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Microparticles: targets and tools in cardiovascular disease
Maria Carmen Martinez1, Simon Tual-Chalot, Daniela Leonetti
1Institut National de la Santé et de la Recherche Médicale (INSERM) Unité 694, Faculté de Médecine, Université d'Angers, Angers, France.
Abstract:
Cells communicate with other cells not only via direct cell-cell contact and the production of signaling molecules but also through release of microparticles (MPs). MPs are small vesicles released from stimulated and/or apoptotic cells. They harbor membrane proteins that are characteristic of the original parent cell and intracellular components involved in cell signaling. MPs are considered to be both biomarkers and effectors of cell signaling that maintain and/or initiate cell dysfunction. Thus, MPs can evoke endothelial dysfunction by decreasing nitric oxide (NO) production and promoting vascular inflammation which favor the prothrombotic state in atherosclerosis. Novel pharmacological approaches targeting MP production or properties could be used to treat cardiovascular pathologies. Paradoxically, another useful approach might be to employ engineered MPs with modified compositions as therapeutic agents to correct cardiovascular pathologies. This review is focused on the mechanisms of MP formation and their effects on target cells under physiological or pathophysiological conditions.
Insights
Microparticles (MPs) are released from cells and can cause cell dysfunction, contributing to cardiovascular diseases. Targeting MPs offers potential therapeutic strategies for these conditions.
Area of Science:
- Cell Biology
- Biochemistry
- Cardiovascular Science
Background:
- Cells communicate through direct contact, signaling molecules, and microparticles (MPs).
- MPs are small vesicles released from stimulated or apoptotic cells, carrying parent cell characteristics and signaling components.
- MPs act as biomarkers and effectors of cell signaling, potentially initiating or maintaining cell dysfunction.
Purpose of the Study:
- To review the mechanisms of microparticle formation.
- To discuss the effects of microparticles on target cells in physiological and pathophysiological conditions.
- To explore therapeutic strategies involving microparticles for cardiovascular pathologies.
Main Methods:
- Literature review of microparticle formation mechanisms.
- Analysis of microparticle effects on endothelial cells and vascular inflammation.
- Exploration of pharmacological and engineered microparticle-based therapies.
Main Results:
- Microparticles can evoke endothelial dysfunction by reducing nitric oxide (NO) production.
- Microparticles promote vascular inflammation, contributing to a prothrombotic state in atherosclerosis.
- Microparticles are implicated in maintaining and initiating cell dysfunction.
Conclusions:
- Microparticle production and properties present novel therapeutic targets for cardiovascular diseases.
- Engineered microparticles with modified compositions may serve as therapeutic agents.
- Understanding microparticle formation and function is crucial for treating cardiovascular pathologies.
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