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Extracellular killing of Leishmania promastigotes and amastigotes by macrophage precursors derived from bone marrow cultures

Flagellates of the genus Leishmania are obligate intracellular parasites of vertebrates including man. The microorganisms reside and multiply inside the phagolysosomes of cells of the mononuclear phagocyte lineage. We here report on the spontaneous leishmanicidal activity exerted extracellularly by...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188919/
https://www.ncbi.nlm.nih.gov/pubmed/3356968
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description Flagellates of the genus Leishmania are obligate intracellular parasites of vertebrates including man. The microorganisms reside and multiply inside the phagolysosomes of cells of the mononuclear phagocyte lineage. We here report on the spontaneous leishmanicidal activity exerted extracellularly by immature cells of the mononuclear phagocyte lineage. Highly purified, bone marrow-derived macrophage precursor cells displayed a strong spontaneous leishmanicidal activity already at very low effector/target rations (3:1, 6:1). This leishmanicidal activity was effective against both promastigotes and amastigotes as targets. The cytotoxic effect was evident within 4 h and maximal after 12 h of effector-target organism cocultivation, as determined by a radiolabel-release assay. An intimate cell-cell contact seemed necessary for the parasites to be killed.
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spelling pubmed-21889192008-04-17 Extracellular killing of Leishmania promastigotes and amastigotes by macrophage precursors derived from bone marrow cultures J Exp Med Articles Flagellates of the genus Leishmania are obligate intracellular parasites of vertebrates including man. The microorganisms reside and multiply inside the phagolysosomes of cells of the mononuclear phagocyte lineage. We here report on the spontaneous leishmanicidal activity exerted extracellularly by immature cells of the mononuclear phagocyte lineage. Highly purified, bone marrow-derived macrophage precursor cells displayed a strong spontaneous leishmanicidal activity already at very low effector/target rations (3:1, 6:1). This leishmanicidal activity was effective against both promastigotes and amastigotes as targets. The cytotoxic effect was evident within 4 h and maximal after 12 h of effector-target organism cocultivation, as determined by a radiolabel-release assay. An intimate cell-cell contact seemed necessary for the parasites to be killed. The Rockefeller University Press 1988-04-01 /pmc/articles/PMC2188919/ /pubmed/3356968 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
Extracellular killing of Leishmania promastigotes and amastigotes by macrophage precursors derived from bone marrow cultures
title Extracellular killing of Leishmania promastigotes and amastigotes by macrophage precursors derived from bone marrow cultures
title_full Extracellular killing of Leishmania promastigotes and amastigotes by macrophage precursors derived from bone marrow cultures
title_fullStr Extracellular killing of Leishmania promastigotes and amastigotes by macrophage precursors derived from bone marrow cultures
title_full_unstemmed Extracellular killing of Leishmania promastigotes and amastigotes by macrophage precursors derived from bone marrow cultures
title_short Extracellular killing of Leishmania promastigotes and amastigotes by macrophage precursors derived from bone marrow cultures
title_sort extracellular killing of leishmania promastigotes and amastigotes by macrophage precursors derived from bone marrow cultures
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188919/
https://www.ncbi.nlm.nih.gov/pubmed/3356968