Analysis of chromatin remodeling in cellular senescence and organismal aging
| Project/Area Number |
23590346
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
General medical chemistry
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| Research Institution | Teikyo University |
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Principal Investigator |
ADACHI Mimi 帝京大学, 医学部, 准教授 (10323693)
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| Project Period (FY) |
2011-04-28 – 2015-03-31
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| Project Status |
Completed (Fiscal Year 2014)
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| Budget Amount *help |
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2013: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2011: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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| Keywords | 老化 / 細胞老化 / クロマチン / プロテオーム / 糖質コルチコイド / 鉱質コルチコイド / プロテオミクス / バイオマーカー / MASS / アルドラーゼA / 解糖系 / ヘテロクロマチン / ヒストン / miRNA |
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| Outline of Final Research Achievements |
(1)We reported that protein content and density in nuclei of senescent human and mouse fibroblasts in vitro, and in liver nuclei of aged mice in vivo by using NanoOrange staining and high resolution fluorescence microscopy. Thus we have identified some proteins increasing in cultured human diploid fibroblast as they approach replicative senescence using 2D-DIGE and MALDI-TOFMS. Some proteins including Aldolase A in those expressed higher in the lung and liver of old mice (25-31 months) than of young mice (3-5 months). However there was no relationship between those proteins and aging.
(2)We found that the amount of glucocorticoid in serum is higher in old mice, and that serum mineral corticoid is lower. Further, in human adrenocortical tumor cell line, H295R cells, which were induced to replicative or drug-induced senescence, glucocorticoid production and most of steroidogenic factors gene expression were increased.
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Report
(5 results)
Research Products
(16 results)
