ASXL2 Regulates Glucose, Lipid, and Skeletal Homeostasis
Author(s) -
Takashi Izawa,
Nidhi Rohatgi,
T. Fukunaga,
Qun-Tian Wang,
Matthew J. Silva,
Michael J. Gardner,
Michael L. McDaniel,
Nada A. Abumrad,
Clay F. Semenkovich,
Steven L. Teitelbaum,
Wei Zou
Publication year - 2015
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2015.05.019
Subject(s) - osteoclast , glucose homeostasis , bone resorption , regulator , microbiology and biotechnology , bone remodeling , homeostasis , biology , medicine , endocrinology , insulin , receptor , genetics , insulin resistance , gene
ASXL2 is an ETP family protein that interacts with PPARγ. We find that ASXL2-/- mice are insulin resistant, lipodystrophic, and fail to respond to a high-fat diet. Consistent with genetic variation at the ASXL2 locus and human bone mineral density, ASXL2-/- mice are also severely osteopetrotic because of failed osteoclast differentiation attended by normal bone formation. ASXL2 regulates the osteoclast via two distinct signaling pathways. It induces osteoclast formation in a PPARγ/c-Fos-dependent manner and is required for RANK ligand- and thiazolidinedione-induced bone resorption independent of PGC-1β. ASXL2 also promotes osteoclast mitochondrial biogenesis in a process mediated by PGC-1β but independent of c-Fos. Thus, ASXL2 is a master regulator of skeletal, lipid, and glucose homeostasis.
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