Insulin/IGF-1 and TNF-alpha stimulate phosphorylation of IRS-1 at inhibitory Ser(307) via distinct pathways

Serine/threonine phosphorylation of IRS-1 might inhibit insulin signaling, but the relevant phosphorylation sites are difficult to identify in culture d cells and to validate in isolated tissues. Recently, we discovered that r ecombinant NH2-terminal Jun kinase phosphorylates IRS-1 at Ser(307), which inhibits insulin-stimulated tyrosine phosphorylation of IRS-1. To monitor p hosphorylation of Ser(307) in various cell and tissue backgrounds, we prepa red a phosphospecific polyclonal antibody designated alpha pSer(307). This antibody revealed that TNF-alpha, IGF-1, or insulin stimulated phosphorylat ion of IRS-1 at Ser(307) in 3T3-L1 preadipocytes and adipocytes. Insulin in jected into mice or rats also stimulated phosphorylation of Ser(307) on IRS -1 immunoprecipitated from muscle; moreover, Ser(307) was phosphorylated in human muscle during the hyperinsulinemic euglycemic clamp. Experiments in 3T3-L1 preadipocytes and adipocytes revealed that insulin-stimulated phosph orylation of Ser(307) was inhibited by LY294002 or wortmannin, whereas TNF- alpha -stimulated phosphorylation was inhibited by PD98059. Thus, distinct kinase pathways might converge at Ser(307) to mediate feedback or heterolog ous inhibition of IRS-1 signaling to counterregulate the insulin response.