The ability to manipulate the mouse genome through transgenic and knock-out or knock-in technologies has revolutionized modern Immunology. The purpose of this core facility (Core B) is to integrate the transgenic and gene targeting approach into the studies of host-pathogen interaction, a major thrust of the program project """"""""Mouse models for understanding host-pathogen interactions"""""""". This Transgenic/Knockout Mouse Core will provide the critical technical capability to generate and to maintain transgenic and mutant mice commonly used by two or more investigators of the program project (PPG). In particular, this Core will complement Core C to provide transgenic mice expressing fluorescent proteins to be used for imaging studies. Core B will also generate and distribute transgenic strains of mice as needed by the individual investigator in the PPG.
In aim 1, C57Bl/6 transgenic mice expressing fluorescent genes, whose expression is driven by different promoter/enhancers will be generated and maintained for use in video imaging experiments. These include mice expressing membrane Cyan Fluorescent Protein (CFP) in dendritic cells or macrophages and mice with CFP or YFP (Yellow Fluorescent Protein) expressed in all cell types.
In aim 2, knock-out/knock-in mice with genes involved in innate immunity will be maintained as well as back-crossed to C57BI/6 or Balb/c if necessary. These mice, including DC- and macrophage-specific FADD-/-, MyD88-/-, IFN-alpha/betaR-/-, TRAIL-R-/-, NK deficient mice, NKG2D-/-, IL-12/GFP (Green Fluorescent Protein) knock-in and lFN-gamma/GFP knock-in mice, will be provided to investigators in the PPG for their biochemical, infection or imaging experiments.
In aim 3, Core B will generate and provide transgenic mice for the specific needs of the individual PPG investigator. Completion of these aims is necessary and essential for the success of the PPG designed to understand how the immune system interacts with model pathogens.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI065831-04
Application #
7892568
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
Budget Start
2009-07-01
Budget End
2010-06-30
Support Year
4
Fiscal Year
2009
Total Cost
$253,908
Indirect Cost
Name
University of California Berkeley
Department
Type
DUNS #
124726725
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Chu, H Hamlet; Chan, Shiao-Wei; Gosling, John Paul et al. (2016) Continuous Effector CD8(+) T Cell Production in a Controlled Persistent Infection Is Sustained by a Proliferative Intermediate Population. Immunity 45:159-71
Han, Seong-Ji; Melichar, Heather J; Coombes, Janine L et al. (2014) Internalization and TLR-dependent type I interferon production by monocytes in response to Toxoplasma gondii. Immunol Cell Biol 92:872-81
Grover, Harshita Satija; Chu, H Hamlet; Kelly, Felice D et al. (2014) Impact of regulated secretion on antiparasitic CD8 T cell responses. Cell Rep 7:1716-1728
Young, Jennifer A; He, Tina H; Reizis, Boris et al. (2013) Commensal microbiota are required for systemic inflammation triggered by necrotic dendritic cells. Cell Rep 3:1932-44
Coombes, Janine L; Charsar, Brittany A; Han, Seong-Ji et al. (2013) Motile invaded neutrophils in the small intestine of Toxoplasma gondii-infected mice reveal a potential mechanism for parasite spread. Proc Natl Acad Sci U S A 110:E1913-22
Grover, Harshita Satija; Blanchard, Nicolas; Gonzalez, Federico et al. (2012) The Toxoplasma gondii peptide AS15 elicits CD4 T cells that can control parasite burden. Infect Immun 80:3279-88
Coombes, Janine L; Han, Seong-Ji; van Rooijen, Nico et al. (2012) Infection-induced regulation of natural killer cells by macrophages and collagen at the lymph node subcapsular sinus. Cell Rep 2:124-35
Dzhagalov, Ivan L; Melichar, Heather J; Ross, Jenny O et al. (2012) Two-photon imaging of the immune system. Curr Protoc Cytom Chapter 12:Unit12.26
Tam, Connie; LeDue, Jeffrey; Mun, James J et al. (2011) 3D quantitative imaging of unprocessed live tissue reveals epithelial defense against bacterial adhesion and subsequent traversal requires MyD88. PLoS One 6:e24008
Melichar, Heather J; Li, Ou; Herzmark, Paul et al. (2011) Quantifying subcellular distribution of fluorescent fusion proteins in cells migrating within tissues. Immunol Cell Biol 89:549-57

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