2013 Fiscal Year Final Research Report
Mechanisms of morphological changes of mitochondria during neural differentiation and under disease condition by using cell-resealing technique
Project/Area Number |
23657124
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Multi-year Fund |
Research Field |
Cell biology
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Research Institution | The University of Tokyo |
Principal Investigator |
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Project Period (FY) |
2011 – 2012
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Keywords | シグナル伝達 / 神経科学 / 細胞・組織 / セミインタクト細胞 |
Research Abstract |
We established a neural cell line N14.5-Tom5 cells, in which mitochondrial protein GFP-Tom5 is stably expressed. By using N14.5-Tom5, we found that activation of GSK3beta or Akt was involved in mitochondrial fission during neural differentiation, and identified the phosphorylation of Drp1, dynamin-related GTPase, by GSK3beta regulated the fission. Interestingly, the phosphorylation of Drp1 is reported be required for the mitochondrial fission at the onset of mitosis in mammalian cells. Next, we constructed model cells that replicated the conditions in neurons of Alzheimer's disease by using the resealing-cell technique and cytosol prepared from ApoE(-/-) mouse. As a result, we found that inactivity of Akt in the model cells caused the elongation of mitochondria and resulted in depressed mitochondrial function. Collectively, the persistent phosphorylation of both GSK3beta and Akt plays a crucial role for the maintaining normal mitochondrial morphology and function.
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Research Products
(13 results)
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[Journal Article] PPARγ-induced PARylation promotes local DNA demethylation by production of 5-hydroxymethylcytosine2013
Author(s)
Fujiki, K., Shinoda, A., Kano, F., Sato, R., Shirahige, K., Murata, M
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Journal Title
Nature Communications
Volume: 4
Pages: 2262
DOI
Peer Reviewed
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[Journal Article] PKCd and e regulate the morphological integrity of the ER-Golgi intermediate compartment (ERGIC) but not the anterograde and retrograde transports via the Golgi apparatus2012
Author(s)
Sugawara, T., Nakatsu, D., Kii, H., Maiya, N., Adachi, A., Yamamoto, A., Kano, F., Murata, M
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Journal Title
Biochem. Biophys. Acta (Molecular Cell Research)
Volume: 1823(4)
Pages: 861-875
Peer Reviewed
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