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2018 Fiscal Year Final Research Report

The effects of CC25 on bone formation in new born mouse

Research Project

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Project/Area Number 16K12720
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Eating habits
Research InstitutionShizuoka University

Principal Investigator

Yukita Akira  静岡大学, 教育学部, 准教授 (80401214)

Co-Investigator(Kenkyū-buntansha) 茶山 和敏  静岡大学, 農学部, 准教授 (30260582)
中村 浩彰  松本歯科大学, 歯学部, 教授 (50227930)
二宮 禎  日本大学, 歯学部, 准教授 (00360222)
Project Period (FY) 2016-04-01 – 2019-03-31
KeywordsCCL25 / 母乳 / 骨形成 / 骨代謝 / ケモカイン
Outline of Final Research Achievements

Previous studies have shown that CCL25, which is known to be involved in intestinal immunity, is contained in breast milk. By the artificial lactation experiment we established before, we found that CCL25 in artificial milk can activate bone formation and bone resorption, and promote bone growth in the longitudinal direction of infant mice. On the other hand, although we attempted to extend the period of artificial nursing, it was very difficult to extend the period of 10 days or more. Therefore, we investigated the role of CCL25 in bone tissue using a CCL25 gene-deficient mouse. As a result, although there was no significant difference in skeletal abnormalities and long bone length in both 10-day-old and 10-week-old mice, increase in bone mass was observed in 10-week-old mice.

Free Research Field

組織学、細胞学、分子生物学

Academic Significance and Societal Importance of the Research Achievements

本研究は腸管免疫に関わるタンパク質であるCCL25が骨の形成にも関わることを初めて示した。特に成獣期において、体内のCCL25が減少すると骨形成が活発になり骨量が増えることから、過剰なCCL25は骨形成の不全や骨量の低下の原因となる可能性が考えらる。さらなる研究が必要ではあるが、CCL25の体内量の調節を介して、全く新しい骨疾患の治療薬が開発できるのではないかと期待している。

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Published: 2020-03-30  

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