Assessing a Potential Role of Host Pannexin 1 during Chlamydia trachomatis Infection

被引:8
|
作者
McKuen, Mary J. [1 ,2 ]
Dahl, Gerhard [3 ,4 ]
Fields, Kenneth A. [1 ,2 ]
机构
[1] Univ Miami, Miller Sch Med, Dept Microbiol, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Dept Immunol, Miami, FL 33136 USA
[3] Univ Miami, Miller Sch Med, Dept Physiol, Miami, FL 33136 USA
[4] Univ Miami, Miller Sch Med, Dept Biophys, Miami, FL 33136 USA
来源
PLOS ONE | 2013年 / 8卷 / 06期
基金
美国国家卫生研究院;
关键词
NEISSERIA-GONORRHOEAE; INFLAMMASOME; INCLUSION; MEMBRANE; ATP; ACTIVATION; CHANNELS; CELLS; INHIBITION; EXPRESSION;
D O I
10.1371/journal.pone.0063732
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
Pannexin 1 (Panx1) is a plasma membrane channel glycoprotein that plays a role in innate immune response through association with the inflammasome complex. Probenecid, a classic pharmacological agent for gout, has also been used historically in combination therapy with antibiotics to prevent cellular drug efflux and has been reported to inhibit Panx1. As the inflammasome has been implicated in the progression of Chlamydia infections, and with chlamydial infections at record levels in the US, we therefore investigated whether probenecid would have a direct effect on Chlamydia trachomatis development through inhibition of Panx1. We found chlamydial development to be inhibited in a dose-dependent, yet reversible manner in the presence of probenecid. Drug treatment induced an aberrant chlamydial morphology consistent with persistent bodies. Although Panx1 was shown to localize to the chlamydial inclusion, no difference was seen in chlamydial development during infection of cells derived from wild-type and Panx1 knockout mice. Therefore, probenecid may inhibit C. trachomatis growth by an as yet unresolved mechanism.
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页数:9
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