Thromb Haemost 2010; 103(03): 556-563
DOI: 10.1160/TH09-07-0478
Theme Issue Article
Schattauer GmbH

Integrin cleavage regulates bidirectional signalling in vascular smooth muscle cells

Kai Kappert
1   Department of Medicine/ Cardiology, Deutsches Herzzentrum Berlin, Berlin, Germany
2   Department of Pharmacology, Center for Cardiovascular Research (CCR), Charité Universitätsmedizin-Berlin, Berlin, Germany
,
Vesna Furundzija
1   Department of Medicine/ Cardiology, Deutsches Herzzentrum Berlin, Berlin, Germany
,
Jan Fritzsche
1   Department of Medicine/ Cardiology, Deutsches Herzzentrum Berlin, Berlin, Germany
,
Christian Margeta
3   Division of Angiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria
,
Janine Krüger
2   Department of Pharmacology, Center for Cardiovascular Research (CCR), Charité Universitätsmedizin-Berlin, Berlin, Germany
,
Heike Meyborg
1   Department of Medicine/ Cardiology, Deutsches Herzzentrum Berlin, Berlin, Germany
,
Eckart Fleck
1   Department of Medicine/ Cardiology, Deutsches Herzzentrum Berlin, Berlin, Germany
,
Philipp Stawowy
1   Department of Medicine/ Cardiology, Deutsches Herzzentrum Berlin, Berlin, Germany
› Author Affiliations
Financial support:This work was supported by a grant of the Charité-Universitätsmedizin Berlin to P.S. K.K. is supported by the Deutsche Forschungsgemeinschaft (Ka1820/4–1). E.F. is supported by the Zukunftsfond Berlin/TSB Medici.
Further Information

Publication History

Received: 26 July 2009

Accepted after major revision: 22 January 2009

Publication Date:
22 November 2017 (online)

Summary

Integrins link the cytoskeleton to the extracellular matrix, providing outside-in/inside-out signalling essential for vascular smooth muscle cell (VSMC) migration in atherosclerosis. The integrin αv subunit is synthesised from its precursor via furin-dependent endoproteolytic cleavage. Furin is a proprotein convertase (PC) highly expressed in VSMCs and in human atherosclerotic lesions. Inhibition of αv processing inhibits binding to vitronectin and migration. However, the precise role of furin-dependent αv cleavage on integrin bidirectional signalling and subsequent VSMC functions is unknown. Our present study demonstrates that the furin-like PC inhibitor decanoyl-RVKR-chloromethylke-tone (dec-CMK) inhibited αv cleavage. This reduced vitronectin-induced (outside-in) focal adhesion kinase (FAK)- and paxillin-phosphorylation, and VSMC motility. Inside-out-stimulated, integrin-mediated VSMC adhesion/migration relied on integrin-adaptor protein activation following protein kinase C (PKC) and ERK1/2 phosphorylation. In contrast to outside-in signalling, PKC-dependent phosphorylation of FAK and paxillin was unaffected by the status of integrin cleavage. Still, cytoskeleton and focal adhesion site rearrangements were modulated by the inhibition of furin-dependent integrin cleavage, thereby lessening inside-out dependent migration. Hence, we find that integrin bidirectional signalling is critically controlled by furin. Furin-dependent integrin processing modulates rapid adaptive integrin/cytoskeleton changes, essential to VSMC motility, which represents a crucial component in atherosclerosis and restenosis.

 
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