Matrix-degrading podosomes in smooth muscle cells.

Abstract:

:Activation of protein kinase C by phorbol esters triggers the remodelling of the actin cytoskeleton and the formation of podosomes in smooth muscle cells (SMCs). Regional control of actin dynamics at specialised microdomains results in a local reduction in contractile forces. The molecular basis for this local inhibition of contractility includes the clustering of cortactin during podosome formation (which precedes the rapid, local dispersion of myosin, tropomyosin and h1 calponin), and the specific recruitment of 110-kDa actin filament-associated protein (AFAP-110) and 190-kDa Rho-specific GTPase-activating protein (p190RhoGAP) to the microdomains. Podosome formation also correlates with cell polarisation, the induction of cell motility, and local degradation of the extracellular matrix. These findings may provide explanations for the complex mechanisms underlying SMC invasion in the course of the development of atherosclerotic lesions and restenosis, and support the concept that matrix degradation and the concomitant engagement of the molecular machinery initiating actin-based cell motility drive tissue invasion in smooth muscle.

journal_name

Eur J Cell Biol

authors

Lener T,Burgstaller G,Crimaldi L,Lach S,Gimona M

doi

10.1016/j.ejcb.2005.08.001

subject

Has Abstract

pub_date

2006-04-01 00:00:00

pages

183-9

issue

3-4

eissn

0171-9335

issn

1618-1298

pii

S0171-9335(05)00113-5

journal_volume

85

pub_type

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