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PMID: 6279711 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Inhibition of collagen degradative enzymes by retinoic acid in vitro.

Journal of the American Academy of Dermatology ·Vol. 6 ·No. 4 Pt 2 Suppl ·1982-04-00 ·Pages 603-7

Bauer EA, Seltzer JL, Eisen AZ

Abstract

The effects of a variety of retinoids on collagenase and gelatinase expression have been examined in skin fibroblast cultures derived from normal volunteers and from patients with the hereditary blistering disorder, recessive dystrophic epidermolysis bullosa. Both 13-cis- and all-trans-retinoic acid were effective inhibitors of collagenase production in both cell types. In the case of collagenase, the inhibition of collagenase activity was paralleled by a reduction in immunoreactive enzyme protein, suggesting that these retinoids act by inhibiting synthesis and/or secretion of the enzyme. Retinoic acid also inhibited production of the second enzyme in the collagen degradative pathway, gelatinase. In this case, the decrease in gelatinase activity was equal to or slightly greater than the achieved in collagenase expression. The observation that certain retinoids modulate the two crucial enzymes in the degradation of collagen in the skin suggests that they might be useful therapeutic agents in recessive dystrophic epidermolysis bullosa, a disease in which the pathogenesis of blistering is in part related to connective tissue destruction.

MeSH Terms
Cells, Cultured Epidermolysis Bullosa/enzymology Fibroblasts/enzymology Gelatinases Humans Isomerism Isotretinoin Microbial Collagenase/metabolism Pepsin A/metabolism Skin/cytology,enzymology Tretinoin/pharmacology Vitamin A/pharmacology
Chemicals
Vitamin A Tretinoin Pepsin A Gelatinases Microbial Collagenase Isotretinoin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Bauer E A
Seltzer J L
Eisen A Z
Article Info
Journal
Journal of the American Academy of Dermatology
Abbr.
J Am Acad Dermatol
ISSN
0190-9622
Published
1982-04-00
Pages
603-7
Language
English
Region
United States
NLM ID
7907132
Subset
IM
Grants
NIADDK NIH HHS · AM 07284 · United States
NIADDK NIH HHS · AM 12129 · United States
NIADDK NIH HHS · AM 19537 · United States
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