Platelet-Derived Microvesicles in Cardiovascular Diseases

Microvesicles (MVs) circulating in the blood are small vesicles (100–1,000 nm in diameter) derived from membrane blebs of cells such as activated platelets, endothelial cells, and leukocytes. A growing body of evidence now supports the concept that platelet-derived microvesicles (PMVs), the most abu...

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Main Authors: Maria T. K. Zaldivia, James D. McFadyen, Bock Lim, Xiaowei Wang, Karlheinz Peter
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-11-01
Series:Frontiers in Cardiovascular Medicine
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fcvm.2017.00074/full
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spelling doaj-094f2436732249d2b56ba6e24b2f34692020-11-24T22:45:18ZengFrontiers Media S.A.Frontiers in Cardiovascular Medicine2297-055X2017-11-01410.3389/fcvm.2017.00074300418Platelet-Derived Microvesicles in Cardiovascular DiseasesMaria T. K. Zaldivia0Maria T. K. Zaldivia1James D. McFadyen2James D. McFadyen3James D. McFadyen4Bock Lim5Xiaowei Wang6Xiaowei Wang7Karlheinz Peter8Karlheinz Peter9Karlheinz Peter10Atherothrombosis and Vascular Biology, Baker Heart and Diabetes Institute, Melbourne, VIC, AustraliaDepartment of Medicine, Monash University, Melbourne, VIC, AustraliaAtherothrombosis and Vascular Biology, Baker Heart and Diabetes Institute, Melbourne, VIC, AustraliaDepartment of Medicine, Monash University, Melbourne, VIC, AustraliaDepartment of Haematology, The Alfred Hospital, Melbourne, VIC, AustraliaAtherothrombosis and Vascular Biology, Baker Heart and Diabetes Institute, Melbourne, VIC, AustraliaAtherothrombosis and Vascular Biology, Baker Heart and Diabetes Institute, Melbourne, VIC, AustraliaDepartment of Medicine, Monash University, Melbourne, VIC, AustraliaAtherothrombosis and Vascular Biology, Baker Heart and Diabetes Institute, Melbourne, VIC, AustraliaDepartment of Medicine, Monash University, Melbourne, VIC, AustraliaHeart Centre, The Alfred Hospital, Melbourne, VIC, AustraliaMicrovesicles (MVs) circulating in the blood are small vesicles (100–1,000 nm in diameter) derived from membrane blebs of cells such as activated platelets, endothelial cells, and leukocytes. A growing body of evidence now supports the concept that platelet-derived microvesicles (PMVs), the most abundant MVs in the circulation, are important regulators of hemostasis, inflammation, and angiogenesis. Compared with healthy individuals, a large increase of circulating PMVs has been observed, particularly in patients with cardiovascular diseases. As observed in MVs from other parent cells, PMVs exert their biological effects in multiple ways, such as triggering various intercellular signaling cascades and by participating in transcellular communication by the transfer of their “cargo” of cytoplasmic components and surface receptors to other cell types. This review describes our current understanding of the potential role of PMVs in mediating hemostasis, inflammation, and angiogenesis and their consequences on the pathogenesis of cardiovascular diseases, such as atherosclerosis, myocardial infarction, and venous thrombosis. Furthermore, new developments of the therapeutic potential of PMVs for the treatment of cardiovascular diseases will be discussed.http://journal.frontiersin.org/article/10.3389/fcvm.2017.00074/fullmicrovesiclesplatelet-derived microvesiclescardiovascular diseasetherapeutic potentialhemostasisinflammation
collection DOAJ
language English
format Article
sources DOAJ
author Maria T. K. Zaldivia
Maria T. K. Zaldivia
James D. McFadyen
James D. McFadyen
James D. McFadyen
Bock Lim
Xiaowei Wang
Xiaowei Wang
Karlheinz Peter
Karlheinz Peter
Karlheinz Peter
spellingShingle Maria T. K. Zaldivia
Maria T. K. Zaldivia
James D. McFadyen
James D. McFadyen
James D. McFadyen
Bock Lim
Xiaowei Wang
Xiaowei Wang
Karlheinz Peter
Karlheinz Peter
Karlheinz Peter
Platelet-Derived Microvesicles in Cardiovascular Diseases
Frontiers in Cardiovascular Medicine
microvesicles
platelet-derived microvesicles
cardiovascular disease
therapeutic potential
hemostasis
inflammation
author_facet Maria T. K. Zaldivia
Maria T. K. Zaldivia
James D. McFadyen
James D. McFadyen
James D. McFadyen
Bock Lim
Xiaowei Wang
Xiaowei Wang
Karlheinz Peter
Karlheinz Peter
Karlheinz Peter
author_sort Maria T. K. Zaldivia
title Platelet-Derived Microvesicles in Cardiovascular Diseases
title_short Platelet-Derived Microvesicles in Cardiovascular Diseases
title_full Platelet-Derived Microvesicles in Cardiovascular Diseases
title_fullStr Platelet-Derived Microvesicles in Cardiovascular Diseases
title_full_unstemmed Platelet-Derived Microvesicles in Cardiovascular Diseases
title_sort platelet-derived microvesicles in cardiovascular diseases
publisher Frontiers Media S.A.
series Frontiers in Cardiovascular Medicine
issn 2297-055X
publishDate 2017-11-01
description Microvesicles (MVs) circulating in the blood are small vesicles (100–1,000 nm in diameter) derived from membrane blebs of cells such as activated platelets, endothelial cells, and leukocytes. A growing body of evidence now supports the concept that platelet-derived microvesicles (PMVs), the most abundant MVs in the circulation, are important regulators of hemostasis, inflammation, and angiogenesis. Compared with healthy individuals, a large increase of circulating PMVs has been observed, particularly in patients with cardiovascular diseases. As observed in MVs from other parent cells, PMVs exert their biological effects in multiple ways, such as triggering various intercellular signaling cascades and by participating in transcellular communication by the transfer of their “cargo” of cytoplasmic components and surface receptors to other cell types. This review describes our current understanding of the potential role of PMVs in mediating hemostasis, inflammation, and angiogenesis and their consequences on the pathogenesis of cardiovascular diseases, such as atherosclerosis, myocardial infarction, and venous thrombosis. Furthermore, new developments of the therapeutic potential of PMVs for the treatment of cardiovascular diseases will be discussed.
topic microvesicles
platelet-derived microvesicles
cardiovascular disease
therapeutic potential
hemostasis
inflammation
url http://journal.frontiersin.org/article/10.3389/fcvm.2017.00074/full
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