| Literature DB >> 26051940 |
Takashi Izawa1, Nidhi Rohatgi1, Tomohiro Fukunaga1, Qun-Tian Wang2, Matthew J Silva3, Michael J Gardner3, Michael L McDaniel1, Nada A Abumrad4, Clay F Semenkovich5, Steven L Teitelbaum6, Wei Zou7.
Abstract
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.Entities:
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Year: 2015 PMID: 26051940 PMCID: PMC4472564 DOI: 10.1016/j.celrep.2015.05.019
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423