Cargando…

A potassium ionophore (Nigericin) inhibits stimulation of human lymphocytes by mitogens

Nigericin, an ionophore that exchanges K+ for H+ across most biologic membranes, reversibly inhibited the proliferative response of human lymphocytes to phytohemagglutinin (PHA). Inhibition occurred at nigericin concentrations of 10(-8) M or greater, and only during the early event of mitogenesis. T...

Descripción completa

Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1978
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184504/
https://www.ncbi.nlm.nih.gov/pubmed/146727
_version_ 1782145687091150848
collection PubMed
description Nigericin, an ionophore that exchanges K+ for H+ across most biologic membranes, reversibly inhibited the proliferative response of human lymphocytes to phytohemagglutinin (PHA). Inhibition occurred at nigericin concentrations of 10(-8) M or greater, and only during the early event of mitogenesis. There was no effect if nigericin was added 24 h or later after the initiation of PHA-stimulated cultures. The effect was not the result of toxicity or impaired mitochondrial respiration. At similar concentrations, nigericin also inhibited lymphocyte responses in mixed lymphocyte cultures and to other mitogens including concanavalin A, pokeweed mitogen, and the calcium ionophore A23187. The findings support the view that one or more transmembranous events, mediated by changes in cation flux and/or membrane potential, are critical in the initial stages of lymphocyte mitogenesis.
format Text
id pubmed-2184504
institution National Center for Biotechnology Information
language English
publishDate 1978
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21845042008-04-17 A potassium ionophore (Nigericin) inhibits stimulation of human lymphocytes by mitogens J Exp Med Articles Nigericin, an ionophore that exchanges K+ for H+ across most biologic membranes, reversibly inhibited the proliferative response of human lymphocytes to phytohemagglutinin (PHA). Inhibition occurred at nigericin concentrations of 10(-8) M or greater, and only during the early event of mitogenesis. There was no effect if nigericin was added 24 h or later after the initiation of PHA-stimulated cultures. The effect was not the result of toxicity or impaired mitochondrial respiration. At similar concentrations, nigericin also inhibited lymphocyte responses in mixed lymphocyte cultures and to other mitogens including concanavalin A, pokeweed mitogen, and the calcium ionophore A23187. The findings support the view that one or more transmembranous events, mediated by changes in cation flux and/or membrane potential, are critical in the initial stages of lymphocyte mitogenesis. The Rockefeller University Press 1978-02-01 /pmc/articles/PMC2184504/ /pubmed/146727 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 Articles
A potassium ionophore (Nigericin) inhibits stimulation of human lymphocytes by mitogens
title A potassium ionophore (Nigericin) inhibits stimulation of human lymphocytes by mitogens
title_full A potassium ionophore (Nigericin) inhibits stimulation of human lymphocytes by mitogens
title_fullStr A potassium ionophore (Nigericin) inhibits stimulation of human lymphocytes by mitogens
title_full_unstemmed A potassium ionophore (Nigericin) inhibits stimulation of human lymphocytes by mitogens
title_short A potassium ionophore (Nigericin) inhibits stimulation of human lymphocytes by mitogens
title_sort potassium ionophore (nigericin) inhibits stimulation of human lymphocytes by mitogens
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184504/
https://www.ncbi.nlm.nih.gov/pubmed/146727