Tadayuki Tsujita

Dr. Tadayuki Tsujita

Faculty of Agriculture, Saga University, Saga, Japan
orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2008 in The Journal of Immunology
Verified
Journal Article
Closed access
PDF file
AMAya Matsuo
Aya Matsuo
HOHiroyuki Oshiumi
Hiroyuki Oshiumi
TTTadayuki Tsujita
Tadayuki Tsujita
HMHiroshi Mitani
Hiroshi Mitani
HKHisae Kasai
Hisae Kasai
TSTsukasa Seya
Tsukasa Seya
TLR22 occurs exclusively in aquatic animals and its role is unknown. Herein we show that the fugu (Takifugu rubripes) (fg)TLR3 and fgTLR22 link the IFN-inducing pathway via the fg Toll-IL-1R homology domain-containing adaptor protein 1(fgTICAM-1, or TRIF) adaptor in fish cells. fgTLR3 resides in endoplasmic reticulum and recognizes relatively short-sized dsRNA, whereas fgTLR22 recognizes long-sized dsRNA on the cell surface. On poly(I:C)-stimulated fish cells, both recruit fgTICAM-1, which in turn moves from the TLR to a cytoplasmic signalosome region. Thus, fgTICAM-1 acts as a shuttling platform for IFN signaling. When fish cells expressing fgTLR22 are exposed to dsRNA or aquatic dsRNA viruses, cells induce IFN responses to acquire resistance to virus infection. Thus, fish have a novel TICAM-1-coupling TLR that is distinct from the mammalian TLR3 in cellular localization, ligand selection, and tissue distribution. TLR22 may be a functional substitute of human cell-surface TLR3 and serve as a surveillant for infection with dsRNA virus to alert the immune system for antiviral protection in fish.

15 January 2003 in Immunogenetics
Verified
Journal Article
Closed access
HOHiroyuki Oshiumi
Hiroyuki Oshiumi
TTTadayuki Tsujita
Tadayuki Tsujita
KSKyoko Shida
Kyoko Shida
MMMisako Matsumoto
Misako Matsumoto
KIKazuho Ikeo
Kazuho Ikeo
TSTsukasa Seya
Tsukasa Seya

15 January 2010 in Free Radical Biology and Medicine
Verified
Journal Article
Closed access
SCSudhir Chowdhry
Sudhir Chowdhry
MNMaiiada H. Nazmy
Maiiada H. Nazmy
PMPaul James Meakin
Paul James Meakin
ADAlbena T Dinkova-Kostova
Albena T Dinkova-Kostova
SWShaun V. Walsh
Shaun V. Walsh
JHJohn Hayes
John Hayes

1 November 2004 in Journal of Biological Chemistry
Verified
Journal Article
Open access
PDF file
TTTadayuki Tsujita
Tadayuki Tsujita
HTHironobu Tsukada
Hironobu Tsukada
MNMiki Nakao
Miki Nakao
HOHiroyuki Oshiumi
Hiroyuki Oshiumi
MMMisako Matsumoto
Misako Matsumoto
TSTsukasa Seya
Tsukasa Seya
Rainbow trout (Onchorhynchus mikiss) possess two genes encoding putative leucine-rich repeat (LRR)-containing proteins similar to human TLR5. Molecular cloning of these two LRR proteins suggested the presence of a TLR5-like membrane form (rtTLR5M) and a soluble form (rtTLR5S). Here we elucidated the primary structures and the unique combinational functions of these fish versions of TLR5. The LRR regions of rtTLR5S and rtTLR5M exhibited 81% homology and relatively high (35.6 and 33.7%) homology to the extracellular domains of human TLR5 (huTLR5). Thus, two distinct genes encode the TLR5 orthologs in fish, one of which has a consensus intracellular domain (TIR). In order to test their functions, we constructed fusion proteins with the LRR region of rtTLR5S (S-chimera) or that of rtTLR5M and the TIR of huTLR5 (M-chimera). The S- and M-chimeras expressed in HeLa or CHO cells signaled the presence of Vibrio anguillarum flagellin, resulting in NF-κB activation. rtTLR5M was ubiquitously expressed, whereas rtTLR5S was predominantly expressed in the liver. In the hepatoma cell lines of the rainbow trout RTH-149, stimulation of rtTLR5M with V. anguillarum or its flagellin allowed the up-regulation of rtTLR5S. Flagellin-mediated NF-κB activation was more significant in the presence of or simultaneous expression of rtTLR5S. Therefore, a two-step flagellin response occurred for host defense against bacterial infection in fish: (a) flagellin first induced basal activation of NF-κB via membrane TLR5, facilitating the production of soluble TLR5 and minimal acute phase proteins, and (b) the inducible soluble TLR5 amplifies membrane TLR5-mediated cellular responses in a positive feedback fashion.

23 February 2015 in Nature Medicine
Verified
Journal Article
Closed access
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KNKeizo Nishikawa
Keizo Nishikawa
YIYoriko Iwamoto
Yoriko Iwamoto
YKYasuhiro Kobayashi
Yasuhiro Kobayashi
FKFumiki Katsuoka
Fumiki Katsuoka
Shin-ichi KawaguchiShin-ichi Kawaguchi
Shin-ichi Kawaguchi
MIMasaru Ishii
Masaru Ishii

1 February 2017 in Free Radical Biology and Medicine
Verified
Journal Article
Closed access
KTKouhei Tsuchida
Kouhei Tsuchida
TTTadayuki Tsujita
Tadayuki Tsujita
MHMakiko Hayashi
Makiko Hayashi
AOAsaka Ojima
Asaka Ojima
NKNadine Keleku-Lukwete
Nadine Keleku-Lukwete
MYMasayuki Yamamoto
Masayuki Yamamoto