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      Cellular senescence in knee osteoarthritis: molecular mechanisms and therapeutic implications.

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          Abstract

          Cellular senescence is the inability of cells to proliferate, which has both beneficial and detrimental effects on tissue development and homeostasis. Chronic accumulation of senescent cells is associated with age-related disease, including osteoarthritis, a common joint disease responsible for joint pain and disability in older adults. The pathology of this disease includes loss of cartilage, synovium inflammation, and subchondral bone remodeling. Senescent cells are present in the cartilage of people with advanced osteoarthritis, but the link between cellular senescence and this disease is unclear. In this review, we summarize current evidence for the role of cellular senescence of different cell types in the onset and progression of osteoarthritis. We focus on the underlying mechanisms of senescence in chondrocytes, which maintain the cartilage in joints, and review the role of the Forkhead family of transcription factors, which are involved in cartilage maintenance and osteoarthritis. Finally, we discuss the potential therapeutic value and implications of targeting senescent cells using senolytic agents or immune therapies, targeting the senescence-associated secretory phenotype of these cells using senomorphic agents, and renewing the plasticity of stem cells and chondrocytes. Our review highlights current gaps in understanding of the mechanism of senescence that may, when addressed, provided new options for modifying and treating disease in osteoarthritis.

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          Author and article information

          Journal
          Ageing Res Rev
          Ageing research reviews
          Elsevier BV
          1872-9649
          1568-1637
          September 2021
          : 70
          Affiliations
          [1 ] Department of Orthopaedic Surgery, National Clinical Research Center for Geriatrics, West China Hospital of Sichuan University, Chengdu, Sichuan Province, China; Laboratory of Endocrinology and Metabolism, Department of Department of Endocrinology and Metabolism, West China Hospital of Sichuan University, Chengdu, Sichuan Province, China.
          [2 ] Core Facility of West China Hospital, Sichuan University, Chengdu, Sichuan Province, China.
          [3 ] Department of Integrated Traditional Chinese and Western Medicine, West China Hospital of Sichuan University, Chengdu, Sichuan Province, China; Laboratory of Endocrinology and Metabolism, Department of Department of Endocrinology and Metabolism, West China Hospital of Sichuan University, Chengdu, Sichuan Province, China.
          [4 ] Laboratory of Endocrinology and Metabolism, Department of Department of Endocrinology and Metabolism, West China Hospital of Sichuan University, Chengdu, Sichuan Province, China.
          [5 ] Laboratory of Endocrinology and Metabolism, Department of Department of Endocrinology and Metabolism, West China Hospital of Sichuan University, Chengdu, Sichuan Province, China. Electronic address: xijieyu@hotmail.com.
          [6 ] Department of Orthopaedic Surgery, National Clinical Research Center for Geriatrics, West China Hospital of Sichuan University, Chengdu, Sichuan Province, China. Electronic address: peifuxinghuaxi@126.com.
          Article
          S1568-1637(21)00160-4
          10.1016/j.arr.2021.101413
          34298194
          16e73167-7d73-4197-aa42-75d418a7e331
          History

          Cellular senescence,Chondrocyte,Osteoarthritis,Senescence associated secretory phenotype

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