CD44 and β3 integrin organize two functionally distinct actin-based domains in osteoclasts

被引:112
作者
Chabadel, Anne [1 ]
Banon-Rodriguez, Inmaculada [2 ]
Cluet, David [3 ]
Rudkin, Brian B. [3 ]
Wehrle-Haller, Bernhard [4 ]
Genot, Elisabeth [5 ]
Jurdic, Pierre [1 ]
Anton, Ines M. [2 ]
Saltel, Frederic [1 ,5 ]
机构
[1] Univ Lyon 1, Univ Lyon, Ecole Normale Super Lyon,Inst Federatif Biosci Ge, Inst Genom Fonctionnelle Lyon,CNRS,INRA, F-69364 Lyon, France
[2] Univ Autonoma Madrid, Ctr Biol Mol Severo Ochoa, CSIC, E-28049 Madrid, Spain
[3] Univ Lyon 1, Ecole Normale Super Lyon, Inst Federatif Rech BioSci Lyon Gerland, Lab Biol Mol Cellule,UMR 5239,CNRS, F-69364 Lyon 07, France
[4] Ctr Med Univ Geneva, Dept Cellular Physiol & Metab, CH-1211 Geneva, Switzerland
[5] Univ Victor Segalen Bordeaux 2, Inst Federatif Rech 66, European Inst Chem & Biol, INSERM,U889, F-33600 Pessac, France
关键词
D O I
10.1091/mbc.E07-04-0378
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The actin cytoskeleton of mature osteoclasts (OCs) adhering to nonmineralized substrates is organized in a belt of podosomes reminiscent of the sealing zone (SZ) found in bone resorbing OCs. In this study, we demonstrate that the belt is composed of two functionally different actin-based domains: podosome cores linked with CD44, which are involved in cell adhesion, and a diffuse cloud associated with 133 integrin, which is involved in cell adhesion and contraction. Wiskott Aldrich Syndrome Protein (WASp) Interacting Protein (WIP)-/- OCs were devoid of podosomes, but they still exhibited actin clouds. Indeed, WIP-/- OCs show diminished expression of WASp, which is required for podosome formation. CD44 is a novel marker of OC podosome cores and the first nonintegrin receptor detected in these structures. The importance of CD44 is revealed by showing that its clustering restores podosome cores and WASp expression in WIP-/- OCs. However, although CD44 signals are sufficient to form a SZ, the presence of WIP is indispensable for the formation of a fully functional SZ.
引用
收藏
页码:4899 / 4910
页数:12
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