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Blood Cell-Derived Microvesicles in Hematological Diseases and beyond

Microvesicles or ectosomes represent a major type of extracellular vesicles that are formed by outward budding of the plasma membrane. Typically, they are bigger than exosomes but smaller than apoptotic vesicles, although they may overlap with both in size and content. Their release by cells is a me...

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Autores principales: Georgatzakou, Hara T., Fortis, Sotirios P., Papageorgiou, Effie G., Antonelou, Marianna H., Kriebardis, Anastasios G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9220817/
https://www.ncbi.nlm.nih.gov/pubmed/35740926
http://dx.doi.org/10.3390/biom12060803
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author Georgatzakou, Hara T.
Fortis, Sotirios P.
Papageorgiou, Effie G.
Antonelou, Marianna H.
Kriebardis, Anastasios G.
author_facet Georgatzakou, Hara T.
Fortis, Sotirios P.
Papageorgiou, Effie G.
Antonelou, Marianna H.
Kriebardis, Anastasios G.
author_sort Georgatzakou, Hara T.
collection PubMed
description Microvesicles or ectosomes represent a major type of extracellular vesicles that are formed by outward budding of the plasma membrane. Typically, they are bigger than exosomes but smaller than apoptotic vesicles, although they may overlap with both in size and content. Their release by cells is a means to dispose redundant, damaged, or dangerous material; to repair membrane lesions; and, primarily, to mediate intercellular communication. By participating in these vital activities, microvesicles may impact a wide array of cell processes and, consequently, changes in their concentration or components have been associated with several pathologies. Of note, microvesicles released by leukocytes, red blood cells, and platelets, which constitute the vast majority of plasma microvesicles, change under a plethora of diseases affecting not only the hematological, but also the nervous, cardiovascular, and urinary systems, among others. In fact, there is evidence that microvesicles released by blood cells are significant contributors towards pathophysiological states, having inflammatory and/or coagulation and/or immunomodulatory arms, by either promoting or inhibiting the relative disease phenotypes. Consequently, even though microvesicles are typically considered to have adverse links with disease prognosis, progression, or outcomes, not infrequently, they exert protective roles in the affected cells. Based on these functional relations, microvesicles might represent promising disease biomarkers with diagnostic, monitoring, and therapeutic applications, equally to the more thoroughly studied exosomes. In the current review, we provide a summary of the features of microvesicles released by blood cells and their potential implication in hematological and non-hematological diseases.
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spelling pubmed-92208172022-06-24 Blood Cell-Derived Microvesicles in Hematological Diseases and beyond Georgatzakou, Hara T. Fortis, Sotirios P. Papageorgiou, Effie G. Antonelou, Marianna H. Kriebardis, Anastasios G. Biomolecules Review Microvesicles or ectosomes represent a major type of extracellular vesicles that are formed by outward budding of the plasma membrane. Typically, they are bigger than exosomes but smaller than apoptotic vesicles, although they may overlap with both in size and content. Their release by cells is a means to dispose redundant, damaged, or dangerous material; to repair membrane lesions; and, primarily, to mediate intercellular communication. By participating in these vital activities, microvesicles may impact a wide array of cell processes and, consequently, changes in their concentration or components have been associated with several pathologies. Of note, microvesicles released by leukocytes, red blood cells, and platelets, which constitute the vast majority of plasma microvesicles, change under a plethora of diseases affecting not only the hematological, but also the nervous, cardiovascular, and urinary systems, among others. In fact, there is evidence that microvesicles released by blood cells are significant contributors towards pathophysiological states, having inflammatory and/or coagulation and/or immunomodulatory arms, by either promoting or inhibiting the relative disease phenotypes. Consequently, even though microvesicles are typically considered to have adverse links with disease prognosis, progression, or outcomes, not infrequently, they exert protective roles in the affected cells. Based on these functional relations, microvesicles might represent promising disease biomarkers with diagnostic, monitoring, and therapeutic applications, equally to the more thoroughly studied exosomes. In the current review, we provide a summary of the features of microvesicles released by blood cells and their potential implication in hematological and non-hematological diseases. MDPI 2022-06-08 /pmc/articles/PMC9220817/ /pubmed/35740926 http://dx.doi.org/10.3390/biom12060803 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Georgatzakou, Hara T.
Fortis, Sotirios P.
Papageorgiou, Effie G.
Antonelou, Marianna H.
Kriebardis, Anastasios G.
Blood Cell-Derived Microvesicles in Hematological Diseases and beyond
title Blood Cell-Derived Microvesicles in Hematological Diseases and beyond
title_full Blood Cell-Derived Microvesicles in Hematological Diseases and beyond
title_fullStr Blood Cell-Derived Microvesicles in Hematological Diseases and beyond
title_full_unstemmed Blood Cell-Derived Microvesicles in Hematological Diseases and beyond
title_short Blood Cell-Derived Microvesicles in Hematological Diseases and beyond
title_sort blood cell-derived microvesicles in hematological diseases and beyond
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9220817/
https://www.ncbi.nlm.nih.gov/pubmed/35740926
http://dx.doi.org/10.3390/biom12060803
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