The Animal Facility Core will meet the needs of the Program Project Grant members for creating new mouse strains and for established, shared strains. To improve efficiencies the Core will provide and maintain genetically complex animals that are used by multiple projects, assist with backcrosses, and also assist with mice used in genetic mapping projects. There are four SPECIFIC AIMS for this Core. 1. To breed and genetically characterize unique and non-routine mouse strains for use by all the program project members. This service will ensure that animals are readily available for use in experiments for all of the PPG members. 2. To assist program project members with routine backcrossing of newly obtained or derived strains to the appropriate genetic backgrounds for planned studies. Fixed genetic backgrounds will be essential for many of the studies in the PPG. 3. To provide breeding and collection services for genetic mapping projects that are being performed in two of the projects in the PPG (projects 3 and 4). The Core will help with the maintenance and generation of animals in these crosses, as well as collection of DNA for genotyping. 4. To ensure animals provided to program project members are healthy and maintained in a pathogen-free environment for the proposed studies. The availability of the mouse Core will ensure that multiple investigators in the PPG will have sufficient animals available for their studies in a timely and efficient manner.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI035297-19
Application #
8133787
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
Budget Start
2010-08-01
Budget End
2011-07-31
Support Year
19
Fiscal Year
2010
Total Cost
$260,663
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Proekt, Irina; Miller, Corey N; Lionakis, Michail S et al. (2017) Insights into immune tolerance from AIRE deficiency. Curr Opin Immunol 49:71-78
Sanchez Rodriguez, Robert; Pauli, Mariela L; Neuhaus, Isaac M et al. (2014) Memory regulatory T cells reside in human skin. J Clin Invest 124:1027-36
Villalta, S Armando; Rosenthal, Wendy; Martinez, Leonel et al. (2014) Regulatory T cells suppress muscle inflammation and injury in muscular dystrophy. Sci Transl Med 6:258ra142
Stumpf, Melanie; Zhou, Xuyu; Chikuma, Shunsuke et al. (2014) Tyrosine 201 of the cytoplasmic tail of CTLA-4 critically affects T regulatory cell suppressive function. Eur J Immunol 44:1737-46
Bailey-Bucktrout, Samantha L; Martinez-Llordella, Marc; Zhou, Xuyu et al. (2013) Self-antigen-driven activation induces instability of regulatory T cells during an inflammatory autoimmune response. Immunity 39:949-62
Zikherman, Julie; Parameswaran, Ramya; Hermiston, Michelle et al. (2013) The structural wedge domain of the receptor-like tyrosine phosphatase CD45 enforces B cell tolerance by regulating substrate specificity. J Immunol 190:2527-35
Jeker, Lukas T; Bluestone, Jeffrey A (2013) MicroRNA regulation of T-cell differentiation and function. Immunol Rev 253:65-81
de Kouchkovsky, Dimitri; Esensten, Jonathan H; Rosenthal, Wendy L et al. (2013) microRNA-17-92 regulates IL-10 production by regulatory T cells and control of experimental autoimmune encephalomyelitis. J Immunol 191:1594-605
Gratz, Iris K; Truong, Hong-An; Yang, Sara Hsin-Yi et al. (2013) Cutting Edge: memory regulatory t cells require IL-7 and not IL-2 for their maintenance in peripheral tissues. J Immunol 190:4483-7
Baumjohann, Dirk; Kageyama, Robin; Clingan, Jonathan M et al. (2013) The microRNA cluster miR-17?92 promotes TFH cell differentiation and represses subset-inappropriate gene expression. Nat Immunol 14:840-8

Showing the most recent 10 out of 117 publications