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Cloning of Retinal Cells and investigation of growth and in hibitory foctors

Research Project

Project/Area Number 05671455
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field Ophthalmology
Research InstitutionTohoku University

Principal Investigator

ITABASHI Ryuzo  Tohoku Univ., Sch.of Medicine Instructor, 医学部・附属病院, 助手 (20193419)

Co-Investigator(Kenkyū-buntansha) KATO Kei-ichi  Tohoku Univ.Sch.of Medicine Instructor, 医学部・附属病院, 助手 (50260435)
ISHIGURO Sei-ichi  Tohoku Univ., Sch.of Medicine Assistant Professor, 医学部, 講師 (20111271)
阿部 俊明  東北大学, 医学部附属病院, 助手 (90191858)
Project Period (FY) 1993 – 1994
Project Status Completed (Fiscal Year 1994)
Budget Amount *help
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1994: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1993: ¥1,300,000 (Direct Cost: ¥1,300,000)
KeywordsRPE / SV40 Large T / Growth Factor / 網膜色素上皮 / ミュラー細胞 / 視細胞 / 細胞培養 / モノクロナール抗体 / SV40ラージT抗原遺伝子 / SDS電気泳動
Research Abstract

We established a retinal pigment epithelium derived cell line from transgenic mouse harboring temperature-sensitive simian virus 40 large T-antigen. We tried to purify the growth or inhibitory factor from bovine neural retinal extract by using these established cells (PRET cells). Though this retinal extract stimulated RPET cells' growth, this growth effects were poor and not observed under lacking the conditioned medium from the neural retinal cells from transgenic mouse harboring temperature-sensitive simian virus 40 large T-antigen (CM). And more this growth effects of retinal extract on RPET cells were less than on chick retinal pigment epithelial cells. Therefore, it is difficult that purify the endogenous factors in neural retina using PRET cells. On the other hand, the growth effect on PRET cells by CM was dramatic and PRET cells and CM were derived from homogeneous animal. Accordingly, we expect that the combination of PRET cells and CM were the wonderful material for investigating the novel endogenous growth factors. Hereafter we will culture the neural retinal cells from transgenic mouse harboring temperature-sensitive simian virus 40 large T-antigen, collect the large amount of CM and investigate the growth factor for PRET cells in CM.

Report

(3 results)
  • 1994 Annual Research Report   Final Research Report Summary
  • 1993 Annual Research Report
  • Research Products

    (6 results)

All Other

All Publications (6 results)

  • [Publications] 加藤 圭一ら: "SV40 largeT抗原遺伝子導入マウス網膜色素上皮細胞に対する細胞外基質の影響" 日本眼科学会雑誌. 98. 163- (1994)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] Kei-ichi Kato, et al.: "Effect of Extracellurar Hatvices to A Retinal Pigment Epithelial Eell line Habouring Temparature-Sensitive SV40 large T Antigen gene" Acta Societatis Ophthalmolofical Japonical.98. 163 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] 加藤圭一ら: "SV40 largeT抗原遺伝子導入マウス網膜色素上皮細胞に対する細胞外基質の影響" 日本眼科学会雑誌. 98. 163- (1994)

    • Related Report
      1994 Annual Research Report
  • [Publications] Ryuzo Itabashi et al: "Stargardt's disease/Fundus flavimaculatus;psychophysical and electrophysiologic results" Graefe's Arch Clin Exp Ophthalmol. 231. 555-562 (1993)

    • Related Report
      1993 Annual Research Report
  • [Publications] Yuko Suzuki,Sei-ichi Ishiguro 他: "Identification and imnunohistochemistry,of retinal dehydrogenase from borine retinal pigment epithelium" Biochenica et Biophysica Acta. 1163. 201-208 (1993)

    • Related Report
      1993 Annual Research Report
  • [Publications] Kei-ichi Kato et al: "Partial Purification of a novel endogenous growth,factor to Embryonic chick retinal pigment Epithelialcell's from Borine retina" Invest Ophthalmol Vis Sci. 35. 1760-1760 (1994)

    • Related Report
      1993 Annual Research Report

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Published: 1993-04-01   Modified: 2016-04-21  

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