Cargando…
Preformed Membrane-Associated Stores of Interleukin (Il)-12 Are a Previously Unrecognized Source of Bioactive IL-12 That Is Mobilized within Minutes of Contact with an Intracellular Parasite
The prevailing paradigm is that production of the interleukin (IL)-12 p70 heterodimer, a critical T helper cell type 1 (Th1)–inducing cytokine, depends on the induced transcription of the p40 subunit. Concordant with this paradigm, we found that dendritic cells (DCs) produced IL-12 p70 only after at...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2000
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193237/ https://www.ncbi.nlm.nih.gov/pubmed/10952720 |
_version_ | 1782147423523569664 |
---|---|
author | Quinones, Marlon Ahuja, Sunil K. Melby, Peter C. Pate, Lyle Reddick, Robert L. Ahuja, Seema S. |
author_facet | Quinones, Marlon Ahuja, Sunil K. Melby, Peter C. Pate, Lyle Reddick, Robert L. Ahuja, Seema S. |
author_sort | Quinones, Marlon |
collection | PubMed |
description | The prevailing paradigm is that production of the interleukin (IL)-12 p70 heterodimer, a critical T helper cell type 1 (Th1)–inducing cytokine, depends on the induced transcription of the p40 subunit. Concordant with this paradigm, we found that dendritic cells (DCs) produced IL-12 p70 only after at least 2–4 h of stimulation with lipopolysaccharide plus interferon γ. However, using several complementary experimental approaches, including electron and confocal microscopy, we now show that resting murine and human myeloid cells, including macrophages/DCs and DC-rich tissues, contain a novel source of bioactive IL-12 that is preformed and membrane associated. These preformed, membrane-associated IL-12 p70 stores are released within minutes after in vitro or in vivo contact with Leishmania donovani, an intracellular pathogen. Our findings highlight a novel source of bioactive IL-12 that is readily available for the rapid initiation of Th1 host responses to pathogens such as Leishmania species. |
format | Text |
id | pubmed-2193237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21932372008-04-16 Preformed Membrane-Associated Stores of Interleukin (Il)-12 Are a Previously Unrecognized Source of Bioactive IL-12 That Is Mobilized within Minutes of Contact with an Intracellular Parasite Quinones, Marlon Ahuja, Sunil K. Melby, Peter C. Pate, Lyle Reddick, Robert L. Ahuja, Seema S. J Exp Med Original Article The prevailing paradigm is that production of the interleukin (IL)-12 p70 heterodimer, a critical T helper cell type 1 (Th1)–inducing cytokine, depends on the induced transcription of the p40 subunit. Concordant with this paradigm, we found that dendritic cells (DCs) produced IL-12 p70 only after at least 2–4 h of stimulation with lipopolysaccharide plus interferon γ. However, using several complementary experimental approaches, including electron and confocal microscopy, we now show that resting murine and human myeloid cells, including macrophages/DCs and DC-rich tissues, contain a novel source of bioactive IL-12 that is preformed and membrane associated. These preformed, membrane-associated IL-12 p70 stores are released within minutes after in vitro or in vivo contact with Leishmania donovani, an intracellular pathogen. Our findings highlight a novel source of bioactive IL-12 that is readily available for the rapid initiation of Th1 host responses to pathogens such as Leishmania species. The Rockefeller University Press 2000-08-21 /pmc/articles/PMC2193237/ /pubmed/10952720 Text en © 2000 The Rockefeller University Press 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 | Original Article Quinones, Marlon Ahuja, Sunil K. Melby, Peter C. Pate, Lyle Reddick, Robert L. Ahuja, Seema S. Preformed Membrane-Associated Stores of Interleukin (Il)-12 Are a Previously Unrecognized Source of Bioactive IL-12 That Is Mobilized within Minutes of Contact with an Intracellular Parasite |
title | Preformed Membrane-Associated Stores of Interleukin (Il)-12 Are a Previously Unrecognized Source of Bioactive IL-12 That Is Mobilized within Minutes of Contact with an Intracellular Parasite |
title_full | Preformed Membrane-Associated Stores of Interleukin (Il)-12 Are a Previously Unrecognized Source of Bioactive IL-12 That Is Mobilized within Minutes of Contact with an Intracellular Parasite |
title_fullStr | Preformed Membrane-Associated Stores of Interleukin (Il)-12 Are a Previously Unrecognized Source of Bioactive IL-12 That Is Mobilized within Minutes of Contact with an Intracellular Parasite |
title_full_unstemmed | Preformed Membrane-Associated Stores of Interleukin (Il)-12 Are a Previously Unrecognized Source of Bioactive IL-12 That Is Mobilized within Minutes of Contact with an Intracellular Parasite |
title_short | Preformed Membrane-Associated Stores of Interleukin (Il)-12 Are a Previously Unrecognized Source of Bioactive IL-12 That Is Mobilized within Minutes of Contact with an Intracellular Parasite |
title_sort | preformed membrane-associated stores of interleukin (il)-12 are a previously unrecognized source of bioactive il-12 that is mobilized within minutes of contact with an intracellular parasite |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193237/ https://www.ncbi.nlm.nih.gov/pubmed/10952720 |
work_keys_str_mv | AT quinonesmarlon preformedmembraneassociatedstoresofinterleukinil12areapreviouslyunrecognizedsourceofbioactiveil12thatismobilizedwithinminutesofcontactwithanintracellularparasite AT ahujasunilk preformedmembraneassociatedstoresofinterleukinil12areapreviouslyunrecognizedsourceofbioactiveil12thatismobilizedwithinminutesofcontactwithanintracellularparasite AT melbypeterc preformedmembraneassociatedstoresofinterleukinil12areapreviouslyunrecognizedsourceofbioactiveil12thatismobilizedwithinminutesofcontactwithanintracellularparasite AT patelyle preformedmembraneassociatedstoresofinterleukinil12areapreviouslyunrecognizedsourceofbioactiveil12thatismobilizedwithinminutesofcontactwithanintracellularparasite AT reddickrobertl preformedmembraneassociatedstoresofinterleukinil12areapreviouslyunrecognizedsourceofbioactiveil12thatismobilizedwithinminutesofcontactwithanintracellularparasite AT ahujaseemas preformedmembraneassociatedstoresofinterleukinil12areapreviouslyunrecognizedsourceofbioactiveil12thatismobilizedwithinminutesofcontactwithanintracellularparasite |