Division of Immunology & Pathogenesis, Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Division of Immunology & Pathogenesis, Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Immunity. 2018 Sep 18;49(3):560-575.e6. doi: 10.1016/j.immuni.2018.07.016. Epub 2018 Aug 28.
Signaling by Toll-like receptors (TLRs) on intestinal epithelial cells (IECs) is critical for intestinal homeostasis. To visualize epithelial expression of individual TLRs in vivo, we generated five strains of reporter mice. These mice revealed that TLR expression varied dramatically along the length of the intestine. Indeed, small intestine (SI) IECs expressed low levels of multiple TLRs that were highly expressed by colonic IECs. TLR5 expression was restricted to Paneth cells in the SI epithelium. Intestinal organoid experiments revealed that TLR signaling in Paneth cells or colonic IECs induced a core set of host defense genes, but this set did not include antimicrobial peptides, which instead were induced indirectly by inflammatory cytokines. This comprehensive blueprint of TLR expression and function in IECs reveals unexpected diversity in the responsiveness of IECs to microbial stimuli, and together with the associated reporter strains, provides a resource for further study of innate immunity.
肠上皮细胞(IECs)上 Toll 样受体(TLRs)的信号转导对于肠道内稳态至关重要。为了在体内可视化单个 TLR 在肠上皮细胞中的表达,我们构建了五个报告基因小鼠品系。这些小鼠揭示了 TLR 表达沿着肠道的长度呈现出显著的差异。事实上,小肠(SI)IECs 表达多种 TLR 的水平较低,而这些 TLR 在结肠 IECs 中高度表达。TLR5 的表达局限于 SI 上皮中的潘氏细胞。肠道类器官实验表明,潘氏细胞或结肠 IEC 中的 TLR 信号转导诱导了一组核心宿主防御基因,但该组不包括抗菌肽,抗菌肽是由炎症细胞因子间接诱导的。这种 TLR 在 IECs 中表达和功能的综合蓝图揭示了 IECs 对微生物刺激的反应存在意想不到的多样性,与相关的报告基因株一起,为先天免疫的进一步研究提供了资源。