Extensive characterization of IFN-induced GTPases mGBP1 to mGBP10 involved in host defense

被引:168
作者
Degrandi, Daniel
Konermann, Carolin
Beuter-Gunia, Cornelia
Kresse, Alexandra
Wuerthner, Jan
Kurig, Stefanie
Beer, Sandra
Pfeffer, Klaus
机构
[1] Inst Med Microbiol & Hosp Hyg, Dusseldorf, Germany
[2] Univ Dusseldorf, Inst Med Microbiol & Hosp Hyg, Dusseldorf, Germany
关键词
D O I
10.4049/jimmunol.179.11.7729
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
IFN-gamma orchestrates a potent antimicrobial host response. However, the underlying molecular basis for this immunological defense system is largely unknown. In a systematic approach to identify IFN-gamma-regulated host effector molecules, a notable number of transcripts with consensus GTP-binding motives were obtained. Further extensive transcriptome and genome analyses identified five novel family members of murine guanylate-binding proteins (mGBPs) now designated mGBP6, 7, 8, 9, and 10. Moreover, in this study, all 10 mGBP members (mGBP1-10) were extensively characterized. mGBPs are selectively up-regulated in vitro by a set of proinflammatory cytokines and TLR agonists as well as in vivo after Listeria monocytogenes and Toxoplasma gondii infection. After IFN-gamma stimulation, mGBP1, 2, 3, 6, 7, and 9 are associated with intracellular Toxoplasma parasites and, interestingly, virulent Toxoplasma interfere with mGBP recruitment. Taken together, mGBPs comprise an important set of host defense molecules.
引用
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页码:7729 / 7740
页数:12
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