TITLE

Segregation of TRAF6-mediated signaling pathways clarifies its role in osteoclastogenesis

AUTHOR(S)
Kobayashi, Norihiko; Kadono, Yuho; Naito, Asuka; Matsumoto, Kunihiro; Yamamoto, Tadashi; Tanaka, Sakae; Inoue, Jun-ichiro
PUB. DATE
March 2001
SOURCE
EMBO Journal;3/15/2001, Vol. 20 Issue 6, p1271
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Signals emanating from the receptor for interleukin-1 (IL-1), lipopolysaccharide (LPS) or osteoclast differentiation factor/receptor activator of NF?B ligand (ODF/RANKL) stimulate transcription factors AP-1 through mitogen-activated protein kinase (MAPK) activation and NF?B through I?B kinase (IKK) activation. These kinases are thought to be activated by tumor necrosis factor receptor-associated factor 6 (TRAF6). However, molecular mechanisms by which TRAF6 activates various downstream kinases remain to be elucidated. We identified functional domains of TRAF6 under physiological conditions established by appropriate expression of TRAF6 mutants in TRAF6-deficient cells. In IL-1 and LPS signaling pathways, the RING finger and first zinc finger domains are not required for NF?B activation but are required for full activation of MAPK. However, IL-1 and LPS signals utilize distinct regions within the zinc finger domains of TRAF6 to activate NF?B. Furthermore, the RING finger domain is not required for differentiation of splenocytes to multinuclear osteoclasts, but is essential for osteoclast maturation. Thus, TRAF6 plays essential roles in both the differentiation and maturation of osteoclasts by activating various kinases via its multiple domains.
ACCESSION #
12954979

 

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