间充质干细胞
骨质疏松症
骨髓
细胞生物学
癌症研究
间质细胞
生物
同源盒蛋白纳米
胚胎干细胞
衰老
内分泌学
医学
化学
内科学
免疫学
诱导多能干细胞
生物化学
基因
作者
Yuan Wang,Peng Deng,Yuting Liu,Yunshu Wu,Yaqian Chen,Yuchen Guo,Shiwen Zhang,Xiaofei Zheng,Liyan Zhou,Weiqing Liu,Qiwen Li,Weimin Lin,Xingying Qi,Guomin Ou,Cun‐Yu Wang,Quan Yuan
标识
DOI:10.1038/s41467-020-19360-1
摘要
Abstract Age-related osteoporosis is characterized by the deterioration in bone volume and strength, partly due to the dysfunction of bone marrow mesenchymal stromal/stem cells (MSCs) during aging. Alpha-ketoglutarate (αKG) is an essential intermediate in the tricarboxylic acid (TCA) cycle. Studies have revealed that αKG extends the lifespan of worms and maintains the pluripotency of embryonic stem cells (ESCs). Here, we show that the administration of αKG increases the bone mass of aged mice, attenuates age-related bone loss, and accelerates bone regeneration of aged rodents. αKG ameliorates the senescence-associated (SA) phenotypes of bone marrow MSCs derived from aged mice, as well as promoting their proliferation, colony formation, migration, and osteogenic potential. Mechanistically, αKG decreases the accumulations of H3K9me3 and H3K27me3, and subsequently upregulates BMP signaling and Nanog expression. Collectively, our findings illuminate the role of αKG in rejuvenating MSCs and ameliorating age-related osteoporosis, with a promising therapeutic potential in age-related diseases.
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