Cellular and molecular mechanisms involved in amphibian retinal regeneration
| Project/Area Number |
17370080
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Developmental biology
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| Research Institution | Nara Women's University |
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Principal Investigator |
ARAKI Masasuke Nara Women's University, Faculty of Science, Professor (00118449)
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| Project Period (FY) |
2005 – 2007
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| Project Status |
Completed (Fiscal Year 2007)
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| Budget Amount *help |
¥14,620,000 (Direct Cost: ¥13,600,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2007: ¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2006: ¥3,300,000 (Direct Cost: ¥3,300,000)
Fiscal Year 2005: ¥6,900,000 (Direct Cost: ¥6,900,000)
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| Keywords | retinal reveneration / newt / Xenopus laevis / transdifferentiation / retinal pigmented epithelium / FGFs / organ culture / Transgenic animal / 網膜 / 再生 / 両生類 / 組織培養 |
|---|
| Research Abstract |
During the term of the project, we have performed the following studies and obtained a considerable volume of results on the subject of amphibian retinal regeneration.
(1) By a new organ culture model we developed, we analyzed the tissue interaction between the retinal pigment epithelium (RPE) and the choroid. It was shown that the choroid plays an essential role in RPE cell proliferation and neuronal differentiation and that soluble substance (s) are involved in these effects. With FGF signal inhibitors, we analyzed the molecular mechanism of FGF action.
(2) It was long believed that only urodele amphibians like the newt can regenerate the retina from RPE. We, however, discovered that Xenopus laevis can also regenerate the retina even after metamorphosis and in adult stage. This was shown in vivo as well as in vitro.
(3)We developed a novel organ culture method in which RPE tissue was covered (overlaid) by gel matrices. This method enabled us to obtain regeneration of complete retinal structure under culture condition. This is the first report that retinal 3D structure regenerates from a simple epithelium of RPE under a culture condition.
(4) We made three different types of transgenic Xenopus laevis; EF1a promoter, RX promoter and Pax6 promoter were ligated with EGFP as a reporter gene, respectively. We are now analyzing the in vivo and in vitro expression pattern of EGFP during retinal regeneration. This is the first study in which transgenic animal is used for retinal regeneration study.
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Report
(4 results)
Research Products
(56 results)
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[Journal Article] Neuensin-1 expression in the mouse retina during postnatal development and in cultured retinal neurons2006
Author(s)
Nagata, K, Suzuki, H, Niiya, A, Kinoshita, S, Taketani, S, Araki, M
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Journal Title
Brain Res 1081
Pages: 65-71
Description
「研究成果報告書概要(欧文)」より
Related Report
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[Journal Article] Extraocular dorsal signal affects the developmental fate of the optic vesicle and patterns the optic neuroepithelium2005
Author(s)
Kagiyama, Y, Gotouda, K, Sakagami, K, Yasuda, K, Mochii, M, Araki, M
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Journal Title
Dev. Growth Differ 47
Pages: 523-536
NAID
Description
「研究成果報告書概要(欧文)」より
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