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细胞衰老在骨关节炎中的意义:一项关于马关节滑液间充质基质细胞的研究。

Implication of Cellular Senescence in Osteoarthritis: A Study on Equine Synovial Fluid Mesenchymal Stromal Cells.

机构信息

Department of Biomedical and Neuromotor Sciences, University di Bologna, 40126 Bologna, Italy.

Boehringer Ingelheim Vetmedica GmbH, 55218 Ingelheim am Rhein, Germany.

出版信息

Int J Mol Sci. 2023 Feb 4;24(4):3109. doi: 10.3390/ijms24043109.

Abstract

Osteoarthritis (OA) is described as a chronic degenerative disease characterized by the loss of articular cartilage. Senescence is a natural cellular response to stressors. Beneficial in certain conditions, the accumulation of senescent cells has been implicated in the pathophysiology of many diseases associated with aging. Recently, it has been demonstrated that mesenchymal stem/stromal cells isolated from OA patients contain many senescent cells that inhibit cartilage regeneration. However, the link between cellular senescence in MSCs and OA progression is still debated. In this study, we aim to characterize and compare synovial fluid MSCs (sf-MSCs), isolated from OA joints, with healthy sf-MSCs, investigating the senescence hallmarks and how this state could affect cartilage repair. Sf-MSCs were isolated from tibiotarsal joints of healthy and diseased horses with an established diagnosis of OA with an age ranging from 8 to 14 years. Cells were cultured in vitro and characterized for cell proliferation assay, cell cycle analysis, ROS detection assay, ultrastructure analysis, and the expression of senescent markers. To evaluate the influence of senescence on chondrogenic differentiation, OA sf-MSCs were stimulated in vitro for up to 21 days with chondrogenic factors, and the expression of chondrogenic markers was compared with healthy sf-MSCs. Our findings demonstrated the presence of senescent sf-MSCs in OA joints with impaired chondrogenic differentiation abilities, which could have a potential influence on OA progression.

摘要

骨关节炎(OA)被描述为一种以关节软骨丧失为特征的慢性退行性疾病。衰老(senescence)是细胞对压力源的自然反应。在某些情况下有益的衰老细胞的积累与许多与衰老相关的疾病的病理生理学有关。最近,已经证明从 OA 患者中分离的间充质干细胞/基质细胞(MSCs)含有许多抑制软骨再生的衰老细胞。然而,MSCs 中的细胞衰老与 OA 进展之间的联系仍存在争议。在这项研究中,我们旨在表征和比较从 OA 关节中分离的滑液间充质干细胞(sf-MSCs)与健康的 sf-MSCs,研究衰老的特征以及这种状态如何影响软骨修复。sf-MSCs 从患有 OA 且年龄在 8 至 14 岁之间的健康和患病马的胫跗关节中分离出来。将细胞在体外培养并进行细胞增殖测定、细胞周期分析、ROS 检测分析、超微结构分析和衰老标志物的表达分析。为了评估衰老对软骨分化的影响,将 OA sf-MSCs 用软骨形成因子体外刺激长达 21 天,并与健康 sf-MSCs 比较软骨形成标志物的表达。我们的研究结果表明 OA 关节中存在衰老的 sf-MSCs,其软骨分化能力受损,这可能对 OA 的进展有潜在影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/911c/9967174/8e00bdd472a7/ijms-24-03109-g001.jpg

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