2015 Fiscal Year Final Research Report
Study for chromatin dynamics during optic nerve regeneration
Project/Area Number |
25462753
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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 |
Research Field |
Ophthalmology
|
Research Institution | Suzuka University of Medical Science (2014-2015) Kanazawa University (2013) |
Principal Investigator |
|
Project Period (FY) |
2013-04-01 – 2016-03-31
|
Keywords | 神経再生 / エピジェネティクス / レチノイン酸受容体 / ヒストンアセチル化 / 視神経 / 網膜神経節細胞 / 神経回路 / 中枢神経 |
Outline of Final Research Achievements |
Like other CNS neurons, mature retinal ganglion cells (RGCs) cannot regenerate their axons after nerve injury due to loss of regenerative capacity. One of the reasons why they lose their capacity seems to be a dramatic shift in gene expression of RGCs under epigenetic modulation. In here, we found that levels of histone H3 lysine 9 acetylation decreased after birth in RGCs. This decrease showed good correlation with restriction of retinoic acid receptor β (RARβ) expression in RGCs after birth. Furthermore, we demonstrated that a histone deacetylase inhibitor, trichostatin A, induced axonal regeneration of adult rat RGCs through RARβ induction.
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Free Research Field |
神経化学
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