| Literature DB >> 25130399 |
Zixue Jin1, Wei Wei1, Marie Yang1, Yang Du1, Yihong Wan2.
Abstract
<span class="Disease">Mitochondrial complex I (CI) deficiency is associated with multiple neurological and <span class="Disease">metabolic disorders. However, its effect on innate immunity and bone remodeling is unclear. Using deletion of the essential CI subunit Ndufs4 as a model for mitochondrial dysfunction, we report that mitochondria suppress macrophage activation and inflammation while promoting osteoclast differentiation and bone resorption via both cell-autonomous and systemic regulation. Global Ndufs4 deletion causes systemic inflammation and osteopetrosis. Hematopoietic Ndufs4 deletion causes an intrinsic lineage shift from osteoclast to macrophage. Liver Ndufs4 deletion causes a metabolic shift from fatty acid oxidation to glycolysis, accumulating fatty acids and lactate (FA/LAC) in the circulation. FA/LAC further activates Ndufs4(-/-) macrophages via reactive oxygen species induction and diminishes osteoclast lineage commitment in Ndufs4(-/-) progenitors; both inflammation and osteopetrosis in Ndufs4(-/-) mice are attenuated by TLR4/2 deletion. Together, these findings reveal mitochondrial CI as a critical rheostat of innate immunity and skeletal homeostasis.Entities:
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Year: 2014 PMID: 25130399 PMCID: PMC4156549 DOI: 10.1016/j.cmet.2014.07.011
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287