4.7 Article

Validation of Effective Extracellular Vesicles Isolation Methods Adapted to Field Studies in Malaria Endemic Regions

期刊

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2022.812244

关键词

malaria; Plasmodium falciparum; extracellular vesicles; microvesicles; salting-out; polyethylene glycol precipitation

资金

  1. Swiss National Science Foundation [31003A_182729]
  2. Research Pool of the University of Fribourg
  3. Swiss National Science Foundation (SNF) [31003A_182729] Funding Source: Swiss National Science Foundation (SNF)

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Malaria has significant health and economic impact on developing countries, and extracellular vesicles (EVs) may play a role in the disease's pathogenesis and biomarker discovery. However, there is still much to learn about EV biology, and more field studies are needed. The lack of appropriate equipment for EV isolation in low-income regions poses a challenge, and there is a need for accessible extraction protocols.
Malaria affects the poorer regions of the world and is of tremendous health and economic burden for developing countries. Extracellular vesicles (EVs) are small vesicles released by almost any cells in the human body, including malaria infected red blood cells. Recent evidence shows that EVs might contribute to the pathogenesis of malaria. In addition, EVs hold considerable value in biomarker discovery. However, there are still significant gaps in our understanding of EV biology. So far most of our knowledge about EVs in malaria comes from in vitro work. More field studies are required to gain insight into their contribution to the disease and pathogenesis under physiological conditions. However, to perform research on EVs in low-income regions might be challenging due to the lack of appropriate equipment to isolate EVs. Therefore, there is a need to develop and validate EV extraction protocols applicable to poorly equipped laboratories. We established and validated two protocols for EV isolation from cell culture supernatants, rodent and human plasma. We compared polyethylene glycol (PEG) and salting out (SA) with sodium acetate for precipitation of EVs. We then characterized the EVs by Transmission Electron Microscopy (TEM), Western Blot, Size-exclusion chromatography (SEC), bead-based flow cytometry and protein quantification. Both protocols resulted in efficient purification of EVs without the need of expensive material or ultracentrifugation. Furthermore, the procedure is easily scalable to work with large and small sample volumes. Here, we propose that both of our approaches can be used in resource limited countries, therefore further helping to close the gap in knowledge of EVs during malaria.

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