Co-operative Responses of Organella Constituents to Drug stimulation
Co-operative Responses of Organella Constituents to Drug stimulation
批准号:
03304045
负责人:
OHBA Yoshiki
金额:
$10.62万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Co-operative Research (A)
财政年份:
1991
资助国家:
日本
项目状态:
已结题
起止时间:
1991 至 1993
中文摘要
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英文摘要
On considering the efficiency for promoting our project research, this research group was divided into three subgroups depending on the idea that organella consisting domain can be classified to cell membrance, cytoplasm and cell nucleus.(1)The interaction of functional molecules in cell membrane and expression of 2nd messenger with cytosolic factors : the biosynthesis of phospholipid (Akamatsu) and chlesterol (Inoue) and their transport to cell membrance. (2)The active bahavior of functional molecules in cytoplasmic organella : effect of anti-trypanozoma drug to peroxisome formation (Takano), interaction of G protein with mast cells (Ichikawa) and serotonin receptor (Nomura), effects of polyamines to ribosomal function (Igarashi), and contribution of cyclic ADP ribose (Okamoto).(3)The effect of exogenous stimulant to nuclear functional molecules and the response : regulation of gene expression for the response to thyroid (Ohba), steriod (Noda) and glucagon (Ichiyama) hormone stimulation contribution of G protein to the formation of nuclear membrane (Natori)..13EA03 : In the research meeting we discussed on basis of each own result about the processes how exogenous information is converted to 2nd messenger through transduction mechanism and finally attain to the target gene. We concluded that there should be enormous ways of information transfer from cell surface receptor to the target gene, among which contribution of cyclic ADP ribose, discovered by Okamotao must be very important. The further research should be conncentrated to the point that how the steady state passway of information transfer can be disturbed by the foreign information, that is newly administered drugs or inhibitors. These observations may offer many suggestions to the analysis of drug action.
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Y.Ohba: "p13sucl Supresses the catalytic function of p34cdc2 kinase for intermediate filament proteins,in vitro" J.Biol.Chem.263. 20937-20942 (1992)
Y.Ohba:“p13sucl 抑制 p34cdc2 激酶对中间丝蛋白的催化功能,体外”J.Biol.Chem.263。
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H.Okamoto: "Cyclic ADP-ribose in insulin secretion from pancreatic β cell" Science. 259. 370-373 (1993)
H.Okamoto:“胰腺 β 细胞分泌胰岛素中的环状 ADP-核糖”《科学》259. 370-373 (1993)。
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Y.Ohba: "Preference of cdc2 kinase for peptide substate" Peptide Res.5. 281-285 (1992)
Y.Ohba:“cdc2 激酶对肽底物的偏好”肽 Res.5。
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Y.Nomura: "Increase in neurite formation and acetylcholine release by transfection of growth associated protein-43 cDNA into NG108-15 cells" J.Neurochem.61. 526-532 (1993)
Y.Nomura:“通过将生长相关蛋白 43 cDNA 转染至 NG108-15 细胞,增加神经突形成和乙酰胆碱释放”J.Neurochem.61。
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Michihisa Tohda: "The slow cyclic GMP increase caused by serotonin in NG108ー15 cells is not inhibited by antagonist of known serotonin receptors:possible existence of new receptor subtype coupled with membrane‐bound guanylate cyclase" J.Neurochem.57. 714-
Michihisa Tohda:“NG108-15 细胞中血清素引起的缓慢的循环 GMP 增加不受已知血清素受体拮抗剂的抑制:可能存在与膜结合鸟苷酸环化酶结合的新受体亚型”J.Neurochem.57-。
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