Zhu Kecheng, Sheng Chunxiang, Zhang Linlin, Yang Yuying, Chen Xiaojing, Jiang Tao, Song Jiaxi, Zhang Deng, Wang Xiao, Zhao Hongyan, Sun Lihao, Zhou Libin, Tao Bei, Liu Jianmin
Department of Endocrine and Metabolic Diseases, Shanghai Institute of Endocrine and Metabolic Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin Road II, Shanghai, 200025, China.
Shanghai National Clinical Research Center for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission of the PR China, Shanghai Key Laboratory for Endocrine Tumor, State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Cell Commun Signal. 2025 Jan 14;23(1):26. doi: 10.1186/s12964-024-02021-x.
Receptor activator of nuclear factor kappa-B ligand (RANKL) initiates a complex signaling cascade that is crucial for inducing osteoclast differentiation and activation. RANKL-induced signaling has been analyzed in detail, and the involvement of TNF receptor-associated factor 6 (TRAF6), calmodulin-dependent protein kinase (CaMK), NF-κB, mitogen-activated protein kinase (MAPK), activator protein-1 (AP-1), and molecules that contain an immunoreceptor tyrosine-based activation motif (ITAM) has been reported. However, the precise molecular steps that regulate RANKL signaling remain largely unknown. Here, we revealed the indispensable role of a class III histone deacetylase (SIRT5) in the processes of RANKL-induced osteoclast differentiation and activation. SIRT5 expression in osteoclasts was increased during osteoclastogenesis upon stimulation with RANKL. The RANKL-induced signaling activation was suppressed in SIRT5-deficient osteoclasts but enhanced by SIRT5 overexpression. Mice with global or conditional monocytic lineage knockout of SIRT5 had increased bone mass and reduced osteoclast numbers. In the cytoplasm, SIRT5 interacted with the scaffold protein JNK-interacting protein 4 (JIP4) to finely regulate MAPK signaling, which was critical for osteoclast differentiation and activation. Pharmacological inhibition of the catalytic activity of SIRT5 effectively reversed bone loss in ovariectomized mice. Taken together, the results of this study reveal that the SIRT5-JIP4 axis is a novel positive regulator that finely regulates RANKL-induced osteoclast differentiation and suggest that targeting this axis is a therapeutic strategy for preventing osteoporotic bone loss.
核因子κB受体激活剂配体(RANKL)启动了一个复杂的信号级联反应,这对于诱导破骨细胞分化和激活至关重要。RANKL诱导的信号传导已得到详细分析,并且已报道肿瘤坏死因子受体相关因子6(TRAF6)、钙调蛋白依赖性蛋白激酶(CaMK)、核因子κB(NF-κB)、丝裂原活化蛋白激酶(MAPK)、活化蛋白-1(AP-1)以及含有基于免疫受体酪氨酸的激活基序(ITAM)的分子参与其中。然而,调节RANKL信号传导的精确分子步骤在很大程度上仍然未知。在这里,我们揭示了III类组蛋白去乙酰化酶(SIRT5)在RANKL诱导的破骨细胞分化和激活过程中的不可或缺的作用。在用RANKL刺激的破骨细胞生成过程中,破骨细胞中的SIRT5表达增加。在SIRT5缺陷的破骨细胞中,RANKL诱导的信号激活受到抑制,但通过SIRT5过表达而增强。全身性或条件性单核细胞谱系敲除SIRT5的小鼠骨量增加,破骨细胞数量减少。在细胞质中,SIRT5与支架蛋白JNK相互作用蛋白4(JIP4)相互作用,以精细调节MAPK信号传导,这对破骨细胞分化和激活至关重要。对SIRT5催化活性的药理学抑制有效逆转了去卵巢小鼠的骨质流失。综上所述,本研究结果表明,SIRT5-JIP4轴是一种新型的正调节因子,可精细调节RANKL诱导的破骨细胞分化,并表明靶向该轴是预防骨质疏松性骨质流失的治疗策略。