<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Mbagwu, Smart Ikechukwu</dc:creator>
  <dc:creator>Lannes, Nils</dc:creator>
  <dc:creator>Walch, Michael</dc:creator>
  <dc:creator>Filgueira, Luis</dc:creator>
  <dc:creator>Mantel, Pierre-Yves</dc:creator>
  <dc:date>2019-12-24</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Microglia are the chief immune cells of the brain and have been reported to be  activated in severe malaria. Their activation may drive towards neuroinflammation in  cerebral malaria. Malaria-infected red blood cell derived-extracellular vesicles  (MiREVs) are produced during the blood stage of malaria infection. They mediate  intercellular communication and immune regulation, among other functions. During  cerebral malaria, the breakdown of the bloodbrain barrier can promote the migration  of substances such as MiREVs from the periphery into the brain, targeting cells such  as microglia. Microglia and extracellular vesicle interactions in different pathological  conditions have been reported to induce neuroinflammation. Unlike in astrocytes,  microgliaextracellular vesicle interaction has not yet been described in malaria  infection. Therefore, in this study, we aimed to investigate the uptake of MiREVs by  human microglia cells and their cytokine response. Human blood monocyte-derived  microglia (MoMi) were generated from buffy coats of anonymous healthy donors using  Ficoll-Paque density gradient centrifugation. The MiREVs were isolated from the  Plasmodium falciparum cultures. They were purified by ultracentrifugation and labeled  with PKH67 green fluorescent dye. The internalization of MiREVs by MoMi was  observed after 4 h of co-incubation on coverslips placed in a 24-well plate at 37 C  using confocal microscopy. Cytokine-gene expression was investigated using rt- qPCR, following the stimulation of the MoMi cells with supernatants from the parasite  cultures at 2, 4, and 24 h, respectively. MiREVs were internalized by the microglia and  accumulated in the perinuclear region. MiREVs-treated cells increased gene  expression of the inflammatory cytokine TNF and reduced gene expression of the  immune suppressive IL-10. Overall, the results indicate that MiREVs may act on  microglia, which would contribute to enhanced inflammation in cerebral malaria.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/308559</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308559/files/man_hmr.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3390/pathogens9010021</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Pathogens. - 2020, vol. 9, no. 1, p. 21</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Human microglia respond to malaria-induced extracellular vesicles</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
