Department of Infection Biology, University Hospital Erlangen and Friedrich-Alexander University Erlangen-Nuremberg (FAU), Erlangen, Germany.
Department of Medicine 1, University Hospital Erlangen and Friedrich-Alexander University Erlangen-Nuremberg (FAU), Erlangen, Germany.
Mucosal Immunol. 2019 Mar;12(2):413-424. doi: 10.1038/s41385-018-0107-3. Epub 2018 Nov 16.
Intestinal epithelial cells (IECs) constitute an important barrier between host and pathogen. Immune mechanisms that provide protection against gastrointestinal helminths often require IL-4Rα-induced activation of STAT6-regulated genes in IECs. However, it is not known whether STAT6 activation in IECs enhances protective immunity against helminths. Furthermore, the regulation of proliferation and differentiation processes of the intestinal epithelium by IEC-intrinsic STAT6 signaling remains unclear. To address these questions, we generated mice with specific expression of a constitutively active version of STAT6 in IECs. These VillinCre_STAT6vt mice show accumulation of secretory IECs, increased proliferation of IECs and lengthening of the small intestine. They rapidly expelled Nippostrongylus brasiliensis worms even in the absence of T cells. Furthermore, primary infection with Heligmosomoides polygyrus resulted in larval trapping in the submucosa and the fecundity of adult worms was severely impaired. Our results reveal an important IEC-intrinsic role of STAT6-regulated genes for intestinal homeostasis and protective immunity against helminths.
肠上皮细胞 (IECs) 构成了宿主与病原体之间的重要屏障。提供针对胃肠道寄生虫保护的免疫机制通常需要 IEC 中 IL-4Rα 诱导的 STAT6 调节基因的激活。然而,尚不清楚 IEC 中的 STAT6 激活是否增强了针对寄生虫的保护性免疫。此外,IEC 固有 STAT6 信号转导对肠道上皮细胞增殖和分化过程的调节尚不清楚。为了解决这些问题,我们生成了在 IEC 中特异性表达组成型激活形式 STAT6 的小鼠。这些 VillinCre_STAT6vt 小鼠表现出分泌型 IEC 的积累、IEC 增殖增加和小肠变长。即使没有 T 细胞,它们也能迅速排出巴西旋毛虫蠕虫。此外,原发性感染旋毛虫会导致幼虫被困在黏膜下层,成虫的繁殖力严重受损。我们的研究结果揭示了 STAT6 调节基因在肠道稳态和针对寄生虫的保护性免疫中的重要 IEC 内在作用。