4.5 Review

Claudins: unlocking the code to tight junction function during embryogenesis and in disease

期刊

CLINICAL GENETICS
卷 77, 期 4, 页码 314-325

出版社

WILEY
DOI: 10.1111/j.1399-0004.2010.01397.x

关键词

claudin; tight junction; embryogenesis; epithelial cells; paracellular transport

资金

  1. Fonds de la recherche en sante du Quebec (FRSQ)
  2. Kidney Foundation of Canada
  3. Natural Science and Engineering Research Council of Canada
  4. Canadian Institutes of Health Research

向作者/读者索取更多资源

Claudins are the structural and molecular building blocks of tight junctions. Individual cells express more than one claudin family member, which suggests that a combinatorial claudin code that imparts flexibility and dynamic regulation of tight junction function could exist. Although we have learned much from manipulating claudin expression and function in cell lines, loss-of-function and gain-of-function experiments in animal model systems are essential for understanding how claudin-based boundaries function in the context of a living embryo and/or tissue. These in vivo manipulations have pointed to roles for claudins in maintaining the epithelial integrity of cell layers, establishing micro-environments and contributing to the overall shape of an embryo or tissue. In addition, loss-of-function mutations in combination with the characterization of mutations in human disease have demonstrated the importance of claudins in regulating paracellular transport of solutes and water during normal physiological states. In this review, we will discuss specific examples of in vivo studies that illustrate the function of claudin family members during development and in disease.

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

4.5
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