Department of Orthopaedics, First Affiliated Hospital of Soochow University, Suzhou, 215006, Jiangsu, China.
Department of Orthopedics, Hai'an People's Hospital, Hai'an, 226600, Jiangsu, China.
Cell Death Dis. 2024 Aug 27;15(8):624. doi: 10.1038/s41419-024-07018-5.
Osteoporosis (OP) is a disorder of bone remodeling caused by an imbalance between bone resorption by osteoclasts and bone formation by osteoblasts. Therefore, inhibiting excessive osteoclast activity is one of the promising strategies for treating OP. A major transient receptor potential cation channel, known as transient receptor potential ankyrin 1 (TRPA1), was found to alleviate joint pain and cartilage degeneration in osteoarthritis. However, little research has focused on TRPA1 function in OP. As a result, this study aimed to explore the TRPA1 characteristics and its potential therapeutic function during osteoclastogenesis. The TRPA1 expression gradually increased in the osteoclast differentiation process; however, its suppression with small interfering RNA and an inhibitor (HC030031) significantly controlled the osteoclast count and the expression of osteoclast characteristic genes. Its suppression also inhibited endoplasmic reticulum (ER) stress-related pancreatic ER kinase (PERK) pathways. An ER stress inhibitor (thapsigargin) reversed the down-regulated levels of ER stress and osteoclast differentiation by suppressing TRPA1. Transcriptome sequencing results demonstrated that TRPA1 negatively regulated reactive oxygen species (ROS) and significantly increased the expression of an antioxidant gene, SRXN1. The osteoclast differentiation and the levels of ER stress were enhanced with SRXN1 inhibition. Finally, TRPA1 knockdown targeting macrophages by adeno-associated virus-9 could relieve osteoclast differentiation and osteopenia in ovariectomized mice. In summary, silencing TRPA1 restrained osteoclast differentiation through ROS-mediated down-regulation of ER stress via inhibiting PERK pathways. The study also indicated that TRPA1 might become a prospective treatment target for OP.
骨质疏松症(OP)是一种由破骨细胞骨吸收和成骨细胞骨形成之间失衡引起的骨重塑疾病。因此,抑制破骨细胞活性过度是治疗 OP 的一种有前途的策略。瞬时受体电位阳离子通道(TRP)家族中的一个主要成员,即瞬时受体电位锚蛋白 1(TRPA1),被发现可缓解骨关节炎中的关节疼痛和软骨退化。然而,关于 TRPA1 在 OP 中的功能研究甚少。因此,本研究旨在探讨 TRPA1 在破骨细胞分化过程中的特征及其在破骨细胞生成中的潜在治疗作用。TRPA1 的表达在破骨细胞分化过程中逐渐增加;然而,用小干扰 RNA 和抑制剂(HC030031)抑制其表达可显著控制破骨细胞计数和破骨细胞特征基因的表达。其抑制作用还抑制了内质网(ER)应激相关的胰腺 ER 激酶(PERK)途径。ER 应激抑制剂(他普西龙)通过抑制 TRPA1 逆转了 ER 应激和破骨细胞分化的下调水平。转录组测序结果表明,TRPA1 负调控活性氧(ROS),并显著增加抗氧化基因 SRXN1 的表达。SRXN1 抑制可增强破骨细胞分化和 ER 应激水平。最后,腺相关病毒-9 靶向巨噬细胞的 TRPA1 敲低可减轻去卵巢小鼠的破骨细胞分化和骨质疏松症。总之,沉默 TRPA1 通过抑制 PERK 途径下调 ROS 介导的 ER 应激来抑制破骨细胞分化。该研究还表明,TRPA1 可能成为 OP 的一种有前景的治疗靶点。