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Extracellular vesicles from malaria‐infected red blood cells: not all are secreted equal
Author(s) -
Blow Frances,
Buck Amy H
Publication year - 2022
Publication title -
embo reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.584
H-Index - 184
eISSN - 1469-3178
pISSN - 1469-221X
DOI - 10.15252/embr.202255499
Subject(s) - biology , malaria , microbiology and biotechnology , extracellular vesicles , plasmodium falciparum , plasmodium (life cycle) , intracellular , red blood cell , intracellular parasite , extracellular , vesicle , immunology , parasite hosting , biochemistry , membrane , world wide web , computer science
Extracellular vesicles (EVs) mediate the transfer of molecules between cells and play diverse roles in host–pathogen interactions. Malaria is an important disease caused by intracellular Plasmodium species that invade red blood cells and these red blood cells release EVs. The EVs from infected cells have diverse functions in the disease and an obstacle in understanding how they exert their functions is that multiple EV types exist. In this issue of EMBO reports, Abou Karam and colleagues use sophisticated biophysical techniques to isolate and characterize two EV subpopulations produced by red blood cells infected with Plasmodium falciparum (Abou Karam et al , 2022). The authors show that these EV subpopulations have distinct sizes, protein content, membrane packing, and fusion capabilities, suggesting that EV subpopulations from infected cells could target different cell types and subcellular locations. This work underscores the concept that understanding EV heterogeneity will go hand in hand with understanding EV functions.

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