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Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity

Reports from a number of laboratories have shown that mAbs against the T3-Ti receptor complex cause an increase in cytosolic-free Ca2+ [( Ca2+]i) and the hydrolysis of phosphatidylinositolbisphosphate (PIP2) in CTLs. In the present report we show that activation of CTLs by their specific targets cau...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1987
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188645/
https://www.ncbi.nlm.nih.gov/pubmed/3036996
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description Reports from a number of laboratories have shown that mAbs against the T3-Ti receptor complex cause an increase in cytosolic-free Ca2+ [( Ca2+]i) and the hydrolysis of phosphatidylinositolbisphosphate (PIP2) in CTLs. In the present report we show that activation of CTLs by their specific targets causes: (a) release of Ca2+ from intracellular stores; (b) transient formation of inositol trisphosphate (InsP3); and (c) an increased permeability to Ca2+ of CTL plasma membrane. Killing of unrelated targets could be induced by cocentrifugation of the unrelated targets with CTLs in the presence of A23187 or PMA. We conclude that: (a) activation of CTLs by specific antigens triggers the generation of the same intracellular mediators generated by stimulation of lymphocytes with anti-T3-Ti receptor antibodies and/or with polyclonal mitogens; and (b) intracellular signals that mediate the delivery of the lethal hit by CTLs are indistinguishable from those that induce cell proliferation.
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spelling pubmed-21886452008-04-17 Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity J Exp Med Articles Reports from a number of laboratories have shown that mAbs against the T3-Ti receptor complex cause an increase in cytosolic-free Ca2+ [( Ca2+]i) and the hydrolysis of phosphatidylinositolbisphosphate (PIP2) in CTLs. In the present report we show that activation of CTLs by their specific targets causes: (a) release of Ca2+ from intracellular stores; (b) transient formation of inositol trisphosphate (InsP3); and (c) an increased permeability to Ca2+ of CTL plasma membrane. Killing of unrelated targets could be induced by cocentrifugation of the unrelated targets with CTLs in the presence of A23187 or PMA. We conclude that: (a) activation of CTLs by specific antigens triggers the generation of the same intracellular mediators generated by stimulation of lymphocytes with anti-T3-Ti receptor antibodies and/or with polyclonal mitogens; and (b) intracellular signals that mediate the delivery of the lethal hit by CTLs are indistinguishable from those that induce cell proliferation. The Rockefeller University Press 1987-07-01 /pmc/articles/PMC2188645/ /pubmed/3036996 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
Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity
title Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity
title_full Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity
title_fullStr Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity
title_full_unstemmed Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity
title_short Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity
title_sort calcium and inositolphosphates in the activation of t cell-mediated cytotoxicity
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188645/
https://www.ncbi.nlm.nih.gov/pubmed/3036996