The experiments proposed in this grant rely heavily on close collaborative interactions amongst the three PIs. The Core component will greatly facilitate these interactions. Core B is divided into 3 components: a) breeding of transgenic/knockout mice, b) maintenance of conventional transgenic and knockout mice, and c) flow cytometry. Core B is designed to provide aged T cell receptor transgenic, gene knockout and conventional mice that are required by all three projects of the program. Core B will breed and screen transgenic animals (using FACS or PCR analysis) and backcross them as necessary to render them suitable for the experiments detailed in the individual projects of the program. Because this process is very labor intensive, a centralized facility specialized to perform this task is essential. The core will obtain the various aged conventional, transgenic or knockout mice needed for the individual projects, quarantine them if necessary, develop standardized procedures for screening for the transgenic/knockout gene expression in each case, and will breed and backcross the mice to inbred strains. The goals are to have healthy, genetically homogeneous mice for the investigators in the project. Investigators will be able to obtain these mice for experiments but will maintain the animals separately during the course of the sometimes lengthy adoptive transfer experiments. Each of the three projects relies heavily on the use of flow cytometry to assess the expression of various cell surface markers. The costs for FACS analysis is included in Core B because: 1) all three projects will rely heavily on the use of the common FACS facility; 2) screening of the aforementioned animals require the use of flow cytometry and 3) many of the studies involving flow cytometry represent collaborative interactions among the PIs.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
3P01AG001743-20S1
Application #
6216946
Study Section
Project Start
1999-09-30
Project End
2000-08-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
20
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Boyman, Onur; Ramsey, Chris; Kim, David M et al. (2008) IL-7/anti-IL-7 mAb complexes restore T cell development and induce homeostatic T Cell expansion without lymphopenia. J Immunol 180:7265-75
Ramsey, Chris; Rubinstein, Mark P; Kim, David M et al. (2008) The lymphopenic environment of CD132 (common gamma-chain)-deficient hosts elicits rapid homeostatic proliferation of naive T cells via IL-15. J Immunol 180:5320-6
Jelley-Gibbs, Dawn M; Strutt, Tara M; McKinstry, K Kai et al. (2008) Influencing the fates of CD4 T cells on the path to memory: lessons from influenza. Immunol Cell Biol 86:343-52
Purton, Jared F; Tan, Joyce T; Rubinstein, Mark P et al. (2007) Antiviral CD4+ memory T cells are IL-15 dependent. J Exp Med 204:951-61
Kovar, Marek; Boyman, Onur; Shen, Xuefei et al. (2006) Direct stimulation of T cells by membrane vesicles from antigen-presenting cells. Proc Natl Acad Sci U S A 103:11671-6
Rubinstein, Mark P; Kovar, Marek; Purton, Jared F et al. (2006) Converting IL-15 to a superagonist by binding to soluble IL-15R{alpha}. Proc Natl Acad Sci U S A 103:9166-71
Ishimaru, Naozumi; Kishimoto, Hidehiro; Hayashi, Yoshio et al. (2006) Regulation of naive T cell function by the NF-kappaB2 pathway. Nat Immunol 7:763-72
Boyman, Onur; Cho, Jae-Ho; Tan, Joyce T et al. (2006) A major histocompatibility complex class I-dependent subset of memory phenotype CD8+ cells. J Exp Med 203:1817-25
Surh, Charles D; Boyman, Onur; Purton, Jared F et al. (2006) Homeostasis of memory T cells. Immunol Rev 211:154-63
Haynes, Laura; Eaton, Sheri M; Burns, Eve M et al. (2005) Newly generated CD4 T cells in aged animals do not exhibit age-related defects in response to antigen. J Exp Med 201:845-51

Showing the most recent 10 out of 75 publications