A conserved role for a GATA transcription factor in regulating epithelial innate immune responses

被引:220
作者
Shapira, Michael
Hamlin, Brigham J.
Rong, Jiming
Chen, Karen
Ronen, Michal
Tan, Man-Wah [1 ]
机构
[1] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Microbiol, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Immunol, Sch Med, Stanford, CA 94305 USA
关键词
gene expression; innate immunity; infection; ELT-2; Pseudomonas aeruginosa;
D O I
10.1073/pnas.0603424103
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
Innate immunity is an ancient and conserved defense mechanism. Although host responses toward various pathogens have been delineated, how these responses are orchestrated in a whole animal is less understood. Through an unbiased genome-wide study performed in Caenorhabditis elegans, we identified a conserved function for endodermal GATA transcription factors in regulating local epithelial innate immune responses. Gene expression and functional RNAi-based analyses identified the tissue-specific GATA transcription factor ELT-2 as a major regulator of an early intestinal protective response to infection with the human bacterial pathogen Pseudomonas aeruginosa. In the adult worm, ELT-2 is required specifically for infection responses and survival on pathogen but makes no significant contribution to gene expression associated with intestinal maintenance or to resistance to cadmium, heat, and oxidative stress. We further demonstrate that this function is conserved, because the human endodermal transcription factor GATA6 has a protective function in lung epithelial cells exposed to A aeruginosa. These findings expand the repertoire of innate immunity mechanisms and illuminate a yet-unknown function of endodermal GATA proteins.
引用
收藏
页码:14086 / 14091
页数:6
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