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Figure 4. Inhibition of SIRT1 deacetylase increases oxidative stress resistance in neurons
Cortical neurons from E18 rat embryos were cultured onto 96-well plates (A) or 10 cm dishes (B). (A) On 5 DIV neurons were transfected with either control or SIRT1 siRNA. 2 days later some neurons were subjected to H2O2 or menadione, followed by MTT survival assay 24 hrs later. ***P < 0.001 compared with H2O2-treated, **P < 0.01 compared to menadione-treated groups, respectively, t-test. (B) On 5 DIV neurons were transfected with either control or SIRT1 siRNA and 2 days later SIRT1 deacetylase activity was measured (**P < 0.01, n=4, control vs. SIRT1 siRNA, t-test). Data are represented as mean±SEM.
We also tested if SIRT1 inhibition protects against other forms of stress. Inhibition of SIRT1 did not rescue neurons from either ultraviolet irradiation (UV) or methyl methanesulfonate (MMS) induced cell damage, suggesting that protection may be specific for oxidative stress (Fig. 5). This specificity may also in part explain why others have described protective effects for SIRT1 under different stress conditions.
29
Object Description
| Title | Roles of SIRT1 in neuronal oxidative damage and brain function |
| Author | Li, Ying |
| Author email | lying@usc.edu; yingraceli@yahoo.com |
| Degree | Doctor of Philosophy |
| Document type | Dissertation |
| Degree program | Neuroscience |
| School | College of Letters, Arts and Sciences |
| Date defended/completed | 2008-09-12 |
| Date submitted | 2008 |
| Restricted until | Unrestricted |
| Date published | 2008-10-30 |
| Advisor (committee chair) | Longo, Valter D. |
| Advisor (committee member) |
Baudry, Michel Pike, Christian J. Madigan, Stephen A. |
| Abstract | Aging is a common phenomenon of multiple organisms. In humans aging is frequently accompanied by cognitive decline and occurrence of neurodegenerative diseases which reduce the quality of life and impose financial stress on society. Delaying the aging process, extending life span and decreasing the occurrence of age-related brain function deficit have always been aspirations of human kind. Extensive research has advanced our understanding of the mechanisms underlying aging, among which is the ability of calorie restriction to increase longevity, and the pivotal regulatory roles of insulin/IGF-1 signaling pathway. Some recent studies identified silent information regulator 2 (Sir2; SIRT1 is the mammalian homolog) as a key mediator of the beneficial effects of calorie restriction and this prompted development of SIRT1 activators for human consumption to delay aging and accompanying cognitive decline. However, our laboratory previously showed in yeast that Sir2 can increase stress sensitivity and limit life span extension under certain conditions, calling for more detailed characterization of SIRT1. In the research described in this dissertation I extended this study to the mammalian system and focused on the role of SIRT1 on the health of neurons and brain functions, especially learning and memory.; This dissertation consists of three chapters. In chapter 1 I briefly review some recent progress on aging, oxidative stress, insulin/IGF-1 signaling pathway and learning and memory with emphasis on the involvement of SIRT1 in these processes. In chapter 2 I focused on the role of SIRT1 in oxidative stress in neurons and its mechanisms. I found that SIRT1 inhibition increased resistance to oxidative damage and this effect is partially mediated by a reduction in IGF-I/IRS-2/Ras/ERK1/2 signaling. In chapter 3 I studied the functions of SIRT1 in learning and memory. The experiments showed that deletion of SIRT1 impairs a certain form of synaptic plasticity and reduce performance in several different learning and memory tasks while overexpressing SIRT1 did not substantially affect learning and memory.; Together, my studies reveal that SIRT1 exacerbates neuronal oxidative damage but is essential in learning and memory, indicating that SIRT1 plays multiple roles in aging and brain functions and that caution should be exercised in designing anti-aging or therapeutic approaches that involve targeting SIRT1. |
| Keyword | SIRT1; neurons; brain; oxidative damage; learning and memory |
| Language | English |
| Part of collection | University of Southern California dissertations and theses |
| Publisher (of the original version) | University of Southern California |
| Place of publication (of the original version) | Los Angeles, California |
| Publisher (of the digital version) | University of Southern California. Libraries |
| Provenance | Electronically uploaded by the author |
| Type | texts |
| Legacy record ID | usctheses-m1723 |
| Contributing entity | University of Southern California |
| Rights | Li, Ying |
| Repository name | Libraries, University of Southern California |
| Repository address | Los Angeles, California |
| Repository email | cisadmin@lib.usc.edu |
| Filename | etd-LI-2405 |
| Archival file | uscthesesreloadpub_Volume44/etd-LI-2405.pdf |
Description
| Title | Page 39 |
| Contributing entity | University of Southern California |
| Repository email | cisadmin@lib.usc.edu |
| Full text | Figure 4. Inhibition of SIRT1 deacetylase increases oxidative stress resistance in neurons Cortical neurons from E18 rat embryos were cultured onto 96-well plates (A) or 10 cm dishes (B). (A) On 5 DIV neurons were transfected with either control or SIRT1 siRNA. 2 days later some neurons were subjected to H2O2 or menadione, followed by MTT survival assay 24 hrs later. ***P < 0.001 compared with H2O2-treated, **P < 0.01 compared to menadione-treated groups, respectively, t-test. (B) On 5 DIV neurons were transfected with either control or SIRT1 siRNA and 2 days later SIRT1 deacetylase activity was measured (**P < 0.01, n=4, control vs. SIRT1 siRNA, t-test). Data are represented as mean±SEM. We also tested if SIRT1 inhibition protects against other forms of stress. Inhibition of SIRT1 did not rescue neurons from either ultraviolet irradiation (UV) or methyl methanesulfonate (MMS) induced cell damage, suggesting that protection may be specific for oxidative stress (Fig. 5). This specificity may also in part explain why others have described protective effects for SIRT1 under different stress conditions. 29 |
