Cargando…

Molecular Pathways Modulated by Mesenchymal Stromal Cells and Their Extracellular Vesicles in Experimental Models of Liver Fibrosis

End-stage liver fibrosis is common to all chronic liver diseases. Since liver transplantation has several limitations, including lack of donors, immunological rejection, and high medical costs, therapeutic alternatives are needed. The administration of mesenchymal stromal cells (MSCs) has been prove...

Descripción completa

Detalles Bibliográficos
Autores principales: Chiabotto, Giulia, Pasquino, Chiara, Camussi, Giovanni, Bruno, Stefania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794013/
https://www.ncbi.nlm.nih.gov/pubmed/33425900
http://dx.doi.org/10.3389/fcell.2020.594794
_version_ 1783634120625094656
author Chiabotto, Giulia
Pasquino, Chiara
Camussi, Giovanni
Bruno, Stefania
author_facet Chiabotto, Giulia
Pasquino, Chiara
Camussi, Giovanni
Bruno, Stefania
author_sort Chiabotto, Giulia
collection PubMed
description End-stage liver fibrosis is common to all chronic liver diseases. Since liver transplantation has several limitations, including lack of donors, immunological rejection, and high medical costs, therapeutic alternatives are needed. The administration of mesenchymal stromal cells (MSCs) has been proven effective in tissue regeneration after damage. However, the risk of uncontrolled side effects, such as cellular rejection and tumorigenesis, should be taken into consideration. A safer alternative to MSC transplantation is represented by the MSC secretome, which retains the same beneficial effect of the cell of origin, without showing any considerable side effect. The paracrine effect of MSCs is mainly carried out by secreted particles in the nanometer range, known as extracellular vesicles (EVs) that play a fundamental role in intercellular communication. In this review, we discuss the current literature on MSCs and MSC-EVs, focusing on their potential therapeutic action in liver fibrosis and on their molecular content (proteins and RNA), which contributes in reverting fibrosis and prompting tissue regeneration.
format Online
Article
Text
id pubmed-7794013
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-77940132021-01-09 Molecular Pathways Modulated by Mesenchymal Stromal Cells and Their Extracellular Vesicles in Experimental Models of Liver Fibrosis Chiabotto, Giulia Pasquino, Chiara Camussi, Giovanni Bruno, Stefania Front Cell Dev Biol Cell and Developmental Biology End-stage liver fibrosis is common to all chronic liver diseases. Since liver transplantation has several limitations, including lack of donors, immunological rejection, and high medical costs, therapeutic alternatives are needed. The administration of mesenchymal stromal cells (MSCs) has been proven effective in tissue regeneration after damage. However, the risk of uncontrolled side effects, such as cellular rejection and tumorigenesis, should be taken into consideration. A safer alternative to MSC transplantation is represented by the MSC secretome, which retains the same beneficial effect of the cell of origin, without showing any considerable side effect. The paracrine effect of MSCs is mainly carried out by secreted particles in the nanometer range, known as extracellular vesicles (EVs) that play a fundamental role in intercellular communication. In this review, we discuss the current literature on MSCs and MSC-EVs, focusing on their potential therapeutic action in liver fibrosis and on their molecular content (proteins and RNA), which contributes in reverting fibrosis and prompting tissue regeneration. Frontiers Media S.A. 2020-12-08 /pmc/articles/PMC7794013/ /pubmed/33425900 http://dx.doi.org/10.3389/fcell.2020.594794 Text en Copyright © 2020 Chiabotto, Pasquino, Camussi and Bruno. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Chiabotto, Giulia
Pasquino, Chiara
Camussi, Giovanni
Bruno, Stefania
Molecular Pathways Modulated by Mesenchymal Stromal Cells and Their Extracellular Vesicles in Experimental Models of Liver Fibrosis
title Molecular Pathways Modulated by Mesenchymal Stromal Cells and Their Extracellular Vesicles in Experimental Models of Liver Fibrosis
title_full Molecular Pathways Modulated by Mesenchymal Stromal Cells and Their Extracellular Vesicles in Experimental Models of Liver Fibrosis
title_fullStr Molecular Pathways Modulated by Mesenchymal Stromal Cells and Their Extracellular Vesicles in Experimental Models of Liver Fibrosis
title_full_unstemmed Molecular Pathways Modulated by Mesenchymal Stromal Cells and Their Extracellular Vesicles in Experimental Models of Liver Fibrosis
title_short Molecular Pathways Modulated by Mesenchymal Stromal Cells and Their Extracellular Vesicles in Experimental Models of Liver Fibrosis
title_sort molecular pathways modulated by mesenchymal stromal cells and their extracellular vesicles in experimental models of liver fibrosis
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794013/
https://www.ncbi.nlm.nih.gov/pubmed/33425900
http://dx.doi.org/10.3389/fcell.2020.594794
work_keys_str_mv AT chiabottogiulia molecularpathwaysmodulatedbymesenchymalstromalcellsandtheirextracellularvesiclesinexperimentalmodelsofliverfibrosis
AT pasquinochiara molecularpathwaysmodulatedbymesenchymalstromalcellsandtheirextracellularvesiclesinexperimentalmodelsofliverfibrosis
AT camussigiovanni molecularpathwaysmodulatedbymesenchymalstromalcellsandtheirextracellularvesiclesinexperimentalmodelsofliverfibrosis
AT brunostefania molecularpathwaysmodulatedbymesenchymalstromalcellsandtheirextracellularvesiclesinexperimentalmodelsofliverfibrosis