Targeting adipocyte ESRRA promotes osteogenesis and vascular formation in adipocyte-rich bone marrow.
Tongling HuangZhaocheng LuZihui WangLixin ChengLu GaoJun GaoNing ZhangChang-An GengXiaoli ZhaoHuaiyu WangChi-Wai WongKelvin Wai-Kwok YeungHaobo PanWilliam Weijia LuMin GuanPublished in: Nature communications (2024)
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.
Keyphrases
- bone marrow
- insulin resistance
- adipose tissue
- fatty acid
- high fat diet induced
- bone loss
- mesenchymal stem cells
- metabolic syndrome
- skeletal muscle
- transcription factor
- type diabetes
- gene expression
- cell fate
- poor prognosis
- estrogen receptor
- weight gain
- drug delivery
- bone regeneration
- soft tissue
- binding protein
- body composition
- physical activity
- weight loss
- long non coding rna
- postmenopausal women