Unusual Regulation of a STAT Protein by an SLC6 Family Transporter in C. elegans Epidermal Innate Immunity

被引:71
作者
Dierking, Katja [1 ,2 ,3 ,4 ]
Polanowska, Jolanta [1 ,2 ,3 ]
Omi, Shizue [1 ,2 ,3 ]
Engelmann, Ilka [1 ,2 ,3 ]
Gut, Marta [5 ]
Lembo, Frederique [6 ]
Ewbank, Jonathan J. [1 ,2 ,3 ]
Pujol, Nathalie [1 ,2 ,3 ]
机构
[1] Univ Mediterranee, Ctr Immunol Marseille Luminy, F-13288 Marseille, France
[2] INSERM, U631, F-13288 Marseille, France
[3] CNRS, UMR6102, F-13288 Marseille, France
[4] Univ Kiel, Dept Evolutionary Ecol & Genet, D-24118 Kiel, Germany
[5] CNG, F-91057 Evry, France
[6] CRCM, F-13273 Marseille, France
关键词
ANTIMICROBIAL PEPTIDE EXPRESSION; CAENORHABDITIS-ELEGANS; GENOME-WIDE; MEDIATED ENDOCYTOSIS; DOMAIN PROTEIN; INFECTION; RESPONSES; ACTIVATION; RESISTANCE; SIGNATURES;
D O I
10.1016/j.chom.2011.04.011
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The cuticle and epidermis of Caenorhabditis elegans provide the first line of defense against invading pathogens. Upon invasion by the fungal pathogen Drechmeria coniospora, C. elegans responds by upregulating the expression of antimicrobial peptides (AMPs) in the epidermis via activation of at least two pathways, a neuroendocrine TGF-beta pathway and a p38 MAPK pathway. Here, we identify the sodium-neurotransmitter symporter SNF-12, a member of the solute carrier family (SLC6), as being essential for both these immune signaling pathways. We also identify the STAT transcription factor-like protein STA-2 as a direct physical interactor of SNF-12 and show that the two proteins function together to regulate AMP gene expression in the epidermis. Both SNF-12 and STA-2 act cell autonomously and specifically in the epidermis to govern the transcriptional response to fungal infection. These findings reveal an unorthodox mode of regulation for a STAT factor and highlight the molecular plasticity of innate immune signaling.
引用
收藏
页码:425 / 435
页数:11
相关论文
共 43 条
[1]  
[Anonymous], 1988, NEMATODE CAENORHABDI
[2]   Intracellular Toll-like Receptors [J].
Blasius, Amanda L. ;
Beutler, Bruce .
IMMUNITY, 2010, 32 (03) :305-315
[3]   Sequential activation of signaling pathways during innate immune responses in Drosophila [J].
Boutros, M ;
Agaisse, H ;
Perrimon, N .
DEVELOPMENTAL CELL, 2002, 3 (05) :711-722
[4]  
Bromberg JF, 2001, BIOESSAYS, V23, P161, DOI 10.1002/1521-1878(200102)23:2<161::AID-BIES1023>3.0.CO
[5]  
2-0
[6]  
Chase Daniel L, 2007, WormBook, P1
[7]   TLR-independent control of innate immunity in Caenorhabditis elegans by the TIR domain adaptor protein TIR-1, an ortholog of human SARM [J].
Couillault, C ;
Pujol, N ;
Reboul, J ;
Sabatier, L ;
Guichou, JF ;
Kohara, Y ;
Ewbank, JJ .
NATURE IMMUNOLOGY, 2004, 5 (05) :488-494
[8]   ULTRASTRUCTURAL-STUDY OF ADHESION AND INITIAL-STAGES OF INFECTION OF NEMATODES BY CONIDIA OF DRECHMERIA-CONIOSPORA [J].
DIJKSTERHUIS, J ;
VEENHUIS, M ;
HARDER, W .
MYCOLOGICAL RESEARCH, 1990, 94 :1-8
[9]   bZIP transcription factor zip-2 mediates an early response to Pseudomonas aeruginosa infection in Caenorhabditis elegans [J].
Estes, Kathleen A. ;
Dunbar, Tiffany L. ;
Powell, Jennifer R. ;
Ausubel, Frederick M. ;
Troemel, Emily R. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (05) :2153-2158
[10]   Tackling both sides of the host-pathogen equation with Caenorhabditis elegans [J].
Ewbank, JJ .
MICROBES AND INFECTION, 2002, 4 (02) :247-256