Mesenchymal Stem Cell-Derived Extracellular Vesicles to the Rescue of Renal Injury

Acute kidney injury (AKI) and chronic kidney disease (CKD) are rising in global prevalence and cause significant morbidity for patients. Current treatments are limited to slowing instead of stabilising or reversing disease progression. In this review, we describe mesenchymal stem cells (MSCs) and th...

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Main Authors: Lucy Birtwistle, Xin-Ming Chen, Carol Pollock
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/12/6596
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author Lucy Birtwistle
Xin-Ming Chen
Carol Pollock
author_facet Lucy Birtwistle
Xin-Ming Chen
Carol Pollock
author_sort Lucy Birtwistle
collection DOAJ
description Acute kidney injury (AKI) and chronic kidney disease (CKD) are rising in global prevalence and cause significant morbidity for patients. Current treatments are limited to slowing instead of stabilising or reversing disease progression. In this review, we describe mesenchymal stem cells (MSCs) and their constituents, extracellular vesicles (EVs) as being a novel therapeutic for CKD. MSC-derived EVs (MSC-EVs) are membrane-enclosed particles, including exosomes, which carry genetic information that mimics the phenotype of their cell of origin. MSC-EVs deliver their cargo of mRNA, miRNA, cytokines, and growth factors to target cells as a form of paracrine communication. This genetically reprograms pathophysiological pathways, which are upregulated in renal failure. Since the method of exosome preparation significantly affects the quality and function of MSC-exosomes, this review compares the methodologies for isolating exosomes from MSCs and their role in tissue regeneration. More specifically, it summarises the therapeutic efficacy of MSC-EVs in 60 preclinical animal models of AKI and CKD and the cargo of biomolecules they deliver. MSC-EVs promote tubular proliferation and angiogenesis, and inhibit apoptosis, oxidative stress, inflammation, the epithelial-to-mesenchymal transition, and fibrosis, to alleviate AKI and CKD. By reprogramming these pathophysiological pathways, MSC-EVs can slow or even reverse the progression of AKI to CKD, and therefore offer potential to transform clinical practice.
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spelling doaj.art-505c74e7be8d475f84f5d4d92a2c4c8f2023-11-22T00:54:05ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-06-012212659610.3390/ijms22126596Mesenchymal Stem Cell-Derived Extracellular Vesicles to the Rescue of Renal InjuryLucy Birtwistle0Xin-Ming Chen1Carol Pollock2Faculty of Medicine and Health, Sydney Medical School, University of Sydney, Camperdown, NSW 2050, AustraliaKolling Institute, Sydney Medical School, University of Sydney, Royal North Shore Hospital, St Leonards, NSW 2065, AustraliaKolling Institute, Sydney Medical School, University of Sydney, Royal North Shore Hospital, St Leonards, NSW 2065, AustraliaAcute kidney injury (AKI) and chronic kidney disease (CKD) are rising in global prevalence and cause significant morbidity for patients. Current treatments are limited to slowing instead of stabilising or reversing disease progression. In this review, we describe mesenchymal stem cells (MSCs) and their constituents, extracellular vesicles (EVs) as being a novel therapeutic for CKD. MSC-derived EVs (MSC-EVs) are membrane-enclosed particles, including exosomes, which carry genetic information that mimics the phenotype of their cell of origin. MSC-EVs deliver their cargo of mRNA, miRNA, cytokines, and growth factors to target cells as a form of paracrine communication. This genetically reprograms pathophysiological pathways, which are upregulated in renal failure. Since the method of exosome preparation significantly affects the quality and function of MSC-exosomes, this review compares the methodologies for isolating exosomes from MSCs and their role in tissue regeneration. More specifically, it summarises the therapeutic efficacy of MSC-EVs in 60 preclinical animal models of AKI and CKD and the cargo of biomolecules they deliver. MSC-EVs promote tubular proliferation and angiogenesis, and inhibit apoptosis, oxidative stress, inflammation, the epithelial-to-mesenchymal transition, and fibrosis, to alleviate AKI and CKD. By reprogramming these pathophysiological pathways, MSC-EVs can slow or even reverse the progression of AKI to CKD, and therefore offer potential to transform clinical practice.https://www.mdpi.com/1422-0067/22/12/6596extracellular vesicleexosomemesenchymal stem cellsacute kidney injurychronic kidney diseasemiRNA
spellingShingle Lucy Birtwistle
Xin-Ming Chen
Carol Pollock
Mesenchymal Stem Cell-Derived Extracellular Vesicles to the Rescue of Renal Injury
International Journal of Molecular Sciences
extracellular vesicle
exosome
mesenchymal stem cells
acute kidney injury
chronic kidney disease
miRNA
title Mesenchymal Stem Cell-Derived Extracellular Vesicles to the Rescue of Renal Injury
title_full Mesenchymal Stem Cell-Derived Extracellular Vesicles to the Rescue of Renal Injury
title_fullStr Mesenchymal Stem Cell-Derived Extracellular Vesicles to the Rescue of Renal Injury
title_full_unstemmed Mesenchymal Stem Cell-Derived Extracellular Vesicles to the Rescue of Renal Injury
title_short Mesenchymal Stem Cell-Derived Extracellular Vesicles to the Rescue of Renal Injury
title_sort mesenchymal stem cell derived extracellular vesicles to the rescue of renal injury
topic extracellular vesicle
exosome
mesenchymal stem cells
acute kidney injury
chronic kidney disease
miRNA
url https://www.mdpi.com/1422-0067/22/12/6596
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AT xinmingchen mesenchymalstemcellderivedextracellularvesiclestotherescueofrenalinjury
AT carolpollock mesenchymalstemcellderivedextracellularvesiclestotherescueofrenalinjury