Host defense against Pseudomonas aeruginosa requires ceramide-rich membrane rafts

被引:445
作者
Grassmé, H
Jendrossek, V
Riehle, A
von Kürthy, G
Berger, J
Schwarz, H
Weller, M
Kolesnick, R
Gulbins, E [1 ]
机构
[1] Univ Essen Gesamthsch, Dept Biol Mol, Essen, Germany
[2] Univ Tubingen, Dept Radiat Oncol, Tubingen, Germany
[3] Univ Tubingen, Dept Neurol, Tubingen, Germany
[4] Max Planck Inst Dev Biol, Tubingen, Germany
[5] Mem Sloan Kettering Canc Ctr, Lab Signal Transduct, New York, NY 10021 USA
关键词
D O I
10.1038/nm823
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pseudomonas aeruginosa infection is a serious complication in patients with cystic fibrosis and in immunocompromised individuals. Here we show that P. aeruginosa infection triggers activation of the acid sphingomyelinase and the release of ceramide in sphingolipid-rich rafts. Ceramide reorganizes these rafts into larger signaling platforms that are required to internalize P. aeruginosa, induce apoptosis and regulate the cytokine response in infected cells. Failure to generate ceramide-enriched membrane platforms in infected cells results in an unabated inflammatory response, massive release of interleukin (IL)-1 and septic death of mice. Our findings show that ceramide-enriched membrane platforms are central to the host defense against this potentially lethal pathogen.
引用
收藏
页码:322 / 330
页数:9
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