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1993 Fiscal Year Final Research Report Summary

^<31>P MRS Study of Metabolism in Neuroblastoma

Research Project

Project/Area Number 03454268
Research Category

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

Allocation TypeSingle-year Grants
Research Field Pediatrics
Research InstitutionKyoto Prefectural University of Medicine

Principal Investigator

SAWADA Tadashi  Kyoto Prefectural Univ.of Med.Prof, 医学部, 教授 (10079874)

Co-Investigator(Kenkyū-buntansha) SAWADA Tadashi  Kyoto Prefectural Univ.of Med.Prof (10079874)
SAWADA Tadashi  Kyoto Prefectural Univ.of Med.Prof (10079874)
SAWADA Tadashi  Kyoto Prefectural Univ.of Med.Prof (10079874)
SAWADA Tadashi  Kyoto Prefectural Univ.of Med.Prof (10079874)
SAWADA Tadashi  Kyoto Prefectural Univ.of Med.Prof (10079874)
Project Period (FY) 1991 – 1993
Keywords^<31>P-MRS / Hollow fiber / Perfusion culture / PME / PCr / metabolite / metabolism / growth
Research Abstract

The human neuroblastoma cell line was used. The medium was supplemented with 10 % fetal bovine serum. Minivitafiber unit ( Grace Japan, Amicon ) was chosen in this study. Cells were introduced into the hollow-fiber unit and allowed to deposit and reattach for a few hours, and then the intracapillary space ( ICS ) was begun to be perfused. The perfusion of the extracapillary space ( ECS ) was started 48 hours after inoculation. A peristaltic pump was used to maintain the flow rate of 22 ml/min in ICS and 0.3 ml/min in ECS.Phosphorus-31 nuclear magnetic resonance ( ^<31>P-NMR ) spectra were obtained on CSI II operating at 81 MHz for phosphorus. The spectral conditions were a 60゚ pulse, a 2.0 recycle time. Starling 10 days after inocuation of the culture unit, prominent spectra could be obtained by 2000 scans on intact cells aerated by continuous medium perfusion at 37゚C.Peaks were phosphomonoesters ( PME ), inorganic phosphate ( Pi ), phosphodiesters ( PDE ), phosphocreatine ( PCr ), gamma -adennosine triphosphate ( ATP ), alpha -ATP and beta -ATP.
The ^<31>P-NMR spectra of human neuroblastoma cells were obtained on intact cells cultured in hollow fiber. The spectra were dominated by phosphomonoester peaks. The perfusion system was developed to achieve the high cell density and maintain viable intact cells for NMR study.
This system would be useful for study of growth and metabolism in neuroblastoma.

  • Research Products

    (7 results)

All Other

All Publications (7 results)

  • [Publications] 四方卓磨,他: "ホローファイバーを用いた潅流培養法による生きた神経芽腫細胞の^<31>P-MRS" 医学のあゆみ. 166. 623-624 (1993)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 沢田淳,他: "^<31>P-MRSによる培養神経芽腫細胞の代謝-ホローファイバー式培養法を用いて-" 厚生省がん研究「分子細胞遺伝学的情報からみた神経芽細胞腫の集学的治療に関する研究」 主任研究者土田嘉昭:平成3,4年度研究報告. 93-94 (1993)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 四方卓磨,他: "^<31>P-MRSによる培養神経芽腫細胞の代謝に関する検討:ホローファイバー式培養方法を用いて" 日本小児科学会雑誌(第96回日本小児科学会学術集会号). 97. 413 (1993)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 四方卓磨,他: "^<31>P-NMR Spectroscopyによる培養神経芽腫細胞の代謝" 日本小児外科学会雑誌(第30回日本小児外科学会総会日程抄録). 29. 215 (1993)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 四方卓磨,他: "ホローファイバー式培養法による生きた神経芽腫細胞の^<31>P-MRS" 日本磁気共鳴医学会雑誌(第21回日本磁気共鳴医学会大会講演抄録集). 13. 481 (1993)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] A.Shikata,et al.: "Increased expression of trk proto-oncogene by γ-interferon in human neuroblastoma cell lines" Japanese Journal of Cancer Research. 85. 122-126 (1994)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] A.Shikata, T.Sugimoto, H.Hosoi, Y.Sotozono, T.Shikata, T.Sawada and Luis F.Parada: "Increased expression of trk proto-oncogene by gamma-interferon in human neuroblastoma cell lines" Japanese Journal of Cancer Research. 85. 122-126 (1994)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 1995-03-27  

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