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Development of A High-Resolution Non-Confocal Slicing Microscope

Research Project

Project/Area Number 05558099
Research Category

Grant-in-Aid for Developmental Scientific Research (B)

Allocation TypeSingle-year Grants
Research Field Neuroscience in general
Research InstitutionHamamatsu University School of Medicine, Photon Medical Research Center

Principal Investigator

TERAKAWA Susumu  Hamamatsu University School of Medicine, Photon Medical Research Center Professor, 光量子医学研究センター, 教授 (50014246)

Project Period (FY) 1993 – 1994
Project Status Completed (Fiscal Year 1994)
Budget Amount *help
¥8,600,000 (Direct Cost: ¥8,600,000)
Fiscal Year 1994: ¥2,400,000 (Direct Cost: ¥2,400,000)
Fiscal Year 1993: ¥6,200,000 (Direct Cost: ¥6,200,000)
KeywordsVideo microscopy / High resolution optics / Confocal microscope / Numerical aperture / Intracellular organelle / Microvilli / Differential interference microscope / Nomarski microscope / 分解能 / 光学顕微鏡 / エキソサイトシス / 多重光顕法 / Ca-イメージング / エキソサイトーシス / 好中球 / fura-2
Research Abstract

A numerical aperture of 1.4 has been the largest for objective lenses, to date. This set a limit to the spatial resolution at about 0.2mum. It is considered to be theoretically impossible to make an objective lens of any higher numerical aperture, because of limited refractive indices of the materials for optics such as, glass and oil. The spherical aberrtaion is also a practical problem when making a lens of high numerical aperture. In this research, construction of an objective lens of a numerical aperture higher than the conventional value was attempted, with a final purpose to observe exocytosis in the synaptic terminal of neuronal cells using the video microscopy. The idea is to make use of a special glass and oil of high refractive indices, and to ignore the marginal aberration, as the video microscopy requires only the axial image.
Two lenses of a numerical aperture of 1.65 were developed successfully. Both can fit to the threaded revolver of the conventional microscope, attaining a magnification of 100 times with a working distance of 100mum. It improved the spatial resolution by about 20%. Several biological specimens were examined with one of these lenses at the differential interference contrast mode. Mitochondria, Golgi-like structures, nuclear membrane, secretory graules were clearly visible. Some cytoskeletal patterns were visible underneath the erythrocyte membrane. Microvilli of the intestinal epithelium and spines of the platelet were better resolved than before.
Shortcomings were that the immersion oil was unstable against a strong light, and that the best resolution is realized in a very short range near the coverslip. With this optics, synaptic exocytosis is planned to be examined, soon. The lens will become commercially available upon order(Olympus, HR Lens).

Report

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

    (15 results)

All Other

All Publications (15 results)

  • [Publications] TERAKAWA, S,: "Eridence against the swelling hypothesis for initiation of exocytosis in terminals of chronaffin cell processes" Journal of Physiology (Paris). 87. 209-213 (1993)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] Kamijo, A.: "Neurotransmitter-induced exocytosis in goblet and acinar cells of rat nasal mucosa studied by video microscopy" American Journal of Physiology. 265. L200-L209 (1993)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] Terakawa, S.: "Exocytosis in the gronoth come of differentiated chromaffin cells induced by electrical stimulation" Japanese Journal of Physiology. 43. S213-S216 (1993)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] Manivannan, S.: "Rapid sprouting of filopodia in chromaffin cells,PC12cells,and dorsal root neurons induced by electricnl stim" Journal of Neuroscierce. 14. 5917-5928 (1994)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] Terakawa, S.: "Dynamics of exocytosis in the terminal of chromaffin cells revealed by dual-microscopy of DICimage and fluorescero image" Neuroscience Research (Supplement). 19. S36- (1994)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] 寺川 進: "トランスミッターの放出の可視化" ブレインサイエンス. 6. 51-58 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] Terakawa, S., Manivannan, S.& Kumakura, K.: "Evidence against the swelling hypothesis for initiation of exocytosis in terminals of chromaffin cell processes." J.Physiol. (Paris). 87. 209-213 (1993)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] Kamijo, A., Terakawa, S.& Hisamatsu, K: "Neurotransmitter-induced exocytosis in goblet and acinar cells of rat nasal mucosa studied by video microscopy." Am.J.Physiol. 265. L200-L209 (1993)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] Terakawa, S., Manivannan, S.& Kumakura, K.: "Exocytosis in the growth cone of differentiated chromaffin cells induced by electrical stimulation." Jpn.J.Physiol.43. S213-S216 (1993)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] Manivannan S & Terakawa, S.: "Rapid sprouting of filopodia in chromaffin cells, PC12 cells, and dorsal root neurons induced by electrical stimulation." J.Neurosci. 14. 5917-5928 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] Terakawa, S., Kumakura, K: "Dynamics of exocytosis in the terminal of chromaffin cells revealed by dual-microscopy of DIC image and fluorescence image." Neurosci Res. Suppl 19. S36 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] Terakawa, S.: "Visualization of transmitter release" Brain Science. 6. 51-58 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] 寺川進: "トランスミッター放出の可視化" ブレインサイエンス. 6. 51-58 (1995)

    • Related Report
      1994 Annual Research Report
  • [Publications] 寺川 進: "ビデオマイクロスコピーによる膵臓腺房細胞の開口分泌解析" 日本生理学雑誌. 55. 503 (1993)

    • Related Report
      1993 Annual Research Report
  • [Publications] 桜井 孝司: "ビデオ顕微鏡によるランゲルハンス島の分泌パターンの解析" 日本生理学雑誌. 55. 503 (1993)

    • Related Report
      1993 Annual Research Report

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

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