This P30 Core Grant for Vision Research application from the University of Wisconsin Vision Researchers proposes three modules. These are Gene Delivery/Quantitative Molecular Biology,Pathology and Imaging, and Animal Models/ Eye Organ Culture. The ability to efficiently deliver genes to cells is a powerful new therapeutic approach in treating ocular disease. In addition, gene delivery to cells in culture is an essential research tool. The Gene Delivery Module will construct vectors, prepare high titer stocks of these materials for use by researchers, and assist investigators with gene delivery methods. The use of quantitative methods in molecular biology is growing. In particular, the quantitation of gene expression by RT-PCR and the analysis of gene expression changes using array technology. The Quantitative Molecular Biology Module will provide dedicated technical expertise to these areas will enhance the abilities of those researchers currently using these methods but more importantly, the core will make it easier for researchers currently not using these technologies to add them to their research programs. Pathology analysis and sophisticated imaging methods have become increasingly important, as the emphasis on translational research has grown. These methodologies are also critical for studies using animal models. The Pathology and Imaging Module will provide advanced histology, microscopy and image analysis, and morphometry of tissue sections and cultured cells. The development of new therapies and improving our understanding of visual system function relies on transferring work done in vitro to animal models. The Animal Model and Eye Organ Culture Module will assist investigators in using animal models (primate and rodent), experimental glaucoma induction, imaging and ocular physiology. This expertise will aid the efforts of core users in assessing the effects of their agents, manipulations, and vectors/constructs on ocular function in rodents and primates. The services provided by these modules have been functioning for some time, but their ability to assist researchers has been limited by a lack of consistent support, and particularly by a lack of personnel. Funding of this proposal will enable us to improve our productivity and conduct work in a more timely manner, speeding the pace of progress in vision research on campus. It will allow us to expand the assistance available to eye researchers on campus and perhaps attract other investigators to eye research. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Center Core Grants (P30)
Project #
5P30EY016665-04
Application #
7465377
Study Section
Special Emphasis Panel (ZEY1-VSN (03))
Program Officer
Liberman, Ellen S
Project Start
2005-07-01
Project End
2010-06-30
Budget Start
2008-07-01
Budget End
2009-06-30
Support Year
4
Fiscal Year
2008
Total Cost
$598,938
Indirect Cost
Name
University of Wisconsin Madison
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Ghanian, Zahra; Mehrvar, Shima; Jamali, Nasim et al. (2018) Time-lapse microscopy of oxidative stress demonstrates metabolic sensitivity of retinal pericytes under high glucose condition. J Biophotonics 11:e201700289
Rouhimoghadam, Milad; Safarian, Shahrokh; Carroll, Jason S et al. (2018) Tamoxifen-Induced Apoptosis of MCF-7 Cells via GPR30/PI3K/MAPKs Interactions: Verification by ODE Modeling and RNA Sequencing. Front Physiol 9:907
Telle, Mary R; Chen, Nickolas; Shinsako, Daniel et al. (2018) Relationship between corneal sensitivity, corneal thickness, corneal diameter, and intraocular pressure in normal cats and cats with congenital glaucoma. Vet Ophthalmol :
Schmitt, Heather M; Schlamp, Cassandra L; Nickells, Robert W (2018) Targeting HDAC3 Activity with RGFP966 Protects Against Retinal Ganglion Cell Nuclear Atrophy and Apoptosis After Optic Nerve Injury. J Ocul Pharmacol Ther 34:260-273
Chan, Wesley; Almasieh, Mohammadali; Catrinescu, Maria-Magdalena et al. (2018) Cobalamin-Associated Superoxide Scavenging in Neuronal Cells Is a Potential Mechanism for Vitamin B12-Deprivation Optic Neuropathy. Am J Pathol 188:160-172
Janus, David A; Lieven, Christopher J; Crowe, Megan E et al. (2018) Polyester-based microdisc systems for sustained release of neuroprotective phosphine-borane complexes. Pharm Dev Technol 23:882-889
Ashwinbalaji, Soundararajan; Senthilkumari, Srinivasan; Gowripriya, Chidambaranathan et al. (2018) SB772077B, A New Rho Kinase Inhibitor Enhances Aqueous Humour Outflow Facility in Human Eyes. Sci Rep 8:15472
Lawlor, Mitchell; Danesh-Meyer, Helen; Levin, Leonard A et al. (2018) Glaucoma and the brain: Trans-synaptic degeneration, structural change, and implications for neuroprotection. Surv Ophthalmol 63:296-306
Gurel, Zafer; Sheibani, Nader (2018) O-Linked ?-N-acetylglucosamine (O-GlcNAc) modification: a new pathway to decode pathogenesis of diabetic retinopathy. Clin Sci (Lond) 132:185-198
Tan, Junkai; Fan, Ning; Wang, Ningli et al. (2018) Effects of Lentivirus-Mediated C3 Expression on Trabecular Meshwork Cells and Intraocular Pressure. Invest Ophthalmol Vis Sci 59:4937-4944

Showing the most recent 10 out of 402 publications