Cheon Yoon-Hee, Kwak Sung Chul, Chung Chong Hyuk, Lee Chang Hoon, Lee Myeung Su, Kim Ju-Young
Musculoskeletal and Immune Disease Research Institute, School of Medicine, Wonkwang University, Iksan 54538, Republic of Korea.
Division of Rheumatology, Department of Internal Medicine, Wonkwang University Hospital, Iksan 54538, Republic of Korea.
Int J Mol Sci. 2025 Sep 4;26(17):8613. doi: 10.3390/ijms26178613.
Swiprosin-1 (SWS1/EFhd2) is a calcium-binding adaptor protein involved in cytoskeletal regulation, but its physiological role in bone homeostasis remains largely undefined. To elucidate its function in osteoclast biology, we examined SWS1 expression and activity during osteoclastogenesis using primary murine bone marrow-derived macrophages, siRNA-mediated knockdown, and SWS1 knockout (KO) mice. SWS1 was predominantly localized to the nucleus in precursor cells and redistributed to the F-actin ring in mature osteoclasts. Receptor activator of nuclear factor-kappa B ligand stimulation significantly downregulated SWS1 mRNA expression. Loss of SWS1 enhanced osteoclast formation, F-actin ring integrity, and bone resorption, accompanied by elevated expression of osteoclastogenic markers. In vivo, male SWS1 KO mice exhibited deteriorated trabecular bone microarchitecture with increased osteoclast numbers. Mechanistically, SWS1 deficiency intensified αvβ3 integrin-associated cytoskeletal signaling and upregulated Akt, MAPK, NF-κB, and PLCγ2 pathways. These results indicate that SWS1 negatively regulates osteoclast differentiation and function by restraining cytoskeletal reorganization and downstream signaling. Collectively, our findings establish SWS1 as a novel modulator of osteoclast activity and a potential therapeutic target for osteolytic bone disorders.
Swiprosin-1(SWS1/EFhd2)是一种参与细胞骨架调节的钙结合衔接蛋白,但其在骨稳态中的生理作用仍不清楚。为了阐明其在破骨细胞生物学中的功能,我们使用原代小鼠骨髓来源的巨噬细胞、小干扰RNA介导的敲低以及SWS1基因敲除(KO)小鼠,研究了破骨细胞生成过程中SWS1的表达和活性。SWS1主要定位于前体细胞的细胞核中,并在成熟破骨细胞中重新分布到F-肌动蛋白环。核因子κB受体激活剂配体刺激显著下调SWS1 mRNA表达。SWS1缺失增强了破骨细胞形成、F-肌动蛋白环完整性和骨吸收,并伴有破骨细胞生成标志物表达升高。在体内,雄性SWS1 KO小鼠的小梁骨微结构恶化,破骨细胞数量增加。机制上,SWS1缺乏增强了αvβ3整合素相关的细胞骨架信号,并上调了Akt、丝裂原活化蛋白激酶、核因子κB和磷脂酶Cγ2途径。这些结果表明,SWS1通过抑制细胞骨架重组和下游信号传导来负向调节破骨细胞分化和功能。总的来说,我们的研究结果确立了SWS1作为破骨细胞活性的新型调节剂以及溶骨性骨疾病潜在治疗靶点的地位。