Cutting edge:: Infection by the agent of human granulocytic ehrlichiosis prevents the respiratory burst by down-regulating gp91phox1

被引:80
作者
Banerjee, R
Anguita, J
Roos, D
Fikrig, E
机构
[1] Yale Univ, Sch Med, Dept Internal Med, Rheumatol Sect,Lab Clin Invest 608, New Haven, CT 06520 USA
[2] Univ Amsterdam, Acad Med Ctr, Expt & Clin Immunol Lab, Amsterdam, Netherlands
[3] Netherlands Blood Transfus Serv, Cent Lab, Amsterdam, Netherlands
关键词
D O I
10.4049/jimmunol.164.8.3946
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The agent of human granulocytic ehrlichiosis (HGE) is an emerging tick-borne pathogen that resides in neutrophils and can be cultured in a promyelocytic (HL-60) cell line. In response to microbes, polymorphonuclear leukocytes normally activate the NADPH oxidase enzyme complex and generate superoxide anion (O-2(-)). However, HL-60 cells infected with HGE bacteria did not produce O-2(-) upon activation with PMA, RT-PCR demonstrated that HGE organisms inhibited mRNA expression of a single component of NADPH oxidase, gp91(phox) and FAGS analysis showed that plasma membrane-associated gp91(phox) protein was reduced on the infected cells. Infection with HGE organisms also decreased gp91(phox) mRNA levels in splenic neutrophils in a murine model of HGE, demonstrating this phenomenon in vivo. Therefore, HGE bacteria repress the respiratory burst by down-regulating gp91(phox), the first direct inhibition of NADPH oxidase by a pathogen.
引用
收藏
页码:3946 / 3949
页数:4
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