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巨噬细胞在肾脏疾病中的致病和保护作用。

Pathogenic and protective role of macrophages in kidney disease.

机构信息

Centre for Transplantation and Renal Research, Westmead Millennium Institute, University of Sydney, Darcy Rd., Westmead, Sydney, NSW, Australia.

出版信息

Am J Physiol Renal Physiol. 2013 Jul 1;305(1):F3-11. doi: 10.1152/ajprenal.00122.2013. Epub 2013 May 1.

DOI:10.1152/ajprenal.00122.2013
PMID:23637206
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3725671/
Abstract

Macrophages (MΦ) are located throughout kidney tissue, where they play important roles in homeostasis, surveillance, tolerance, and cytoprotection. MΦ are highly heterogeneous cells and exhibit distinct phenotypic and functional characteristics depending on their microenvironment and the disease type and stage. Recent studies have identified a dual role for MΦ in several murine models of kidney disease. In this review, we discuss the pathogenic and protective roles of the various MΦ subsets in experimental and human kidney diseases and summarize current progress toward the therapeutic use of MΦ in kidney diseases.

摘要

巨噬细胞(MΦ)分布于肾脏组织的各个部位,在维持内环境稳定、免疫监视、免疫耐受和细胞保护方面发挥着重要作用。MΦ是高度异质性的细胞,其表型和功能特征取决于其微环境以及疾病的类型和阶段。最近的研究在几种小鼠肾脏疾病模型中发现了 MΦ的双重作用。在这篇综述中,我们讨论了各种 MΦ亚群在实验性和人类肾脏疾病中的致病和保护作用,并总结了目前在肾脏疾病中利用 MΦ进行治疗的研究进展。

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本文引用的文献

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J Clin Invest. 2012 Dec;122(12):4519-32. doi: 10.1172/JCI60363. Epub 2012 Nov 12.
2
Interleukin-18 binding protein therapy is protective in adriamycin nephropathy.白细胞介素-18 结合蛋白治疗对阿霉素肾病具有保护作用。
Am J Physiol Renal Physiol. 2013 Jan 1;304(1):F68-76. doi: 10.1152/ajprenal.00669.2011. Epub 2012 Oct 24.
3
Inflammation in diabetic nephropathy.糖尿病肾病中的炎症。
Mediators Inflamm. 2012;2012:146154. doi: 10.1155/2012/146154. Epub 2012 Aug 21.
4
Translating tolerogenic therapies to the clinic - where do we stand?将耐受原性疗法转化为临床应用——我们处于什么阶段?
Front Immunol. 2012 Aug 20;3:254. doi: 10.3389/fimmu.2012.00254. eCollection 2012.
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The interferon signature and STAT1 expression in rheumatoid arthritis synovial fluid macrophages are induced by tumor necrosis factor α and counter-regulated by the synovial fluid microenvironment.类风湿性关节炎滑液巨噬细胞中的干扰素特征和信号转导及转录激活因子1(STAT1)表达由肿瘤坏死因子α诱导,并受滑液微环境的反向调节。
Arthritis Rheum. 2012 Oct;64(10):3119-28. doi: 10.1002/art.34544.
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Notch-RBP-J signaling regulates the transcription factor IRF8 to promote inflammatory macrophage polarization.Notch-RBP-J 信号通路调控转录因子 IRF8 促进炎性巨噬细胞极化。
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