4.7 Review

V3: an enigmatic isoform of the proteoglycan versican

期刊

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
卷 325, 期 2, 页码 C519-C537

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00059.2023

关键词

atherosclerosis; cell proliferation; hyaluronan; inflammation; versican

向作者/读者索取更多资源

V3 is an understudied isoform of the versican family, lacking glycosaminoglycan chains. Despite limited research, studies have shown expression of V3 during development and disease, with significant phenotypic effects observed in experimental models. However, there are currently no antibodies available to distinguish V3 from other isoforms.
V3 is an isoform of the extracellular matrix (ECM) proteoglycan (PG) versican generated through alternative splicing of the versican gene such that the two major exons coding for sequences in the protein core that support chondroitin sulfate (CS) glycosaminoglycan (GAG) chain attachment are excluded. Thus, versican V3 isoform carries no GAGs. A survey of PubMed reveals only 50 publications specifically on V3 versican, so it is a very understudied member of the versican family, partly because to date there are no antibodies that can distinguish V3 from the CS-carrying isoforms of versican, that is, to facilitate functional and mechanistic studies. However, a number of in vitro and in vivo studies have identified the expression of the V3 transcript during different phases of development and in disease, and selective overexpression of V3 has shown dramatic phenotypic effects in gain and loss of function studies in experimental models. Thus, we thought it would be useful and instructive to discuss the discovery, characterization, and the putative biological importance of the enigmatic V3 isoform of versican.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据