Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1982 Feb 1;92(2):387–397. doi: 10.1083/jcb.92.2.387

Abnormal Epidermal Keratinization in the repeated epilation mutant mouse

KA Holbrook, BA Dale, KS Brown
PMCID: PMC2112075  PMID: 6174530

Abstract

Repeated epilation (Er) is a radiation-induced, autosomal, incomplete dominant mutation in mice which is expressed in heterozygotes but is lethal in the homozygous condition. Many effects of the mutation occur in skin: the epidermis in Er/Er mice is adhesive (oral and nasal orifices fuse, limbs adhere to the body wall), hyperplastic, and fails to undergo terminal differentiation. Skin from fetal +/+, Er/+ and Er/Er mice at ages pre- and postkeratinization examined by light, scanning, and transmission electron microscopy showed marked abnormalities in tissue architecture, differentiation, and cell structure; light and dark basal epidermal cells were separated by wide intercellular spaces, joined by few desmosomes, and contained phagolysomes. The numbers of spinous, granular, and superficial layers were highly variable within any given region and among various regions of the body. In some areas, 2-8 layers of granular cells, containing large or diminutive keratohyalin granules, extended to the epidermal surface; in others, the granular layers were covered by several layers of partially keratinized or nonkeratinized cells. In rare instances, a single or small group of cornified cells was present among the granular layers but was not associated with the epidermal surface. Both the granular and nonkeratinized/partially keratinized upper epidermal layers Er/Er skin gave positive immunofluorescence with antiserum to the histidine-rich, basic protein, filaggrin. Proteins in epidermal extracts from +/+, Er/+ and Er/Er mice were separated and identified by radio- and immunolabeling techniques. The Er/Er extract was missing a 26.5- kdalton protein and had an altered ratio of bands in the keratin region. The 26.5-kdalton band was histidine-rich and cross-reacted with the antiserum to rat filaggrin. Several high molecular weight bands present in both Er/Er and +/+ extracts also reacted with the antiserum. These are presumed to be the precursors of filaggrin and to account for the immunofluorescence om Er/Er epidermis even though the product protein is absent. The morphologic and biochemical data indicated that the genetic defect has a general and profound influence on epidermal differentiation, including alteration of two proteins (filaggrin and keratin) important in normal terminal differentiation, tissue architecture, and cytology. Identification of epidermal abnormalities at early stages of development (prekeratinization) and defective structure of other tissues and gross anatomy suggest that the mutation is responsible for a defect in same regulatory step important in many processes of differentiation and development.

Full Text

The Full Text of this article is available as a PDF (1.9 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Allen T. D., Potten C. S. Fine-structural identification and organization of the epidermal proliferative unit. J Cell Sci. 1974 Jul;15(2):291–319. doi: 10.1242/jcs.15.2.291. [DOI] [PubMed] [Google Scholar]
  2. Argyris T. S. Ribosome accumulation and the regulation of epidermal hyperplastic growth. Life Sci. 1979 Mar 26;24(13):1137–1147. doi: 10.1016/0024-3205(79)90049-3. [DOI] [PubMed] [Google Scholar]
  3. Ball R. D., Walker G. K., Bernstein I. A. Histidine-rich proteins as molecular markers of epidermal differentiation. J Biol Chem. 1978 Aug 25;253(16):5861–5868. [PubMed] [Google Scholar]
  4. Bhisey R. A., Satyavati, Sirsat M. Sequential ultrastructural alterations in the mouse epidermis after a single subcutaneous injection of 20-methylcholanthrene. Indian J Cancer. 1977 Mar;14(1):18–24. [PubMed] [Google Scholar]
  5. Dale B. A., Holbrook K. A., Steinert P. M. Assembly of stratum corneum basic protein and keratin filaments in macrofibrils. Nature. 1978 Dec 14;276(5689):729–731. doi: 10.1038/276729a0. [DOI] [PubMed] [Google Scholar]
  6. Dale B. A., Ling S. Y. Evidence of a precursor form of stratum corneum basic protein in rat epidermis. Biochemistry. 1979 Aug 7;18(16):3539–3546. doi: 10.1021/bi00583a016. [DOI] [PubMed] [Google Scholar]
  7. Dale B. A., Ling S. Y. Immunologic cross-reaction of stratum corneum basic protein and a keratohyalin granule protein. J Invest Dermatol. 1979 May;72(5):257–261. doi: 10.1111/1523-1747.ep12531715. [DOI] [PubMed] [Google Scholar]
  8. Dale B. A., Lonsdale-Eccles J. D., Holbrook K. A. Stratum corneum basic protein: an interfilamentous matrix protein of epidermal keratin. Curr Probl Dermatol. 1980;10:311–325. doi: 10.1159/000396298. [DOI] [PubMed] [Google Scholar]
  9. Dale B. A. Purification and characterization of a basic protein from the stratum corneum of mammalian epidermis. Biochim Biophys Acta. 1977 Mar 28;491(1):193–204. doi: 10.1016/0005-2795(77)90055-1. [DOI] [PubMed] [Google Scholar]
  10. Eng A. M., Worobec S. Cytologic features of hyperplastic epidermis. J Cutan Pathol. 1977 Oct;4(5):258–265. doi: 10.1111/j.1600-0560.1977.tb00914.x. [DOI] [PubMed] [Google Scholar]
  11. FREI J. V., SHELDON H. Corpus intra cristam: a dense body within mitochondria of cells in hyperplastic mouse epidermis. J Biophys Biochem Cytol. 1961 Dec;11:724–729. doi: 10.1083/jcb.11.3.724. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Fuchs E., Green H. Changes in keratin gene expression during terminal differentiation of the keratinocyte. Cell. 1980 Apr;19(4):1033–1042. doi: 10.1016/0092-8674(80)90094-x. [DOI] [PubMed] [Google Scholar]
  13. Guenet J. L., Salzgeber B., Tassin M. T. Repeated epilation: a genetic epidermal syndrome in mice. J Hered. 1979 Mar-Apr;70(2):90–94. doi: 10.1093/oxfordjournals.jhered.a109223. [DOI] [PubMed] [Google Scholar]
  14. Harris R. R., Mackenzie I. C., Williams R. A. An examination of the relationship between experimentally altered rates of epidermal proliferations and rates of epidermal metabolism assayed in vitro. J Invest Dermatol. 1980 Jun;74(6):402–406. doi: 10.1111/1523-1747.ep12544514. [DOI] [PubMed] [Google Scholar]
  15. Jarrett A., Wrench R., Mahmoud B. Granular layer induction following the topical application of proliferating agents. Arch Dermatol Res. 1979 Mar 31;264(2):143–151. doi: 10.1007/BF00431125. [DOI] [PubMed] [Google Scholar]
  16. Kakefuda T., Roberts E., Suntzeff V. Electron microscopic study of methylcholanthrene-induced epidermal carcinogenesis in mice: mitochondrial dense bodies and intracisternal A-particles. Cancer Res. 1970 Apr;30(4):1011–1019. [PubMed] [Google Scholar]
  17. Knowles J. C., Weavers B., Cooper E. H. Accumulation of calcium in the intramitochondrial dense bodies in mice. Exp Cell Res. 1972 Jul;73(1):230–233. doi: 10.1016/0014-4827(72)90124-3. [DOI] [PubMed] [Google Scholar]
  18. LUFT J. H. Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961 Feb;9:409–414. doi: 10.1083/jcb.9.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Laskey R. A., Mills A. D. Quantitative film detection of 3H and 14C in polyacrylamide gels by fluorography. Eur J Biochem. 1975 Aug 15;56(2):335–341. doi: 10.1111/j.1432-1033.1975.tb02238.x. [DOI] [PubMed] [Google Scholar]
  20. Lonsdale-Eccles J. D., Haugen J. A., Dale B. A. A phosphorylated keratohyalin-derived precursor of epidermal stratum corneum basic protein. J Biol Chem. 1980 Mar 25;255(6):2235–2238. [PubMed] [Google Scholar]
  21. Potten C. S., Hendry J. H. Letter: Clonogenic cells and stem cells in epidermis. Int J Radiat Biol Relat Stud Phys Chem Med. 1973 Nov;24(5):537–540. doi: 10.1080/09553007314551441. [DOI] [PubMed] [Google Scholar]
  22. Potten C. S. The epidermal proliferative unit: the possible role of the central basal cell. Cell Tissue Kinet. 1974 Jan;7(1):77–88. doi: 10.1111/j.1365-2184.1974.tb00401.x. [DOI] [PubMed] [Google Scholar]
  23. Raick A. N. Ultrastructural, histological, and biochemical alterations produced by 12-O-tetradecanoyl-phorbol-13-acetate on mouse epidermis and their relevance to skin tumor promotion. Cancer Res. 1973 Feb;33(2):269–286. [PubMed] [Google Scholar]
  24. Renart J., Reiser J., Stark G. R. Transfer of proteins from gels to diazobenzyloxymethyl-paper and detection with antisera: a method for studying antibody specificity and antigen structure. Proc Natl Acad Sci U S A. 1979 Jul;76(7):3116–3120. doi: 10.1073/pnas.76.7.3116. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Rice R. H., Green H. The cornified envelope of terminally differentiated human epidermal keratinocytes consists of cross-linked protein. Cell. 1977 Jun;11(2):417–422. doi: 10.1016/0092-8674(77)90059-9. [DOI] [PubMed] [Google Scholar]
  26. Steinert P. M., Cantieri J. S., Teller D. C., Lonsdale-Eccles J. D., Dale B. A. Characterization of a class of cationic proteins that specifically interact with intermediate filaments. Proc Natl Acad Sci U S A. 1981 Jul;78(7):4097–4101. doi: 10.1073/pnas.78.7.4097. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Tarin D. Assessment of the significance of the intramitochondrial dense body in carcinogenesis. J Invest Dermatol. 1970 Jul;55(1):26–30. doi: 10.1111/1523-1747.ep12290491. [DOI] [PubMed] [Google Scholar]
  28. Weiss L. W., Zelickson A. S. Embryology of the epidermis: ultrastructural aspects. II. Period of differentiation in the mouse with mammalian comparisons. Acta Derm Venereol. 1975;55(5):321–329. [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES