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Study on possible role of cytokines in response to oxidative stress by using cytokine knock out mice

Research Project

Project/Area Number 11672183
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Biological pharmacy
Research InstitutionShowa university

Principal Investigator

OGURO Takiko  Showa Univ., Sch.Pharmaceut.Sci., lecturer, 薬学部, 講師 (10185572)

Co-Investigator(Kenkyū-buntansha) YOSHIDA Takemi  Showa Univ., Sch.Pharmaceut.Sci., Professor, 薬学部, 教授 (20138415)
Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥2,600,000 (Direct Cost: ¥2,600,000)
Fiscal Year 2000: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1999: ¥1,500,000 (Direct Cost: ¥1,500,000)
KeywordsTNFα / LPS / cytokine / MAPK / heme oxygenase / BCG / CYP / metallothionein / 酸化ストレス / ノックアウトマウス
Research Abstract

Cytokines constitute very sophisticated network, by which they play important roles in the activation of responsible cells and production of cytokines themselves. Therefore, it is difficult to determine function of an individual cytokine. In this study, we examined the effect of each cytokine on their target cells, especially the expression of HO-1 in the liver, in IL-1 α/β (IL-1), TNFα and IL-6 knockout mice. We found that in addition to IL-1, TNFα also played an important role in HO-1 gene expression by LPS.Based on these findings, we also examined major signal transduction from LPS in cytokine knockout mice. LPS has been shown to lead HO-1 gene expression via activation of AP-1. Therefore, we determined the effect of LPS on signal transduction from MAPK cascade leading to HO-1 gene expression in TNFα KO mice, which produced little response to the agent. We found the marked decrease in the activation of p38 and JNK, but no differences in the of phosphorylation of ERK, between wild and TNFα KO mice. The results suggest that TNFα plays actively in the LPS-mediated induction of HO-1 gene expression, and its signal is conducted via p38 and/or JNK.Additionally, we clarified the important role of cytokine KO mice in the study on BCG-mediated regulation of cytochrome P450 and metallothionein.

Report

(2 results)
  • 2000 Final Research Report Summary
  • 1999 Annual Research Report

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Published: 1999-04-01   Modified: 2016-04-21  

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