Human red blood cells release microvesicles with distinct sizes and protein composition that alter neutrophil phagocytosis

• Published in: Journal of extracellular biology Vol. 2; no. 11
• Main Authors: Oliveira, Getulio Pereira, Welsh, Joshua A., Pinckney, Brandy, Palu, Cintia C., Lu, Shulin, Zimmerman, Alan, Barbosa, Raquel Hora, Sahu, Parul, Noshin, Maeesha, Gummuluru, Suryaram, Tigges, John, Jones, Jennifer Clare, Ivanov, Alexander R., Ghiran, Ionita C.
• Format: Journal Article
• Language: English
• Published: United States John Wiley & Sons, Inc 01.11.2023; John Wiley and Sons Inc; Wiley
• Subjects: Biosynthesis; Calcimycin; Calcium homeostasis; Calcium ionophores; Calcium transport; Cell interactions; Electron microscopy; Erythrocytes; extracellular vesicles; Flow cytometry; Homeostasis; Internalization; Ionomycin; Ionophores; Leukocytes (neutrophilic); Membrane fusion; Membrane vesicles; Microscopy; Neutrophils; Phagocytosis; Plasma; Protein composition; Protein transport; Proteins; Proteomics; RBCs; Software; Extracellular vesicles; neutrophils; RBCs; calcium ionophores
• ISSN: 2768-2811; 2768-2811
• DOI: 10.1002/jex2.107

Extracellular vesicles (EVs) are membrane‐bound structures released by cells and tissues into biofluids, involved in cell‐cell communication. In humans, circulating red blood cells (RBCs), represent the most common cell‐type in the body, generating daily large numbers of microvesicles. In vitro, RBC vesiculation can be mimicked by stimulating RBCs with calcium ionophores, such as ionomycin and A23187. The fate of microvesicles released during in vivo aging of RBCs and their interactions with circulating cells is hitherto unknown. Using SEC plus DEG isolation methods, we have found that human RBCs generate microvesicles with two distinct sizes, densities and protein composition, identified by flow cytometry, and MRPS, and further validated by immune TEM. Furthermore, proteomic analysis revealed that RBC‐derived microvesicles (RBC‐MVs) are enriched in proteins with important functions in ion channel regulation, calcium homeostasis and vesicular transport, such as of sorcin, stomatin, annexin A7 and RAB proteins. Cryo‐electron microscopy identified two separate pathways of RBC‐MV‐neutrophil interaction, direct fusion with the plasma membrane and internalization, respectively. Functionally, RBC‐MVs decrease neutrophil ability to phagocytose Escherichia coli but do not affect their survival at 24 h. This work brings new insights regarding the complexity of the RBC‐MVs biogenesis, as well as their possible role in circulation.