Schaller Research Group at CellNetworks, Department of Infectious Diseases, Virology, Heidelberg University Hospital, Heidelberg, Germany.
Laboratory for Intestinal Ecosystem, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Nat Microbiol. 2020 Jan;5(1):181-191. doi: 10.1038/s41564-019-0594-3. Epub 2019 Nov 4.
Intestinal epithelial cells (IECs) act as a physical barrier separating the commensal-containing intestinal tract from the sterile interior. These cells have found a complex balance allowing them to be prepared for pathogen attacks while still tolerating the presence of bacterial or viral stimuli present in the lumen of the gut. Using primary human IECs, we probed the mechanisms that allow for such a tolerance. We discovered that viral infections emanating from the basolateral side of IECs elicit a stronger intrinsic immune response in comparison to lumenal apical infections. We determined that this asymmetric immune response is driven by the clathrin-sorting adaptor AP-1B, which mediates the polarized sorting of Toll-like receptor 3 (TLR3) towards the basolateral side of IECs. Mice and human IECs lacking AP-1B showed an exacerbated immune response following apical stimulation. Together, these results suggest a model where the cellular polarity program plays an integral role in the ability of IECs to partially tolerate apical commensals while remaining fully responsive to invasive basolateral pathogens.
肠上皮细胞 (IECs) 作为一种物理屏障,将含有共生菌的肠道与无菌的内部隔开。这些细胞已经找到了一种复杂的平衡,使它们能够为病原体的攻击做好准备,同时仍然能够耐受肠道腔中存在的细菌或病毒刺激。我们使用原代人 IECs 来探究允许这种耐受的机制。我们发现,与腔顶感染相比,源自 IECs 基底外侧的病毒感染会引发更强的固有免疫反应。我们确定这种不对称的免疫反应是由网格蛋白分选衔接蛋白 AP-1B 驱动的,该蛋白介导 Toll 样受体 3 (TLR3) 向 IECs 的基底外侧的极化分选。缺乏 AP-1B 的小鼠和人 IECs 在受到腔顶刺激后表现出过度的免疫反应。总之,这些结果表明,细胞极性程序在 IEC 部分耐受腔顶共生菌的能力中发挥着重要作用,同时仍然对侵入性的基底外侧病原体保持完全反应。