Comparative Overview of Toll-like Receptors in Lower Animals

被引:24
作者
Satake, Honoo [1 ]
Sasaki, Naoko [1 ]
机构
[1] Suntory Inst Bioorgan Res, Osaka 6188503, Japan
关键词
Toll-like receptor; innate immunity; evolution; ascidian; Ciona intestinalis; IMMUNE GENE REPERTOIRE; ANTIMICROBIAL PEPTIDE; SOLITARY TUNICATE; CIONA-INTESTINALIS; GENOMIC ANALYSIS; STRUCTURAL BASIS; INNATE IMMUNITY; EXPRESSION; HEMOCYTES; SYSTEM;
D O I
10.2108/zsj.27.154
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
Toll-like receptors (TLRs) have been shown to play a crucial role in host defense against pathogenic microbes in innate immunity in mammals. Recent genome-wide analyses have suggested that TLRs or related genes are conserved in the genome of non-mammalian organisms such as fishes, cyclostomes, ascidians, cephalochordates, sea urchins, and hydras. However, neither active forms nor functions of authentic invertebrate TLRs had been elucidated. Quite recently, we verified the structures, localization, ligand recognition, activities, and inflammatory cytokine production of two TLRs in the ascidian Ciona intestinalis, designated Ci-TLR1 and Ci-TLR2. Both Ci-TLRs possess a unique structural organization, with moderate sequence similarity to functionally characterized vertebrate TLRs, and are expressed predominantly in the stomach and intestine as well as in hemocytes. Unlike vertebrate TLRs, Ci-TLR1 and Ci-TLR2 are present in both the plasma membrane and endosomes. Furthermore, both Ci-TLR1 and Ci-TLR2 stimulate NF-kappa B induction in response to multiple pathogenic ligands that are differentially recognized by respective vertebrate TLRs. Pathogenic ligands that stimulate the Ci-TLRs also induce the expression of Ci-TNF alpha in the intestine and stomach, where the Ci-TLRs are abundantly expressed. These data reveal the conservation of the TLR-triggered innate immune system in C. intestinalis, and both common and unique biological and immunological functions of the Ci-TLRs. Based on the latest findings, we review recent advances in studies of TLRs or related receptors in fish, cyclostomes, deuterostome invertebrates, and hydra, and also the significance of studies of lower organism TLRs.
引用
收藏
页码:154 / 161
页数:8
相关论文
共 49 条
[21]  
Lee IH, 2001, J PEPT RES, V58, P445
[22]   Dicynthaurin:: an antimicrobial peptide from hemocytes of the solitary tunicate, Halocynthia aurantium [J].
Lee, IH ;
Lee, YS ;
Kim, CH ;
Kim, CR ;
Hong, T ;
Menzel, L ;
Boo, LM ;
Pohl, J ;
Sherman, MA ;
Waring, A ;
Lehrer, RI .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2001, 1527 (03) :141-148
[23]   The dorsoventral regulatory gene cassette spatzle/Toll/cactus controls the potent antifungal response in Drosophila adults [J].
Lemaitre, B ;
Nicolas, E ;
Michaut, L ;
Reichhart, JM ;
Hoffmann, JA .
CELL, 1996, 86 (06) :973-983
[24]   Structural basis of toll-like receptor 3 signaling with double-stranded RNA [J].
Liu, Lin ;
Botos, Istvan ;
Wang, Yan ;
Leonard, Joshua N. ;
Shiloach, Joseph ;
Segal, David M. ;
Davies, David R. .
SCIENCE, 2008, 320 (5874) :379-381
[25]   Teleost TLR22 recognizes RNA duplex to induce IFN and protect cells from birnaviruses [J].
Matsuo, Aya ;
Oshiumi, Hiroyuki ;
Tsujita, Tadayuki ;
Mitani, Hiroshi ;
Kasai, Hisae ;
Yoshimizu, Mamoru ;
Matsumoto, Misako ;
Seya, Tsukasa .
JOURNAL OF IMMUNOLOGY, 2008, 181 (05) :3474-3485
[26]   The innate immune repertoire in Cnidaria - ancestral complexity and stochastic gene loss [J].
Miller, David J. ;
Hemmrich, Georg ;
Ball, Eldon E. ;
Hayward, David C. ;
Khalturin, Konstantin ;
Funayama, Noriko ;
Agata, Kiyokazu ;
Bosch, Thomas C. G. .
GENOME BIOLOGY, 2007, 8 (04)
[27]   Characterization of novel ascidian β integrins as primitive complement receptor subunits [J].
Miyazawa, S ;
Nonaka, M .
IMMUNOGENETICS, 2004, 55 (12) :836-844
[28]   Evolution of the complement system [J].
Nonaka, M .
CURRENT OPINION IN IMMUNOLOGY, 2001, 13 (01) :69-73
[29]   Opsonic complement system of the solitary ascidian, Halocynthia roretzi [J].
Nonaka, M ;
Azumi, K .
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 1999, 23 (4-5) :421-427
[30]  
Nonaka M, 1999, J IMMUNOL, V162, P387