The Mouse Core plays a central role in this proposal, providing for the breeding and management of the large colony of transgenic and knockout mice that will be generated for this project. Five different knockout strains have been or will be created for this project, and these will be each intercrossed with one another, as well as with 3-4 different strains of transgenic lines (tetO-responder lines), to generate multiple substrains. These animals are the source for all of the behavioral, physiological, pharmacological, anatomical and cell-based studies in the Program Project, and are a primary shared resource for all of the collaborative experiments among the three participating laboratories. The need for this core is justified by the large numbers of genetically modified mice that must be generated and maintained solely for the purposes of this project (see Budget Justification). The behavioral phenotyping experiments in particular require large numbers of animals of each strain and genotype, because the greater inherent variability of such experiments requires large numbers of animals to achieve statistical significance. The Mouse Core will leverage the infrastructure, personnel, equipment and other resources available in the Transgenic Animal Facility at Caltech (TAFCIT), while providing exclusive support for the generation, maintenance, breeding and shipping of transgenic and knockout mice strains associated with this Program Project.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS048499-04
Application #
7559608
Study Section
National Institute of Neurological Disorders and Stroke Initial Review Group (NSD)
Project Start
Project End
Budget Start
2008-01-01
Budget End
2008-12-31
Support Year
4
Fiscal Year
2008
Total Cost
$192,004
Indirect Cost
Name
California Institute of Technology
Department
Type
DUNS #
009584210
City
Pasadena
State
CA
Country
United States
Zip Code
91125
Anderson, David J; Adolphs, Ralph (2014) A framework for studying emotions across species. Cell 157:187-200
Vrontou, Sophia; Wong, Allan M; Rau, Kristofer K et al. (2013) Genetic identification of C fibres that detect massage-like stroking of hairy skin in vivo. Nature 493:669-73
Kim, Se-Jeong; Park, Goon Ho; Kim, Donghoon et al. (2011) Analysis of cellular and behavioral responses to imiquimod reveals a unique itch pathway in transient receptor potential vanilloid 1 (TRPV1)-expressing neurons. Proc Natl Acad Sci U S A 108:3371-6
Bráz, João M; Ackerman, Larry; Basbaum, Allan I (2011) Sciatic nerve transection triggers release and intercellular transfer of a genetically expressed macromolecular tracer in dorsal root ganglia. J Comp Neurol 519:2648-57
Bráz, João M; Basbaum, Allan I (2010) Differential ATF3 expression in dorsal root ganglion neurons reveals the profile of primary afferents engaged by diverse noxious chemical stimuli. Pain 150:290-301
Shields, Shannon D; Cavanaugh, Daniel J; Lee, Hyosang et al. (2010) Pain behavior in the formalin test persists after ablation of the great majority of C-fiber nociceptors. Pain 151:422-9
Scherrer, Gregory; Low, Sarah A; Wang, Xidao et al. (2010) VGLUT2 expression in primary afferent neurons is essential for normal acute pain and injury-induced heat hypersensitivity. Proc Natl Acad Sci U S A 107:22296-301
Guan, Yun; Liu, Qin; Tang, Zongxiang et al. (2010) Mas-related G-protein-coupled receptors inhibit pathological pain in mice. Proc Natl Acad Sci U S A 107:15933-8
Bates, E A; Nikai, T; Brennan, K C et al. (2010) Sumatriptan alleviates nitroglycerin-induced mechanical and thermal allodynia in mice. Cephalalgia 30:170-8
Bráz, J M; Basbaum, A I (2009) Triggering genetically-expressed transneuronal tracers by peripheral axotomy reveals convergent and segregated sensory neuron-spinal cord connectivity. Neuroscience 163:1220-32

Showing the most recent 10 out of 25 publications