Cellular senescence in osteoarthritis and anti-aging strategies

被引:44
作者
Hou, Angyang [1 ,2 ]
Chen, Peng [1 ]
Tang, He [1 ]
Meng, Haoye [1 ]
Cheng, Xiaoqing [1 ]
Wang, Yu [1 ]
Zhang, Yuming [2 ]
Peng, Jiang [1 ]
机构
[1] Gen Hosp Chinese PLA, Beijing Key Lab Regenerat Med Orthoped, Orthoped Res Inst Chinese PLA, Fuxing Rd 28, Beijing 100853, Peoples R China
[2] Shanxi Med Univ, Shanxi Prov Peoples Hosp, Taiyuan 030012, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Cellular senescence; Treatment; Osteoarthritis; Aging; Chondrocytes; MESENCHYMAL STEM-CELLS; LIFE-SPAN; CHONDROCYTE SENESCENCE; OXIDATIVE STRESS; PATHOGENESIS; RESVERATROL; CLEARANCE; APOPTOSIS; MATRIX; SIRT1;
D O I
10.1016/j.mad.2018.08.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In older adults, the prevalence of osteoarthritis (OA) increases directly with age and is the most common cause of chronic disability. It is necessary to recognize that OA is a degenerative disease that strongly correlates with age, and often promotes elevated levels of cartilage injury. Chondrocytes undergo an age-dependent decline in proliferative and synthetic capacity. It is thought that cellular senescence may play a significant role in the pathology of OA, with chondrocytes exhibiting a variety of senescence-associated phenotypes. In this review, we discuss cellular senescence and its relationship with OA. More importantly, we introduce novel strategies for the modulation of cellular senescence, including the use of sirtuin 6, mammalian target of rapamycin, N-acetyl-Lcysteine, proteoglycan-4 and senolytic, which may help to delay senescence and improve cartilage regeneration in the aging population.
引用
收藏
页码:83 / 87
页数:5
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