Extracellular vesicles arising from apoptosis: forms, functions, and applications

被引:30
作者
Gregory, Christopher D. [1 ]
Rimmer, Michael P. [2 ]
机构
[1] Univ Edinburgh, Inst Regenerat & Repair, Ctr Inflammat Res, BioQuarter,4-5 Little France Dr, Edinburgh EH16 4UU, Scotland
[2] Univ Edinburgh, Inst Regenerat & Repair, Ctr Reprod Hlth, Edinburgh, Scotland
基金
英国工程与自然科学研究理事会;
关键词
SYSTEMIC-LUPUS-ERYTHEMATOSUS; ENDOTHELIAL PROGENITOR CELLS; FIND-ME SIGNAL; MEMBRANE-VESICLES; MICROPARTICLES; BODIES; EXOSOMES; MACROPHAGE; MICROVESICLES; DEATH;
D O I
10.1002/path.6138
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Extracellular vesicles (EVs) are lipid bilayer-enclosed subcellular bodies produced by most, if not all cells. Research over the last two decades has recognised the importance of EVs in intercellular communication and horizontal transfer of biological material. EVs range in diameter from tens of nanometres up to several micrometres and are able to transfer a spectrum of biologically active cargoes - from whole organelles, through macromolecules including nucleic acids and proteins, to metabolites and small molecules - from their cells of origin to recipient cells, which may consequently become physiologically or pathologically altered. Based on their modes of biogenesis, the most renowned EV classes are (1) microvesicles, (2) exosomes (both produced by healthy cells), and (3) EVs from cells undergoing regulated death by apoptosis (ApoEVs). Microvesicles bud directly from the plasma membrane, while exosomes are derived from endosomal compartments. Current knowledge of the formation and functional properties of ApoEVs lags behind that of microvesicles and exosomes, but burgeoning evidence indicates that ApoEVs carry manifold cargoes, including mitochondria, ribosomes, DNA, RNAs, and proteins, and perform diverse functions in health and disease. Here we review this evidence, which demonstrates substantial diversity in the luminal and surface membrane cargoes of ApoEVs, permitted by their very broad size range (from around 50 nm to >5 mu m; the larger often termed apoptotic bodies), strongly suggests their origins through both microvesicle- and exosome-like biogenesis pathways, and indicates routes through which they interact with recipient cells. We discuss the capacity of ApoEVs to recycle cargoes and modulate inflammatory, immunological, and cell fate programmes in normal physiology and in pathological scenarios such as cancer and atherosclerosis. Finally, we provide a perspective on clinical applications of ApoEVs in diagnostics and therapeutics. (c) 2023 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
引用
收藏
页码:592 / 608
页数:17
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