4.7 Article

Monitoring Distribution Dynamics of EV RNA Cargo Within Recipient Monocytes and Macrophages

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2021.739628

关键词

Palsmodium falciparum; extracellular vesicles (EVs); imaging flow cytometry (IFC); parasite; uptake

资金

  1. Weizmann Institute of Science, Staff Scientists Internal Grant
  2. Benoziyo Endowment Fund for the Advancement of Science
  3. Jeanne and Joseph Nissim Foundation for Life Sciences Research
  4. Samuel M. Soref and Helene K. Soref Foundation
  5. European Research Council (ERC) under the European Union [757743]
  6. Israel Science Foundation (ISF) [619/16, 2235/16]
  7. Israel Precision Medicine Program (IPMP) [1637/20]
  8. European Research Council (ERC) [757743] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Extracellular vesicles (EVs) play a crucial role in cell-cell communication processes and are especially important for pathogens like malaria parasites. Monitoring the uptake of malaria-derived EVs by host cells using imaging flow cytometry has been demonstrated. By staining the RNA cargo and monitoring its distribution, the kinetics of cargo delivery and distribution parameters can be evaluated.
Extracellular vesicles (EVs) are produced by across almost all the living kingdoms and play a crucial role in cell-cell communication processes. EVs are especially important for pathogens, as Plasmodium falciparum (Pf) parasite, the leading causing species in human malaria. Malaria parasites are able to modulate the host immune response from a distance via delivering diverse cargo components inside the EVs, such as proteins and nucleic acids. We have previously shown that imaging flow cytometry (IFC) can be effectively used to monitor the uptake of different cargo components of malaria derived EVs by host human monocytes. Here, we take this approach one step further and demonstrate that we can directly investigate the dynamics of the cargo distribution pattern over time by monitoring its distribution within two different recipient cells of the immune system, monocytes vs macrophages. By staining the RNA cargo of the vesicles and monitor the signal we were able to evaluate the kinetics of its delivery and measure different parameters of the cargo's distribution post internalization. Interestingly, we found that while the level of the EV uptake is similar, the pattern of the signal for RNA cargo distribution is significantly different between these two recipient immune cells. Our results demonstrate that this method can be applied to study the distribution dynamics of the vesicle cargo post uptake to different types of cells. This can benefit significantly to our understanding of the fate of cargo components post vesicle internalization in the complex interface between pathogen-derived vesicles and their host recipient cells.

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