Rheumatic diseases are a complex group of human disorders that cause significant morbidity and mortality. With the identification of gene loci involved in human rheumatic diseases, the next objectives will be to identify the function, localization, and interactions of these gene products and to determine their role in the initiation and progression of rheumatic diseases. To advance research into molecular and cellular basis of the rheumatic diseases, the Analytical Imaging and Immunoreagent Core will support RDCC investigators research programs with state-of-the-art imaging capabilities and through the generation of essential immunoreagents. First, the Immunoreagent Component will assist P30 investigators in the development and characterization of novel monoclonal antibodies that are relevant to the study of rheumatic diseases. Second, the Imaging Component will provide center members with access to high-end imaging capabilities that include multi and single photon confocal, high resolution fluorescence using Stimulated Depletion (STED) and conventional transmission, cryo, and environmental scanning electron microscopy. In addition, the AIIC will provide expertise in the areas of exeperimental design, data collection, and data analysis. The resources provided through the AIIC far exceed the capabilities available to individual laboratories and departments and together will facilitate the detailed analyses of the pathogenic mechanisms leading to rheumatic diseases.

Public Health Relevance

A more thorough understanding of the molecular mechanisms and pathophysiology of rheumatic diseases is needed in order to develop novel therapeutic and management approaches. The AIIC will advance research by providing investigators with access to novel immunoreagentsand and high-end imaging capabilities that are not available in single laboratories or most departments. In addition, the AIIC will provide exepertise in the areas of exeperimental design, data collection and data analysis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
5P30AR048311-13
Application #
8725930
Study Section
Special Emphasis Panel (ZAR1-KM)
Project Start
Project End
Budget Start
2014-09-01
Budget End
2015-08-31
Support Year
13
Fiscal Year
2014
Total Cost
$209,062
Indirect Cost
$67,356
Name
University of Alabama Birmingham
Department
Type
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Hamilton, Jennie A; Wu, Qi; Yang, PingAr et al. (2018) Cutting Edge: Intracellular IFN-? and Distinct Type I IFN Expression Patterns in Circulating Systemic Lupus Erythematosus B Cells. J Immunol 201:2203-2208
Yang, Zhenhua; Shah, Kushani; Busby, Theodore et al. (2018) Hijacking a key chromatin modulator creates epigenetic vulnerability for MYC-driven cancer. J Clin Invest 128:3605-3618
Hough, Kenneth P; Trevor, Jennifer L; Strenkowski, John G et al. (2018) Exosomal transfer of mitochondria from airway myeloid-derived regulatory cells to T cells. Redox Biol 18:54-64
Williams, Adele P; Waters, Alicia M; Stewart, Jerry E et al. (2018) A novel retinoid X receptor agonist, UAB30, inhibits rhabdomyosarcoma cells in vitro. J Surg Res 228:54-62
Ladowski, Joseph M; Martens, Gregory R; Reyes, Luz M et al. (2018) Examining the Biosynthesis and Xenoantigenicity of Class II Swine Leukocyte Antigen Proteins. J Immunol 200:2957-2964
Hough, Kenneth P; Wilson, Landon S; Trevor, Jennifer L et al. (2018) Unique Lipid Signatures of Extracellular Vesicles from the Airways of Asthmatics. Sci Rep 8:10340
Chou, Chu-Fang; Hsieh, Yu-Hua; Grubbs, Clinton J et al. (2018) The retinoid X receptor agonist, 9-cis UAB30, inhibits cutaneous T-cell lymphoma proliferation through the SKP2-p27kip1 axis. J Dermatol Sci 90:343-356
Friedman, Gregory K; Bernstock, Joshua D; Chen, Dongquan et al. (2018) Enhanced Sensitivity of Patient-Derived Pediatric High-Grade Brain Tumor Xenografts to Oncolytic HSV-1 Virotherapy Correlates with Nectin-1 Expression. Sci Rep 8:13930
Garner, Evan F; Williams, Adele P; Stafman, Laura L et al. (2018) FTY720 Decreases Tumorigenesis in Group 3 Medulloblastoma Patient-Derived Xenografts. Sci Rep 8:6913
Ladowski, Joseph M; Reyes, Luz M; Martens, Gregory R et al. (2018) Swine Leukocyte Antigen Class II Is a Xenoantigen. Transplantation 102:249-254

Showing the most recent 10 out of 340 publications