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2022 Fiscal Year Final Research Report

Etiological and pathological analysis of rats with congenitally abnormal bone and cartilage formation

Research Project

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Project/Area Number 19K09584
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 56020:Orthopedics-related
Research InstitutionKanazawa Medical University

Principal Investigator

SHIMADA Hiroki  金沢医科大学, 看護学部, 教授 (60278108)

Project Period (FY) 2019-04-01 – 2023-03-31
Keywords骨軟骨形成 / 白内障 / 脱毛 / 脂質代謝
Outline of Final Research Achievements

We have previously established a strain of rats that exhibits congenital osteochondrodysplasia-related pathologies such as short face and severe curvature of the spine, as well as systemic pathologies such as cataracts, partial alopecia, and hyperkeratosis of the skin. This rat strain is very similar to the X-linked dominant Conradi-Hunermann type of petechial chondrodysplasia, which is caused by mutations in the cholesterol metabolism enzyme gene EBP.
The purpose of this study was to elucidate the etiology and pathogenesis of these rats.
Whole genome analysis revealed no mutation in the Ebp gene on the x sex chromosome between the control and the pathological groups. On the other hand, there were genes with missense mutations on the x chromosome that are thought to be related to lipid metabolism and bone formation.

Free Research Field

発生学

Academic Significance and Societal Importance of the Research Achievements

本研究で解析したラットは骨軟骨形成異常の病因解明を明らかにする上で非常に有用であると考えられる。さらにこの系統は骨軟骨形成異常のみならず,白内障,皮膚疾患等,広範囲な疾患の病因,病態を研究するうえで重要なモデルとなりうる。

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Published: 2024-01-30  

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