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Epidermolysis bullosa simplex: Expression of gelatinase activity in cultured human skin fibroblasts

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Abstract

We have measured the baseline level of gelatinase in fibroblast-conditioned medium from 41 Scandinavian individuals. They comprised 12 healthy persons, 11 individuals with the skin disorder dominant epidermolysis bullosa simplex (DEBS), 16 patients with other types of epidermolysis bullosa (EB) and 2 siblings with prolidase deficiency. These results divide the cell strains into those with low and those with high activity levels. Although this dual biochemical trait occurred in all the groups of individuals, the high-activity trait was more frequent among the DEBS patients. The localized DEBS forms showed an elevated activity level, in contrast to the previously reported generalized DEBS Köbner forms. Although a high level was found in some individuals with other EB forms, the high incidence in four families with localized DEBS Weber-Cockayne (eight of eight) and a single family with generalized DEBS—mottled pigmentation (two of two) may result from a close linkage between an EB gene and a gene responsible for the biochemical trait. In addition, in the single complete family tested, the level of gelatinase activity in cultured fibroblasts seemed to be regulated by codominant alleles or genes. A raised baseline level of gelatinase activity in cultured skin fibroblasts may be the result of either an altered expression of gelatinase or an allelic variant of this enzyme with increased specific activity. Further studies of gelatinase in cultured fibroblasts may provide insight into the regulatory mechanism and genetics behind this activity and allow formal linkage studies versus DEBS.

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References

  • Bauer, E. A., and Eisen, A. Z. (1978). Recessive dystrophic epidermolysis bullosa. Evidence for increased collagenase as a genetic characteristic in cell culture.J. Exp. Med. 1481378.

    Google Scholar 

  • Bonifas, J., Rothman, A. L., and Epstein, E. (1991). Linkage of epidermis bullosa simplex to probes in the region of keratin gene clusters on chromosomes 12q and 17q.J. Invest. Dermatol. 96:550a.

    Google Scholar 

  • Cawston, T. E., Galloway, W. A., and Marmer, E. (1981). Purification of rabbit bone inhibitor of collagenase.Biochem. J. 195159.

    Google Scholar 

  • Clark, I. M., and Cawston, T. E. (1989). Fragments of human fibroblast collagenase: Purification and characterization.Biochem. J. 263201.

    Google Scholar 

  • Collier, I. E., Wilhelm, S. M., Eisen, A. Z., Marmer, B. L., Grant, G. A., Seltzer, J. L., Kronberger, A. M., He, C., Bauer, E. A., and Goldberg, G. I. (1988). H-ras oncogene-transformed human bronchial epithelial cells (TBE-1) secrets a single metalloprotease capable of degrading basement membrane collagen.J. Biol. Chem. 2636579.

    Google Scholar 

  • Coulombe, P. A., Hutton, M. E., Letai, A., Hebert, A., Paller, A. S., and Fuchs, E. (1991). Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analysis.Cell 661301.

    Google Scholar 

  • Eisen, A. Z., Jeffrey, J. J., and Gross, J. (1968). Human skin collagenase. Isolation and mechanism of attack on the collagen molecule.Biochim. Biophys. Acta 151637.

    Google Scholar 

  • Fields, G. B., Netzel-Arnett, S. J., Windsdor, L. J., Engler, J. A., Birkedal-Hansen, H., and Van Wart, H. E. (1990). Proteolytic activities of human fibroblast collagenase: Hydrolysis of a broad range of substrates at a single active site.Biochemistry 296670.

    Google Scholar 

  • Fine, J.-D., and Griffith, R. D. (1985). A specific defect in glycosylation of epidermal cell membranes. Definition in skin from patients with epidermolysis bullosa simplex.Arch. Dermatol. 1211292.

    Google Scholar 

  • Fisher, T., and Gedde-Dahl, T., Jr. (1979). Epidermolysis bullosa simplex and mottled pigmentation: A new dominant syndrome. I. Clinical and histological features.Clin. Genet. 15228.

    Google Scholar 

  • Gedde-Dahl, T., Jr. (1971).Epidermolysis Bullosa; A Clinical Genetic and Epidemiological Study Universitets-forlaget, Oslo, and John Hopkins Press, Baltimore.

    Google Scholar 

  • Gedde-Dahl, T., Jr. (1978). Classification of epidermolysis bullosa. In Herzberg, J. J., and Korting, G. W. (eds.),Pädiatrische Dermatologie FK Schattauer, Stuttgart, pp. 65–91.

    Google Scholar 

  • Gedde-Dahl, T., Jr. (1981). Sixteen types of epidermolysis bullosa.Acta. Derm. Venerol. (Stockh.) (Suppl. 9574.

    Google Scholar 

  • Gedde-Dahl, T., Jr. (1990). Intraepidermal epidermolysis bullosa and allied conditions. In Wojnarowska, F., and Briggaman, R. A. (eds.),The Management of Blistering Diseases Chapman and Hall, London, pp. 189–212.

    Google Scholar 

  • Gedde-Dahl, T., Jr., Olaisen, B., Aarum, G., Brevik, K., and Bye, R. (1984). Linkage relations of chromosome 16 marker PGP to GPT: EBS1 and unassigned markers.Cytogenet. Cell. Genet. 37474.

    Google Scholar 

  • Haneke, E., and Anton-Lamprecht, I. (1982). Ultrastructure of blister formation in epidermolysis bullosa hereditaria: V. Epidermolysis bullosa simplex localisata type Weber-Cockayne.J. Invest. Dermatol. 78219.

    Google Scholar 

  • Harris, E. D., and Krane, S. M. (1972). An endopeptidase from rheumatoid synovial tissue culture.Biochim. Biophys. Acta 258566.

    Google Scholar 

  • Hashimoto, I., Gedde-Dahl, T., Jr., Schnyder, U. W., and Anton-Lamprecht, I. (1976). Ultrastructural studies in epidermolysis bullosa hereditaria. II. Dominant dystrophic type of Cockayne-Touraine.Arch. Dermatol. Res. 255285.

    Google Scholar 

  • Heim, S. (1983).In vitro growth characteristics of skin fibroblasts from patients with adenomatosis of the colon rectum and their relatives.Clin. Genet. 2341.

    Google Scholar 

  • Ito, M., Okuda, C., Shimizu, N., Tazawa, T., and Sato, Y. (1991). Epidermolysis bullosa simplex (Koebner) is a keratin disorder.Arch. Dermatol. 127367.

    Google Scholar 

  • Johnson-Wint, B., and Hollies, S. (1982). A rapid in situ deoxyribonucleic acid assay for determining cell number in culture and tissue.Anal. Biochem. 122338.

    Google Scholar 

  • Lane, E. B., Rugg, E. L., Navsaria, H., Leigh, I. M., Heagerty, A. H. M., Ishida-Yamamoto, A., and Eady, R. A. J. (1992). A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering.Nature 356244.

    Google Scholar 

  • May, B. K., and Elliott, W. H. (1968). Characteristics of extracellular protease formation bybacillus subtilis and it's control by amino acid repression.Biochim. Biophys. Acta 157607.

    Google Scholar 

  • Murphy, G., Cockett, M. I., Ward, R. V., and Docherty, A. J. P. (1991). Matrix metalloproteinase degradation of elastin, type IV collagen and proteoglycan.Biochem. J. 277277.

    Google Scholar 

  • O'Connell, P., Nakamura, Y., Lathrop, G. M., Leppart, M., Cartwright, P., Lalouel, J.-M., and White, R. (1988). Three genetic linkage groups on chromosome 8.Cytogenet. Cell. Genet. 46672.

    Google Scholar 

  • Olaisen, B., and Gedde-Dahl, T., Jr. (1973). GPT-epidermolysis bullosa simplex (EBS-Ogna) linkage in man.Hum. Hered. 23189.

    Google Scholar 

  • Pearson, R. W. (1967). Epidermolysis bullosa, Porphyria cutanea tarda and erythema multiforme. In Zelickson, A. S. (ed.),Ultrastructure of Normal and Abnormal Skin Lea and Febiger, Philadelphia, pp. 320–334.

    Google Scholar 

  • Rice, R. H., and Means, G. E. (1971). Radioactive labeling of proteinsin vitro.J. Biol. Chem. 246831.

    Google Scholar 

  • Rosenberg, M., Fuchs, E., Le Beau, M. M., Eddy, R., and Shows, T. B. (1991). Three epidermal and one epithelial keratin gene map to human chromosome 12.Cell Cytogenet. 5733.

    Google Scholar 

  • Sanchez, G., Seltzer, J. L., Eisen, A. Z., Stapler, P., and Bauer, E. A. (1983). Generalized dominant epidermolysis bullosa simplex: Decreased activity of a gelatinolytic protease in cultured fibroblasts as a phenotypic marker.J. Invest. Dermatol. 81576.

    Google Scholar 

  • Savolainen, E.-R., Kero, M., Philalaniemi, T., and Kivirikko, K. (1981). Deficiency of galactosyl-hydroxylysyl glucosyltransferase, an enzyme of collagen synthesis in a family with dominant epidermolysis bullosa simplex.N. Engl. J. Med. 304197.

    Google Scholar 

  • Seltzer, J. L., Adams, S. A., Grant, G. G., and Eisen, A. Z. (1981). Purification and properties of a gelatin-specific neutral protease from human skin.J. Biol. Chem. 2564662.

    Google Scholar 

  • Seltzer, J. L., Eschbach, M. L., Winberg, J. O., Bauer, E. A., Eisen, A. Z., and Weingarten, H. (1987). Erichrome black T inhibition of human skin collagenase, but not gelatinase, using both protein and synthetic substrates.Collagen Rel. Res. 7399.

    Google Scholar 

  • Seltzer, J. L., Weingarten, H., Akers, K. T., Eschbach, M. L., Grant, G. A., and Eisen, A. Z. (1989). Cleavage specificity of type IV collagenase (gelatinase) from human skin.J. Biol. Chem. 26419583.

    Google Scholar 

  • Stack, M. S., and Gray, R. D. (1989). Comparison of vertebrate collagenase and gelatinase using a new fluorogenic substrate peptide.J. Biol. Chem. 2644277.

    Google Scholar 

  • Tipton, D. A., Stricklin, G. P., and Dabbous, M. Kh. (1991). Fibroblast heterogeneity in collagenolytic response to cyclosporine.J. Cell. Biochem. 46152.

    Google Scholar 

  • Welgus, H. G., Jeffrey, J. J., Stricklin, G. P., and Eisen, A. Z. (1982). The gelatinolytic activity of human skin fibroblast collagenase.J. Biol. Chem. 25711534.

    Google Scholar 

  • Welgus, H. G., Grant, G. A., Sacchettini, J. C., Roswit, W. T., and Jeffrey, J. J. (1985). The gelatinolytic activity of rat uterus collagenase.J. Biol. Chem. 26013601.

    Google Scholar 

  • Wilhelm, S. M., Collier, I. E., Kronberger, A. M., Eisen, A. Z., Marmer, B. L., Grant, G. A., Bauer, E. A., and Goldberg, G. I. (1987). Human skin fibroblast stromelysin: Structure, glycosylation, substrate specificity, and differential expression in normal and tumorigenic cells.Proc. Natl. Acad. Sci. USA 846725.

    Google Scholar 

  • Winberg, J. O., and Gedde-Dahl, T., Jr. (1986). Gelatinase expression in generalized epidermolysis bullosa simplex fibroblasts.J. Invest. Dermatol. 87326.

    Google Scholar 

  • Winberg, J. O., Gedde-Dahl, T., Jr., and Bauer, E. A. (1989). Collagenase expression in skin fibroblasts from families with recessive dystrophic epidermolysis bullosa.J. Invest. Dermatol. 9282.

    Google Scholar 

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This work was supported in part by the Norwegian Research Council for Science and the Humanities (NAVF) and the Concerted Action on Hereditary Connective Tissue Diseases of the European Community (1990–1992, project leader, M. Matton).

Part of this work was performed at the Department of Genetics, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo.

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Winberg, JO., Gedde-Dahl, T. Epidermolysis bullosa simplex: Expression of gelatinase activity in cultured human skin fibroblasts. Biochem Genet 30, 401–420 (1992). https://doi.org/10.1007/BF00569330

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  • DOI: https://doi.org/10.1007/BF00569330

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