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代谢性炎症相关骨关节炎中的嘌呤能系统信号传导

Purinergic System Signaling in Metainflammation-Associated Osteoarthritis.

作者信息

Gratal Paula, Lamuedra Ana, Medina Juan Pablo, Bermejo-Álvarez Ismael, Largo Raquel, Herrero-Beaumont Gabriel, Mediero Aránzazu

机构信息

Bone and Joint Research Unit, IIS-Fundación Jiménez Díaz UAM, Madrid, Spain.

出版信息

Front Med (Lausanne). 2020 Aug 28;7:506. doi: 10.3389/fmed.2020.00506. eCollection 2020.

Abstract

Inflammation triggered by metabolic imbalance, also called metainflammation, is low-grade inflammation caused by the components involved in metabolic syndrome (MetS), including central obesity and impaired glucose tolerance. This phenomenon is mainly due to excess nutrients and energy, and it contributes to the pathogenesis of osteoarthritis (OA). OA is characterized by the progressive degeneration of articular cartilage, which suffers erosion and progressively becomes thinner. Purinergic signaling is involved in several physiological and pathological processes, such as cell proliferation in development and tissue regeneration, neurotransmission and inflammation. Adenosine and ATP receptors, and other members of the signaling pathway, such as AMP-activated protein kinase (AMPK), are involved in obesity, type 2 diabetes (T2D) and OA progression. In this review, we focus on purinergic regulation in osteoarthritic cartilage and how different components of MetS, such as obesity and T2D, modulate the purinergic system in OA. In that regard, we describe the critical role in this disease of receptors, such as adenosine A2A receptor (A2AR) and ATP P2X7 receptor. Finally, we also assess how nucleotides regulate the inflammasome in OA.

摘要

由代谢失衡引发的炎症,也称为代谢性炎症,是一种由代谢综合征(MetS)相关成分引起的低度炎症,这些成分包括中心性肥胖和糖耐量受损。这种现象主要归因于营养物质和能量过剩,并且它促进骨关节炎(OA)的发病机制。OA的特征是关节软骨进行性退变,软骨遭受侵蚀并逐渐变薄。嘌呤能信号传导参与多种生理和病理过程,如发育过程中的细胞增殖、组织再生、神经传递和炎症。腺苷和ATP受体以及信号通路的其他成员,如AMP活化蛋白激酶(AMPK),参与肥胖、2型糖尿病(T2D)和OA的进展。在本综述中,我们聚焦于骨关节炎软骨中的嘌呤能调节以及MetS的不同成分,如肥胖和T2D,如何在OA中调节嘌呤能系统。在这方面,我们描述了诸如腺苷A2A受体(A2AR)和ATP P2X7受体等受体在该疾病中的关键作用。最后,我们还评估了核苷酸如何调节OA中的炎性小体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a73a/7485330/99986aed49e7/fmed-07-00506-g0001.jpg

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