Heparan sulfate and development: differential roles of the N-acetylglucosamine N-deacetylase/N-sulfotransferase isozymes

Biochim Biophys Acta. 2002 Dec 19;1573(3):209-15. doi: 10.1016/s0304-4165(02)00386-0.

Abstract

Heparan sulfates (HSs) are N- and O-sulfated polysaccharide components of proteoglycans, which are important constituents of the cell surface as well as the extracellular matrix. Heparin, with extensive clinical application as an anticoagulant, is a highly sulfated form of HS present within the granules of connective tissue type mast cells. The diverse functions of HS, which include the modulation of growth factor/cytokine activity, interaction with matrix proteins and binding of enzymes to cell surfaces, depend greatly on the presence of specific, high affinity regions on the chains. N-acetylglucosamine N-deacetylase/N-sulfotransferases, NDSTs, are an important group of enzymes in HS biosynthesis, initiating the sulfation of the polysaccharide chains and thus determining the generation of the high affinity sites. Here, we review the role of the four vertebrate NDSTs in HS biosynthesis as well as their regulated expression. The main emphasis is the phenotypes of mice lacking one or more of the NDSTs.

Publication types

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

MeSH terms

  • Amidohydrolases / genetics
  • Amidohydrolases / metabolism*
  • Animals
  • Carbohydrate Sequence
  • Disease Models, Animal
  • Gene Expression Regulation, Enzymologic*
  • Heparan Sulfate Proteoglycans / metabolism
  • Heparitin Sulfate / biosynthesis*
  • Humans
  • Isoenzymes
  • Mice
  • Protein Biosynthesis
  • Sulfotransferases / genetics
  • Sulfotransferases / metabolism*
  • Transcription, Genetic

Substances

  • Heparan Sulfate Proteoglycans
  • Isoenzymes
  • Heparitin Sulfate
  • Sulfotransferases
  • heparitin sulfotransferase
  • Amidohydrolases