Regulation of collagen biosynthesis by ascorbic acid: a review

Yale J Biol Med. 1985 Nov-Dec;58(6):553-9.

Abstract

L-ascorbic acid is an essential cofactor for lysyl hydroxylase and prolyl hydroxylase, enzymes essential for collagen biosynthesis. In addition, L-ascorbic acid preferentially stimulates collagen synthesis in a manner which appears unrelated to the effect of L-ascorbic acid on hydroxylation reactions. This reaction is stereospecific and unrelated to intracellular degradation of collagen. The effect apparently occurs at a transcriptional or translational level, since L-ascorbic acid preferentially stimulates collagen-specific mRNA. In addition, it stimulates lysyl hydroxylase activity but inhibits prolyl hydroxylase activity in human skin fibroblasts in culture.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Ascorbic Acid / analogs & derivatives
  • Ascorbic Acid / pharmacology*
  • Cells, Cultured
  • Collagen / biosynthesis*
  • Collagen / metabolism
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Humans
  • Hydroxylysine / biosynthesis
  • Hydroxyproline / biosynthesis
  • Kinetics
  • Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase / metabolism
  • Procollagen-Proline Dioxygenase / metabolism
  • Skin / drug effects
  • Skin / metabolism*

Substances

  • Hydroxylysine
  • Collagen
  • Procollagen-Proline Dioxygenase
  • Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase
  • Ascorbic Acid
  • Hydroxyproline