Biosynthesis and function of chondroitin sulfate

被引:371
|
作者
Mikami, Tadahisa [1 ]
Kitagawa, Hiroshi [1 ]
机构
[1] Kobe Pharmaceut Univ, Dept Biochem, Higashinada Ku, Kobe, Hyogo 6588558, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2013年 / 1830卷 / 10期
关键词
Chondroitin sulfate; Glycosaminoglycan; Glycosyltransferase; Proteoglycan; Sulfotransferase; Biosynthesis/catabolism; PROTEIN LINKAGE REGION; EHLERS-DANLOS-SYNDROME; HERPES-SIMPLEX-VIRUS; ACETYLGALACTOSAMINE; 4-SULFATE; 6-O-SULFOTRANSFERASE; TRANSFERS N-ACETYLGALACTOSAMINE; DERMATAN; 4-O-SULFOTRANSFERASE; NUCLEOTIDE-SUGAR TRANSPORTER; ELEGANS VULVAL MORPHOGENESIS; E-DISACCHARIDE EXPRESSION; OF-FUNCTION MUTATIONS;
D O I
10.1016/j.bbagen.2013.06.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Chondroitin sulfate proteoglycans (CSPGs) are principal pericellular and extracellular components that form regulatory milieu involving numerous biological and pathophysiological phenomena. Diverse functions of CSPGs can be mainly attributed to structural variability of their polysaccharide moieties, chondroitin sulfate glycosaminoglycans (CS-GAG). Comprehensive understanding of the regulatory mechanisms for CS biosynthesis and its catabolic processes is required in order to understand those functions. Scope of review: Here, we focus on recent advances in the study of enzymatic regulatory pathways for CS biosynthesis including successive modification/degradation, distinct CS functions, and disease phenotypes that have been revealed by perturbation of the respective enzymes in vitro and in vivo. Major conclusions: Fine-tuned machineries for CS production/degradation are crucial for the functional expression of CS chains in developmental and pathophysiological processes. General significance: Control of enzymes responsible for CS biosynthesis/catabolism is a potential target for therapeutic intervention for the CS-associated disorders. (c) 2013 Elsevier B.V. All rights reserved.
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页码:4719 / 4733
页数:15
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