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Mesenchymal stromal cell-derived extracellular vesicles for bone regeneration therapy
Vishnu Priya Murali1, Christina A Holmes1
1Department of Chemical and Biomedical Engineering, College of Engineering, Florida A&M University-Florida State University, 2525 Pottsdamer Street, Room A131, Tallahassee, FL 32310, USA.
Bone Reports
|June 7, 2021
Summary
Mesenchymal stromal cell (MSC)-derived extracellular vesicles (EVs) show promise for bone regeneration. However, inconsistent EV characterization and a lack of mechanistic studies hinder clinical translation.
Area of Science:
- Biomedical Engineering
- Regenerative Medicine
- Cell Biology
Background:
- Mesenchymal stromal cells (MSCs) are crucial for bone regeneration.
- Extracellular vesicles (EVs) derived from MSCs are emerging as cell-free therapeutic agents.
- Understanding the mechanisms of MSC-EVs in bone repair is essential for clinical application.
Purpose of the Study:
- To review preclinical studies on MSC-derived EVs for bone regeneration.
- To identify commonalities in EV biomarker expression, miRNA cargo, and pathway activation.
- To elucidate the therapeutic mechanisms of MSC-EVs in bone regeneration.
Main Methods:
- Systematic review of preclinical studies involving MSC-derived EVs in bone regeneration.
- Analysis of EV characterization data, including biomarker expression and miRNA cargo.
- Evaluation of reported mechanisms of MSC-EV action.
Main Results:
- MSCs-EVs demonstrated efficacy in inducing bone formation across various preclinical models.
- A significant number of studies lacked comprehensive EV characterization.
- Diverse miRNA cargo profiles were observed, even within EVs from similar sources.
- Limited research has explored the underlying mechanisms of MSC-EV therapeutic effects.
Conclusions:
- There is a critical need for mechanistic preclinical studies with thorough EV characterization.
- Identifying optimal MSC-EV sources for bone regeneration requires further investigation.
- Addressing challenges in EV delivery, scalable production, and storage is vital for clinical translation.
Keywords:
BiomaterialsBone regenerationExtracellular vesiclesMesenchymal stromal cellsTissue engineeringmiRNAMore Related Videos
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