自噬及自噬基因Atg16l1在小鼠和人类肠道潘氏细胞中的关键作用。

A key role for autophagy and the autophagy gene Atg16l1 in mouse and human intestinal Paneth cells.

作者信息

Cadwell Ken, Liu John Y, Brown Sarah L, Miyoshi Hiroyuki, Loh Joy, Lennerz Jochen K, Kishi Chieko, Kc Wumesh, Carrero Javier A, Hunt Steven, Stone Christian D, Brunt Elizabeth M, Xavier Ramnik J, Sleckman Barry P, Li Ellen, Mizushima Noboru, Stappenbeck Thaddeus S, Virgin Herbert W

机构信息

Department of Pathology and Immunology, Washington University School of Medicine, St Louis, Missouri 63110, USA.

出版信息

Nature. 2008 Nov 13;456(7219):259-63. doi: 10.1038/nature07416. Epub 2008 Oct 5.

Abstract

Susceptibility to Crohn's disease, a complex inflammatory disease involving the small intestine, is controlled by over 30 loci. One Crohn's disease risk allele is in ATG16L1, a gene homologous to the essential yeast autophagy gene ATG16 (ref. 2). It is not known how ATG16L1 or autophagy contributes to intestinal biology or Crohn's disease pathogenesis. To address these questions, we generated and characterized mice that are hypomorphic for ATG16L1 protein expression, and validated conclusions on the basis of studies in these mice by analysing intestinal tissues that we collected from Crohn's disease patients carrying the Crohn's disease risk allele of ATG16L1. Here we show that ATG16L1 is a bona fide autophagy protein. Within the ileal epithelium, both ATG16L1 and a second essential autophagy protein ATG5 are selectively important for the biology of the Paneth cell, a specialized epithelial cell that functions in part by secretion of granule contents containing antimicrobial peptides and other proteins that alter the intestinal environment. ATG16L1- and ATG5-deficient Paneth cells exhibited notable abnormalities in the granule exocytosis pathway. In addition, transcriptional analysis revealed an unexpected gain of function specific to ATG16L1-deficient Paneth cells including increased expression of genes involved in peroxisome proliferator-activated receptor (PPAR) signalling and lipid metabolism, of acute phase reactants and of two adipocytokines, leptin and adiponectin, known to directly influence intestinal injury responses. Importantly, Crohn's disease patients homozygous for the ATG16L1 Crohn's disease risk allele displayed Paneth cell granule abnormalities similar to those observed in autophagy-protein-deficient mice and expressed increased levels of leptin protein. Thus, ATG16L1, and probably the process of autophagy, have a role within the intestinal epithelium of mice and Crohn's disease patients by selective effects on the cell biology and specialized regulatory properties of Paneth cells.

摘要

克罗恩病是一种累及小肠的复杂炎症性疾病,对其易感性由30多个基因座控制。一种克罗恩病风险等位基因位于ATG16L1中,该基因与酵母自噬必需基因ATG16同源(参考文献2)。目前尚不清楚ATG16L1或自噬如何影响肠道生物学或克罗恩病的发病机制。为了解决这些问题,我们构建并鉴定了ATG16L1蛋白表达不足的小鼠,并通过分析从携带ATG16L1克罗恩病风险等位基因的克罗恩病患者收集的肠道组织,对基于这些小鼠研究得出的结论进行了验证。在此我们表明,ATG16L1是一种真正的自噬蛋白。在回肠上皮内,ATG16L1和另一种自噬必需蛋白ATG5对潘氏细胞的生物学特性均具有选择性重要意义,潘氏细胞是一种特殊的上皮细胞,其部分功能是通过分泌含有抗菌肽和其他改变肠道环境的蛋白质的颗粒内容物来实现的。ATG16L1和ATG5缺陷的潘氏细胞在颗粒胞吐途径中表现出明显异常。此外,转录分析揭示了ATG16L1缺陷的潘氏细胞特有的意外功能获得,包括参与过氧化物酶体增殖物激活受体(PPAR)信号传导和脂质代谢的基因、急性期反应物以及已知直接影响肠道损伤反应的两种脂肪细胞因子瘦素和脂联素的表达增加。重要的是,携带ATG16L1克罗恩病风险等位基因纯合的克罗恩病患者表现出与自噬蛋白缺陷小鼠中观察到的类似的潘氏细胞颗粒异常,并且瘦素蛋白水平升高。因此,ATG16L1以及可能的自噬过程,通过对潘氏细胞的细胞生物学和特殊调节特性的选择性作用,在小鼠和克罗恩病患者的肠道上皮中发挥作用。

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