Our long-term goal is to study the role of mitochondria in aging. The overall goal of this grant application is to test the mitochondria! theror/ of aging and, in particular, to investigate the role of mitochondrial DNA(mtDNA) mutations in mouse brain during aging. As one of the most favored hypotheses, the mitochondrial theory of aging, predicts that somatic mitochondria DNA (mtDNA) mutations accumulate with time, and the compromised mitochondrial function resulting from these mutations is then responsible for various aging phenotypes. However, there has been no comprehensive study of the overall accumulation of mtDNA mutations during aging, and the physiological consequences of aging-related mtDNA mutations are largely unclear. We recently established a method to transfer mtDNA from mouse nerve endings, i.e., synaptosomes to a cell system, and we have improved methods to isolate and characterize mtDNA mutations. Combined with established mitochondrial molecular genetic and biochemical technologies, we can, for the first time, investigate the accumulation of mtDNA mutations in neuronal cells during aging by evaluating individual mtDNA from the synaptosomes.The particular hypothesis to be tested in this proposal is that mutations in the mitochondrial genome accumulate during aging in mouse neuronal cells; these mtDNA mutations in turn compromise mitochondrial function and may result in oxidative damage to various cellular components including mtDNA in neuronal cells. We will perform genetic and functional analyses of aging-related mtDNA mutations by transferring synaptosomal mtDNA to a cell line system. This will reveal low frequncy mtDNA mutations that could not be identified by other methods. By generating neuronal cell models that carry aging-related mtDNA mutations, we will also charaterize the physiological consequences of the mutations, in particular those related to oxidative damage. The successful completion of this project will not only help to test the mitochondrial theory of aging, but could also provide insights into the underlying mechanisms of the aging process.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG025223-03
Application #
7371075
Study Section
Special Emphasis Panel (ZRG1-NDBG (09))
Program Officer
Wise, Bradley C
Project Start
2006-03-01
Project End
2011-01-31
Budget Start
2008-02-15
Budget End
2009-01-31
Support Year
3
Fiscal Year
2008
Total Cost
$286,789
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Biology
Type
Schools of Medicine
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Tiwari, Meenakshi; Sharma, Lokendra K; Vanegas, Difernando et al. (2014) A nonapoptotic role for CASP2/caspase 2: modulation of autophagy. Autophagy 10:1054-70
Li, Hongzhi; Kumar Sharma, Lokendra; Li, Youfen et al. (2013) Comparative bioenergetic study of neuronal and muscle mitochondria during aging. Free Radic Biol Med 63:30-40
Liu, Danhui; Li, Hongzhi; Lu, Jianxin et al. (2013) Tissue-specific implications of mitochondrial alterations in aging. Front Biosci (Elite Ed) 5:734-47
Zhang, Chengkang; Huang, Vincent H; Simon, Mariella et al. (2012) Heteroplasmic mutations of the mitochondrial genome cause paradoxical effects on mitochondrial functions. FASEB J 26:4914-24
Li, Hongzhi; Liu, Danhui; Lu, Jianxin et al. (2012) Physiology and pathophysiology of mitochondrial DNA. Adv Exp Med Biol 942:39-51
Shen, Lijun; Wei, Jia; Chen, Tao et al. (2011) Evaluating mitochondrial DNA in patients with breast cancer and benign breast disease. J Cancer Res Clin Oncol 137:669-75
Yang, Yongjie; Cimen, Huseyin; Han, Min-Joon et al. (2010) NAD+-dependent deacetylase SIRT3 regulates mitochondrial protein synthesis by deacetylation of the ribosomal protein MRPL10. J Biol Chem 285:7417-29
Li, Youfen; Li, Hong-Zhi; Hu, Peiqing et al. (2010) Generation and bioenergetic analysis of cybrids containing mitochondrial DNA from mouse skeletal muscle during aging. Nucleic Acids Res 38:1913-21
Shen, Lijun; Fang, Hezhi; Chen, Tao et al. (2010) Evaluating mitochondrial DNA in cancer occurrence and development. Ann N Y Acad Sci 1201:26-33
Park, Jeong Soon; Sharma, Lokendra Kumar; Li, Hongzhi et al. (2009) A heteroplasmic, not homoplasmic, mitochondrial DNA mutation promotes tumorigenesis via alteration in reactive oxygen species generation and apoptosis. Hum Mol Genet 18:1578-89

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