HIV-1 Nef associated PAK and PI3-kinases stimulate Akt-independent Bad-phosphorylation to induce anti-apoptotic signals

D Wolf, V Witte, B Laffert, K Blume, E Stromer… - Nature medicine, 2001 - nature.com
D Wolf, V Witte, B Laffert, K Blume, E Stromer, S Trapp, P d'Aloja, A Schürmann, AS Baur
Nature medicine, 2001nature.com
A highly conserved signaling property of Nef proteins encoded by human or simian
immunodeficiency virus is the binding and activation of a PAK kinase whose function is
unclear. Here we show that Nef-mediated p21-activated kinase (PAK) activation involves
phosphatidylinositol 3-kinase, which acts upstream of PAK and is bound and activated by
Nef similar to the manner of Polyoma virus middle T antigen. The Nef-associated
phosphatidylinositol-3–PAK complex phosphorylated the pro-apoptotic Bad protein without …
Abstract
A highly conserved signaling property of Nef proteins encoded by human or simian immunodeficiency virus is the binding and activation of a PAK kinase whose function is unclear. Here we show that Nef-mediated p21-activated kinase (PAK) activation involves phosphatidylinositol 3-kinase, which acts upstream of PAK and is bound and activated by Nef similar to the manner of Polyoma virus middle T antigen. The Nef-associated phosphatidylinositol-3–PAK complex phosphorylated the pro-apoptotic Bad protein without involving the protein kinase B–Akt kinase, which is generally believed to inactivate Bad by serine phosphorylation. Consequently, Nef, but not a Nef mutant incapable of activating PAK, blocked apoptosis in T cells induced by serum starvation or HIV replication. Nef anti-apoptotic effects are likely a crucial mechanism for viral replication in the host and thus in AIDS pathogenesis.
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