| Project/Area Number |
11671731
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Ophthalmology
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| Research Institution | Nagoya University |
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Principal Investigator |
IWAMOTO Takashi School of Medicine, Nagoya University Research Associate, 医学部, 助手 (60223426)
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| Co-Investigator(Kenkyū-buntansha) |
ITO Masafumi School of Medicine, Nagoya University Associate Professor, 医学部, 助教授 (50184693)
KITAMURA Toshio Tokyo University, Dept. of Hematopoietic Factors, Institute of Medical Science, Associate Professor, 医科学研究所, 客員助教授 (20282527)
MIYAKE Yozo School of Medicine, Nagoya University Professor, 医学部, 教授 (30166136)
HAMAGUCHI Michinari School of Medicine, Nagoya University Professor, 医学部, 教授 (90135351)
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| Project Period (FY) |
1999 – 2000
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| Project Status |
Completed (Fiscal Year 2000)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2000: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1999: ¥2,400,000 (Direct Cost: ¥2,400,000)
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| Keywords | Interleukin 6 / gp130 / receptor / Tiel / TNFα / vascular endothelial cell / TGFβ / 血管内皮 |
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| Research Abstract |
1.Cloning of Interleukin 6(I1-6)receptor/gp130 and Tiel
The DNA fragment coding the intracellular region of gp130 and that coding the extracellular region of Tiel were amplified by PCR.
2.Construction of a chimera gene of gp130 and Tiel and its introduction into pro-B cells
The DNA fragments of gp130 and Tiel were subcloned into an expression vector of pcDNA3 to construct a chimera gene. Then we transfected this plasmid to IL-3 dependent pro-B cells(Ba/F3)by electroporation method. However, we could not detect the chimera protein by immunoblotting with anit-gp130 antibody. Since RNA expression of a chimera gene was detected, its stability at protein level appeared to be unstable.
3.Molecular cloning of the genes that are induced by gp130
We cloned several IL-6 induced genes by subtraction method, one of which was Ral guanine nucleotide dissociation stimulator(RalGDS). The induction was fully dependent on Stat3 activation. The analysis of RalGDS function in signal transduction through gp130 now is under way.
factor(TNF)α, one vascular endothelial growth factor.
4.Cloning of inhibitory molecules for signal transduction of tumor necrosis
While TNFα induces the apoptosis in NIH3T3 mouse fibroblasts, v-Src-transformed NIH3T3 cells are resistant. We constructed a retroviral cDNA expression library from v-Src-transformed cells and infected it to NIH3T3 cells. Then we selected several clones in the presence of TNFα and recovered cDNA from each clone. One of them was an antisense-fragment coding a novel possible serine threonine phosphatase. Full length of the cDNA was cloned by PCR method, sequenced, and named as PET.When antisense of PET was introduced into NIH3T3 cells, they became partially resistant to TNFα. Now, the analysis of its expression in mouse tissues and function are under way.
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