The TBK1 adaptor and autophagy receptor NDP52 restricts the proliferation of ubiquitin-coated bacteria

被引:676
作者
Thurston, Teresa L. M. [1 ]
Ryzhakov, Grigory [1 ]
Bloor, Stuart [1 ]
von Muhlinen, Natalia [1 ]
Randow, Felix [1 ]
机构
[1] MRC, Mol Biol Lab, Div Prot & Nucle Acid Chem, Cambridge CB2 2QH, England
基金
英国医学研究理事会;
关键词
KINASE-RELATED KINASES; KAPPA-B; ENDOPLASMIC-RETICULUM; PROTEIN; BINDING; RECOGNITION; INNATE; DOMAIN; HOST; IKK;
D O I
10.1038/ni.1800
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cell-autonomous innate immune responses against bacteria attempting to colonize the cytosol of mammalian cells are incompletely understood. Polyubiquitylated proteins can accumulate on the surface of such bacteria, and bacterial growth is restricted by Tank-binding kinase (TBK1). Here we show that NDP52, not previously known to contribute to innate immunity, recognizes ubiquitin-coated Salmonella enterica in human cells and, by binding the adaptor proteins Nap1 and Sintbad, recruits TBK1. Knockdown of NDP52 and TBK1 facilitated bacterial proliferation and increased the number of cells containing ubiquitin-coated salmonella. NDP52 also recruited LC3, an autophagosomal marker, and knockdown of NDP52 impaired autophagy of salmonella. We conclude that human cells utilize the ubiquitin system and NDP52 to activate autophagy against bacteria attempting to colonize their cytosol.
引用
收藏
页码:1215 / U103
页数:8
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