共 25 条
Deacylation and palmitoylation of lipid A by Salmonellae outer membrane enzymes modulate host signaling through Toll-like receptor 4
被引:42
作者:

Kawasaki, K
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h-index: 0
机构: Univ Washington, Dept Microbiol, Seattle, WA 98195 USA

Ernst, RK
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h-index: 0
机构: Univ Washington, Dept Microbiol, Seattle, WA 98195 USA

Miller, SI
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h-index: 0
机构:
Univ Washington, Dept Microbiol, Seattle, WA 98195 USA Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
机构:
[1] Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
[2] Univ Washington, Dept Med, Seattle, WA USA
[3] Univ Washington, Dept Genome Sci, Seattle, WA USA
来源:
JOURNAL OF ENDOTOXIN RESEARCH
|
2004年
/
10卷
/
06期
关键词:
deacylation;
palmitoylation;
lipid A;
Salmonellae;
outer membrane enzymes;
Toll-like receptor 4;
D O I:
10.1179/096805104225006264
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:
The Salmonella typhimurium virulence gene products, PhoP/PhoQ sense host micro-environments to regulate the expression of a lipid A 3-O-deacylase, PagL, and a lipid A palmitoyltransferase, PagP. Therefore, deacylation and/or palmitoylation of lipid A could occur in Salmonellae adapted to host environments. The acylation state of lipid A can alter host recognition and signaling by Toll-like receptor (TLR) 4, and may play an important role in host defenses against Salmonellae infection. Deacylated lipid A, deacylated and palmitoylated lipid A, palmitoylated lipid A, and unmodified lipid A species were purified, and the activity was examined using cell lines expressing recombinant human or mouse TLR4. Compared with unmodified lipid A, the modified lipid A species are 10-100-fold less active. These results suggest that PagL and PagP modify lipid A to reduce TLR4-signaling as part of Salmonellae adaptation to the host environment.
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页码:439 / 444
页数:6
相关论文
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