Nature communications · 2019
TMCO1-mediated Ca2+ leak underlies osteoblast functions via CaMKII signaling.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Li Jianwei, Liu Caizhi, Li Yuheng, Zheng Qiaoxia, Xu Youjia, Liu Beibei, Sun Weijia, Li Yuan, Ji Shuhui, Liu Mingwei, Zhang Jing, Zhao Dingsheng, Du Ruikai, Liu Zizhong, Zhong Guohui, Sun Cuiwei, Wang Yanqing, Song Jinping, Zhang Shu, Qin Jun, Ling Shukuan, Wang Xianhua, Li Yingxian
Аннотация
Transmembrane and coiled-coil domains 1 (TMCO1) is a recently identified Ca2+ leak channel in the endoplasmic reticulum. TMCO1 dysfunction in humans is associated with dysmorphism, mental retardation, glaucoma and the occurrence of cancer. Here we show an essential role of TMCO1 in osteogenesis mediated by local Ca2+/CaMKII signaling in osteoblasts. TMCO1 levels were significantly decreased in bone from both osteoporosis patients and bone-loss mouse models. Tmco1-/- mice exhibited loss of bone mass and altered microarchitecture characteristic of osteoporosis. In the absence of TMCO1, decreased HDAC4 phosphorylation resulted in nuclear enrichment of HADC4, which leads to deacetylation and degradation of RUNX2, the master regulator of osteogenesis. We further demonstrate that TMCO1-mediated Ca2+ leak provides local Ca2+ signals to activate the CaMKII-HDAC4-RUNX2 signaling axis. The establishment of TMCO1 as a pivotal player in osteogenesis uncovers a novel potential therapeutic target for ameliorating osteoporosis.
Предметные рубрики MeSH
AgedAnimalsCalcium ChannelsCalcium SignalingCalcium-Calmodulin-Dependent Protein Kinase Type 2Core Binding Factor Alpha 1 SubunitFemaleHistone DeacetylasesHumansMembrane ProteinsMice, Inbred C57BLMice, Mutant StrainsMiddle AgedOsteoblastsOsteogenesisOsteoporosisOvariectomyProtein StabilitySignal Transduction