Apoptotic Tumor Cell-Derived Extracellular Vesicles as Important Regulators of the Onco-Regenerative Niche

被引:46
|
作者
Gregory, Christopher D. [1 ]
Dransfield, Ian [1 ]
机构
[1] Univ Edinburgh, Queens Med Res Inst, Med Res Council, Ctr Inflammat Res, Edinburgh, Midlothian, Scotland
来源
FRONTIERS IN IMMUNOLOGY | 2018年 / 9卷
基金
英国医学研究理事会;
关键词
extracellular vesicles; apoptosis; inflammation and cancer; tumor microenvironment; angiogenesis; tissue repair and regeneration; macrophage activation; tumor biology; HORIZONTAL TRANSFER; DNA-DAMAGE; BODIES; CANCER; DEATH; MICROVESICLES; PATHWAY; PHAGOCYTOSIS; ACTIVATION; EXPRESSION;
D O I
10.3389/fimmu.2018.01111
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cells undergoing apoptosis produce heterogeneous populations of membrane delimited extracellular vesicles (Apo-EVs) which vary not only in size-from tens of nanometers to several microns-but also in molecular composition and cargo Apo-Evs carry a variety of potentially biologically active components, including small molecules, proteins, and nucleic acids Larger forms of Apo-EVs, commonly termed "apoptotic bodies," can carry organelles, such as mitochondria and nuclear fragments Molecules displayed on the surface of extracellular vesicles (EVs) can contribute substantially to their size, as well as their functions Thus far, relatively little is known of the functional significance of Apo-EVs apart from their roles in fragmentation of dying cells and indicated immunomodulatory activities Here, we discuss EV production by dying tumor cells and consider the possible roles of Apo-EVs in a cell death-driven sector of the tumor microenvironment known as the onco-regenerative niche (ORN) We propose that tumor-derived Apo-EVs are significant vehicles of the ORN, functioning as critical intercellular communicators that activate oncogenic tissue repair and regeneration pathways We highlight important outstanding questions and suggest that Apo-EVs may harbor novel therapeutic targets.
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页数:7
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