The Flow Cytometry and High-speed Cell Sorting Core (FCCS) is a state- of-the-art facility designed to enhance the power and productivity of the research of Rheumatic Disease Core Center (RDCC) investigators by providing flow cytometry for cell analyses and purification at a reasonable cost. To accomplish this goal, the Core provides the equipment, service and expertise necessary for the application of flow cytometry and related technologies to cutting edge research in the rheumatic diseases. Through the support of our users and with the advice of our Scientific Advisory Committee, we have used nationally peer- reviewed federal instrumentation grants and UAB resources to obtain top- of-the-line equipment that provides a wide range of applications for RDCC investigators by providing flow cytometry for cell analyses and purification at a reasonable cost. To accomplish this goal, the Core provides the equipment, service and expertise necessary for the application for flow cytometry and related technologies to cutting edge research in the rheumatic diseases. Through the support of our users and with the advice of our Scientific Advisory Committee, we have used nationally peer-reviewed federal instrumentation grants and UAB resources to obtain top-of-the-line equipment that provides a wide range of applications for RDCC investigators. This includes a nine-detector, sort enhanced FACS Vantage, a six detector, loader equipped FACS Caliber, a researcher-operated FACScan, a SLM8000 UV-capable spectroufluorimeter, and computers for data independent analysis. With this equipment, we have developed new techniques as well as provided basic sample analysis, with the result that the FCCS Core has served over 120 independently funded UAB investigators and contributed to many publications. Our goals for the core are to continue efforts at (1) outreach and education, to alert RDCC investigators to the potential for flow technology to increase the power of their research, (2) service, to improve efficiency and to maintain the highest possible standards of quality, and (3) application development, to continue to bring new technologies and protocols to the RDCC research community to expand the ways that flow cytometry can contribute to rheumatic disease research. To achieve these goals, we will stress a Lab Manager with high awareness of new protocols through courses and cytometry meetings, two-way teaching between the Core and the RDCC community, a Scientific Advisory Committee that combines both knowledgeable users and those involved in senior research positions at UAB, an external advisory who is well informed about newer equipment and applications, and an integration with the larger UAB institution to maintain support and development. With these efforts, we will maintain flow cytometry as a fundamental and vital tool for state-of-the-art research in the rheumatic diseases at UAB.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
1P30AR048311-01
Application #
6547723
Study Section
Special Emphasis Panel (ZAR1)
Project Start
2001-09-28
Project End
2006-08-31
Budget Start
Budget End
Support Year
1
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
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
Harms, Ashley S; Thome, Aaron D; Yan, Zhaoqi et al. (2018) Peripheral monocyte entry is required for alpha-Synuclein induced inflammation and Neurodegeneration in a model of Parkinson disease. Exp Neurol 300:179-187
Lever, Jeremie M; Yang, Zhengqin; Boddu, Ravindra et al. (2018) Parabiosis reveals leukocyte dynamics in the kidney. Lab Invest 98:391-402
Chakraborty, Asmi; Dorsett, Kaitlyn A; Trummell, Hoa Q et al. (2018) ST6Gal-I sialyltransferase promotes chemoresistance in pancreatic ductal adenocarcinoma by abrogating gemcitabine-mediated DNA damage. J Biol Chem 293:984-994
Su, Hairui; Sun, Chiao-Wang; Liu, Szu-Mam et al. (2018) Defining the epigenetic status of blood cells using a cyanine-based fluorescent probe for PRMT1. Blood Adv 2:2829-2836
Shin, Boyoung; Kress, Robert L; Kramer, Philip A et al. (2018) Effector CD4 T cells with progenitor potential mediate chronic intestinal inflammation. J Exp Med 215:1803-1812
Gibson, Sara A; Yang, Wei; Yan, Zhaoqi et al. (2018) CK2 Controls Th17 and Regulatory T Cell Differentiation Through Inhibition of FoxO1. J Immunol 201:383-392

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