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Physiological roles of GTP binding protein associated with pertussis toxin (IAP) for the study of medicinal and diagnostic functions

Research Project

Project/Area Number 61870093
Research Category

Grant-in-Aid for Developmental Scientific Research

Allocation TypeSingle-year Grants
Research Field Biological pharmacy
Research InstitutionHokkaido University

Principal Investigator

TOKUMITSU Yukiko  Faculty of Pharmaceutical Sciences, Hokkaido University, 薬学部, 助教授 (60001046)

Co-Investigator(Kenkyū-buntansha) UI Michio  Faculty of Pharmaceutical Sciences, Tokyo University, 薬学部, 教授 (50001037)
KAMATAKI Tetsuya  Faculty of Pharmaceutical Sciences, Hokkaido University, 薬学部, 教授 (00009177)
MURAYAMA Toshihiko  Faculty of Pharmaceutical Sciences, Hokkaido University, 薬学部, 助手 (90174317)
OKADA Fumihiko  Health Center, Hokkaido University, 保健管理センター, 助教授 (40109517)
NOMURA Yasuyuki  Faculty of Pharmaceutical Sciences, Hokkaido University, 薬学部, 教授 (00034041)
堅田 利明  北海道大学, 薬学部, 助手 (10088859)
岡島 史和  群馬大学, 内分泌研究所, 助教授 (30142748)
Project Period (FY) 1986 – 1988
Project Status Completed (Fiscal Year 1989)
Budget Amount *help
¥14,000,000 (Direct Cost: ¥14,000,000)
Fiscal Year 1988: ¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 1987: ¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 1986: ¥7,000,000 (Direct Cost: ¥7,000,000)
KeywordsIAP / GTP binding protein / Proliferation and differentiation of cells / Phospholipase A_2 / Signal transduction / NIH3T3^<ras> / Adenylate cyclase system / c-myc / 肝細胞 / アデニル酸シクラーゼ血小板トロンビン / ホスホリパーゼA_2 / セロトニン受容体 / IAPの化学修飾 / 免疫細胞系 / 増殖作用 / アデニレートシクラーゼ系 / 3T3線維芽細胞 / 甲状腺細胞
Research Abstract

Many kinds of hormones and neurotransmitters interact with their specific receptors coupled to guanine nucleotide-binding protein (G protein) and lead to physiological actions. Pertussis toxin (IAP) lose their function of G protein in various types of cells. IAP is a useful probe to study the mechanism of signal transduction via G protein. Therefore, we examined the roles of G protein serving as IAP substrates and other G protein. The results obtained were as follows. (1) Serum-induced DNA synthesis in 3T3 fibroblasts was inhibited via loss of function of IAP substrates, thereby leading to cell proliferation. (2) IAP-sensitive G protein plays a role in c-myc gene expression of rat hepatocytes. (3) A new G protein sensitive to IAP was induced during differentiation of HL-60 cells into neutrophil type of cells. (4) IAP inhibited differentiation of 3T3L1 cells into adipocytes via IAP-sensitive G protein. (5) One of two types of the P2-purinergic receptors was coupled to IAP-sensitive G protein, resulting in inhibition of cAMP formation. (6) Adenylate cyclase activity in NIH-3T3^<src> cells decreased via reduction of the number of beta-adrenoceptors and phosphorylation of Gs protein but not ADP-ribosylation of Gi or Go. (7) Thrombin and epinephrine in platelets activated phospholipase A2 via IAP-sensitive G protein. (8) Adenylate cyclase activity in NIH-3T3^<ras> cells increased via rbduction of the amount of IAP-sensitive G protein. (9) Purified muscarinic receptors were coupled to purified IAP-sensitive G protein reconstituted. (10) Serotonin 1A receptors were coupled to IAP-sensitive G protein in rat brain cortex and hippocampus. (11) Amino acid sequences were determined, and GTP-binding sites and ADP-ribosylation sites were identified by molecular cloning of rat brain Gi and Go cDNA.

Report

(3 results)
  • 1989 Final Research Report Summary
  • 1988 Annual Research Report
  • 1986 Annual Research Report
  • Research Products

    (23 results)

All Other

All Publications (23 results)

  • [Publications] T.Murayama and M.Uni: "Possible involvement of a GTP-binding protein,the substrate of islet-activating protein,in receptor-mediated signaling for cell proliferation." J.Biol.Chem.262. 12463-12467 (1987)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] M.Oinuma,T.Katada and M.Ui: "A new GTP-binding protein in differentiated human leukemic(HL-60)cells serving as the specific substrate of isletactivating protein,pertussis toxin." J.Biol.Chem.262. 8347-8353 (1987)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] F.Okajima,Y.Tokumitsu and M.Ui: "P2-purinergic receptors are coupled to two signal transduction system leading to inhibition of cAMP generation and to production of inositol triphosphate in rat hepatocytes." J.Biol.Chem.262. 13483-13490 (1987)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] F.Okada,Y.Tokumitsu and M.Ui: "Possible involvement of pertussis toxin substrates(Gi,Go)in desipramine-induced refractoriness of adenylate cyclase in cerebral cortices of rats." J.Neurochem.51. 194-199 (1988)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] Y.Fujinaga,N.Morozumi,K.Sato,Y.Tokumitsu,K.Fujinaga,Y.Kondo,M.Ui and F.Okajima: "A pertussis toxin-sensitive GTP-binding protein plays a role in the Go-Gi transition of rat hepatocytes following establishment in primary culture." FEBS Lett.245. 117-121 (1989)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] Y.Kitamura,M.Mochii,R.Kodama,K.Agata,K.Watanabe,G.Eguchi and Y.Nomura: "Ontogenesis of α_2-adrenoceptor coupling with GTP-binding proteins in the rat telencephalon." J.Neurochem.53. (1989)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] T.Murayama and M.Ui: "Possible involvement of a GTP-binding protein, the substrate of islet-activating protein, in receptor-mediated signaling for cell proliferation." J.Biol.Chem.262. 12463-12467 (1987)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] M.Oinuma, T.Katada and M.Ui: "A new GTP-binding protein in differentiated human leukemic (HL-60) cells serving as the specific substrate of islet- activating protein, pertussis toxin." J.Biol.Chem.262. 8347-8353 (1987)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] F.Okajima, Y.Tokumitsu and M.Ui: "P2-purinergic receptors are coupled to two signal transduction system leading to inhibition of cAMP generation and to production of inositol triphosphate in rat hepatocytes." J.Biol.Chem.262. 13483-13490 (1987)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] F.Okajima, Y.Tokumitsu and M.Ui: "Possible involvement of pertussis toxin substrates (Gi, Go) in desipramine-induced refractoriness of adenylate cyclase in cerebral cortices of rats." J.Neurochem.51. 194-199 (1988)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] Y.Fujinaga, N.Morozumi, K.Sato, Y, Tokumitsu, K.Fujinaga, Y.Kondo, M.Ui and F.Okajima: "A pertussis toxin-sensitive GTP-binding protein plays a role in the G_0-G_1 transition of rat hepatocytes following establishment in primary culture." FEBS Lett.245. 117-121 (1989)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] Yukako Fujinaga: FEBS Lett. 244. (1989)

    • Related Report
      1988 Annual Research Report
  • [Publications] Fumihiko Okada: J.Neurochem.

    • Related Report
      1988 Annual Research Report
  • [Publications] Yoshihisa Kitamura: J.Neurochem.

    • Related Report
      1988 Annual Research Report
  • [Publications] Shirakura Shiro: Biochim.Biophys.Acta.

    • Related Report
      1988 Annual Research Report
  • [Publications] Lisa Konishi: Biochem.Biophys.Res.Commur.153. 1214-1222 (1988)

    • Related Report
      1988 Annual Research Report
  • [Publications] Fumihiko Okada: J.Neurochem.51. 194-199 (1988)

    • Related Report
      1988 Annual Research Report
  • [Publications] 岡島史和: 生化学. 58. 982 (1986)

    • Related Report
      1986 Annual Research Report
  • [Publications] Akira,Kikuchi: The Journal of Biological Chemistry. 261(25). 211558-1156 (1986)

    • Related Report
      1986 Annual Research Report
  • [Publications] Toshihiko Murayama: J.Biol.Chem.262. - (1987)

    • Related Report
      1986 Annual Research Report
  • [Publications] Fumihiko Okada: J.Neurochem. 47. 454-459 (1986)

    • Related Report
      1986 Annual Research Report
  • [Publications] Masahiro Tsuchimoto: Comp.Biochem.Physiol.87A. 377-383 (1985)

    • Related Report
      1986 Annual Research Report
  • [Publications] Kazuko Haga: Nature(London). 316-6030. 731-732 (1985)

    • Related Report
      1986 Annual Research Report

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Published: 1987-03-31   Modified: 2016-04-21  

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