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Ptk6-/- 雄性小鼠小肠中琥珀酸诱导的 2 型免疫和分泌细胞产生受损。

Impaired activation of succinate-induced type 2 immunity and secretory cell production in the small intestines of Ptk6-/- male mice.

机构信息

Department of Biochemistry and Molecular Genetics, University of Illinois College of Medicine, University of Illinois at Chicago, Chicago, IL, 60607, USA.

University of Washington, Seattle, WA, USA.

出版信息

Cell Death Dis. 2024 Oct 26;15(10):777. doi: 10.1038/s41419-024-07149-9.

Abstract

Protein tyrosine kinase 6 (PTK6) is an intracellular tyrosine kinase that is distantly related to the SRC family of tyrosine kinases. It is expressed in epithelial linings and regulates regeneration and repair of the intestinal epithelium. Analysis of publicly available datasets showed Ptk6 is upregulated in tuft cells upon activation of type 2 immunity. We found that disruption of Ptk6 influences gene expression involved in intestinal immune responses. Administration of succinate, which mimics infection and activates tuft cells, revealed PTK6-dependent activation of innate immune responses in male but not female mice. In contrast to all wild type and Ptk6-/- female mice, Ptk6-/- male mice do not activate innate immunity or upregulate differentiation of the tuft and goblet secretory cell lineages following succinate treatment. Mechanistically, we found that PTK6 regulates Il25 and Irag2, genes that are required for tuft cell effector functions and activation of type 2 innate immunity, in organoids derived from intestines of male but not female mice. In patients with Crohn's disease, PTK6 is upregulated in tuft cells in noninflamed regions of intestine. These data highlight roles for PTK6 in contributing to sex differences in intestinal innate immunity and provide new insights into the regulation of IL-25.

摘要

蛋白酪氨酸激酶 6(PTK6)是一种细胞内酪氨酸激酶,与 SRC 家族的酪氨酸激酶有较远的亲缘关系。它在上皮衬里中表达,并调节肠道上皮的再生和修复。对公开可用数据集的分析表明,PTK6 在 2 型免疫激活时在类肠细胞中上调。我们发现,PTK6 的破坏会影响参与肠道免疫反应的基因表达。琥珀酸盐的给药,模拟感染并激活类肠细胞,揭示了 PTK6 依赖性的先天免疫反应在雄性而不是雌性小鼠中的激活。与所有野生型和 Ptk6-/-雌性小鼠不同,Ptk6-/-雄性小鼠在琥珀酸盐处理后不会激活先天免疫或上调类肠细胞和杯状分泌细胞谱系的分化。从机制上讲,我们发现 PTK6 在源自雄性而非雌性小鼠肠道的类器官中调节 Il25 和 Irag2 基因,这些基因是类肠细胞效应功能和 2 型先天免疫激活所必需的。在克罗恩病患者中,PTK6 在肠道非炎症区域的类肠细胞中上调。这些数据突出了 PTK6 在肠道先天免疫的性别差异中的作用,并为 IL-25 的调节提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c48/11513114/329aaf7f7aae/41419_2024_7149_Fig1_HTML.jpg

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