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Gene expression in the mouse growth plate

Research Project

Project/Area Number 18591678
Research Category

Grant-in-Aid for Scientific Research (C)

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

Principal Investigator

SATO Kazuki  Keio University, Department of Orthopedic Surgery, Assistant (60235322)

Co-Investigator(Kenkyū-buntansha) ISSHIKI Honoka  Keio University, Department of Orthopedic, Assistant (00348674)
UMEZAWA Akihiro  KEIO UNIVERSITY, Department of Reproductive Biology, National Research Institute for Child Health and Development, Director (70213486)
TOYAMA Yoshiaki  Keio University, Department of Orthopedic Surgery, Professor (40129549)
Project Period (FY) 2006 – 2007
Project Status Completed (Fiscal Year 2007)
Budget Amount *help
¥3,920,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥420,000)
Fiscal Year 2007: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2006: ¥2,100,000 (Direct Cost: ¥2,100,000)
Keywordsepiphyseal plate / gene expression / mouse
Research Abstract

Longitudinal bone growth is a complex process that begins chondrocyte proliferation and subsequent hypertrophy and secretion of extracellular matrix. Subsequently matrix mineralization, vascular invasion, chondrocyte apoptosis, and replacement of chondrocytes by osteocytes lead to the formation of bone. The chondrocytes of the growth plate have been classified into four anatomic zones, reflecting their cellular features and the tissue architecture. In the resting zone (RZ),the ratio of extracellular matrix to cell volume is quite high. The chondrocytes take on a flattened appearance, begin to divide, and organize into columns that extend from proliferating zone (PZ) to maturing zone (MZ). The dividing cells separate from each other and grow larger in the hypertrophic zone (HZ).
There are notable biochemical and morphological differences among chondrocytes in each zone. In order to better characterize the genetic program controlling bone growth, gene expression was analyzed in chondrocytes microdissected from four previously defined zones of the growth plate. This study is the first to examine the growth plate at such resolution and further extends previous work by measuring expression of ~34,000 putative transcripts. We identified significant differences in gene expression among zones in growth plate, which likely contribute to the regulation of chondrocyte maturation in the growth plate.

Report

(3 results)
  • 2007 Annual Research Report   Final Research Report Summary
  • 2006 Annual Research Report
  • Research Products

    (2 results)

All 2006

All Presentation (2 results)

  • [Presentation] マウス成長板における遺伝子発現解析2006

    • Author(s)
      一色ほのか, 佐藤和毅, 戸山芳昭
    • Organizer
      第21回日本整形外科学会基礎学術集会
    • Place of Presentation
      長崎
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] Gene expression analysis in the mouse growth plate2006

    • Author(s)
      Honoka Isshiki, Kazuki Sato, Yoshiaki Toyama
    • Organizer
      The 21thst Annual Orthopaedic Research Meeting of the Japanese Orthopaedic Association
    • Place of Presentation
      Nagasaki, Japan
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary

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Published: 2006-04-01   Modified: 2016-04-21  

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