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
相关论文
共 195 条
  • [1] Apoptotic Cells Promote Their Own Clearance and Immune Tolerance through Activation of the Nuclear Receptor LXR
    A-Gonzalez, Noelia
    Bensinger, Steven J.
    Hong, Cynthia
    Beceiro, Susana
    Bradley, Michelle N.
    Zelcer, Noam
    Deniz, Jose
    Ramirez, Cristina
    Diaz, Mercedes
    Gallardo, German
    Ruiz de Galarreta, Carlos
    Salazar, Jon
    Lopez, Felix
    Edwards, Peter
    Parks, John
    Andujar, Miguel
    Tontonoz, Peter
    Castrillo, Antonio
    [J]. IMMUNITY, 2009, 31 (02) : 245 - 258
  • [2] Biogenesis of extracellular vesicles (EV): exosomes, microvesicles, retrovirus-like vesicles, and apoptotic bodies
    Akers, Johnny C.
    Gonda, David
    Kim, Ryan
    Carter, Bob S.
    Chen, Clark C.
    [J]. JOURNAL OF NEURO-ONCOLOGY, 2013, 113 (01) : 1 - 11
  • [3] Intercellular transfer of the oncogenic receptor EGFrvIII by microvesicles derived from tumour cells
    Al-Nedawi, Khalid
    Meehan, Brian
    Micallef, Johann
    Lhotak, Vladimir
    May, Linda
    Guha, Abhijit
    Rak, Janusz
    [J]. NATURE CELL BIOLOGY, 2008, 10 (05) : 619 - U24
  • [4] Macrophages use apoptotic cell-derived methionine and DNMT3A during efferocytosis to promote tissue resolution
    Ampomah, Patrick B.
    Cai, Bishuang
    Sukka, Santosh R.
    Gerlach, Brennan D.
    Yurdagul, Arif, Jr.
    Wang, Xiaobo
    Kuriakose, George
    Darville, Lancia N. F.
    Sun, Yan
    Sidoli, Simone
    Koomen, John M.
    Tall, Alan R.
    Tabas, Ira
    [J]. NATURE METABOLISM, 2022, 4 (04) : 444 - +
  • [5] Apoptotic cells represent a dynamic stem cell niche governing proliferation and tissue regeneration
    Ankawa, Roi
    Goldberger, Nitzan
    Yosefzon, Yahav
    Koren, Elle
    Yusupova, Marianna
    Rosner, Daniel
    Feldman, Alona
    Baror-Sebban, Shulamit
    Buganim, Yosef
    Simon, David J.
    Tessier-Lavigne, Marc
    Fuchs, Yaron
    [J]. DEVELOPMENTAL CELL, 2021, 56 (13) : 1900 - +
  • [6] Phagocytosis of apoptotic cells in homeostasis
    Arandjelovic, Sanja
    Ravichandran, Kodi S.
    [J]. NATURE IMMUNOLOGY, 2015, 16 (09) : 907 - 917
  • [7] Annexin I is an endogenous ligand that mediates apoptotic cell engulfment
    Arur, S
    Uche, UE
    Rezaul, K
    Fong, M
    Scranton, V
    Cowan, AE
    Mohler, W
    Han, DK
    [J]. DEVELOPMENTAL CELL, 2003, 4 (04) : 587 - 598
  • [8] Plexin B2 Is a Regulator of Monocyte Apoptotic Cell Disassembly
    Atkin-Smith, Georgia K.
    Miles, Mark A.
    Tixeira, Rochelle
    Lay, Fung T.
    Duan, Mubing
    Hawkins, Christine J.
    Thanh Kha Phan
    Paone, Stephanie
    Mathivanan, Suresh
    Hulett, Mark D.
    Chen, Weisan
    Poon, Ivan K. H.
    [J]. CELL REPORTS, 2019, 29 (07): : 1821 - +
  • [9] Disassembly of the Dying: Mechanisms and Functions
    Atkin-Smith, Georgia K.
    Poon, Ivan K. H.
    [J]. TRENDS IN CELL BIOLOGY, 2017, 27 (02) : 151 - 162
  • [10] Isolation of cell type-specific apoptotic bodies by fluorescence-activated cell sorting
    Atkin-Smith, Georgia K.
    Paone, Stephanie
    Zanker, Damien J.
    Duan, Mubing
    Phan, Than K.
    Chen, Weisan
    Hulett, Mark D.
    Poon, Ivan K. H.
    [J]. SCIENTIFIC REPORTS, 2017, 7