The heart of this application is a smoothly functioning, high-through-put Animal Core that can provide animal care that meets or exceeds The Guide standards while meeting the needs of the phenotyping core investigator and the phenotyping core laboratories. The Animal Core for the Mouse Metabolic Phenotyping Center (MMPC) at UCD (MMPC-UCD) will be comprised of space, resource, and personnel within the UCD Mouse Biology Program (MBP). MBP focuses on expanding knowledge ofthe biology of laboratory mice and on the application of genetically-altered mice in biomedical research. Among the many projects relying on MBP support and vivarium services are the NIH/NCRR's Mutant Mouse Regional Resources Centers (MMRRC) and the trans-NIH Knock Out Mouse Project (KOMP) Repository. MBP is already engaged in working with investigators around the globe coordinating rodent imports and exports;creating, expanding and cryoarchiving lines of genetically altered mice;assisting research planning using genetically altered mice (age, gender, number, genetic background, special husbandry requirements, etc);and providing stewardship and oversight of animal care and health for all mice housed in MBP. With the MBP operational and management program within the University and our close working relationship with the UCD Institutional Animal Care and Use Committee (lACUC), the Attending Veterinarian, and rodent infectious disease specialists, MBP has wide latitude in the importation, quarantine and housing of mice of varying health statuses. With this experience and these operational programs in place, we are uniquely qualified to provide rodent importation, acclimation/quarantine, housing, health monitoring and project scheduling that will be conducive for rapid and efficient evaluation of strains submitted to MMPC-UCD for phenotyping. This Animal Core will have the institutional resources and authority to import and acclimate/quarantine mice for further phenotypic analysis with minimal delay. This will broaden the availability of metabolic phenotyping tests by allowing more investigator mice to be imported and analyzed, and expedite generation of data and completion of research using these mice in a more timely fashion.

Public Health Relevance

Mouse models of diabetes, diabetic complications, obesity and other related disorders have been invaluable for elucidating the disease potential, pathogenesis and treatment of these conditions in the human population. This animal core will provide stewardship and oversight for these animals that meets and exceeds federal and institutional policies and guidelines on the care and use of animals used in biomedical research.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Resource-Related Research Projects--Cooperative Agreements (U24)
Project #
5U24DK092993-03
Application #
8517706
Study Section
Special Emphasis Panel (ZDK1-GRB-S)
Project Start
Project End
Budget Start
2013-06-01
Budget End
2014-05-31
Support Year
3
Fiscal Year
2013
Total Cost
$140,732
Indirect Cost
$37,253
Name
University of California Davis
Department
Type
DUNS #
047120084
City
Davis
State
CA
Country
United States
Zip Code
95618
Majtan, Tomas; Jones Jr, Wendell; Krijt, Jakub et al. (2018) Enzyme Replacement Therapy Ameliorates Multiple Symptoms of Murine Homocystinuria. Mol Ther 26:834-844
Yokoyama, Amy S; Dunaway, Keith; Rutkowsky, Jennifer et al. (2018) Chronic consumption of a western diet modifies the DNA methylation profile in the frontal cortex of mice. Food Funct 9:1187-1198
Rutkowsky, Jennifer M; Lee, Linda L; Puchowicz, Michelle et al. (2018) Reduced cognitive function, increased blood-brain-barrier transport and inflammatory responses, and altered brain metabolites in LDLr -/-and C57BL/6 mice fed a western diet. PLoS One 13:e0191909
Cheng, Yingduan; Yuan, Quan; Vergnes, Laurent et al. (2018) KDM4B protects against obesity and metabolic dysfunction. Proc Natl Acad Sci U S A 115:E5566-E5575
Rozman, Jan; Rathkolb, Birgit; Oestereicher, Manuela A et al. (2018) Identification of genetic elements in metabolism by high-throughput mouse phenotyping. Nat Commun 9:288
Hsu, Ming-Fo; Bettaieb, Ahmed; Ito, Yoshihiro et al. (2017) Protein tyrosine phosphatase Shp2 deficiency in podocytes attenuates lipopolysaccharide-induced proteinuria. Sci Rep 7:461
McGavigan, Anne K; Garibay, Darline; Henseler, Zachariah M et al. (2017) TGR5 contributes to glucoregulatory improvements after vertical sleeve gastrectomy in mice. Gut 66:226-234
Ito, Yoshihiro; Hsu, Ming-Fo; Bettaieb, Ahmed et al. (2017) Protein tyrosine phosphatase 1B deficiency in podocytes mitigates hyperglycemia-induced renal injury. Metabolism 76:56-69
López-Yoldi, Miguel; Stanhope, Kimber L; Garaulet, Marta et al. (2017) Role of cardiotrophin-1 in the regulation of metabolic circadian rhythms and adipose core clock genes in mice and characterization of 24-h circulating CT-1 profiles in normal-weight and overweight/obese subjects. FASEB J 31:1639-1649
Jung, Chris J; Zhang, Junli; Trenchard, Elizabeth et al. (2017) Efficient gene targeting in mouse zygotes mediated by CRISPR/Cas9-protein. Transgenic Res 26:263-277

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