2023 Fiscal Year Final Research Report
Endothelial colony forming cells in retinal vasculature
Project/Area Number |
21K09674
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Review Section |
Basic Section 56060:Ophthalmology-related
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Research Institution | Osaka University |
Principal Investigator |
Sakimoto Susumu 大阪大学, 大学院医学系研究科, 特任准教授(常勤) (60633047)
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Project Period (FY) |
2021-04-01 – 2024-03-31
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Keywords | 網膜血管 / 血管内皮細胞 / 血管内皮コロニー形成細胞 / 糖尿病網膜症 |
Outline of Final Research Achievements |
We analyzed the retinal vascular remodeling mechanism of gene A, which belongs to the CREB family. Retinal vascular endothelial cells were isolated using flow cytometry in wild-type mice during retinal vascular development and in an ischemic retinopathy model, and gene A expression was confirmed by qPCR. Angiogenesis assays using gene A knockdown (KD) human retinal vascular endothelial cells showed a significant decrease in vascular density. Analysis using gene A knockout (KO) mice showed decreased vascular elongation and an increase in the vascular-free field in the OIR model. Results suggest that gene A is involved in retinal vascular architecture.
Translated with www.DeepL.com/Translator (free version)
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Free Research Field |
眼科学
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Academic Significance and Societal Importance of the Research Achievements |
血管内皮コロニー形成細胞(Endothelial colony-forming cells: ECFCs)は、細胞治療に用いるヒトないしは自家血管内皮細胞のソースとして知られているが、近年広義のECFCとして、生体内における血管内皮幹/前駆細胞の存在が注目されている。申請者は、最近報告されているCD201などのマーカーに着目し、網膜血管におけるECFCの同定とニッチ環境の解明を行っており、本研究成果はECFCを調節する遺伝子の役割を明らかにすることができた。
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