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Paracrine effects of human adipose-derived mesenchymal stem cells in inflammatory stress-induced senescence features of osteoarthritic chondrocytes

机译:人脂肪来源的间充质干细胞的旁分泌作用在炎性应激诱导的骨关节炎软骨细胞衰老特征中的作用

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摘要

Aging and exposure to stress would determine the chondrocyte phenotype in osteoarthritis (OA). In particular, chronic inflammation may contribute to stress-induced senescence of chondrocytes and cartilage degeneration during OA progression. Recent studies have shown that adipose-derived mesenchymal stem cells exert paracrine effects protecting against degenerative changes in chondrocytes. We have investigated whether the conditioned medium (CM) from adipose-derived mesenchymal stem cells may regulate senescence features induced by inflammatory stress in OA chondrocytes. Our results indicate that CM down-regulated senescence markers induced by interleukin-1β including senescence-associated β-galactosidase activity, accumulation of γH2AX foci and morphological changes with enhanced formation of actin stress fibers. Treatment of chondrocytes with CM also decreased the production of oxidative stress, the activation of mitogen-activated protein kinases, and the expression of caveolin-1 and p21. The effects of CM were related to the reduction in p53 acetylation which would be dependent on the enhancement of Sirtuin 1 expression. Therefore, CM may exert protective effects in degenerative joint conditions by countering the premature senescence of OA chondrocytes induced by inflammatory stress.
机译:衰老和暴露于压力下将决定骨关节炎(OA)中的软骨细胞表型。尤其是,慢性炎症可能会导致在OA进展期间应激诱导的软骨细胞衰老和软骨变性。最近的研究表明,脂肪来源的间充质干细胞发挥旁分泌作用,防止软骨细胞的变性变化。我们已经研究了来自脂肪间充质干细胞的条件培养基(CM)是否可以调节OA软骨细胞中炎性应激诱导的衰老特征。我们的结果表明,白介素-1β诱导的CM下调了衰老标记,包括衰老相关的β-半乳糖苷酶活性,γH2AX聚集和形态变化,肌动蛋白应激纤维形成增强。 CM处理软骨细胞还可以降低氧化应激的产生,促分裂原激活的蛋白激酶的激活以及Caveolin-1和p21的表达。 CM的作用与p53乙酰化的降低有关,这取决于Sirtuin 1表达的增强。因此,CM可通过抵抗炎症应激诱导的OA软骨细胞的过早衰老,在退行性关节疾病中发挥保护作用。

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