Molecular make-up of the glomerular filtration barrier

被引:108
作者
Patrakka, Jaakko [1 ,2 ]
Tryggvason, Karl [1 ]
机构
[1] Karolinska Inst, Div Matrix Biol, Dept Med Biochem & Biophys, S-17177 Stockholm, Sweden
[2] Karolinska Univ Hosp, Dept Renal Med, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Glomerulus filtration barrier; Podocyte; Slit diaphragm; Glomerular basement membrane; Glomerular endothelial cell; FOCAL SEGMENTAL GLOMERULOSCLEROSIS; CONGENITAL NEPHROTIC SYNDROME; INTEGRIN-LINKED KINASE; MICE LACKING; BASEMENT-MEMBRANE; SLIT DIAPHRAGM; ACTIN CYTOSKELETON; MUTANT ALPHA-ACTININ-4; PERINATAL LETHALITY; PODOCYTE STRUCTURE;
D O I
10.1016/j.bbrc.2010.04.069
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
The glomerular filtration barrier is composed of glomerular endothelial cells, the glomerulus basement membrane and the podocyte cell layer. The filtration barrier is a target of injury in several systemic and renal diseases, and this often leads to progressive renal disease and kidney failure. Therefore, it is essential to understand the molecular biology of the glomerulus. During the last two decades, a lot of new information about molecular components of the glomerulus filtration barrier has been generated. Many of the key discoveries have been obtained through studies on the genetic background of inherited glomerular diseases. These studies have emphasized the role of podocytes in the filtration barrier function. During the last decade, the use of knockout mouse technology has become more available and given important new insights into the functional significance of glomerular components. Large-scale approaches, such as microarray profiling, have also given data about molecules involved in the biology and pathology of the glomerulus. In the coming decade, the use of global expression profiling platforms, transgenic mouse lines, and other in vivo gene delivery methods will rapidly expand our understanding of biology and pathology of the glomerular filtration barrier, and hopefully expose novel target molecules for therapy in progressive renal diseases. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:164 / 169
页数:6
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