Two Differently Regulated Nuclear Factor κ B Activation Pathways Triggered by the Cytoplasmic Tail of CD40

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 96; no. 4; pp. 1234 - 1239
• Main Authors: Tsukamoto, Nobuo, Kobayashi, Norihiko, Azuma, Sakura, Yamamoto, Tadashi, Inoue, Jun-ichiro
• Format: Journal Article
• Language: English
• Published: National Academy of Sciences of the United States of America 16.02.1999; National Acad Sciences; The National Academy of Sciences
• Subjects: Antibodies; B lymphocytes; Biochemistry; Biological Sciences; Cell extracts; Gels; Genetic mutation; Physiological regulation; Plasmids; Proteins; T lymphocytes
• DOI: 10.1073/pnas.96.4.1234
• ISSN: 0027-8424

CD40 signaling modulates the immune response at least in part by activation of nuclear factor κ B (NFκ B). It has been shown that two distinct domains in the CD40 cytoplasmic tail (cyt), namely cyt-N and cyt-C, independently activate NFκ B. Although four members of the tumor necrosis factor receptor-associated factor (TRAF) family, including TRAF2, TRAF3, TRAF5, and TRAF6, bind to the CD40 cyt, how each TRAF protein contributes to the NFκ B activation by CD40 is not clear. Here we report that TRAF2, TRAF3, and TRAF5 bind cyt-C, whereas TRAF6 binds cyt-N. cyt-N is conserved poorly between human and mouse CD40, while cyt-C is highly conserved. However, single aa substitution of Glu-235 in cyt-N of human CD40 with Ala abolishes the binding of TRAF6 to cyt-N and NFκ B activation by cyt-N. Conservation of this Glu between mouse and human CD40 strongly suggests that TRAF6 could link cyt-N to signals essential for CD40-mediated immune response. Furthermore, NFκ B activation by cyt-C is inhibited by a kinase-negative form of NFκ B-inducing kinase more efficiently than that by cyt-N, consistent with the result that NFκ B activation by TRAF2 and TRAF5 is inhibited by a kinase-negative form of NFκ B-inducing kinase more efficiently than that by TRAF6. These results indicate that NFκ B activating signals emanating from cyt-N and cyt-C are mediated by the different members of the TRAF family and could be regulated in a distinct manner.