کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3353467 1216860 2011 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Negative Regulation by Amidase PGRPs Shapes the Drosophila Antibacterial Response and Protects the Fly from Innocuous Infection
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ایمونولوژی
پیش نمایش صفحه اول مقاله
Negative Regulation by Amidase PGRPs Shapes the Drosophila Antibacterial Response and Protects the Fly from Innocuous Infection
چکیده انگلیسی

SummaryPeptidoglycan recognition proteins (PGRPs) are key regulators of insect immune responses. In addition to recognition PGRPs, which activate the Toll and Imd pathways, the Drosophila genome encodes six catalytic PGRPs with the capacity to scavenge peptidoglycan. We have performed a systematic analysis of catalytic PGRP function using deletions, separately and in combination. Our findings support the role of PGRP-LB as a negative regulator of the Imd pathway and brought to light a synergy of PGRP-SCs with PGRP-LB in the systemic response. Flies lacking all six catalytic PGRPs were still viable but exhibited deleterious immune responses to innocuous gut infections. Together with recent studies on mammalian PGRPs, our study uncovers a conserved role for PGRPs in gut homeostasis. Analysis of the immune phenotype of flies lacking all catalytic PGRPs and the Imd regulator Pirk reveals that the Imd-mediated immune response is highly constrained by the existence of multiple negative feedbacks.

Graphical AbstractFigure optionsDownload high-quality image (351 K)Download as PowerPoint slideHighlights
► Amidase PGRPs prevent the activation of deleterious immune responses by commensals
► The role of mammalian and insect PGRPs in gut homeostasis is conserved
► Amidase PGRPs synergize with Pirk to downregulate the immune response
► Drosophila immunity is highly constrained by multiple negative feedback loops

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: - Volume 35, Issue 5, 23 November 2011, Pages 770–779
نویسندگان
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