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Analysis of the induction of cytokine production by Pseudomonas aeruginosa pilin in the lung of mice

Research Project

Project/Area Number 15591060
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field 膠原病・アレルギー・感染症内科学
Research InstitutionOita University (2004)
大分医科大学 (2003)

Principal Investigator

NASU Masaru  Oita University, Faculty of Medicine, Professor, 医学部, 教授 (70039874)

Co-Investigator(Kenkyū-buntansha) HIRAMATSU Kazufumi  Oita University, Faculty of Medicine, Research associate, 医学部, 助手 (80301381)
KADOTA Jun-ichi  Oita University, Faculty of Medicine, Associate professor, 医学部, 助教授 (50233838)
Project Period (FY) 2003 – 2004
Project Status Completed (Fiscal Year 2004)
Budget Amount *help
¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 2004: ¥1,600,000 (Direct Cost: ¥1,600,000)
Fiscal Year 2003: ¥1,500,000 (Direct Cost: ¥1,500,000)
KeywordsPseudomonas aeruginosa / inflammation / pilin / respiratory infection / cytokines
Research Abstract

It is well known that pili of Pseudomonas aeruginosa has important role for adherence to epithelial cell. Some studies have been revealed that pili induced IL-8 production from epithelial cell in vitro experiments. In this study, we investigated that the affects of intratracheal inoculation of pilin, which is a component protein of pili, in murine model. Pilin was extracted from SDS-PAGE gel after sucrose gradient centrifugation. Purified pilin of P.aeruginosa, BSA or lipopolysaccharide(LPS) were inoculated to 6 weeks old Balb/c mice intratracheally. The mice were sacrificed and performed bronchoalveolar lavage(BAL). BAL fluid were analysed for cell counts and cytokines(TNF-α, MIP-2, IL-4, IFN-γ) concentrations. Additionally, to investigate the critical epitope for infiltration of inflammatory cells, we sythesized thirteen peptides(residues 1-20,11-30,21-40,31-50,41-60,51-70,61-80,71-90,81-100,91-110,101-120,111-130,121-143 based on PAO-1 amino acids sequence) and inoculated these pept … More ides intratracheally followed by BAL for examination of WBC counts and cytokine concentration. White blood cells in BAL fluid whose mice were inoculated pilin increased after 6 hr inoculation compared with the BSA-inoculated control mice. Peak counts of WBC in BAL fluid of pilin inoculated at 72hr after inoculation. More than ninety percent of WBC were neutrophils. Intratracheal inoculation of pilin induced TNF-α and MIP-2 concentrations in BAL fluid compared with BSA inoculated group although there was no significant difference between pilin inoculated and BSA inoculated groups in the concentrations of IL-4 and IFN-γ in BAL fluid. On the other hand, all thirteen peptides did not affect any response of inflammatory cell and cytokine concentration in BAL fluid significantly although some peptides slightly induced neutrophils and TNF-α in BAL fluid. These findings suggest that pilin of P.aeruginosa is one of the important factors' for induction of inflammation in the P.aeruginosa respiratory infection. Less

Report

(3 results)
  • 2004 Annual Research Report   Final Research Report Summary
  • 2003 Annual Research Report

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Published: 2003-04-01   Modified: 2016-04-21  

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