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¹ Division of Immunology, Children's Hospital and Department of Pediatrics, Harvard Medical School, Boston, MA 02115
² Department of Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01655

Address correspondence to Raif S. Geha, Div. of Immunology, 1 Blackfan Circle, Boston, MA 02115. Tel: (617) 919-2482; Fax: (617) 730-0528; email: raif.geha{at}childrens.harvard.edu

Receptor-interacting protein (RIP) has been reported to associate with tumor necrosis–associated factor (TRAF)2 and TRAF6. Since TRAF2 and TRAF6 play important roles in CD40 signaling and TRAF6 plays an important role in TLR4 signaling, we examined the role of RIP in signaling via CD40 and TLR4. Splenocytes from RIP^–/– mice proliferated and underwent isotype switching normally in response to anti-CD40–IL-4 but completely failed to do so in response to LPS–IL-4. However, they normally up-regulated TNF- and IL-6 gene expression and CD54 and CD86 surface expression after LPS stimulation. RIP^–/– splenocytes exhibited increased apoptosis and impaired Akt phosphorylation after LPS stimulation. These results suggest that RIP is essential for cell survival after TLR4 signaling and links TLR4 to the phosphatidylinositol 3 kinase–Akt pathway.

Key Words: NFB • IB • p38 MAP kinase • IL-6 • TNF-

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