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The basic study of transplantation of encapsulated cryopreserved mouse primordial follicles

Research Project

Project/Area Number 10671510
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Obstetrics and gynecology
Research InstitutionASAHIKAWA MEDICAL COLLEGE

Principal Investigator

SENGOKU Kazuo  Asahikawa Medical College, Dept. of OB/GYN, Associate Professor, 医学部, 助教授 (30163124)

Co-Investigator(Kenkyū-buntansha) TAMATE Kenichi  Asahikawa Medical College, Dept. of OB/GYN, Associate Professor, 医学部, 講師 (90207233)
Project Period (FY) 1998 – 1999
Project Status Completed (Fiscal Year 1999)
Budget Amount *help
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1999: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1998: ¥1,200,000 (Direct Cost: ¥1,200,000)
KeywordsPrimordial follicle / Cryopreservation / Microcapsule / Oocyte maturation / 原始卵胞卵 / 胚発育 / HB-EGF / 活性酸素 / 多精子受精防御
Research Abstract

We studied the probability of the successful cryopreservation of mouse primordial follicles. In addition, we evaluated the effectiveness of encapsulation of primordial follicles for successful transplantation, and obtained the following results.
1. Mouse primordial follicles were successfully cryopreserved with slow freeze-rapid thaw protocols using propandiol and sucrose as a cryoprotectant. Furthermore, primordial follicles treated with Hb, NO scavenger, and SOD, superoxide scavenger, showed significant higher survival rates compared with non-treated group after freeze-thawing.
2. Frozen-thawed follicles were encapsulated within alginate microcapsule and then implanted into peritoneal cavity in mouse and rat. Frozen-thawed mouse primordial follicules grafted in mouse demonstrated follicular growth, but the most advanced follicles had a maximum three or four granulosa cell layers. On the other hand, follicular growth was not found when primordial follicles were grafted to rats.
3. We confirmed the expression of GDF-9 mRNA in all of primordial, primary and secondary oocytes. However, relative amount of GDF-9 mRNA could not determined in this experiment.
Although mature follicles and oocytes were not obtained from encapsulated primordial follicle grafts, our preliminary results may offer important aspects of ovarian tissues and follicle banking.

Report

(3 results)
  • 1999 Annual Research Report   Final Research Report Summary
  • 1998 Annual Research Report
  • Research Products

    (4 results)

All Other

All Publications (4 results)

  • [Publications] K.Sengoku: "Requirement of sperm-oocyte plasma membrane fusion for establishment of the plasma membrane block to polyspermy in human pronuclear oocytes"Molecular Reproduction Development. 52・2. 183-188 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] K. Sengoku, K. Tamate, Y. Takaoka, M. Horikawa, K. Goishi, R. Okada, K. Tsuchiya, M. Ishikawa: "Requirement of sperm-oocyte plasma membrane fusion for establishment of the plasma membrane block to polyspermy in human pronuclear oocytes"Moleclular Reproduction Development. 52(2). 183-188 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] K.Sengoku: "Requirement of sperm-oocyte plasma membrane fusion for establishment of the plasma membrane block to polyspermy in human pronuclear oocytes"Molecular Reproduction Development. 52・2. 183-188 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] K.Sengoku: "Requirement of sperm-oocyte plasma membrane fusion for establishment of the plasma membrane block to polyspermy in human pronuclear oocytes" Molecular Reproduction Development. 52・2. 183-188 (1999)

    • Related Report
      1998 Annual Research Report

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Published: 1998-04-01   Modified: 2016-04-21  

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