The role of microvesicles and its active molecules in regulating cellular biology
- PMID: 31559684
- PMCID: PMC6850934
- DOI: 10.1111/jcmm.14667
The role of microvesicles and its active molecules in regulating cellular biology
Abstract
Cell-derived microvesicles are membrane vesicles produced by the outward budding of the plasma membrane and released by almost all types of cells. These have been considered as another mechanism of intercellular communication, because they carry active molecules, such as proteins, lipids and nucleic acids. Furthermore, these are present in circulating fluids, such as blood and urine, and are closely correlated to the progression of pathophysiological conditions in many diseases. Recent studies have revealed that microvesicles have a dual effect of damage and protection of receptor cells. However, the nature of the active molecules involved in this effect remains unclear. The present study mainly emphasized the mechanism of microvesicles and the active molecules mediating the different biological effects of receptor cells by affecting autophagy, apoptosis and inflammation pathways. The effective ways of blocking microvesicles and its active molecules in mediating cell damage when microvesicles exert harmful effects were also discussed.
Keywords: active molecules; apoptosis; autophagy; inflammation; lipids; miRNA; microvesicles; proteins.
© 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.
Conflict of interest statement
The authors declare no conflict of interest.
Figures



References
-
- Chargaff E, West R. The biological significance of the thromboplastic protein of blood. J Biol Chem. 1946;166:189‐197. - PubMed
-
- Chiva‐Blanch G, Crespo J, Suades R, et al. CD142+/CD61+, CD146+ and CD45+ microparticles predict cardiovascular events in high risk patients following a Mediterranean diet supplemented with nuts. Thromb Haemost. 2016;116:103‐114. - PubMed
-
- Jia L, Fan J, Cui W, et al. Endothelial cell‐derived microparticles from patients with obstructive sleep apnea hypoxia syndrome and coronary artery disease increase aortic endothelial cell dysfunction. Cell Physiol Biochem. 2017;43:2562‐2570. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources