首页> 外文期刊>European Journal of Immunology >Interleukin-4-triggered, STAT6-dependent production of a factor that induces mouse mast cell apoptosis.
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Interleukin-4-triggered, STAT6-dependent production of a factor that induces mouse mast cell apoptosis.

机译:Interleukin-4-triggered, STAT6-dependent生产诱发小鼠肥大的一个因素细胞凋亡。

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摘要

IL-4 can suppress mast cell development from mouse spleen, bone marrow and peritoneal cells by an indirect process that is dependent on the presence of macrophages. Mast cells undergo apoptosis when exposed to supernatants collected from cultures of IL-4-stimulated peritoneal cells due to the IL-4-induced production of an apoptosis-inducing factor in the cultures. This effect of IL-4 is shown to be dependent on STAT6 signaling, because IL-4 and IL-13 do not suppress mast cell development from the spleen and peritoneal cells of STAT6-/- mice. Moreover, supernatants from cultures of IL-4- and IL-13-stimulated peritoneal cells of STAT6-/- mice do not exhibit apoptosis-inducing activity. We confirm, by using deficient mice, neutralizing antibodies and recombinant cytokines, that IL-4-induced apoptosis is not related to the well-known apoptosis-inducing factors Fas, Fas ligand, TNF-alpha, TRAIL, TGF-beta or perforin. These results demonstrate a novel mechanism whereby IL-4 and IL-13 can suppress mast cell development by inducing the production of an apoptosis-inducing factor from macrophages.
机译:从小鼠il - 4可以抑制肥大细胞的发展脾脏、骨髓和腹膜细胞的间接的依赖的过程巨噬细胞的存在。细胞凋亡时接触到上层的收集从文化IL-4-stimulated腹膜细胞由于IL-4-induced生产的凋亡诱导因素的文化。效果依赖STAT6 il - 4所示信号,因为il - 4和IL-13不抑制从脾和肥大细胞的发展STAT6 - / -小鼠腹膜细胞。上层清液il - 4和文化IL-13-stimulated腹膜细胞STAT6 - / -老鼠不表现出凋亡诱导活性。我们确认,通过使用有缺陷的老鼠,中和抗体和细胞因子,重组IL-4-induced凋亡并不相关著名的凋亡诱导因素Fas, Fas配体、tnf、跟踪,及或穿孔素。这些结果表明一种新的机制, il - 4和IL-13可以抑制肥大细胞通过诱导的生产发展从巨噬细胞凋亡诱导因素。

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