par Blero, Daniel
;De Smedt, Florence
;Pesesse, Xavier
;Paternotte, Nathalie
;Payrastre, Bernard;Erneux, Christophe
;Moreau, Colette 
Référence Biochemical and biophysical research communications, 282, 3, page (839-843)
Publication Publié, 2001-04






Référence Biochemical and biophysical research communications, 282, 3, page (839-843)
Publication Publié, 2001-04
Article révisé par les pairs
Résumé : | The lipid phosphatase SHIP2 (SH2 domain containing inositol 5-phosphatase 2) has recently been shown to be a potent negative regulator of insulin signaling and insulin sensitivity in vivo. We show here that SHIP2 is expressed in Chinese hamster ovary cells overexpressing the insulin receptor (CHO-IR cells) and tyrosine phosphorylated upon insulin stimulation. We show that SHIP2, which is recruited in anti-phosphotyrosine immunoprecipitates in insulin-stimulated cells, accounts for the insulin sensitivity or apparent increase in activity reported by Guilherme et al. (J. Biol. Chem. 271, 29533-29536, 1996). Overexpression of SHIP2 led to a decrease of the insulin-dependent PIP3 production as well as Akt/PKB activation and MAPK stimulation. |