Exosomes: An emerging factor in stress-induced immunomodulation

被引:119
作者
Beninson, Lida A. [1 ]
Fleshner, Monika [1 ]
机构
[1] Univ Colorado, Dept Integrat Physiol, Boulder, CO 80309 USA
基金
美国国家科学基金会;
关键词
Exosomes; Stress; Innate immunity; Hsp72; microRNA; HEAT-SHOCK PROTEINS; EXTRACELLULAR HSP72; DENDRITIC CELLS; RETICULOCYTE MATURATION; MOLECULAR CHAPERONES; DIAGNOSTIC MARKER; PLASMA-MEMBRANE; DANGER SIGNAL; TUMOR-CELLS; IN-VITRO;
D O I
10.1016/j.smim.2013.12.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Cells constitutively release small (40-100 nm) vesicles known as exosomes, but their composition and function changes in response to a variety of physiological challenges, such as injury, infection, and disease. Advances in our understanding of the immunological relevance of exosomes have been made, however, few studies have explored their role in stress physiology. Exposure to a variety of acute stressors facilitates the efficacy of innate immune responses, but the mechanisms for these effects are not fully understood. Since exosomes are emerging as important inflammatory mediators, they likely exhibit a similar role when an organism is exposed to an acute stressor. Here, we review our current knowledge of the basic properties and immunological functions of exosomes and provide emerging data supporting the role of stress-modified exosomes in regulating the innate immune response, potentially enabling long-distance cellular communication and obviating the need for direct cell-to-cell contact. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:394 / 401
页数:8
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