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

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
Volume 1573, Issue 3, Pages 209-215

Publisher

ELSEVIER
DOI: 10.1016/S0304-4165(02)00386-0

Keywords

heparan sulfate; mast cell; heparin; embryonic development; translational regulation; gene targeting

Funding

  1. NHLBI NIH HHS [HL57345] Funding Source: Medline
  2. NIGMS NIH HHS [GM33063] Funding Source: Medline

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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. (C) 2002 Elsevier Science B.V. All rights reserved.

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