1] Department of Immunology and Cell Biology, Graduate School of Medicine and Frontier Biosciences, Osaka University, Osaka, Japan. [2] WPI-Immunology Frontier Research Center, Osaka University, Osaka, Japan. [3] Japan Science and Technology Agency, CREST, Tokyo, Japan.
1] Department of Immunology and Cell Biology, Graduate School of Medicine and Frontier Biosciences, Osaka University, Osaka, Japan. [2] WPI-Immunology Frontier Research Center, Osaka University, Osaka, Japan. [3] Japan Science and Technology Agency, CREST, Tokyo, Japan. [4] Department of Otorhinolaryngology-Head and Neck Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.
Nat Med. 2015 Mar;21(3):281-7. doi: 10.1038/nm.3774. Epub 2015 Feb 23.
Metabolic reprogramming occurs in response to the cellular environment to mediate differentiation, but the fundamental mechanisms linking metabolic processes to differentiation programs remain to be elucidated. During osteoclast differentiation, a shift toward more oxidative metabolic processes occurs. In this study we identified the de novo DNA methyltransferase 3a (Dnmt3a) as a transcription factor that couples these metabolic changes to osteoclast differentiation. We also found that receptor activator of nuclear factor-κB ligand (RANKL), an essential cytokine for osteoclastogenesis, induces this metabolic shift towards oxidative metabolism, which is accompanied by an increase in S-adenosylmethionine (SAM) production. We found that SAM-mediated DNA methylation by Dnmt3a regulates osteoclastogenesis via epigenetic repression of anti-osteoclastogenic genes. The importance of Dnmt3a in bone homeostasis was underscored by the observations that Dnmt3a-deficient osteoclast precursor cells do not differentiate efficiently into osteoclasts and that mice with an osteoclast-specific deficiency in Dnmt3a have elevated bone mass due to a smaller number of osteoclasts. Furthermore, inhibition of DNA methylation by theaflavin-3,3'-digallate abrogated bone loss in models of osteoporosis. Thus, this study reveals the role of epigenetic processes in the regulation of cellular metabolism and differentiation, which may provide the molecular basis for a new therapeutic strategy for a variety of bone disorders.
代谢重编程发生在细胞环境中,以介导分化,但将代谢过程与分化程序联系起来的基本机制仍有待阐明。在破骨细胞分化过程中,代谢过程向更氧化的方向转变。在这项研究中,我们确定了从头 DNA 甲基转移酶 3a(Dnmt3a)是一种转录因子,它将这些代谢变化与破骨细胞分化联系起来。我们还发现,核因子-κB 配体(RANKL)是破骨细胞生成的必需细胞因子,它诱导这种代谢向氧化代谢转变,伴随着 S-腺苷甲硫氨酸(SAM)产量的增加。我们发现,Dnmt3a 通过 SAM 介导的 DNA 甲基化通过表观遗传抑制抗破骨生成基因来调节破骨细胞生成。Dnmt3a 在骨稳态中的重要性体现在以下观察结果中:缺乏 Dnmt3a 的破骨细胞前体细胞不能有效地分化为破骨细胞,并且破骨细胞特异性缺乏 Dnmt3a 的小鼠由于破骨细胞数量减少而导致骨量增加。此外,茶黄素-3,3'-二没食子酸酯抑制 DNA 甲基化可阻断骨质疏松症模型中的骨质流失。因此,这项研究揭示了表观遗传过程在细胞代谢和分化调节中的作用,这可能为各种骨疾病的新治疗策略提供分子基础。