Macrophages, Dendritic Cells, and Kidney Ischemia-Reperfusion Injury

被引:181
作者
Li, Li
Okusa, Mark D.
机构
[1] Univ Virginia, Dept Med, Charlottesville, VA USA
[2] Univ Virginia, Ctr Immun Inflammat & Regenerat Med, Charlottesville, VA USA
基金
美国国家卫生研究院;
关键词
Antigen presentation; leukocyte; innate immunity; inflammation; ACUTE-RENAL-FAILURE; SKEWS MONOCYTE DIFFERENTIATION; IMMUNE-RESPONSE; ISCHEMIA/REPERFUSION INJURY; INNATE; RECEPTORS; DANGER; MICE; INFLAMMASOME; PATHOGENESIS;
D O I
10.1016/j.semnephrol.2010.03.005
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Dendritic cells and macrophages are critical early initiators of innate immunity in the kidney and orchestrate inflammation subsequent to ischemia-reperfusion injury. They are the most abundant leukocytes present in the kidney, and they represent a heterogeneous population of cells that are capable of inducing sterile inflammation after reperfusion directly through the production of proinflammatory cytokines and other soluble inflammatory mediators or indirectly through activation of effector T lymphocytes and natural killer T cells. In addition, recent studies have indicated that kidney and immune cell micro-RNAs control gene expression and have the ability to regulate the initial inflammatory response to injury. Although dendritic cells and macrophages contribute to both innate and adaptive immunity and to injury and repair, this review focuses on the initial innate response to kidney ischemia-reperfusion injury. © 2010 Elsevier Inc.
引用
收藏
页码:268 / 277
页数:10
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