(Tissue Culture/Molecular) Continuing funds are requested by 17 vision scientists (holding 13 eligible NEI R01 grants) and their personnel to support three resource/service cores and an administrative core in the newly merged Department of Ophthalmology, Visual and Anatomical Sciences (former Ophthalmology and Anatomy/Cell Biology Departments). The Tissue Culture/Molecular (TC/M) core will be directed by Dr. Jena Steinle, an R01-funded investigator with significant expertise in tissue culture and molecular biology techniques. Together with the PI, and a research assistant, the environment and capability to conduct vision research at Wayne State University and affiliated institutions will be enhanced through prioritization of the work of NEI R01 funded investigators, their staff and students (graduate and fellows) in numerous aspects of both tissue culture and molecular biology. The TC/M core will provide vision scientists (priority for NEI R01 funded) with facilities and technical assistance that will assure quality and cost effectiveness of the work performed. This core will maintain and propagate ocular and other cell types, as well as provide investigators with genotyping, reverse transcription-polymerase chain reaction (RT) and quantitative polymerase chain reaction (q)-PCR, gene silencing- siRNA, shRNA, CRISPR/Cas9, nested PCR and adherence assays. It will also provide for consultation/assistance on recombinant (r) AAV virus vector design and construction and assistance to the PI, students or staff for in vitro functional assessments. Overall, the TC/M core will assist NEI R01-funded investigators and their staff/students in studies that require the use of tissue culture and molecular biology techniques; foster collaboration between vision scientists using tissue culture and molecular biological techniques; and bring new investigators into vision research by providing assistance in tissue culture and molecular techniques that can expand their research focus.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Center Core Grants (P30)
Project #
5P30EY004068-37
Application #
10000934
Study Section
Special Emphasis Panel (ZEY1)
Project Start
1997-04-01
Project End
2024-08-31
Budget Start
2020-09-01
Budget End
2021-08-31
Support Year
37
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Wayne State University
Department
Type
DUNS #
001962224
City
Detroit
State
MI
Country
United States
Zip Code
48202
Berkowitz, Bruce A (2018) Oxidative stress measured in vivo without an exogenous contrast agent using QUEST MRI. J Magn Reson 291:94-100
Shi, Haoshen; Ebrahim, Abdul S; Berger, Elizabeth A (2018) A Contrast in Pathogenic Responses between C57BL/6J and BALB/cJ Mice Using a Model of Retinal Injury. Am J Pathol 188:2717-2728
Curtiss, Elizabeth; Liu, Li; Steinle, Jena J (2018) miR15a regulates NLRP3 inflammasome proteins in the retinal vasculature. Exp Eye Res 176:98-102
Gao, Nan; Me, Rao; Dai, Chenyang et al. (2018) Opposing Effects of IL-1Ra and IL-36Ra on Innate Immune Response to Pseudomonas aeruginosa Infection in C57BL/6 Mouse Corneas. J Immunol 201:688-699
Curtiss, Elizabeth; Jiang, Youde; Liu, Li et al. (2018) Epac1 Restores Normal Insulin Signaling through a Reduction in Inflammatory Cytokines. Mediators Inflamm 2018:3809092
Singh, Pawan Kumar; Khatri, Indu; Jha, Alokkumar et al. (2018) Determination of system level alterations in host transcriptome due to Zika virus (ZIKV) Infection in retinal pigment epithelium. Sci Rep 8:11209
Han, Jing; Li, Yue; Liu, Xiuli et al. (2018) Metformin suppresses retinal angiogenesis and inflammation in vitro and in vivo. PLoS One 13:e0193031
Berkowitz, Bruce A; Podolsky, Robert H; Berri, Ali M et al. (2018) Dark Rearing Does Not Prevent Rod Oxidative Stress In Vivo in Pde6brd10 Mice. Invest Ophthalmol Vis Sci 59:1659-1665
Jiang, Youde; Liu, Li; Steinle, Jena J (2018) miRNA15a regulates insulin signal transduction in the retinal vasculature. Cell Signal 44:28-32
Liu, Li; Patel, Paragi; Steinle, Jena J (2018) PKA regulates HMGB1 through activation of IGFBP-3 and SIRT1 in human retinal endothelial cells cultured in high glucose. Inflamm Res 67:1013-1019

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