| Project/Area Number |
02670103
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
General medical chemistry
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| Research Institution | University of Tsukuba |
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Principal Investigator |
ISHII Tetsuro Univ. Tsukuba, Inst. Basic Med. Sci., Lecturer, 基礎医学系, 講師 (20111370)
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| Co-Investigator(Kenkyū-buntansha) |
BANNAI Shiro Univ. Tsukuba, Ints. Basic Med. Sci., Professor, 基礎医学系, 教授 (70019579)
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| Project Period (FY) |
1990 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1991: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1990: ¥1,000,000 (Direct Cost: ¥1,000,000)
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| Keywords | cystine / amino acid transport / diethylmaleate / stress protein / Xenopus / cDNA cloning / ジェチルマレイン酸 / グルタミン酸 / 細胞膜 |
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| Research Abstract |
The amino acid transport activity designated System x_C^- is a Na^+-independent system and is highly specific for cystine and glutamate. In cell culture systems, the uptake of cystine mediated by this system is usually important in maintaining intracellular glutathione levels, because cystine and/or cysteine is the rate limiting precursor amino acid of glutathione synthesis. This transport activity can be induced in mouse peritoneal macrophages during culture by diethylmaleate, a sulfhydryl-reactive agent. We prepared mRNA from those macrophages and injected into Xenopus oocytes and demonstrated the expression of System x_C^-, i. e., a Na^+-independent, glutamate-inhibitable cystine transport system. The expressed cystine transport activity depended on the assay temperature, in that cystine uptake measured at 37ﾟC was several-fold higher than that measured at 20ﾟC. Injection of size- fractionated mRNA indicated that the System x_C^--transporter of the mouse macrophage is encoded by mRNA of 1.5 to 2.9 kb.
In the next step, we constructed a lambdaZAPII cDNA library from the macrophage mRNA. Using a differential hybridization technique, we have isolated hundreds of cDNA clones which appeared to be induced under diethylmaleate treatment in macrophages. We are examining those selected cDNA clones expecting to find out a cDNA clone encoding cystine transporter.
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