The c-kit ligand, stem cell factor, can enhance innate immunity through effects on mast cells

被引:126
作者
Maurer, M
Echtenacher, B
Hültner, L
Kollias, G
Männel, DN
Langley, KE
Galli, SJ
机构
[1] Beth Israel Deaconess Med Ctr E, Dept Pathol, Div Expt Pathol, Boston, MA 02215 USA
[2] Univ Regensburg, Inst Pathol Tumorimmunol, D-93042 Regensburg, Germany
[3] GSF Forschungszentrum Umwelt & Gesundheit, Inst Expt Hamatol, D-81337 Munich, Germany
[4] Hellen Pasteur Inst, Dept Mol Genet, Athens 11521, Greece
[5] Amgen Inc, Thousand Oaks, CA 91320 USA
关键词
c-kit; innate immunity; mast cells; stem cell factor; tumor necrosis; factor-alpha;
D O I
10.1084/jem.188.12.2343
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 call 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 WBB6F1-Kit(W)/Kit(W-v) mice indicate that this effect of SCF treatment reflects, at least in part, the actions of SCF oil mast cells. Repetitive administration of SCF also carl enhance survival in mice that genetically lack tumor necrosis factor (TNF)-alpha, 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-alpha, These findings identify c-kit and mast cells as potential therapeutic targets for enhancing innate immune responses.
引用
收藏
页码:2343 / 2348
页数:6
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