Module 4. Specialized Animal Resource - Generating and maintaining transgenic mouse colonies - Visual Function and non-invasive retinal imaging Timothy Kern, PhD Director;Tadao Maeda, MD, PhD, co-Director Heather Butler, Kathryn Franke, Managers Overview: The Specialized Animal Resource (SAR) Module has been extensively utilized since the first funding cycle in 1997. The function of this Module has been to generate and maintain transgenic mouse colonies for VSRC investigators, and Heather Butler has managed the core since 2005. This core currently breeds and manages more than 60 mouse lines, with some requiring continuous cross-breeding and record keeping. In the last 4 years since the previous submission, the SAR has bred approximately 46,000 mice. In the previous submission in 2006, we added a second full-time technician, Kathryn Franke, to meet the increased needs of VSRC investigators for transgenic mice. In the current submission, we have added a Visual Function and noninvasive retinal imaging sub-Module to provide investigators with the ability to monitor visual function in rodents (thus complementing the histological and structural data that is provided by the Histology Core). Both functions of this Module are located in dedicated space in the Animal Resource Center (ARC) in the basement of the School of Medicine. This facility is a newly renovated, state-of-the-art barrier animal facility dedicated to virus-free mice. The facility is controlled for airflow, temperature and humidity, and these parameters are monitored continuously by remote sensors. The VSRC has dedicated breeding rooms are located adjacent to investigator assigned rooms in the ARC, and animals are transferred daily by the SAR Managers to each investigator's colony. The ARC is fully accredited and employs a highly skilled staff, including three full-time veterinarians and full-time veterinary technicians, in addition to ARC staff required for animal husbandry. SAR Core part A. Specialized Breeding and Animal Generation. Breeding, record keeping of breeding history, and collection of tissue for genotyping (via the Molecular Core) are the primary functions of this Module, and remains unchanged in the present grant submission. SAR Core part B. Small animal visual function and non-invasive retinal imaging sub-Module. This function of this new Module will provide expertise in, and use of 2 ERG units, 2 SLOs, an OCT unit, and an Optomotor machine (which measures the optokinetic response in rodents, yielding measurements analogous to visual acuity and contrast sensitivity). To facilitate use of this sub-Module, the SAR Module Managers, Heather Butler and Katherine Franke, have been trained to use the ERG by Dr. Tadao Maeda, who has extensive experience. Dr. Kern has trained the Managers to use the Optomotor Unit, and staff from the company who sold the unit (Cerebral Mechanics) provided additional in depth training. All of the equipment has been purchased and is already in place in the ARC. No additional staff positions are requested.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Center Core Grants (P30)
Project #
5P30EY011373-18
Application #
8734429
Study Section
Special Emphasis Panel (ZEY1)
Project Start
Project End
Budget Start
2014-09-01
Budget End
2015-08-31
Support Year
18
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Type
DUNS #
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Gragg, Megan; Park, Paul S-H (2018) Misfolded rhodopsin mutants display variable aggregation properties. Biochim Biophys Acta Mol Basis Dis 1864:2938-2948
Parmar, Vipul M; Parmar, Tanu; Arai, Eisuke et al. (2018) A2E-associated cell death and inflammation in retinal pigmented epithelial cells from human induced pluripotent stem cells. Stem Cell Res 27:95-104
Cheng, Yu-Shiuan; Linetsky, Mikhail; Gu, Xilin et al. (2018) Light-induced generation and toxicity of docosahexaenoate-derived oxidation products in retinal pigmented epithelial cells. Exp Eye Res :
Palczewska, Grazyna; Stremplewski, Patrycjusz; Suh, Susie et al. (2018) Two-photon imaging of the mammalian retina with ultrafast pulsing laser. JCI Insight 3:
Mallory, D Paul; Gutierrez, Elizabeth; Pinkevitch, Margaret et al. (2018) The Retinitis Pigmentosa-Linked Mutations in Transmembrane Helix 5 of Rhodopsin Disrupt Cellular Trafficking Regardless of Oligomerization State. Biochemistry 57:5188-5201
Linetsky, Mikhail; Bondelid, Karina S; Losovskiy, Sofiya et al. (2018) 4-Hydroxy-7-oxo-5-heptenoic Acid Lactone Is a Potent Inducer of the Complement Pathway in Human Retinal Pigmented Epithelial Cells. Chem Res Toxicol 31:666-679
Choi, Elliot H; Suh, Susie; Sander, Christopher L et al. (2018) Insights into the pathogenesis of dominant retinitis pigmentosa associated with a D477G mutation in RPE65. Hum Mol Genet 27:2225-2243
Zhang, Lingjun; Li, Yan; Qiu, Wen et al. (2018) Targeting CD6 for the treatment of experimental autoimmune uveitis. J Autoimmun 90:84-93
Orban, Tivadar; Leinonen, Henri; Getter, Tamar et al. (2018) A Combination of G Protein-Coupled Receptor Modulators Protects Photoreceptors from Degeneration. J Pharmacol Exp Ther 364:207-220
Samanta, Amrita; Kiselar, Janna; Pumroy, Ruth A et al. (2018) Structural insights into the molecular mechanism of mouse TRPA1 activation and inhibition. J Gen Physiol 150:751-762

Showing the most recent 10 out of 510 publications