HMGB1: a potential new target for tendinopathy treatment

被引:1
|
作者
Lu, Panpan [1 ,2 ,3 ,4 ]
Li, Yingjuan [2 ,5 ]
Dai, Guangchun [1 ,2 ,3 ,4 ]
Zhang, Yuanwei [1 ,2 ,3 ,4 ]
Shi, Liu [1 ,2 ,3 ,4 ]
Zhang, Ming [1 ,2 ,3 ,4 ]
Wang, Hao [1 ,2 ,3 ,4 ]
Rui, Yunfeng [1 ,2 ,3 ,4 ,6 ]
机构
[1] Southeast Univ, Zhongda Hosp, Dept Orthopaed, Nanjing, Peoples R China
[2] Southeast Univ, Sch Med, Nanjing, Peoples R China
[3] Southeast Univ, Orthopaed Trauma Inst OTI, Nanjing, Peoples R China
[4] Southeast Univ, Zhongda Hosp, Trauma Ctr, Nanjing, Peoples R China
[5] Southeast Univ, Zhongda Hosp, Dept Geriatr, Nanjing, Peoples R China
[6] Southeast Univ, Zhongda Hosp, Dept Orthopaed, 87 Ding Jia Qiao, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
HMGB1; tendinopathy; mechanism; therapeutic; tendon stem; progenitor cell; GROUP BOX 1; NUCLEAR-PROTEIN HMGB1; EXTRACELLULAR HMGB1; STEM-CELLS; TENDON; AUTOPHAGY; RECEPTOR; DIFFERENTIATION; IDENTIFICATION; INFLAMMATION;
D O I
10.1080/03008207.2023.2199089
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tendinopathy describes a complex pathology of the tendon characterized by abnormalities in the microstructure, composition, and cellularity of the tendon, leading to pain, limitation of activity and reduced function. Nevertheless, the mechanism of tendinopathy has not been fully elucidated, and the treatment of tendinopathy remains a challenge. High mobility group box 1 (HMGB1), a highly conserved and multifaceted nuclear protein, exerts multiple roles and high functional variability and is involved in many biological and pathological processes. In recent years, several studies have suggested that HMGB1 is associated with tendinopathy and may play a key role in the pathogenesis of tendinopathy. Therefore, this review summarizes the expression and distribution of HMGB1 in tendinopathy, focuses on the roles of HMGB1 and HMGB1-based potential mechanisms involved in tendinopathy, and finally summarizes the findings on HMGB1-based therapeutic approaches in tendinopathy, probably providing new insight into the mechanism and further potential therapeutic targets of tendinopathy.
引用
收藏
页码:362 / 375
页数:14
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