RANKL coordinates multiple osteoclastogenic pathways by regulating expression of ubiquitin ligase RNF146

Yoshinori Matsumoto, Jose Larose, Oliver A. Kent, Melissa Lim, Adele Changoor, Lucia Zhang, Yaryna Storozhuk, Xiaohong Mao, Marc D. Grynpas, Feng Cong, Robert Rottapel

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13 Citations (Scopus)

Abstract

Bone undergoes continuous remodeling due to balanced bone formation and resorption mediated by osteoblasts and osteoclasts, respectively. Osteoclasts arise from the macrophage lineage, and their differentiation is dependent on RANKL, a member of the TNF family of cytokines. Here, we have provided evidence that RANKL controls the expression of 3BP2, an adapter protein that is required for activation of SRC tyrosine kinase and simultaneously coordinates the attenuation of ?-catenin, both of which are required to execute the osteoclast developmental program. We found that RANKL represses the transcription of the E3 ubiquitin ligase RNF146 through an NF-?B-related inhibitory element in the RNF146 promoter. RANKL-mediated suppression of RNF146 results in the stabilization of its substrates, 3BP2 and AXIN1, which consequently triggers the activation of SRC and attenuates the expression of ?-catenin, respectively. Depletion of RNF146 caused hypersensitivity to LPS-induced TNF-? production in vivo. RNF146 thus acts as an inhibitory switch to control osteoclastogenesis and cytokine production and may be a control point underlying the pathogenesis of chronic inflammatory diseases.

Original languageEnglish
Pages (from-to)1303-1315
Number of pages13
JournalJournal of Clinical Investigation
Volume127
Issue number4
DOIs
Publication statusPublished - Apr 3 2017
Externally publishedYes

ASJC Scopus subject areas

  • Medicine(all)

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    Matsumoto, Y., Larose, J., Kent, O. A., Lim, M., Changoor, A., Zhang, L., Storozhuk, Y., Mao, X., Grynpas, M. D., Cong, F., & Rottapel, R. (2017). RANKL coordinates multiple osteoclastogenic pathways by regulating expression of ubiquitin ligase RNF146. Journal of Clinical Investigation, 127(4), 1303-1315. https://doi.org/10.1172/JCI90527