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dc.contributor.authorRuivo, Margarida T. Grilo
dc.contributor.authorVera, Iset Medina
dc.contributor.authorSales-Dias, Joana
dc.contributor.authorMeireles, Patrícia
dc.contributor.authorMota, Maria M.
dc.contributor.authorMancio-Silva, Liliana
dc.contributor.authorGural, Nil
dc.contributor.authorBhatia, Sangeeta N
dc.date.accessioned2017-01-10T15:39:12Z
dc.date.available2017-01-10T15:39:12Z
dc.date.issued2016-08
dc.date.submitted2016-04
dc.identifier.issn22111247
dc.identifier.urihttp://hdl.handle.net/1721.1/106319
dc.description.abstractManipulation of the master regulator of energy homeostasis AMP-activated protein kinase (AMPK) activity is a strategy used by many intracellular pathogens for successful replication. Infection by most pathogens leads to an activation of host AMPK activity due to the energetic demands placed on the infected cell. Here, we demonstrate that the opposite is observed in cells infected with rodent malaria parasites. Indeed, AMPK activity upon the infection of hepatic cells is suppressed and dispensable for successful infection. By contrast, an overactive AMPK is deleterious to intracellular growth and replication of different Plasmodium spp., including the human malaria parasite, P. falciparum. The negative impact of host AMPK activity on infection was further confirmed in mice under conditions that activate its function. Overall, this work establishes the role of host AMPK signaling as a suppressive pathway of Plasmodium hepatic infection and as a potential target for host-based antimalarial interventions.en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.celrep.2016.08.001en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceElsevieren_US
dc.titleHost AMPK Is a Modulator of Plasmodium Liver Infectionen_US
dc.typeArticleen_US
dc.identifier.citationRuivo, Margarida T. Grilo et al. “Host AMPK Is a Modulator of Plasmodium Liver Infection.” Cell Reports 16.10 (2016): 2539–2545.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.mitauthorGural, Nil
dc.contributor.mitauthorBhatia, Sangeeta N
dc.relation.journalCell Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsRuivo, Margarida T. Grilo; Vera, Iset Medina; Sales-Dias, Joana; Meireles, Patrícia; Gural, Nil; Bhatia, Sangeeta N.; Mota, Maria M.; Mancio-Silva, Lilianaen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1315-3885
dc.identifier.orcidhttps://orcid.org/0000-0002-1293-2097
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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