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Fundamental research for the complex lipid change during wound healing

Research Project

Project/Area Number 04454309
Research Category

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

Allocation TypeSingle-year Grants
Research Field General surgery
Research InstitutionUniversity of Tokyo

Principal Investigator

HARII Kiyonori  University of Tokyo Medical Department Professor, 医学部(病), 教授 (50111539)

Co-Investigator(Kenkyū-buntansha) SUGAWARA Yasushi  University of Tokyo Medical Department Staff, 医学部(病), 医員
YOSHIMURA Koutaro  University of Tokyo Medical Department Staff, 医学部(病), 助手 (60210762)
KAWASHOMA Takao  University of Tokyo Medical Department Staff, 医学部(病), 助手 (20214637)
伊藤 優  東京大学, 医学部(病)形成外科, 教務職員 (30240716)
田幡 雅彦  東京大学, 医学部(病)形成外科, 医員 (30236723)
岩森 正男  東京大学, 医学部生化学, 助教授 (90110022)
Project Period (FY) 1992 – 1993
Project Status Completed (Fiscal Year 1993)
Budget Amount *help
¥6,700,000 (Direct Cost: ¥6,700,000)
Fiscal Year 1993: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1992: ¥6,100,000 (Direct Cost: ¥6,100,000)
KeywordsWound healing / Epidermal lipid / Cholesterol sulfate / Cholesterol ester / 脂質 / 胎児皮膚 / 創傷治癒
Research Abstract

Little is known about changes in the lipid composition of the skin during fetal development and wound healing. In these studies, we investigated the lipid composition of human fetal epidermmis ranging from 14 week to 28 week estimated gestational ages epidermis(EGA) and fetal mouse epidermis ranging 14 day EGA to delibvery. The lipid composition of epidermal fractions from human skin samples between 14w to 17w EGA was exhibiting a predominance of free sterols, free fatty acid, phospholipids and squalene. After 20 w EGA fetal epidermis became enriched in cholesterol derivatives, ceramids and glycosylceramids. Moreover cholesterol ester became prominent comparing with newborn and adult epidermis. In mouse epidermis, along with the formation of the multilayred structure of the epidermis, cholesterol sulfate concentration of cholesterol sulfate increased. Cholesterol sulfotransferase showed a 6-fold increase from 14 to day 16 EAG with appearance of cholesterol sulfate.
Abnormal wound healing process causes keloid, exhibiting hyperproliferation of extracellular matrix. Keloid was obtained surgically, and the epidermal thickness of keloid was measured and compared the normal looking skin of the same patient. Keloidal epidermis showed marked thickness but the proportion of the four epidermal layrs was not changed. The lipid composition of keloid epidermis was determined and compared with normal looking skin around the lesion. There was a significant decrease in squalene and triglyceride contents compared with the normal epidermis. Squalene and triglyceride are major components of sebaceous gland lipids. Lack of them may make epidermis dry, which in turn causes barrier dysfunction. Recently barrier abnormality results in epidermal hyperproliferation, scaling and inflammation. The lack of sebaceous lipids in keloid may cause the hyperproliferation of epidermis. Keloid may serve a unique model to clarify the role of sebaceous lipids in the whole epidermal lipid function.

Report

(3 results)
  • 1993 Annual Research Report   Final Research Report Summary
  • 1992 Annual Research Report
  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] 館正弘: "ケロイド(肥厚性瘢痕)の脂質成分の分析" Progress in Medicine. 12. 2896-2897 (1992)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1993 Final Research Report Summary
  • [Publications] 館正弘: "肥厚性瘢痕表皮に認められる脂質変化" Progress in Medicine. 13. 2606-2608 (1993)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1993 Final Research Report Summary
  • [Publications] Kagehara M.: "Programmed expression of choelsterol sulfotransferase and transglutaminase during epidermal differentiation of murine skin development." Biochim Biophys Acta. (in press).

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1993 Final Research Report Summary
  • [Publications] Tachi M.: "Lipid analysis of Keloid(Hypertrophic scar)" Progress in Medicine. 12. 2896-2897 (1992)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1993 Final Research Report Summary
  • [Publications] Tachi M.: "Epidermal lipids of keloid" Progress in Medicine. 13. 2606-2608 (1993)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1993 Final Research Report Summary
  • [Publications] Kagehara M.: "Programd expression of cholesterol sulfotransferase during differentiation of murine skin development" Biochim Biophys Acta. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1993 Final Research Report Summary
  • [Publications] 館正弘: "ケロイド(肥厚性瘢痕)の脂質成分の分析" Progress in Medicine. 12. 2896-2897 (1992)

    • Related Report
      1993 Annual Research Report
  • [Publications] 館正弘: "肥厚性瘢痕表皮に認められる脂質変化." Progress in Medicine. 13. 2606-2608 (1993)

    • Related Report
      1993 Annual Research Report
  • [Publications] Kagehara M: "Programmed expression of choelsterol sulfotransferase and transglutaminase during epidermal differentiation of murine skin development." Biochim Biophys Acta(in press).

    • Related Report
      1993 Annual Research Report
  • [Publications] 館正弘(共著): "形成外科アドバンスシリーズ1-3創傷の治療:最近の進歩" 克誠堂出版, 170 (1993)

    • Related Report
      1993 Annual Research Report
  • [Publications] 館正弘(共著): "疾患別モデル動物の作成と新薬開発のための試験実験法" 技術情報協会, 380 (1993)

    • Related Report
      1993 Annual Research Report
  • [Publications] 館 正弘: "ケロイド(肥厚性瘢痕)の脂質成分の分析" Progress in Medicine. 12. 2896-2897 (1992)

    • Related Report
      1992 Annual Research Report

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Published: 1992-04-01   Modified: 2016-04-21  

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