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寒冷暴露通过下调软骨中的载脂蛋白E促进骨关节炎的进展。

Cold exposure promotes the progression of osteoarthritis through downregulating APOE in cartilage.

作者信息

Zhang Yueqi, Fu Mei, Zhou Chun, Wang Xiao, Jiang Zengxin, Jiang Chang, Guo Shengyang, Pang Zhiying, Wang Chenzhong, Yu Tao, An Senbo, Wang Xiuhui, Wang Zhe

机构信息

Department of Traumatic Surgery, Shanghai East Hospital, School of Medicine, Tongji University, 200092, Shanghai, China.

Department of Emergency Medicine, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, 200127, Shanghai, China.

出版信息

EMBO Mol Med. 2025 Jul 15. doi: 10.1038/s44321-025-00268-6.

Abstract

Osteoarthritis (OA) is a degenerative joint disease with limited effective therapies. Cold weathers have been shown to affect joint pain in OA patients. However, the impact of cold climate on OA progression is debated, with the underlying mechanisms not fully understood. This study aims to elucidate the role of Apolipoprotein E (Apoe) in chondrocytes in relation to OA progression under cold exposure. Both human chondrocytes RNA sequencing and DMM mice OA model revealed that lower temperatures significantly downregulated Apoe expression, correlating with OA exacerbation. Conditional knockout of Apoe in cartilage aggravated cartilage degeneration, leading to lipid accumulation, increased ROS production, mitochondrial dysfunction, and elevated chondrocyte apoptosis. Treatment with RGX-104, an LXRβ agonist, reversely restored APOE expression, mitigated aberrant lipid accumulation and countered the detrimental effects of cold exposure on OA progression. These results suggest that targeting lipid transfer and metabolism, especially through Apoe modulation, may offer therapeutic strategies for OA patients residing in colder climates, such as those at high altitudes and latitudes, and even winter season.

摘要

骨关节炎(OA)是一种退行性关节疾病,有效治疗方法有限。已有研究表明,寒冷天气会影响OA患者的关节疼痛。然而,寒冷气候对OA进展的影响存在争议,其潜在机制尚未完全明确。本研究旨在阐明载脂蛋白E(Apoe)在寒冷暴露下软骨细胞中与OA进展相关的作用。人类软骨细胞RNA测序和DMM小鼠OA模型均显示,较低温度显著下调Apoe表达,这与OA病情加重相关。软骨中Apoe的条件性敲除加剧了软骨退变,导致脂质积累、活性氧生成增加、线粒体功能障碍以及软骨细胞凋亡增加。用LXRβ激动剂RGX-104治疗可逆转恢复APOE表达,减轻异常脂质积累,并对抗寒冷暴露对OA进展的有害影响。这些结果表明,针对脂质转运和代谢,尤其是通过调节Apoe,可能为居住在寒冷气候地区的OA患者提供治疗策略,例如高海拔和高纬度地区的患者,甚至在冬季。

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