Back to Search Start Over

The sheddase activity of ADAM17/TACE is regulated by the tetraspanin CD9

Authors :
Francisco Sánchez-Madrid
Carmen Domínguez
Carlos Cabañas
Alvaro Gilsanz
Esther M. Lafuente
Susana Ovalle
Isidoro González-Álvaro
María Dolores Gutiérrez-López
María Yáñez-Mó
Peter N. Monk
Ministerio de Ciencia e Innovación (España)
Fundación Mutua Madrileña
Instituto de Salud Carlos III
Consejo Superior de Investigaciones Científicas (España)
Source :
Digital.CSIC. Repositorio Institucional del CSIC, instname
Publication Year :
2011
Publisher :
Springer Science and Business Media LLC, 2011.

Abstract

ADAM17/TACE is a metalloproteinase responsible for the shedding of the proinflammatory cytokine TNF-a and many other cell surface proteins involved in development, cell adhesion, migration, differentiation, and proliferation. Despite the important biological function of ADAM17, the mechanisms of regulation of its metalloproteinase activity remain largely unknown. We report here that the tetraspanin CD9 and ADAM17 partially co-localize on the surface of endothelial and monocytic cells. In situ proximity ligation, co-immunoprecipitation, crosslinking, and pull-down experiments collectively demonstrate a direct association between these molecules. Functional studies reveal that treatment with CD9-specific antibodies or neoexpression of CD9 exert negative regulatory effects on ADAM17 sheddase activity. Conversely, CD9 silencing increased the activity of ADAM17 against its substrates TNF-a and ICAM-1. Taken together, our results show that CD9 associates with ADAM17 and, through this interaction, negatively regulates the sheddase activity of ADAM17<br />s. This work was supported by grants BFU2007-66443/BMC and BFU2010-19144/BMC from Ministerio de Ciencia e Innovación, a grant from Fundación de Investigación Médica Mutua Madrileña and by RETICS Program RD08/0075-RIER (Red de Inflamacio´n y Enfermedades Reumáticas) from Instituto de Salud Carlos III (to C.C.), a grant from Fundación de Investigación Médica Mutua Madrileña (to M.D.G.L.), and grants PI080794 from Instituto de Salud Carlos III (to M.Y-M) and SAF2007-60578 from Ministerio de Ciencia e Innovación (to E.M.L.). M.D.G.L. was supported by a contract associated to grant SAF2004-01715 from Ministerio de Ciencia e Innovacio´n. S.O. was supported by an I3P predoctoral Fellowship from Consejo Superior de Investigaciones Científicas (CSIC) and by a contract associated to grant BFU2007-66443/BMC from Ministerio de Ciencia e Innovacio´n. A.G. has been supported by a predoctoral Fellowship from Instituto de Salud Carlos III and by grant BFU2007-66443/BMC from Ministerio de Ciencia e Innovación.

Details

ISSN :
14209071 and 1420682X
Volume :
68
Database :
OpenAIRE
Journal :
Cellular and Molecular Life Sciences
Accession number :
edsair.doi.dedup.....7737a01c45e7b71d150d37eca2cec1a1
Full Text :
https://doi.org/10.1007/s00018-011-0639-0