Stretch, tension and adhesion - Adaptive mechanisms of the actin cytoskeleton in podocytes

被引:64
作者
Endlich, N
Endlich, K
机构
[1] Ernst Moritz Arndt Univ Greifswald, Dept Anat, D-17487 Greifswald, Germany
[2] Heidelberg Univ, Dept Anat & Cell Biol, Heidelberg, Germany
关键词
D O I
10.1016/j.ejcb.2005.09.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Podocytes form an epithelial layer on the outer aspect of the basement membrane of glomerular capillaries. The interdigitating pattern of podocyte foot processes (PFPs) generates a unique and extremely long cell-cell contact area the filtration slit. Thus, the interdigitating PFPs are the morphological basis for the high hydraulic conductivity of the glomerular capillaries. Any disturbance in this interdigitating pattern results in a drop of glomerular filtration rate impairing renal function. PFPs are based on the actin cytoskeleton, consisting of a subplasmalemmal network and a central core of filament bundles. Besides giving PFPs their morphology, the actin cytoskeleton anchors cell-cell contact and cell-matrix proteins in podocytes. Several human genetic diseases as well as transgenic mouse models provide evidence for the crucial role of the actin cytoskeleton in podocytes. Varying flow rates of the filtrate, increased glomerular capillary pressure in glomerular hypertension, and varying activation states of contractile proteins in PFPs impose a mechanical load on the actin cytoskeleton, challenging the intricate arrangement of PFPs and podocyte adhesion. Here we review data about the actin cytoskeleton of podocytes and the response of podocytes to mechanical load. From these data possible mechanisms are emerging how the actin cytoskeleton may allow podocytes to adapt to states of increased mechanical load. (c) 2005 Elsevier GmbH. All rights reserved.
引用
收藏
页码:229 / 234
页数:6
相关论文
共 41 条
[1]  
Arrondel C, 2002, J AM SOC NEPHROL, V13, P65, DOI 10.1681/ASN.V13165
[2]   Synaptopodin regulates the actin-bundling activity of α-actinin in an isoform-specific manner [J].
Asanuma, K ;
Kim, K ;
Oh, J ;
Giardino, L ;
Chabanis, S ;
Faul, C ;
Reiser, J ;
Mundel, P .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (05) :1188-1198
[3]   Alterations of podocytes in a murine model of crescentic glomerulonephritis [J].
Besse-Eschmann, V ;
Le Hir, M ;
Endlich, N ;
Endlich, K .
HISTOCHEMISTRY AND CELL BIOLOGY, 2004, 122 (02) :139-149
[4]   Long-term renal consequences of hypertension for normal and diseased kidneys [J].
Bidani, AK ;
Griffin, KA .
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2002, 11 (01) :73-80
[5]   Mice lacking the giant protocadherin mFAT1 exhibit renal slit junction abnormalities and a partially penetrant cyclopia and anophthalmia phenotype [J].
Ciani, L ;
Patel, A ;
Allen, ND ;
Ffrench-Constant, C .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (10) :3575-3582
[6]  
DRENCKHAHN D, 1988, LAB INVEST, V59, P673
[7]   Mechanical strain increases SPARC levels in podocytes: implications for glomerulosclerosis [J].
Durvasula, RV ;
Shankland, SJ .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2005, 289 (03) :F577-F584
[8]  
Endlich N, 2001, J AM SOC NEPHROL, V12, P413, DOI 10.1681/ASN.V123413
[9]   Analysis of differential gene expression in stretched podocytes:: osteopontin enhances adaptation of podocytes to mechanical stress [J].
Endlich, N ;
Sunohara, M ;
Nietfeld, W ;
Wolski, EW ;
Schiwek, D ;
Kränzlin, B ;
Gretz, N ;
Kriz, W ;
Eickhoff, H ;
Endlich, K .
FASEB JOURNAL, 2002, 16 (11) :1850-+
[10]  
Endlich N., 2001, Pfluegers Archiv European Journal of Physiology, V441, pR259