Project/Area Number |
13680693
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Structural biochemistry
|
Research Institution | Kyushu University |
Principal Investigator |
KAWABATA Shun-ichiro Kyushu University, Department of Biology, Associate Professor, 大学院・理学研究院, 助教授 (90183037)
|
Co-Investigator(Kenkyū-buntansha) |
KAWANO Keiichi Toyama Medical and Pharmaceutical University, Faculty of Pharmaceutical Science, Professor, 薬学部, 教授 (10136492)
|
Project Period (FY) |
2001 – 2002
|
Project Status |
Completed (Fiscal Year 2002)
|
Budget Amount *help |
¥4,200,000 (Direct Cost: ¥4,200,000)
Fiscal Year 2002: ¥1,600,000 (Direct Cost: ¥1,600,000)
Fiscal Year 2001: ¥2,600,000 (Direct Cost: ¥2,600,000)
|
Keywords | Gram-negative bacteria / Exocytosis / Lipopolysaccharide / LPS receptor / G protein / カブトガニ / LPS / リピドA |
Research Abstract |
The innate immune system is a sensitive non-self-recognizing cascade triggered by microbial cell wall constituents called pathogen-associated molecular patterns (PAMPs), such as lipopolysaccharides (LPS) of Gram-negative bacteria, β-1,3-glucans of fungi, and peptidoglycans of Gram-positive bacteria. These PAMPs are recognized via a set of germ line-encoded receptros of innate immune system called pattern recognition receptors. Recent studies have revealed that insects and mannals conserve a signaling pathway of the innate immune system through cell-surface receptors, Toll and Toll-like receptors (TLRs). In mammals, TLRs on specialized antigen-presenting cells function as signal transducers by way of NF-kB, leading to the production of pro-inflammatory cytokines and the expression of constimulatory molecules on the cell surface, which are necessary to activate naive T cells; TLRs are possibly assembled at the cell membrane as signaling receptor complexes. In the horseshoe crab innate immunity, LPS-induced exocytosis of granular hemocytes is a key phenomenon to fight infectious microorganisms: the stimulation by LPS induces the secretion of various defense molecules stored in granules of hemocytes. Here we show that a granular component factor C, an LPS-recognizing serine protease zymogen initiating the hemolymph coagulation cascade, also exists on the surface of hemocytes. Our data demonstrate that the complex of the activated factor C with LPS is not required but the proteolytic activity is required and sufficient to trigger the exocytosis through a heterotrimeric GTP-binding protein-mediating signaling pathway. We conclude that the serine protease zymogen on hemocytes functions as a pattern recognition receptor for LPS.
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