Cargando…

Differential Stimulation of the Na(+)/H(+) Exchanger Determines Chloroquine Uptake in Plasmodium falciparum

Here we describe the identification and characterization of a physiological marker that is associated with the chloroquine-resistant (CQR) phenotype in the human malarial parasite Plasmodium falciparum. Single cell in vivo pH measurements revealed that CQR parasites consistently have an elevated cyt...

Descripción completa

Detalles Bibliográficos
Autores principales: Wünsch, Stefan, Sanchez, Cecilia P., Gekle, Michael, Große-Wortmann, Lars, Wiesner, Jochen, Lanzer, Michael
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2132566/
https://www.ncbi.nlm.nih.gov/pubmed/9442109
_version_ 1782142475453857792
author Wünsch, Stefan
Sanchez, Cecilia P.
Gekle, Michael
Große-Wortmann, Lars
Wiesner, Jochen
Lanzer, Michael
author_facet Wünsch, Stefan
Sanchez, Cecilia P.
Gekle, Michael
Große-Wortmann, Lars
Wiesner, Jochen
Lanzer, Michael
author_sort Wünsch, Stefan
collection PubMed
description Here we describe the identification and characterization of a physiological marker that is associated with the chloroquine-resistant (CQR) phenotype in the human malarial parasite Plasmodium falciparum. Single cell in vivo pH measurements revealed that CQR parasites consistently have an elevated cytoplasmic pH compared to that of chloroquine-sensitive (CQS) parasites because of a constitutively activated Na(+)/H(+) exchanger (NHE). Together, biochemical and physiological data suggest that chloroquine activates the plasmodial NHE of CQS parasites, resulting in a transitory phase of rapid sodium/hydrogen ion exchange during which chloroquine is taken up by this protein. The constitutively stimulated NHE of CQR parasites are capable of little or no further activation by chloroquine. We propose that the inability of chloroquine to stimulate its own uptake through the constitutively activated NHE of resistant parasites constitutes a minimal and necessary event in the generation of the chloroquine-resistant phenotype.
format Text
id pubmed-2132566
institution National Center for Biotechnology Information
language English
publishDate 1998
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21325662008-05-01 Differential Stimulation of the Na(+)/H(+) Exchanger Determines Chloroquine Uptake in Plasmodium falciparum Wünsch, Stefan Sanchez, Cecilia P. Gekle, Michael Große-Wortmann, Lars Wiesner, Jochen Lanzer, Michael J Cell Biol Article Here we describe the identification and characterization of a physiological marker that is associated with the chloroquine-resistant (CQR) phenotype in the human malarial parasite Plasmodium falciparum. Single cell in vivo pH measurements revealed that CQR parasites consistently have an elevated cytoplasmic pH compared to that of chloroquine-sensitive (CQS) parasites because of a constitutively activated Na(+)/H(+) exchanger (NHE). Together, biochemical and physiological data suggest that chloroquine activates the plasmodial NHE of CQS parasites, resulting in a transitory phase of rapid sodium/hydrogen ion exchange during which chloroquine is taken up by this protein. The constitutively stimulated NHE of CQR parasites are capable of little or no further activation by chloroquine. We propose that the inability of chloroquine to stimulate its own uptake through the constitutively activated NHE of resistant parasites constitutes a minimal and necessary event in the generation of the chloroquine-resistant phenotype. The Rockefeller University Press 1998-01-26 /pmc/articles/PMC2132566/ /pubmed/9442109 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Wünsch, Stefan
Sanchez, Cecilia P.
Gekle, Michael
Große-Wortmann, Lars
Wiesner, Jochen
Lanzer, Michael
Differential Stimulation of the Na(+)/H(+) Exchanger Determines Chloroquine Uptake in Plasmodium falciparum
title Differential Stimulation of the Na(+)/H(+) Exchanger Determines Chloroquine Uptake in Plasmodium falciparum
title_full Differential Stimulation of the Na(+)/H(+) Exchanger Determines Chloroquine Uptake in Plasmodium falciparum
title_fullStr Differential Stimulation of the Na(+)/H(+) Exchanger Determines Chloroquine Uptake in Plasmodium falciparum
title_full_unstemmed Differential Stimulation of the Na(+)/H(+) Exchanger Determines Chloroquine Uptake in Plasmodium falciparum
title_short Differential Stimulation of the Na(+)/H(+) Exchanger Determines Chloroquine Uptake in Plasmodium falciparum
title_sort differential stimulation of the na(+)/h(+) exchanger determines chloroquine uptake in plasmodium falciparum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2132566/
https://www.ncbi.nlm.nih.gov/pubmed/9442109
work_keys_str_mv AT wunschstefan differentialstimulationofthenahexchangerdetermineschloroquineuptakeinplasmodiumfalciparum
AT sanchezceciliap differentialstimulationofthenahexchangerdetermineschloroquineuptakeinplasmodiumfalciparum
AT geklemichael differentialstimulationofthenahexchangerdetermineschloroquineuptakeinplasmodiumfalciparum
AT großewortmannlars differentialstimulationofthenahexchangerdetermineschloroquineuptakeinplasmodiumfalciparum
AT wiesnerjochen differentialstimulationofthenahexchangerdetermineschloroquineuptakeinplasmodiumfalciparum
AT lanzermichael differentialstimulationofthenahexchangerdetermineschloroquineuptakeinplasmodiumfalciparum