NHC Key Lab of Hormones and Development, Tianjin Key Lab of Metabolic Diseases, Tianjin Medical University Chu Hsien-I Memorial Hospital & Institute of Endocrinology, Tianjin, China.
College of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Cell Death Dis. 2024 Feb 12;15(2):136. doi: 10.1038/s41419-024-06521-z.
Histone methylation plays a crucial role in various cellular processes. We previously reported the in vitro function of histone lysine demethylase 7 A (KDM7A) in osteoblast and adipocyte differentiation. The current study was undertaken to investigate the physiological role of KDM7A in bone homeostasis and elucidate the underlying mechanisms. A conditional strategy was employed to delete the Kdm7a gene specifically in osterix-expressing osteoprogenitor cells in mice. The resulting mutant mice exhibited a significant increase in cancellous bone mass, accompanied by an increase in osteoblasts and bone formation, as well as a reduction in osteoclasts, marrow adipocytes and bone resorption. The bone marrow stromal cells (BMSCs) and calvarial pre-osteoblastic cells derived from the mutant mice exhibited enhanced osteogenic differentiation and suppressed adipogenic differentiation. Additionally, osteoclastic precursor cells from the mutant mice exhibited impaired osteoclast differentiation. Co-culturing BMSCs from the mutant mice with wild-type osteoclast precursor cells resulted in the inhibition of osteoclast differentiation. Mechanistic investigation revealed that KDM7A was able to upregulate the expression of fibroblast activation protein α (FAP) and receptor activator of nuclear factor κB ligand (RANKL) in BMSCs through removing repressive di-methylation marks of H3K9 and H3K27 from Fap and Rankl promoters. Moreover, recombinant FAP attenuated the dysregulation of osteoblast and adipocyte differentiation in BMSCs from Kdm7a deficient mice. Finally, Kdm7a deficiency prevented ovariectomy-induced bone loss in mice. This study establish the role of KDM7A in bone homeostasis through its epigenetic regulation of osteoblast and osteoclast differentiation. Consequently, inhibiting KDM7A may prove beneficial in ameliorating osteoporosis. KDM7A suppresses osteoblast differentiation and bone formation through. upregulating FAP expression and inactivating canonical Wnt signaling, and conversely promotes osteoclast differentiation and bone resorption through upregulating RANKL expression. These are based on its epigenetic removal of the repressive H3K9me2 and H3K27me2 marks from Fap and Rankl promoters. As a result, the expression of KDM7A in osteoprogenitor cells tends to negatively modulate bone mass.
组蛋白甲基化在各种细胞过程中起着至关重要的作用。我们之前报道了组蛋白赖氨酸去甲基酶 7A(KDM7A)在成骨细胞和脂肪细胞分化中的体外功能。本研究旨在探讨 KDM7A 在骨稳态中的生理作用,并阐明其潜在机制。本研究采用条件策略特异性删除小鼠中骨钙素表达的成骨前体细胞中的 Kdm7a 基因。结果表明,突变小鼠骨小梁骨量显著增加,成骨细胞和骨形成增加,破骨细胞、骨髓脂肪细胞和骨吸收减少。突变小鼠的骨髓基质细胞(BMSCs)和颅骨前成骨细胞表现出增强的成骨分化和抑制的成脂分化。此外,突变小鼠的破骨细胞前体细胞表现出破骨细胞分化受损。将突变小鼠的 BMSCs 与野生型破骨细胞前体细胞共培养可抑制破骨细胞分化。机制研究表明,KDM7A 能够通过去除 Fap 和 Rankl 启动子上 H3K9 和 H3K27 的抑制性二甲基化标记,在 BMSCs 中上调成纤维细胞激活蛋白 α(FAP)和核因子 κB 配体受体激活剂(RANKL)的表达。此外,重组 FAP 可减轻 Kdm7a 缺陷小鼠 BMSCs 中成骨细胞和脂肪细胞分化的失调。最后,Kdm7a 缺陷可防止去卵巢诱导的小鼠骨丢失。本研究通过 KDM7A 对成骨细胞和破骨细胞分化的表观遗传调控,确立了 KDM7A 在骨稳态中的作用。因此,抑制 KDM7A 可能有益于改善骨质疏松症。KDM7A 通过上调 FAP 表达和失活经典 Wnt 信号通路来抑制成骨细胞分化和骨形成,通过上调 RANKL 表达来促进破骨细胞分化和骨吸收。这些都是基于其从 Fap 和 Rankl 启动子上去除抑制性 H3K9me2 和 H3K27me2 标记。因此,成骨前体细胞中 KDM7A 的表达倾向于负调节骨量。