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Development of New Objective Lens with Double Cylinders

Research Project

Project/Area Number 11558087
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section展開研究
Research Field Biophysics
Research InstitutionTokyo University of Agriculture and Technology

Principal Investigator

OHTA Yoshihiro  Department of Biotechnology, Associate Professor, 工学部, 助教授 (10223843)

Co-Investigator(Kenkyū-buntansha) ABE Katsuyuki  Olympus Optical Co. Ltd, Assistant Manager, 光学技術部・主任(研究職)
Project Period (FY) 1999 – 2001
Project Status Completed (Fiscal Year 2001)
Budget Amount *help
¥11,900,000 (Direct Cost: ¥11,900,000)
Fiscal Year 2001: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 2000: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 1999: ¥8,900,000 (Direct Cost: ¥8,900,000)
KeywordsObjective lens / fluorescence microscope / mitochondoria / membrane potential / calcium signaling / multiple staining / CCDカメラ / 2重染色 / 細胞 / 経時変化 / フィルタホイール / 反射ミラー / 暗視野照明
Research Abstract

We have developed a florescence microscope by using objective lens with the double cylinders. Since this objective enabled us to detect the time course of fluorescence at different wavelengths simultaneously, we performed the following two experiments, 1) In adrenocortical cells and C6 glioma cells, we observed calcium signaling and mitochondrial membrane potentials. When the intracellular calcium concentration shows a local and rapid increase near mitochondria, the mitochondria show the transient and sudden depolarization, leading to the release of intramitochondrial calcium. When the calcium concentration increases gradually near the mitochondria, however, mitochondria show the uptake of calcium ion and decrease the calcium concentration at cytosol. 2) The changes in mitochondrial membrane potential were detected during the mitosis. The stage of mitosis was identified with Hoechst 33342. The mitochondrial membrane potential decreased during mitosis. On the other hand, the membrane potential recovered after the mitosis. This results might suggest that the intracellular ATP concentration could decrease during mitosis and that it could increase after the mitosis.

Report

(4 results)
  • 2001 Annual Research Report   Final Research Report Summary
  • 2000 Annual Research Report
  • 1999 Annual Research Report
  • Research Products

    (6 results)

All Other

All Publications (6 results)

  • [Publications] Nakayama et al.: "Fluorescence Imaging of Metabolic Responses in Single Mitochondria"Biochem.Biophys.Res.Commun.. 290. 23-28 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] Nakayama et al.: "Fluorescence Imaging of Metabolic Respcnses in Single Mitochondria"Biochem. Biophys. Res. Commun.. 290. 23-28 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] Nakayama, et al.: "Fluorescence Imaging of Metabolic Responses in Single Mitochondria"Biochem. Biophys Res. Commun.. 290. 23-28 (2002)

    • Related Report
      2001 Annual Research Report
  • [Publications] Makoto Yamada: "Dynamic mobility of genetically expressed fusion protein between cytochrome P450IAI and NADPH-cytochrome P450 reductase in yeast microsomes"Biochemistry. 38. 9465-9470 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] 渡辺功一: "蛍光顕微鏡による単離ミトコンドリアの観察方法"生物物理. 224. 258-260 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Miyuki Hoolahan: "Molecular Steroidogenesis"Universal Academy Press Inc.. 442 (2000)

    • Related Report
      1999 Annual Research Report

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Published: 1999-04-01   Modified: 2016-04-21  

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