Toll-like Receptors of the Ascidian Ciona intestinalis PROTOTYPES WITH HYBRID FUNCTIONALITIES OF VERTEBRATE TOLL-LIKE RECEPTORS

被引:72
作者
Sasaki, Naoko [1 ]
Ogasawara, Michio [2 ]
Sekiguchi, Toshio [1 ]
Kusumoto, Shoichi [1 ]
Satake, Honoo [1 ]
机构
[1] Suntory Inst Bioorgan Res, Osaka 6188503, Japan
[2] Chiba Univ, Grad Sch Adv Integrat Sci, Inage Ku, Chiba 2638522, Japan
关键词
IMMUNE GENE REPERTOIRE; PURPLE SEA-URCHIN; INFLAMMATORY RESPONSE; EVOLUTIONARY ORIGIN; EXPRESSION PATTERNS; SIGNALING PATHWAY; GENOMIC ANALYSIS; STRUCTURAL BASIS; HOST-DEFENSE; RECOGNITION;
D O I
10.1074/jbc.M109.032433
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Key transmembrane proteins in the innate immune system, Toll-like receptors (TLRs), have been suggested to occur in the genome of non-mammalian organisms including invertebrates. However, authentic invertebrate TLRs have been neither structurally nor functionally investigated. In this paper, we originally present the structures, localization, ligand recognition, activities, and inflammatory cytokine production of all TLRs of the ascidian Ciona intestinalis, designated as Ci-TLR1 and Ci-TLR2. The amino acid sequence of Ci-TLR1 and Ci-TLR2 were found to possess unique structural organization with moderate sequence similarity to functionally characterized vertebrate TLRs. ci-tlr1 and ci-tlr2 genes were expressed predominantly in the stomach and intestine as well as in hemocytes. Ci-TLR1 and Ci-TLR2 expressed in HEK293 cells, unlike vertebrate TLRs, were localized to both the plasma membrane and endosomes. Intriguingly, both Ci-TLR1 and Ci-TLR2 stimulate NF-kappa B induction in response to multiple pathogenic ligands such as double-stranded RNA, and bacterial cell wall components that are differentially recognized by respective vertebrate TLRs, revealing that Ci-TLRs recognize broader pathogen-associated molecular patterns than vertebrate TLRs. The Ci-TLR-stimulating pathogenic ligands also induced the expression of Ci-TNF alpha in the intestine and stomach where Ci-TLRs are expressed. These results provide evidence that the TLR-triggered innate immune systems are essentially conserved in ascidians, and that Ci-TLRs possess "hybrid" biological and immunological functions, compared with vertebrate TLRs. Moreover, it is presumed that chordate TLR ancestors also acquired the Ci-TLR-like multiple cellular localization and pathogen-associated molecular pattern recognition.
引用
收藏
页码:27336 / 27343
页数:8
相关论文
共 44 条
[1]   Toll-like receptor signalling [J].
Akira, S ;
Takeda, K .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) :499-511
[2]   A novel biological role of tachykinins as an up-regulator of oocyte growth:: Identification of an evolutionary origin of tachykininergic functions in the ovary of the ascidian, Ciona intestinalis [J].
Aoyama, Masato ;
Kawada, Tsuyoshi ;
Fujie, Manabu ;
Hotta, Kohji ;
Sakai, Tsubasa ;
Sekiguchi, Toshio ;
Oka, Kotaro ;
Satoh, Nori ;
Satake, Honoo .
ENDOCRINOLOGY, 2008, 149 (09) :4346-4356
[3]   Genomic analysis of immunity in a Urochordate and the emergence of the vertebrate immune system: "waiting for Godot" [J].
Azumi, K ;
De Santis, R ;
De Tomaso, A ;
Rigoutsos, I ;
Yoshizaki, F ;
Pinto, MR ;
Marino, R ;
Shida, K ;
Ikeda, M ;
Ikeda, M ;
Arai, M ;
Inoue, Y ;
Shimizu, T ;
Satoh, N ;
Rokhsar, DS ;
Du Pasquier, L ;
Kasahara, M ;
Satake, M ;
Nonaka, M .
IMMUNOGENETICS, 2003, 55 (08) :570-581
[4]   Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition [J].
Bauer, S ;
Kirschning, CJ ;
Häcker, H ;
Redecke, V ;
Hausmann, S ;
Akira, S ;
Wagner, H ;
Lipford, GB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) :9237-9242
[5]   The dsRNA binding site of human toll-like receptor 3 [J].
Bell, Jessica K. ;
Askins, Janine ;
Hall, Pamela R. ;
Davies, David R. ;
Segal, David M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (23) :8792-8797
[6]   Uncovering the evolutionary history of innate immunity: The simple metazoan Hydra uses epithelial cells for host defence [J].
Bosch, Thomas C. G. ;
Augustin, Rene ;
Anton-Erxleben, Friederike ;
Fraune, Sebastian ;
Hemmrich, Georg ;
Zill, Holger ;
Rosenstiel, Philip ;
Jacobs, Gunnar ;
Schreiber, Stefan ;
Leippe, Matthias ;
Stanisak, Mareike ;
Groetzinger, Joachim ;
Jung, Sascha ;
Podschun, Rainer ;
Bartels, Joachim ;
Harder, Juergen ;
Schroeder, Jens-M. .
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 2009, 33 (04) :559-569
[7]   JNK2 and IKKβ are required for activating the innate response to viral infection [J].
Chu, WM ;
Ostertag, D ;
Li, ZW ;
Chang, LF ;
Chen, Y ;
Hu, YL ;
Williams, B ;
Perrault, J ;
Karin, M .
IMMUNITY, 1999, 11 (06) :721-731
[8]   Adaptor usage and Toll-like receptor signaling specificity [J].
Dunne, A ;
O'Neill, LAJ .
FEBS LETTERS, 2005, 579 (15) :3330-3335
[9]   Characterization of heme as activator of toll-like receptor 4 [J].
Figueiredo, Rodrigo T. ;
Fernandez, Patricia L. ;
Mourao-Sa, Diego S. ;
Porto, Barbara N. ;
Dutra, Fabianno F. ;
Alves, Leticia S. ;
Oliveira, Marcus F. ;
Oliveira, Pedro L. ;
Graca-Souza, Aurelio V. ;
Bozza, Marcelo T. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (28) :20221-20229
[10]   Human Toll-like receptor 2 mediates monocyte activation by Listeria monocytogenes, but not by group B streptococci or lipopolysaccharide [J].
Flo, TH ;
Halaas, O ;
Lien, E ;
Ryan, L ;
Teti, G ;
Golenbock, DT ;
Sundan, A ;
Espevik, T .
JOURNAL OF IMMUNOLOGY, 2000, 164 (04) :2064-2069