The Mutant and Transgenic Rodent Core (MTRC) is directed by Maria Moalli. The major purpose of MTRC, is to provide Nathan Shock Center (NSC) scientists with aged mice of genotypes that provide otherwise unavailable opportunities to investigate the basic biology of aging or the pathophysiology of age-related disease states. A facility such as the MTRC operated by the NSC at the UM does not exist anywhere else in the country. The NSC's MTRC is specifically dedicated to exploiting for gerontological research the wide range of mutant and transgenic currently available, but not yet studied in the context of aging. The MTRC functions as a service core with the following specific aims: (1) the support of the per diem costs of aging a wide variety of mutant/transgenic rodents, (2) the provision of gross necropsies and histopathologic data on age-related lesions for specific genotypes of mice, (3) the maintenance of select colonies of mutant/transgenic aging mice for NSC scientists, and (4) the development of new models based on transgenic, mutant, or knockout mice. Over the four years of support, the MTRC has supported eleven projects with five faculty sponsors. Most projects were funded for two years, which was the usual time required to obtain mice at the ages required for the study. The projects funded during the current grant period included: the aging of mdx and transgenic-mdx mice, the relationship of early growth rate and longevity, the longevity of dwarf mice, the role of the androgen receptor in breast cancer, a comparison of wild and laboratory inbred mice, the aging of factor IX transgenic mice, studies of rhodopsin transgenic and knockout, DNA methyltransferase knockout, and IL-6 knockout mice, estrogen receptors, and a genetically heterogeneous strain the UM-HET3 mice. In conjunction with the MTRC, the UM Transgenic Animal Core (directed by Sally Camper) has generated a number of novel transgenic-mdx lines that have been used extensively by Chamberlain and his colleagues locally and in six other laboratories world-wide. The MTRC supported projects have led to twelve publications, six grant applications to NIH, with two funded and one pending R0-1 grants, and two funded and one pending P0-1 grants. The MTRC has had a significant impact on the use of transgenic mice and of naturally occurring and engineered mutant mice both among NSC scientists on the UM campus and among their colleagues in the USA and at foreign institutions.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
5P30AG013283-08
Application #
6605433
Study Section
Project Start
2002-07-01
Project End
2003-06-30
Budget Start
Budget End
Support Year
8
Fiscal Year
2002
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Xiong, Yi; Torsoni, Adriana Souza; Wu, Feihua et al. (2018) Hepatic NF-kB-inducing kinase (NIK) suppresses mouse liver regeneration in acute and chronic liver diseases. Elife 7:
Liu, Yan; Jiang, Lin; Sun, Chengxin et al. (2018) Insulin/Snail1 axis ameliorates fatty liver disease by epigenetically suppressing lipogenesis. Nat Commun 9:2751
Ghosh, Amiya Kumar; Mau, Theresa; O'Brien, Martin et al. (2018) Novel role of autophagy-associated Pik3c3 gene in gonadal white adipose tissue browning in aged C57/Bl6 male mice. Aging (Albany NY) 10:764-774
Shen, Hong; Sheng, Liang; Xiong, Yi et al. (2017) Thymic NF-?B-inducing kinase regulates CD4+ T cell-elicited liver injury and fibrosis in mice. J Hepatol 67:100-109
Julius, Annabelle; Desai, Anjali; Yung, Raymond L (2017) Recombinant human erythropoietin stimulates melanoma tumor growth through activation of initiation factor eIF4E. Oncotarget 8:30317-30327
Kim, Evelyn H; Galchev, Vladimir I; Kim, Jin Young et al. (2016) Differential protein expression and basal lamina remodeling in human heart failure. Proteomics Clin Appl 10:585-96
Ghosh, Amiya Kumar; Mau, Theresa; O'Brien, Martin et al. (2016) Impaired autophagy activity is linked to elevated ER-stress and inflammation in aging adipose tissue. Aging (Albany NY) 8:2525-2537
Feinstein, Lydia; Ferrando-Martínez, Sara; Leal, Manuel et al. (2016) Population Distributions of Thymic Function in Adults: Variation by Sociodemographic Characteristics and Health Status. Biodemography Soc Biol 62:208-21
Figueroa-Romero, Claudia; Hur, Junguk; Lunn, J Simon et al. (2016) Expression of microRNAs in human post-mortem amyotrophic lateral sclerosis spinal cords provides insight into disease mechanisms. Mol Cell Neurosci 71:34-45
Sharma, Naveen; Arias, Edward B; Cartee, Gregory D (2016) Inhibition of Akt2 phosphorylation abolishes the calorie restriction-induced improvement in insulin-stimulated glucose uptake by rat soleus muscle. Appl Physiol Nutr Metab 41:1208-1211

Showing the most recent 10 out of 219 publications