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非受体型2蛋白酪氨酸磷酸酶作为动脉粥样硬化疾病的治疗靶点:过去、现在与未来

Protein tyrosine phosphatase non-receptor type 2 as the therapeutic target of atherosclerotic diseases: past, present and future.

作者信息

Tang Xiao-Er, Cheng Ya-Qiong, Tang Chao-Ke

机构信息

Department of Pathophysiology, Shaoyang University, Shaoyang, Hunan, China.

Institute of Cardiovascular Research, Key Laboratory for Atherosclerology of Hunan Province, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, University of South China, Hengyang, Hunan, China.

出版信息

Front Pharmacol. 2023 Aug 21;14:1219690. doi: 10.3389/fphar.2023.1219690. eCollection 2023.

Abstract

Tyrosine-protein phosphatase non-receptor type 2(PTPN2), an important member of the protein tyrosine phosphatase family, can regulate various signaling pathways and biological processes by dephosphorylating receptor protein tyrosine kinases. Accumulating evidence has demonstrated that PTPN2 is involved in the occurrence and development of atherosclerotic cardiovascular disease. Recently, it has been reported that PTPN2 exerts an anti-atherosclerotic effect by regulating vascular endothelial injury, monocyte proliferation and migration, macrophage polarization, T cell polarization, autophagy, pyroptosis, and insulin resistance. In this review, we summarize the latest findings on the role of PTPN2 in the pathogenesis of atherosclerosis to provide a rationale for better future research and therapeutic interventions.

摘要

非受体型2酪氨酸蛋白磷酸酶(PTPN2)是蛋白酪氨酸磷酸酶家族的重要成员,可通过使受体蛋白酪氨酸激酶去磷酸化来调节各种信号通路和生物学过程。越来越多的证据表明,PTPN2参与动脉粥样硬化性心血管疾病的发生和发展。最近,有报道称PTPN2通过调节血管内皮损伤、单核细胞增殖和迁移、巨噬细胞极化、T细胞极化、自噬、焦亡和胰岛素抵抗发挥抗动脉粥样硬化作用。在本综述中,我们总结了PTPN2在动脉粥样硬化发病机制中作用的最新发现,为未来更好的研究和治疗干预提供理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ced/10475599/efef43e3db26/fphar-14-1219690-g001.jpg

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