of microsomes in the incorporation of amino acids into proteins. J Histochem Cytochem. 1954 Sep;2(5):378–386. doi: 10.1177/2.5.378. [DOI] [PubMed] [Google Scholar]
  4. LOWTHER D. A., GREEN N. M., CHAPMAN J. A. Morphological and chemical studies of collagen formation. II. Metabolic activity of collagen associated with subcellular fractions of guinea pig granulomata. J Biophys Biochem Cytol. 1961 Jul;10:373–388. doi: 10.1083/jcb.10.3.373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. MITOMA C., SMITH T. E. Studies on the role of ascorbic acid in collagen synthesis. J Biol Chem. 1960 Feb;235:426–428. [PubMed] [Google Scholar]
  6. PALADE G. E., SIEKEVITZ P. Liver microsomes; an integrated morphological and biochemical study. J Biophys Biochem Cytol. 1956 Mar 25;2(2):171–200. doi: 10.1083/jcb.2.2.171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. PALADE G. E., SIEKEVITZ P. Pancreatic microsomes; an integrated morphological and biochemical study. J Biophys Biochem Cytol. 1956 Nov 25;2(6):671–690. doi: 10.1083/jcb.2.6.671. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. PETERKOFSKY B., UDENFRIEND S. Conversion of proline-C14 to peptide-bound hydroxyproline-C14 in a cell-free system from chick embryo. Biochem Biophys Res Commun. 1961 Nov 20;6:184–190. doi: 10.1016/0006-291x(61)90126-7. [DOI] [PubMed] [Google Scholar]
  9. RICHARDSON K. C., JARETT L., FINKE E. H. Embedding in epoxy resins for ultrathin sectioning in electron microscopy. Stain Technol. 1960 Nov;35:313–323. doi: 10.3109/10520296009114754. [DOI] [PubMed] [Google Scholar]
  10. ROSS R., BENDITT E. P. Wound healing and collagen formation. I. Sequential changes in components of guinea pig skin wounds observed in the electron microscope. J Biophys Biochem Cytol. 1961 Dec;11:677–700. doi: 10.1083/jcb.11.3.677. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. ROSS R., BENDITT E. P. Wound healing and collagen formation. II. Fine structure in experimental scurvy. J Cell Biol. 1962 Mar;12:533–551. doi: 10.1083/jcb.12.3.533. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. SMITH R. H., JACKSON S. F. Studies on the biosynthesis of collagen. II. The conversion of 14C-L-proline to 14C-hydroxyproline by fowl osteoblasts in tissue culture. J Biophys Biochem Cytol. 1957 Nov 25;3(6):913–922. doi: 10.1083/jcb.3.6.913. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. STETTEN M. R. Some aspects of the metabolism of hydroxyproline, studied with the aid of isotopic nitrogen. J Biol Chem. 1949 Nov;181(1):31–37. [PubMed] [Google Scholar]
  14. VAN ROBERTSON W. B., HIWETT J., HERMAN C. The relation of ascorbic acid to the conversion of proline to hydroxyproline in the synthesis of collagen in the carrageenan granuloma. J Biol Chem. 1959 Jan;234(1):105–108. [PubMed] [Google Scholar]

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