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dc.provenanceCONICET-
dc.creatorMuchnik, Rosa-
dc.creatorAgusti, Rosalia-
dc.creatorDocampo, Roberto-
dc.date2019-01-28T20:19:20Z-
dc.date2019-01-28T20:19:20Z-
dc.date2011-03-
dc.date2019-01-28T14:01:51Z-
dc.date.accessioned2019-04-29T15:38:51Z-
dc.date.available2019-04-29T15:38:51Z-
dc.date.issued2011-03-
dc.identifierMuchnik, Rosa; Agusti, Rosalia; Docampo, Roberto; Inositolphosphoceramide metabolism in Trypanosoma cruzi as compared with other trypanosomatids; Wiley Blackwell Publishing, Inc; Journal of Eukaryotic Microbiology; 58; 2; 3-2011; 79-87-
dc.identifier1066-5234-
dc.identifierhttp://hdl.handle.net/11336/68818-
dc.identifierCONICET Digital-
dc.identifierCONICET-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/298471-
dc.descriptionChagas disease is caused by Trypanosoma cruzi and is endemic to North, Central and South American countries. Current therapy against this disease is only partially effective and produces adverse side effects. Studies on the metabolic pathways of T. cruzi, in particular those with no equivalent in mammalian cells, might identify targets for the development of new drugs. Ceramide is metabolized to inositolphosphoceramide (IPC) in T. cruzi and other kinetoplastid protists whereas in mammals it is mainly incorporated into sphingomyelin. In T. cruzi, in contrast to Trypanosoma brucei and Leishmania spp., IPC functions as lipid anchor constituent of glycoproteins and free glycosylinositolphospholipids (GIPLs). Inhibition of IPC and GIPLs biosynthesis impairs differentiation of trypomastigotes into the intracellular amastigote forms. The gene encoding IPC synthase in T. cruzi has been identified and the enzyme has been expressed in a cell-free system. The enzyme involved in IPC degradation and the remodelases responsible for the incorporation of ceramide into free GIPLs or into the glycosylphosphatidylinositols anchoring glycoproteins, and in fatty acid modifications of these molecules of T. cruzi have been understudied. Inositolphosphoceramide metabolism and remodeling could be exploited as targets for Chagas disease chemotherapy.-
dc.descriptionFil: Muchnik, Rosa. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones en Hidratos de Carbono; Argentina-
dc.descriptionFil: Agusti, Rosalia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones en Hidratos de Carbono; Argentina-
dc.descriptionFil: Docampo, Roberto. University of Georgia; Estados Unidos-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherWiley Blackwell Publishing, Inc-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1550-7408.2011.00533.x-
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1111/j.1550-7408.2011.00533.x-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/-
dc.sourcereponame:CONICET Digital (CONICET)-
dc.sourceinstname:Consejo Nacional de Investigaciones Científicas y Técnicas-
dc.sourceinstacron:CONICET-
dc.source.urihttp://hdl.handle.net/11336/68818-
dc.subjectGLYCOSYLINOSITOLPHOSPHOLIPIDS-
dc.subjectGLYCOSYLPHOSPHATIDYLINOSITOL-
dc.subjectINOSITOLPHOSPHOCERAMIDE-
dc.subjectPHOSPHOLIPASE C-
dc.subjectSPHINGOLIPIDS-
dc.subjectTRYPANOSOMA-
dc.subjectOtras Ciencias Químicas-
dc.subjectCiencias Químicas-
dc.subjectCIENCIAS NATURALES Y EXACTAS-
dc.titleInositolphosphoceramide metabolism in Trypanosoma cruzi as compared with other trypanosomatids-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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