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The c-kit Ligand, Stem Cell Factor, Can Enhance Innate Immunity Through Effects on Mast Cells
Mast cells are thought to contribute significantly to the pathology and mortality associated with anaphylaxis and other allergic disorders. However, studies using genetically mast cell–deficient WBB6F(1)-Kit(W)/Kit(W-v) and congenic wild-type (WBB6F(1)-+/+) mice indicate that mast cells can also pro...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1998
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212432/ https://www.ncbi.nlm.nih.gov/pubmed/9858520 |
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author | Maurer, Marcus Echtenacher, Bernd Hültner, Lothar Kollias, George Männel, Daniela N. Langley, Keith E. Galli, Stephen J. |
author_facet | Maurer, Marcus Echtenacher, Bernd Hültner, Lothar Kollias, George Männel, Daniela N. Langley, Keith E. Galli, Stephen J. |
author_sort | Maurer, Marcus |
collection | PubMed |
description | Mast cells are thought to contribute significantly to the pathology and mortality associated with anaphylaxis and other allergic disorders. However, studies using genetically mast cell–deficient WBB6F(1)-Kit(W)/Kit(W-v) and congenic wild-type (WBB6F(1)-+/+) mice indicate that mast cells can also promote health, by participating in natural immune responses to bacterial infection. We previously reported that repetitive administration of the c-kit ligand, stem cell factor (SCF), can increase mast cell numbers in normal mice in vivo. In vitro studies have indicated that SCF can also modulate mast cell effector function. We now report that treatment with SCF can significantly improve the survival of normal C57BL/6 mice in a model of acute bacterial peritonitis, cecal ligation and puncture (CLP). Experiments in mast cell–reconstituted WBB6F(1)-Kit(W)/Kit(W-v) mice indicate that this effect of SCF treatment reflects, at least in part, the actions of SCF on mast cells. Repetitive administration of SCF also can enhance survival in mice that genetically lack tumor necrosis factor (TNF)-α, demonstrating that the ability of SCF treatment to improve survival after CLP does not solely reflect effects of SCF on mast cell– dependent (or –independent) production of TNF-α. These findings identify c-kit and mast cells as potential therapeutic targets for enhancing innate immune responses. |
format | Text |
id | pubmed-2212432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22124322008-04-16 The c-kit Ligand, Stem Cell Factor, Can Enhance Innate Immunity Through Effects on Mast Cells Maurer, Marcus Echtenacher, Bernd Hültner, Lothar Kollias, George Männel, Daniela N. Langley, Keith E. Galli, Stephen J. J Exp Med Articles Mast cells are thought to contribute significantly to the pathology and mortality associated with anaphylaxis and other allergic disorders. However, studies using genetically mast cell–deficient WBB6F(1)-Kit(W)/Kit(W-v) and congenic wild-type (WBB6F(1)-+/+) mice indicate that mast cells can also promote health, by participating in natural immune responses to bacterial infection. We previously reported that repetitive administration of the c-kit ligand, stem cell factor (SCF), can increase mast cell numbers in normal mice in vivo. In vitro studies have indicated that SCF can also modulate mast cell effector function. We now report that treatment with SCF can significantly improve the survival of normal C57BL/6 mice in a model of acute bacterial peritonitis, cecal ligation and puncture (CLP). Experiments in mast cell–reconstituted WBB6F(1)-Kit(W)/Kit(W-v) mice indicate that this effect of SCF treatment reflects, at least in part, the actions of SCF on mast cells. Repetitive administration of SCF also can enhance survival in mice that genetically lack tumor necrosis factor (TNF)-α, demonstrating that the ability of SCF treatment to improve survival after CLP does not solely reflect effects of SCF on mast cell– dependent (or –independent) production of TNF-α. These findings identify c-kit and mast cells as potential therapeutic targets for enhancing innate immune responses. The Rockefeller University Press 1998-12-21 /pmc/articles/PMC2212432/ /pubmed/9858520 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 Maurer, Marcus Echtenacher, Bernd Hültner, Lothar Kollias, George Männel, Daniela N. Langley, Keith E. Galli, Stephen J. The c-kit Ligand, Stem Cell Factor, Can Enhance Innate Immunity Through Effects on Mast Cells |
title | The c-kit Ligand, Stem Cell Factor, Can Enhance Innate Immunity Through Effects on Mast Cells |
title_full | The c-kit Ligand, Stem Cell Factor, Can Enhance Innate Immunity Through Effects on Mast Cells |
title_fullStr | The c-kit Ligand, Stem Cell Factor, Can Enhance Innate Immunity Through Effects on Mast Cells |
title_full_unstemmed | The c-kit Ligand, Stem Cell Factor, Can Enhance Innate Immunity Through Effects on Mast Cells |
title_short | The c-kit Ligand, Stem Cell Factor, Can Enhance Innate Immunity Through Effects on Mast Cells |
title_sort | c-kit ligand, stem cell factor, can enhance innate immunity through effects on mast cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212432/ https://www.ncbi.nlm.nih.gov/pubmed/9858520 |
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