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Cell-cell comunication in developing skeletal muscle
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- NISHIMUTA TAKANORI
- Principal Investigator
- 北海道大学
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- 保坂 善真
- Co-Investigator
- 鳥取大学
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- 辰巳 隆一
- Co-Investigator
- 九州大学
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- 尾嶋 孝一
- Co-Investigator
- 国立研究開発法人農業・食品産業技術総合研究機構
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- MIZUNOYA Wataru
- Research Collaborator
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- SUZUKI Takahiro
- Research Collaborator
About This Project
- Japan Grant Number
- JP16H02585 (JGN)
- Funding Program
- Grants-in-Aid for Scientific Research
- Funding Organization
- Japan Society for the Promotion of Science
Kakenhi Information
- Project/Area Number
- 16H02585
- Research Category
- Grant-in-Aid for Scientific Research (A)
- Allocation Type
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- Single-year Grants
- Review Section / Research Field
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- Biological Sciences > Agriculture > Animal life science > Animal production science
- Research Institution
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- Hokkaido University
- Project Period (FY)
- 2016-04-01 〜 2019-03-31
- Project Status
- Completed
- Budget Amount*help
- 40,560,000 Yen (Direct Cost: 31,200,000 Yen Indirect Cost: 9,360,000 Yen)
Research Abstract
In order to elucidate the regulatory mechanism of muscle hypertrophy and intramuscular fat accumulation, we investigated the cell-cell communication in skeletal muscle. 1. We found that exosomes secreted by muscle cells and adipocytes were taken up into heterologous cells and affected the gene expression of the cells that took up exosomes. 2. Adipocytes suppress the differentiation of muscle cells and promote muscle atrophy by inducing the expression and secretion of IL-6 in muscle cells. 3. We show that APOBEC2 suppresses the pathway in which differentiated satellite cells fuse to form myotubes and promote self-renewal during muscle regeneration. 4. TGF-b1 has been shown to exert potent inhibitory effects at the early stages of muscle regeneration and lipogenesis.
Keywords
Details 詳細情報について
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- CRID
- 1040282256873099648
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- Text Lang
- ja
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- Data Source
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- KAKEN