脂肪细胞
骨髓
内分泌学
内科学
间质细胞
瘦素
生物
细胞生物学
脂肪组织
化学
医学
肥胖
作者
Tongling Huang,Zhaocheng Lu,Zihui Wang,Lixin Cheng,Lu Gao,Jun Gao,Ning Zhang,Chang‐An Geng,Xiaoli Zhao,Huaiyu Wang,Chi‐Wai Wong,Kwk Yeung,Haobo Pan,William W. Lu,Min Guan
标识
DOI:10.1038/s41467-024-48255-8
摘要
Abstract Excessive bone marrow adipocytes (BMAds) accumulation often occurs under diverse pathophysiological conditions associated with bone deterioration. Estrogen-related receptor α (ESRRA) is a key regulator responding to metabolic stress. Here, we show that adipocyte-specific ESRRA deficiency preserves osteogenesis and vascular formation in adipocyte-rich bone marrow upon estrogen deficiency or obesity. Mechanistically, adipocyte ESRRA interferes with E2/ESR1 signaling resulting in transcriptional repression of secreted phosphoprotein 1 ( Spp1 ); yet positively modulates leptin expression by binding to its promoter. ESRRA abrogation results in enhanced SPP1 and decreased leptin secretion from both visceral adipocytes and BMAds, concertedly dictating bone marrow stromal stem cell fate commitment and restoring type H vessel formation, constituting a feed-forward loop for bone formation. Pharmacological inhibition of ESRRA protects obese mice against bone loss and high marrow adiposity. Thus, our findings highlight a therapeutic approach via targeting adipocyte ESRRA to preserve bone formation especially in detrimental adipocyte-rich bone milieu.
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