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程序性死亡配体 2 缺乏加剧了小鼠实验性自身免疫性心肌炎。

Programmed Death-Ligand 2 Deficiency Exacerbates Experimental Autoimmune Myocarditis in Mice.

机构信息

Department of Cardiology, Faculty of Medicine, University of Tsukuba, Tsukuba 305-8575, Japan.

Department of Pathogenobioligy, College of Basic Medical Sciences, Jilin University, Changchun 130012, China.

出版信息

Int J Mol Sci. 2021 Jan 31;22(3):1426. doi: 10.3390/ijms22031426.

Abstract

Programmed death ligand 2 (PD-L2) is the second ligand of programmed death 1 (PD-1) protein. In autoimmune myocarditis, the protective roles of PD-1 and its first ligand programmed death ligand 1 (PD-L1) have been well documented; however, the role of PD-L2 remains unknown. In this study, we report that PD-L2 deficiency exacerbates myocardial inflammation in mice with experimental autoimmune myocarditis (EAM). EAM was established in wild-type (WT) and PD-L2-deficient mice by immunization with murine cardiac myosin peptide. We found that PD-L2-deficient mice had more serious inflammatory infiltration in the heart and a significantly higher myocarditis severity score than WT mice. PD-L2-deficient dendritic cells (DCs) enhanced CD4 T cell proliferation in the presence of T cell receptor and CD28 signaling. These data suggest that PD-L2 on DCs protects against autoreactive CD4 T cell expansion and severe inflammation in mice with EAM.

摘要

程序性死亡配体 2(PD-L2)是程序性死亡 1(PD-1)蛋白的第二个配体。在自身免疫性心肌炎中,PD-1 及其第一个配体程序性死亡配体 1(PD-L1)的保护作用已得到充分证实;然而,PD-L2 的作用尚不清楚。在这项研究中,我们报告 PD-L2 缺乏会加剧实验性自身免疫性心肌炎(EAM)小鼠的心肌炎症。通过用鼠心肌肽免疫,在野生型(WT)和 PD-L2 缺陷型小鼠中建立 EAM。我们发现 PD-L2 缺陷型小鼠心脏的炎症浸润更严重,心肌炎严重程度评分明显高于 WT 小鼠。PD-L2 缺陷型树突状细胞(DCs)在 T 细胞受体和 CD28 信号存在的情况下增强 CD4 T 细胞的增殖。这些数据表明,DC 上的 PD-L2 可防止 EAM 小鼠自身反应性 CD4 T 细胞的扩增和严重炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1c6/7866985/fdb06e8b6661/ijms-22-01426-g001.jpg

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