The Birc1e cytosolic pattern-recognition receptor contributes to the detection and control of Legionella pneumophila infection

被引:405
作者
Zamboni, DS
Kobayashi, KS
Kohlsdorf, T
Ogura, Y
Long, EM
Vance, RE
Kuida, K
Mariathasan, S
Dixit, VM
Flavell, RA
Dietrich, WF
Roy, CR [1 ]
机构
[1] Yale Univ, Sch Med, Sect Microbial Pathogenesis, New Haven, CT 06536 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Canc Immunol & AIDS, Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Yale Univ, Sch Med, Howard Hughes Med Inst, Immunobiol Sect, New Haven, CT 06510 USA
[5] Yale Univ, Sch Med, Dept Ecol & Evolutionary Biol, New Haven, CT 06510 USA
[6] Harvard Univ, Sch Med, Dept Genet, Howard Hughes Med Inst, Boston, MA 02115 USA
[7] Vertex Pharmaceut, Cambridge, MA 02139 USA
[8] Genentech Inc, Dept Mol Oncol, San Francisco, CA 94080 USA
关键词
D O I
10.1038/ni1305
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Baculovirus inhibitor of apoptosis repeat-containing 1 (Birc1) proteins have homology to several germline-encoded receptors of the innate immune system. However, their function in immune surveillance is not clear. Here we describe a Birc1e-dependent signaling pathway that restricted replication of the intracellular pathogen Legionella pneumophila in mouse macrophages. Translocation of bacterial products into host-cell cytosol was essential for Birc1e-mediated control of bacterial replication. Caspase-1 was required for Birc1e-dependent antibacterial responses ex vivo in macrophages and in a mouse model of Legionnaires' disease. The interleukin 1 beta converting enzyme-protease-activating factor was necessary for L. pneumophila growth restriction, but interleukin 1 beta was not required. These results establish Birc1e as a nucleotide-binding oligomerization-leucine-rich repeat protein involved in the detection and control of intracellular L. pneumophila.
引用
收藏
页码:318 / 325
页数:8
相关论文
共 35 条
[21]   The road less traveled:: transport of Legionella to the endoplasmic reticulum [J].
Roy, CR ;
Tilney, LG .
JOURNAL OF CELL BIOLOGY, 2002, 158 (03) :415-419
[22]   THE GENE FOR NEURONAL APOPTOSIS INHIBITORY PROTEIN IS PARTIALLY DELETED IN INDIVIDUALS WITH SPINAL MUSCULAR-ATROPHY [J].
ROY, N ;
MAHADEVAN, MS ;
MCLEAN, M ;
SHUTLER, G ;
YARAGHI, Z ;
FARAHANI, R ;
BAIRD, S ;
BESNERJOHNSTON, A ;
LEFEBVRE, C ;
KANG, XL ;
SALIH, M ;
AUBRY, H ;
TAMAI, K ;
GUAN, XP ;
IOANNOU, P ;
CRAWFORD, TO ;
DEJONG, PJ ;
SURH, L ;
IKEDA, JE ;
KORNELUK, RG ;
MACKENZIE, A .
CELL, 1995, 80 (01) :167-178
[23]   IAP suppression of apoptosis involves distinct mechanisms: The TAK1/JNK1 signaling cascade and caspase inhibition [J].
Sanna, MG ;
Correia, JD ;
Ducrey, O ;
Lee, J ;
Nomoto, K ;
Schrantz, N ;
Deveraux, QL ;
Ulevitch, RJ .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (06) :1754-1766
[24]   Host cell killing and bacterial conjugation require overlapping sets of genes within a 22-kb region of the Legionella pneumophila genome [J].
Segal, G ;
Purcell, M ;
Shuman, HA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1669-1674
[25]   Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp red fluorescent protein [J].
Shaner, NC ;
Campbell, RE ;
Steinbach, PA ;
Giepmans, BNG ;
Palmer, AE ;
Tsien, RY .
NATURE BIOTECHNOLOGY, 2004, 22 (12) :1567-1572
[26]  
Smolewski P, 2001, CYTOMETRY, V44, P73, DOI 10.1002/1097-0320(20010501)44:1<73::AID-CYTO1084>3.0.CO
[27]  
2-S
[28]   Caterpiller: A novel gene family important in immunity, cell death, and diseases [J].
Ting, JPY ;
Davis, BK .
ANNUAL REVIEW OF IMMUNOLOGY, 2005, 23 :387-414
[29]   NALPs: A novel protein family involved in inflammation [J].
Tschopp, J ;
Martinon, F ;
Burns, K .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (02) :95-104
[30]   Nods and 'intracellular' innate immunity [J].
Viala, M ;
Sansonetti, P ;
Philpott, DJ .
COMPTES RENDUS BIOLOGIES, 2004, 327 (06) :551-555