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Pyroptosis Plays a Role in Osteoarthritis

机译:抛火剂在骨关节炎中起着作用

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摘要

Recent studies have revealed novel forms of cell death beyond the canonical types of cellular apoptosis and necrosis, and these novel forms of cell death are induced by extreme microenvironmental factors. Pyroptosis, a type of regulated cell death, occurs when pattern recognition receptors (PRRs) induce the activation of cysteine-aspartic protease 1 (caspase-1) or caspase-11, which can trigger the release of the pyrogenic cytokines interleukin-1β (IL-1β) and IL-18. Osteoarthritis (OA), the most common joint disease worldwide, is characterized by low-grade inflammation and increased levels of cytokines, including IL-1β and IL-18. Additionally, some damaged chondrocytes associated with OA exhibit morphological changes consistent with pyroptosis, suggesting that this form of regulated cell death may contribute significantly to the pathology of OA. This review summarizes the molecular mechanisms of pyroptosis and shows the critical role of NLRP3 (NLR family, pyrin domain containing 3; NLR refers to “nucleotide-binding domain, leucine-rich repeat”) inflammasomes. We also provide evidence describing potential role of pyroptosis in OA, including the relationship with OA risk factors and the contribution to cartilage degradation, synovitis and OA pain.
机译:最近的研究揭示了多种细胞凋亡和坏死的细胞死亡形式的细胞死亡,并且这些新颖的细胞死亡形式被极端微环境诱导。当图案识别受体(PRRS)诱导半胱氨酸 - 天冬氨酸蛋白酶1(Caspase-1)或Caspase-11的激活时,发生糊菌,其受调节细胞死亡发生,其可以引发释放热源细胞因子白细胞介素-1β(IL -1β)和IL-18。骨关节炎(OA)是全球最常见的联合疾病,其特征在于低级炎症和增加的细胞因子,包括IL-1β和IL-18。此外,与OA相关的一些受损的软骨细胞表现出与釜凋亡一致的形态变化,表明这种形式的监管细胞死亡可能会对OA的病理有显着贡献。本综述总结了糊化酶的分子机制,显示了NLRP3(NLR家族,含有3; NLR的NLR系列,吡林结构域的吡啶结构域是指“核苷酸结合结构域,富含亮氨酸的重复”)炎症的关键作用。我们还提供了描述γ凋亡在OA的潜在作用的证据,包括与OA风险因素的关系以及对软骨降解,滑膜炎和OA疼痛的贡献。

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