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Peptidoglycan Sensing by the Receptor PGRP-LE in the Drosophila Gut Induces Immune Responses to Infectious Bacteria and Tolerance to Microbiota

机译:果蝇肠道中受体PGRP-LE的肽聚糖传感诱导对传染性细菌的免疫反应和对微生物群的耐受性。

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摘要

Gut epithelial cells contact both commensal and pathogenic bacteria, and proper responses to these bacteria require a balance of positive and negative regulatory signals. In the Drosophila intestine, peptidoglycan-recognition proteins (PGRPs), including PGRP-LE, play central roles in bacterial recognition and activation of immune responses, including induction of the IMD-NF-kappa B pathway. We show that bacteria recognition is regionalized in the Drosophila gut with various functional regions requiring different PGRPs. Specifically, peptidoglycan recognition by PGRP-LE in the gut induces NF-kappa B-dependent responses to infectious bacteria but also immune tolerance to microbiota through upregulation of pirk and PGRP-LB, which negatively regulate IMD pathway activation. Loss of PGRP-LE-mediated detection of bacteria in the gut results in systemic immune activation, which can be rescued by overexpressing PGRP-LB in the gut. Together these data indicate that PGRP-LE functions as a master gut bacterial sensor that induces balanced responses to infectious bacteria and tolerance to microbiota.
机译:肠上皮细胞接触共生细菌和致病细菌,对这些细菌的正确反应需要平衡正调控信号和负调控信号。在果蝇肠道中,包括PGRP-LE在内的肽聚糖识别蛋白(PGRP)在细菌识别和激活免疫反应(包括诱导IMD-NF-κB途径)中起着核心作用。我们显示细菌识别在果蝇肠道区域化,需要不同的PGRPs的各种功能区域。具体而言,肠道中PGRP-LE对肽聚糖的识别会诱导对传染性细菌的NF-κB依赖性反应,但也会通过上调猪和PGRP-LB的表达而对微生物群产生免疫耐受,从而对IMD途径的激活产生负面影响。 PGRP-LE介导的肠道细菌检测的丢失会导致全身免疫激活,可通过在肠道中过表达PGRP-LB来挽救。这些数据加在一起表明PGRP-LE作为主要的肠道细菌传感器,可诱导对传染性细菌的平衡反应和对微生物群的耐受性。

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