Prolyl Isomerase Pin1 Protects Mice from Endotoxin Shock

被引:16
作者
Akiyama, Hirotada [1 ]
Misawa, Takuma [1 ]
Ono, Masao [2 ]
Uchida, Chiyoko [3 ]
Uchida, Takafumi [1 ,3 ]
机构
[1] Tohoku Univ, Grad Sch Agr Sci, Dept Mol Cell Sci, Sendai, Miyagi 980, Japan
[2] Tohoku Univ, Grad Sch Med, Dept Pathol, Sendai, Miyagi 980, Japan
[3] Tohoku Univ, Interdisciplinary Res Ctr, Sendai, Miyagi 980, Japan
来源
PLOS ONE | 2011年 / 6卷 / 02期
关键词
EXPRESSION; BINDING; GENE; PHOSPHORYLATION; MACROPHAGES; MECHANISMS; DISEASE; STAT3;
D O I
10.1371/journal.pone.0014656
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Prolyl isomerase Pin1 may be involved in innate immunity against microbial infection, but the mechanism how Pin1 controls the innate immunity is poorly understood. Methodology/Principal Findings: Injection of lipopolysaccharide (LPS) into the mice induces inflammatory pulmonary disorder and sometimes the serious damages lead to death. Comparing to the wild-type (WT) mice, the Pin1(-/-) mice showed more serious damages in lung and the lower survival rate after the LPS injection. We compared the levels of typical inflammatory cytokines. Pin1(-/-) mice overreacted to the LPS injection to produce inflammatory cytokines, especially IL-6 more than WT mice. We showed that Pin1 binds phosphorylated PU. 1 and they localize together in a nucleus. These results suggest that Pin1 controls the transcriptional activity of PU. 1 and suppresses overreaction of macrophage that causes serious damages in lung. Conclusions/Significance: Pin1 may protect the mice from serious inflammation by LPS injection by attenuating the increase of IL-6 transcription of the mouse macrophages.
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页数:7
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