Cutting edge: Bacterial modulation of epithelial signaling via changes in neddylation of cullin-1

被引:95
作者
Collier-Hyams, LS [1 ]
Sloane, V [1 ]
Batten, BC [1 ]
Neish, AS [1 ]
机构
[1] Emory Univ, Sch Med, Dept Pathol & Lab Med, Epithelial Pathobiol Unit, Atlanta, GA 30322 USA
关键词
D O I
10.4049/jimmunol.175.7.4194
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The human enteric flora plays a significant role in intestinal health and disease. Certain enteric bacteria can inhibit the NF-kappa B pathway by blockade of I kappa B-alpha ubiquitination. I kappa B-alpha ubiquitination is catalyzed by the E3-SCF beta TrCP ubiquitin ligase, which is itself regulated via covalent modification of the cullin-1 subunit by the ubiquitin-like protein NEDD8. Neddaylation is a biochemical event associated with diverse cellular processes related to cell signaling, however, physiological regulation of cullin neddylation has not been described in mammalian systems. We report that interaction of nonpathogenic bacteria with epithelial cells resulted in a rapid loss of neddylated Cul-1 and consequent repression of the NF-kappa B pathway. This observation may explain the ability of intestinal bacterial communities to influence diverse eukaryotic processes in general and inflammatory tolerance of the mammalian intestinal epithelia specifically.
引用
收藏
页码:4194 / 4198
页数:5
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