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BMP Signaling on Cartilage Repair Response in Full-thickness Articular Cartilage Defects

Research Project

Project/Area Number 12671425
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Orthopaedic surgery
Research InstitutionKumamoto University

Principal Investigator

NAKAMURA Eiichi  Kumamoto University Hospital, Dept.of Orthopaedic Surgery, Lecturer, 医学部付属病院, 助手 (70274719)

Co-Investigator(Kenkyū-buntansha) MIZUTA Hiroshi  Kumamoto University, Graduate School of Medical Sciences, Dept.of Orthopaedic Surgery, Associate Professor, 医学部, 助教授 (60174025)
Project Period (FY) 2000 – 2002
Project Status Completed (Fiscal Year 2002)
Budget Amount *help
¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 2002: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 2001: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 2000: ¥1,400,000 (Direct Cost: ¥1,400,000)
KeywordsArticular Cartilage / Bone Morphogenetic Protein / Chondrocyte / 骨形戒因子
Research Abstract

We investigated BMP signaling on cartilage repair response in full-thickness articular cartilage defects. In the previous study, we established a rat model to clarify cartilage repair response full-thickness articular cartilage defects. The repair process in the center of the defects was analyzed by immunostaining and in situ hybridyzation method at 2,4,7,14 days after surgery using our rat model with a small defect (0.7mm width) and a large defect (1.5mm width). In the center of a small defect, at 2 days after surgery, the messenger RNA of BMP-4 was found, but this protein was not observed. After that, the messenger RNA and protein of BMP-4 was found through all periods. The messenger RNA and protein of BMP-6 was first found at 7 days after surgery. The messenger RNA and protein of GDF-5 was slightly first found at 4 days after surgery. The messenger RNA and protein of those receptors was expressed through all periods. On the other hand, in the center of a large defect, at 2 days after surgery, the messenger RNA of BMP-4 was found without no protein. At 4days after surgery, the messenger RNA and protein of BMP-4 was slightly expressed. At 7 days after surgery, the messenger RNA of BMP-4 was only observed. At 7 days after surgery, the messenger RNA and protein of BMP-4 were not found. The messenger RNA and protein of BMP-6 and GDF-5 was not observed through all periods. The messenger RNA and protein of those receptors was found through all periods as well as those in a small defects. Based on the results of this study, it was certified that, on cartilaginous repair in full-thickness articular cartilage defects, BMP-4 signaling is important for the initiation of the process, BMP-6 signaling may be involved in chondrocyte maturation and hypertrophy, GDF-5 signaling may be involved in chondrocyte hypertrophy

Report

(4 results)
  • 2002 Annual Research Report   Final Research Report Summary
  • 2001 Annual Research Report
  • 2000 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] 中村英一, 水田博志, 安楽喜久, 工藤智志, 高木克公: "関節軟骨全層欠損自然修復過程における骨形成因子(BMP)シグナリングについて"日本整形外科学会雑誌. 76. S946 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Eiichi Nakamura, Hiroshi Mizuta, Yoshihisa Anraku, Satoshi Kudo, Katsumasa Takagi: "BMP Signaling on Cartilage Repair Response in Full-thickness Articular Cartilage Defects"The Proceedings of the 17th Annual Orthopaedic Research Meeting of the Japanese Orthopaedic Association. 76(8). S946 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] 中村英一: "関節軟骨全層欠損自然修復過程における骨形成因子(BMP)シグナリングについて"日本整形外科学会雑誌. 76巻・8号. S946 (2002)

    • Related Report
      2002 Annual Research Report

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Published: 2000-04-01   Modified: 2016-04-21  

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