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Updated: Nov 9, 2025

Characterization of Immune Cell-derived Extracellular Vesicles and Studying Functional Impact on Cell Environment
Published on: June 2, 2020
Mechanobiology of microvesicle release, uptake, and microvesicle-mediated activation
Samantha C Schwager1, Cynthia A Reinhart-King1
1Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, United States.
Abstract:
Microvesicles are small, membrane-bound vesicles that are shed from the plasma membrane of cells into the extracellular space. Microvesicles contain a variety of cargo not typically thought to be released from cells, including receptor tyrosine kinases, cytosolic signaling proteins, and microRNAs, which are transferred from donor cells to recipient cells. The transfer of microvesicle cargo can result in the transformation of recipient cells thereby supporting disease progression, including modified fibroblast metabolism, epithelial cell contractility, vascular remodeling, and immune cell inflammatory signaling. Additionally, microvesicles are believed to play prominent roles in cell-cell communication and disease progression as they are detected at elevated concentrations in diseased tissues. As microvesicle uptake by recipient cells can modulate cell function to promote disease progression, understanding the mechanisms and mechanosensitivity of microvesicle release, internalization, and the resulting signaling is crucial to fully comprehend their functions in disease. Here, we review recent advances in the understanding of actomyosin-regulated microvesicle biogenesis, microvesicle uptake via pinocytosis, and the resulting cellular transformation. We discuss the effects of altered cell contractility, mode of cell migration, and extracellular matrix compliance on microvesicle signaling, with direct implications in disease progression and identifying future therapeutic targets.
Insights
Microvesicles, tiny cell-released sacs, transfer molecules that drive disease progression. Understanding their release and uptake is key to developing new therapies for various diseases.
Area of Science:
- Cell biology
- Extracellular vesicles
- Disease mechanisms
Background:
- Microvesicles are shed from cell membranes and carry diverse cargo like proteins and microRNAs.
- This cargo transfer between cells influences recipient cell functions, promoting disease progression.
- Elevated microvesicle levels are observed in diseased tissues, highlighting their role in cell communication and pathology.
Purpose of the Study:
- To review recent advances in understanding microvesicle biogenesis, uptake, and signaling.
- To explore the mechanosensitivity of microvesicle release and internalization.
- To discuss the implications of microvesicle function in disease progression and therapeutic targeting.
Main Methods:
- Review of current literature on actomyosin-regulated microvesicle biogenesis.
- Analysis of microvesicle uptake mechanisms, including pinocytosis.
- Discussion of cellular signaling pathways modulated by microvesicle cargo.
Main Results:
- Microvesicle cargo transfer can transform recipient cells, affecting metabolism, contractility, and immune signaling.
- Mechanisms of microvesicle release and uptake are sensitive to cellular mechanical properties.
- Altered cell contractility and extracellular matrix influence microvesicle-mediated signaling.
Conclusions:
- Understanding microvesicle dynamics is crucial for comprehending their role in disease.
- Cellular mechanics significantly impact microvesicle-mediated cell communication and disease.
- Microvesicles represent potential therapeutic targets for diseases driven by aberrant cell signaling.
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