Abstract
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-kappaB 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-TNFalpha 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.
Highlights
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
Ci-TLR1 contains one leucine-rich repeat (LRR) C-terminal domain, which is flanked by a cysteine-rich domain, three LRR C-terminal domains are present in Ci-TLR2 (Fig. 1)
Ci-TLR1 and -2 are responsive to identical multiple pathogen-associated molecular patterns (PAMPs) (Fig. 6), which are differentially recognized by respective vertebrate TLRs: poly(I-C) for hTLR3, flagellin for hTLR5, zymosan for hTLR2, and HKLP for hTLR2 [1,2,3, 9, 21, 22, 24, 26, 29]
Summary
We identified the structures, tissue distribution, cellular localizations, and ligand-specific activities of all Ciona TLRs, Ci-TLR1 and -2. To the best of our knowledge, this is the first report on molecular and functional characterization of TLRs that are localized to the plasma membrane and endosomes and recognize multiple PAMPs
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