Mesenchymal stromal cell-derived extracellular vesicles for bone regeneration therapy
Purpose: To analyze preclinical bone regeneration studies employing mesenchymal stromal cell (MSC)- derived extracellular vesicles (EVs) and highlight any commonalities in EV biomarker expression, miRNA cargo(s) or pathway activation that will aid in understanding the underlying therapeutic mechanis...
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2021-06-01
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doaj-b1b9148a0b8647fbae27d99a8f0991402021-06-03T04:57:29ZengElsevierBone Reports2352-18722021-06-0114101093Mesenchymal stromal cell-derived extracellular vesicles for bone regeneration therapyVishnu Priya Murali0Christina A. Holmes1Department of Chemical and Biomedical Engineering, College of Engineering, Florida A&M University-Florida State University, 2525 Pottsdamer Street, Room A131, Tallahassee, FL 32310, USACorresponding author.; Department of Chemical and Biomedical Engineering, College of Engineering, Florida A&M University-Florida State University, 2525 Pottsdamer Street, Room A131, Tallahassee, FL 32310, USAPurpose: To analyze preclinical bone regeneration studies employing mesenchymal stromal cell (MSC)- derived extracellular vesicles (EVs) and highlight any commonalities in EV biomarker expression, miRNA cargo(s) or pathway activation that will aid in understanding the underlying therapeutic mechanisms. Methods: Articles employing EVs derived from either MSCs or MSC-like osteogenic stromal cells in preclinical bone regeneration studies are included in this review. Results: EVs derived from a variety of MSC types were able to successfully induce bone formation in preclinical models. Many studies failed to perform in-depth EV characterization. The studies with detailed EV characterization data report very different miRNA cargos, even in EVs isolated from the same species and cell types. Few preclinical studies have analyzed the underlying mechanisms of MSC-EV therapeutic action. Conclusion: There is a critical need for mechanistic preclinical studies with thorough EV characterization to determine the best therapeutic MSC-EV source for bone regeneration therapies. Issues including controlled EV delivery, large scale production, and proper storage also need to be addressed before EV-based bone regeneration therapies can be translated for clinical bone repair.http://www.sciencedirect.com/science/article/pii/S2352187221003491Extracellular vesiclesBone regenerationMesenchymal stromal cellsTissue engineeringmiRNABiomaterials |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Vishnu Priya Murali Christina A. Holmes |
spellingShingle |
Vishnu Priya Murali Christina A. Holmes Mesenchymal stromal cell-derived extracellular vesicles for bone regeneration therapy Bone Reports Extracellular vesicles Bone regeneration Mesenchymal stromal cells Tissue engineering miRNA Biomaterials |
author_facet |
Vishnu Priya Murali Christina A. Holmes |
author_sort |
Vishnu Priya Murali |
title |
Mesenchymal stromal cell-derived extracellular vesicles for bone regeneration therapy |
title_short |
Mesenchymal stromal cell-derived extracellular vesicles for bone regeneration therapy |
title_full |
Mesenchymal stromal cell-derived extracellular vesicles for bone regeneration therapy |
title_fullStr |
Mesenchymal stromal cell-derived extracellular vesicles for bone regeneration therapy |
title_full_unstemmed |
Mesenchymal stromal cell-derived extracellular vesicles for bone regeneration therapy |
title_sort |
mesenchymal stromal cell-derived extracellular vesicles for bone regeneration therapy |
publisher |
Elsevier |
series |
Bone Reports |
issn |
2352-1872 |
publishDate |
2021-06-01 |
description |
Purpose: To analyze preclinical bone regeneration studies employing mesenchymal stromal cell (MSC)- derived extracellular vesicles (EVs) and highlight any commonalities in EV biomarker expression, miRNA cargo(s) or pathway activation that will aid in understanding the underlying therapeutic mechanisms. Methods: Articles employing EVs derived from either MSCs or MSC-like osteogenic stromal cells in preclinical bone regeneration studies are included in this review. Results: EVs derived from a variety of MSC types were able to successfully induce bone formation in preclinical models. Many studies failed to perform in-depth EV characterization. The studies with detailed EV characterization data report very different miRNA cargos, even in EVs isolated from the same species and cell types. Few preclinical studies have analyzed the underlying mechanisms of MSC-EV therapeutic action. Conclusion: There is a critical need for mechanistic preclinical studies with thorough EV characterization to determine the best therapeutic MSC-EV source for bone regeneration therapies. Issues including controlled EV delivery, large scale production, and proper storage also need to be addressed before EV-based bone regeneration therapies can be translated for clinical bone repair. |
topic |
Extracellular vesicles Bone regeneration Mesenchymal stromal cells Tissue engineering miRNA Biomaterials |
url |
http://www.sciencedirect.com/science/article/pii/S2352187221003491 |
work_keys_str_mv |
AT vishnupriyamurali mesenchymalstromalcellderivedextracellularvesiclesforboneregenerationtherapy AT christinaaholmes mesenchymalstromalcellderivedextracellularvesiclesforboneregenerationtherapy |
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