The goal of the Histology, Microscopy, and Imaging Module is to enhance the capabilities of individual vision research laboratories by enabling them to conduct studies that require understanding the ocular tissue function at the cellular level. This goal is accomplished by providing the infrastructure for two types of services - histology and imaging. The Histology Facility of the Module prepares in a timely fashion cryo or paraffin sections of eyes and mounts them on slides for histo/immunohistochemistry analyses or laser capture microdissection. This Facility also conducts routine histological stains. The Microscopy Facility of the Module helps investigators to produce publication quality images or videos from histological slides, fixed cells, live cells or in vivo mouse eyes. A physical space, resources, and expertise of the Module, operated and supervised by highly experienced personnel, serve as the basis for the following Specific Aims: 1) to process, embed, and section eyes followed by section mounting on slides and staining (if requested); 2) to guide users in the proper dissection, fixation and staining techniques, thus ensuring the production of high quality histological specimens; 3) to provide access to Module's microscopes along with training and consultation in all aspects of a microscopy-based experiments; 4) to provide access to and training on the use of Metamorph imaging software to properly analyze and generate relevant data from images; 5) to assist in production of publication quality images and/or videos. The Histology, Microscopy & Imaging Module has the heaviest usage of all P30 Core Grant Modules and will continue assisting VSRC investigators in producing high-quality and high-profile vision-related publications.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Center Core Grants (P30)
Project #
2P30EY011373-21
Application #
9358190
Study Section
Special Emphasis Panel (ZEY1)
Project Start
Project End
Budget Start
2017-09-01
Budget End
2018-08-31
Support Year
21
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Type
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
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
Saadane, Aicha; Petrov, Alexey; Mast, Natalia et al. (2018) Mechanisms that minimize retinal impact of apolipoprotein E absence. J Lipid Res 59:2368-2382
Sun, Yan; Abbondante, Serena; Karmakar, Mausita et al. (2018) Neutrophil Caspase-11 Is Required for Cleavage of Caspase-1 and Secretion of IL-1? in Aspergillus fumigatus Infection. J Immunol 201:2767-2775
Nahomi, Rooban B; Sampathkumar, Sruthi; Myers, Angela M et al. (2018) The Absence of Indoleamine 2,3-Dioxygenase Inhibits Retinal Capillary Degeneration in Diabetic Mice. Invest Ophthalmol Vis Sci 59:2042-2053
Kiser, Philip D; Zhang, Jianye; Sharma, Aditya et al. (2018) Retinoid isomerase inhibitors impair but do not block mammalian cone photoreceptor function. J Gen Physiol 150:571-590
Basak, Sandip; Gicheru, Yvonne; Samanta, Amrita et al. (2018) Cryo-EM structure of 5-HT3A receptor in its resting conformation. Nat Commun 9:514
Mamidi, Ranganath; Li, Jiayang; Doh, Chang Yoon et al. (2018) Impact of the Myosin Modulator Mavacamten on Force Generation and Cross-Bridge Behavior in a Murine Model of Hypercontractility. J Am Heart Assoc 7:e009627

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