In this effort we aim to generate a mouse model for age-associated systemic inflammation. Towards this end we will use genetically manipulated mice as well as mice treated with chemical agents that generate inflammation. We will assess inflammation by assaying for cytokine production as well as the presence of agents associated with age-associated systemic inflammation in humans. We expect that this mouse model will be useful in studying the cellular and molecular basis for the cause and effect of systemic inflammation in the aging of various tissues, age-associated chronic diseases and obesity.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Investigator-Initiated Intramural Research Projects (ZIA)
Project #
1ZIAAG000771-07
Application #
8931593
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
7
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Aging
Department
Type
DUNS #
City
State
Country
Zip Code
Sharma, Archna; Berga-Bolanos, Rosa; Sultana, Dil Afroz et al. (2013) IL-4 and IL-4 receptor expression is dispensable for the development and function of natural killer T cells. PLoS One 8:e71872
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Yu, Qing; Sharma, Archna; Sen, Jyoti Misra (2010) TCF1 and beta-catenin regulate T cell development and function. Immunol Res 47:45-55
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Xu, Mai; Yu, Qing; Subrahmanyam, Ramesh et al. (2008) Beta-catenin expression results in p53-independent DNA damage and oncogene-induced senescence in prelymphomagenic thymocytes in vivo. Mol Cell Biol 28:1713-23