dc.contributor.author | Noulin, F. | |
dc.contributor.author | Manesia, J. K. | |
dc.contributor.author | Rosanas-Urgell, A. | |
dc.contributor.author | Erhart, A. | |
dc.contributor.author | Borlon, C. | |
dc.contributor.author | Van Den Abbeele, J. | |
dc.contributor.author | D'Alessandro, U. | |
dc.contributor.author | Verfaillie, C. M. | |
dc.date.accessioned | 2015-02-10T15:18:56Z | |
dc.date.available | 2015-02-10T15:18:56Z | |
dc.date.issued | 2014 | |
dc.identifier.issn | 1932-6203 | |
dc.identifier.doi | http://dx.doi.org/10.1371/journal.pone.0112496 | |
dc.identifier.other | ITG-B1B | |
dc.identifier.other | ITG-B3A | |
dc.identifier.other | ITG-B4A | |
dc.identifier.other | ITG-B5B | |
dc.identifier.other | ITG-B6A | |
dc.identifier.other | ITG-N7H | |
dc.identifier.other | DBM | |
dc.identifier.other | U-MALAR | |
dc.identifier.other | U-VPROT | |
dc.identifier.other | JIF | |
dc.identifier.other | DOI | |
dc.identifier.other | FTA | |
dc.identifier.other | OAJ | |
dc.identifier.other | E-only | |
dc.identifier.other | Abstract | |
dc.identifier.other | UPD57 | |
dc.identifier.uri | http://hdl.handle.net/10390/8262 | |
dc.description.abstract | The predilection of Plasmodium vivax (P. vivax) for reticulocytes is a major obstacle for its establishment in a long-term culture system, as this requires a continuous supply of large quantities of reticulocytes, representing only 1-2% of circulating red blood cells. We here compared the production of reticulocytes using an established in vitro culture system from three different sources of hematopoietic stem/progenitor cells (HSPC), i.e. umbilical cord blood (UCB), bone marrow (BM) and adult peripheral blood (PB). Compared to CD34+-enriched populations of PB and BM, CD34+-enriched populations of UCB produced the highest amount of reticulocytes that could be invaded by P. vivax. In addition, when CD34+-enriched cells were first expanded, a further extensive increase in reticulocytes was seen for UCB, to a lesser degree BM but not PB. As invasion by P. vivax was significantly better in reticulocytes generated in vitro, we also suggest that P. vivax may have a preference for invading immature reticulocytes, which should be confirmed in future studies. | en_US |
dc.language | English | en_US |
dc.subject | Protozoal diseases | en_US |
dc.subject | Malaria | en_US |
dc.subject | Plasmodium vivax | en_US |
dc.subject | Vectors | en_US |
dc.subject | Mosquitoes | en_US |
dc.subject | Anopheles | en_US |
dc.subject | In vitro | en_US |
dc.subject | Culture | en_US |
dc.subject | Reticulocytes | en_US |
dc.subject | Red blood cells | en_US |
dc.subject | Hematopoietic stem cells | en_US |
dc.subject | Peripheral blood | en_US |
dc.subject | Bone marrow | en_US |
dc.subject | CD34+ | en_US |
dc.subject | Laboratory techniques and procedures | en_US |
dc.title | Hematopoietic stem/progenitor cell sources to generate reticulocytes for Plasmodium vivax culture | en_US |
dc.type | Article-E | en_US |
dc.citation.issue | 11 | en_US |
dc.citation.jtitle | PLoS ONE | en_US |
dc.citation.volume | 9 | en_US |
dc.citation.pages | e112496 | en_US |
dc.identifier.pmid | http://www.ncbi.nlm.nih.gov/pubmed/25393299 | |
dc.citation.jabbreviation | PLoS ONE | en_US |