Blood Cell-Derived Microvesicles in Hematological Diseases and beyond

Biomolecules. 2022 Jun 8;12(6):803. doi: 10.3390/biom12060803.

Abstract

Microvesicles or ectosomes represent a major type of extracellular vesicles that are formed by outward budding of the plasma membrane. Typically, they are bigger than exosomes but smaller than apoptotic vesicles, although they may overlap with both in size and content. Their release by cells is a means to dispose redundant, damaged, or dangerous material; to repair membrane lesions; and, primarily, to mediate intercellular communication. By participating in these vital activities, microvesicles may impact a wide array of cell processes and, consequently, changes in their concentration or components have been associated with several pathologies. Of note, microvesicles released by leukocytes, red blood cells, and platelets, which constitute the vast majority of plasma microvesicles, change under a plethora of diseases affecting not only the hematological, but also the nervous, cardiovascular, and urinary systems, among others. In fact, there is evidence that microvesicles released by blood cells are significant contributors towards pathophysiological states, having inflammatory and/or coagulation and/or immunomodulatory arms, by either promoting or inhibiting the relative disease phenotypes. Consequently, even though microvesicles are typically considered to have adverse links with disease prognosis, progression, or outcomes, not infrequently, they exert protective roles in the affected cells. Based on these functional relations, microvesicles might represent promising disease biomarkers with diagnostic, monitoring, and therapeutic applications, equally to the more thoroughly studied exosomes. In the current review, we provide a summary of the features of microvesicles released by blood cells and their potential implication in hematological and non-hematological diseases.

Keywords: blood; disease biomarker; extracellular vesicles; hematological disorder; medium/large vesicles; microparticles; microvesicles.

Publication types

  • Review

MeSH terms

  • Blood Platelets
  • Cell-Derived Microparticles* / metabolism
  • Exosomes* / metabolism
  • Extracellular Vesicles* / metabolism
  • Hematologic Diseases* / metabolism
  • Humans

Grants and funding

This research received no external funding.