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压力下的心脏:纤维化重塑中的免疫细胞

The heart under pressure: immune cells in fibrotic remodeling.

作者信息

Theall Brandon, Alcaide Pilar

机构信息

Department of Immunology, Tufts University School of Medicine, Boston, MA.

Immunology Program, Graduate School of Biomedical Sciences, Tufts University School of Medicine, Boston, MA.

出版信息

Curr Opin Physiol. 2022 Feb;25. doi: 10.1016/j.cophys.2022.100484. Epub 2022 Jan 22.

DOI:10.1016/j.cophys.2022.100484
PMID:35224321
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8881013/
Abstract

The complex syndrome of heart failure (HF) is characterized by increased left ventricular pressures. Cardiomyocytes increase in size, cardiac fibroblasts transform and make extracellular matrix, and leukocytes infiltrate the cardiac tissue and alter cardiomyocyte and cardiac fibroblast function. Here we review recent advances in our understanding of the cellular composition of the heart during homeostasis and in response to cardiac pressure overload, with an emphasis on immune cell communication with cardiac fibroblasts and its consequences in cardiac remodeling.

摘要

心力衰竭(HF)这一复杂综合征的特征是左心室压力升高。心肌细胞体积增大,心脏成纤维细胞发生转化并生成细胞外基质,白细胞浸润心脏组织并改变心肌细胞和心脏成纤维细胞的功能。在此,我们综述了在稳态及心脏压力过载情况下,我们对心脏细胞组成理解的最新进展,重点关注免疫细胞与心脏成纤维细胞的通讯及其在心脏重塑中的后果。

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The heart under pressure: immune cells in fibrotic remodeling.压力下的心脏:纤维化重塑中的免疫细胞
Curr Opin Physiol. 2022 Feb;25. doi: 10.1016/j.cophys.2022.100484. Epub 2022 Jan 22.
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J Mol Cell Cardiol. 2016 Dec;101:145-155. doi: 10.1016/j.yjmcc.2016.10.011. Epub 2016 Oct 24.
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本文引用的文献

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NF-κB activation in cardiac fibroblasts results in the recruitment of inflammatory Ly6C monocytes in pressure-overloaded hearts.心肌成纤维细胞中 NF-κB 的激活导致在压力超负荷心脏中募集炎症性 Ly6C 单核细胞。
Sci Signal. 2021 Oct 12;14(704):eabe4932. doi: 10.1126/scisignal.abe4932.
2
Cardiac macrophage subsets differentially regulate lymphatic network remodeling during pressure overload.心脏巨噬细胞亚群在压力超负荷时差异调节淋巴管网络重塑。
Sci Rep. 2021 Aug 19;11(1):16801. doi: 10.1038/s41598-021-95723-y.
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Innate Immune Cells in Pressure Overload-Induced Cardiac Hypertrophy and Remodeling.
T 细胞 MyD88 是通过调节 T 细胞激活来调控心脏纤维化的新型调节剂。
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Subtyping based on immune cell fractions reveal heterogeneity of cardiac fibrosis in end-stage heart failure.基于免疫细胞亚群的分型揭示了终末期心力衰竭中心脏纤维化的异质性。
Front Immunol. 2023 Feb 15;14:1053793. doi: 10.3389/fimmu.2023.1053793. eCollection 2023.
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Emerging epigenetic therapies of cardiac fibrosis and remodelling in heart failure: from basic mechanisms to early clinical development.心力衰竭中心脏纤维化和重构的新兴表观遗传学治疗方法:从基础机制到早期临床开发。
Cardiovasc Res. 2023 Feb 3;118(18):3482-3498. doi: 10.1093/cvr/cvac142.
压力超负荷诱导的心脏肥大和重塑中的固有免疫细胞
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Front Cell Dev Biol. 2021 Apr 9;9:583492. doi: 10.3389/fcell.2021.583492. eCollection 2021.
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