The Immunologic Monitoring (IM) Core will serve as a shared resource to assist the target faculty of the COBRE to pursue high quality research by monitoring immune cell functions following treatment with the dietary supplements in naive and experimental models of inflammatory disease. The Core will be useful to characterize the immune status before, during and after treatment of diseased animals with the plant products so as to provide insights into their prognostic and therapeutic effects. In addition, while the individual projects deal with specialized studies related to the effects of plant products on macrophages that play a pivotal role in inflammation, it is critical to know how these would affect the other immune cells and the overall immunity. This is especially important because inflammatory diseases are systemic and involve multiple types of immune cells. Furthermore, such information on the immunologic effects of the plant derivates is critical in the development of bench-to-bedside research. Specifically, the IM Core will 1) offer a wide range of state-of-the-art resources to pursue cellular and molecular immunological assays so as to enable the investigators to pursue cutting-edge research on the projects. 2) provide technological assistance and training in the use of major equipment by the users 3) participate in the design of the experiments, selection of the appropriate assays, trouble-shoot and interpretation of results. 4) develop and standardize new technologies based on the changing needs of the users by optimization and evaluation of sensitivity, specificity and reproducibility. 5) aid in data collection, evaluation and analysis as well as sharing of the data to enhance collaborations. There are two major components of this core. The core will 1) Serve as a resource of multi-user equipment 2) Perform Immune Function Assessment by 1) Evaluation of the general health status 2) Level I immunological testing which includes a variety of assays that examine the functions of T cells, B cells, NK cells, dendritic cells and macrophages. 3) Level II immunological testing of the genetic, transcriptional and epigenetic mechanisms underlying immune cell dysregulation. This functional assessment performed by the IM Core will complement the cell phenotyping and animal imaging studies performed by other cores and thereby lead to comprehensive integration between projects and cores. These shared resources could be used for translational studies in the future. In summary, the IM Core will provide effective and economical shared resources and service to conduct high-quality research that will lead to increased productivity and enhanced interactions between investigators of all the projects resulting in their ability to attract independent, extramural funding, and advancement of scientific careers.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
5P20GM103641-03
Application #
8733737
Study Section
Special Emphasis Panel (ZRR1-RI-4)
Project Start
Project End
Budget Start
2014-06-01
Budget End
2015-05-31
Support Year
3
Fiscal Year
2014
Total Cost
$205,500
Indirect Cost
$55,500
Name
University of South Carolina at Columbia
Department
Type
DUNS #
041387846
City
Columbia
State
SC
Country
United States
Zip Code
29208
Miranda, Kathryn; Yang, Xiaoming; Bam, Marpe et al. (2018) MicroRNA-30 modulates metabolic inflammation by regulating Notch signaling in adipose tissue macrophages. Int J Obes (Lond) 42:1140-1150
Alhasson, Firas; Seth, Ratanesh Kumar; Sarkar, Sutapa et al. (2018) High circulatory leptin mediated NOX-2-peroxynitrite-miR21 axis activate mesangial cells and promotes renal inflammatory pathology in nonalcoholic fatty liver disease. Redox Biol 17:1-15
Bam, Marpe; Yang, Xiaoming; Sen, Souvik et al. (2018) Characterization of Dysregulated miRNA in Peripheral Blood Mononuclear Cells from Ischemic Stroke Patients. Mol Neurobiol 55:1419-1429
Elliott, David M; Singh, Narendra; Nagarkatti, Mitzi et al. (2018) Cannabidiol Attenuates Experimental Autoimmune Encephalomyelitis Model of Multiple Sclerosis Through Induction of Myeloid-Derived Suppressor Cells. Front Immunol 9:1782
Liese, Angela D; Ma, Xiaonan; Ma, Xiaoguang et al. (2018) Dietary quality and markers of inflammation: No association in youth with type 1 diabetes. J Diabetes Complications 32:179-184
Alghetaa, Hasan; Mohammed, Amira; Sultan, Muthanna et al. (2018) Resveratrol protects mice against SEB-induced acute lung injury and mortality by miR-193a modulation that targets TGF-? signalling. J Cell Mol Med 22:2644-2655
Zhang, Tao; Zhou, Juhua; Man, Gene Chi Wai et al. (2018) MDSCs drive the process of endometriosis by enhancing angiogenesis and are a new potential therapeutic target. Eur J Immunol 48:1059-1073
Seth, Ratanesh Kumar; Kimono, Diana; Alhasson, Firas et al. (2018) Increased butyrate priming in the gut stalls microbiome associated-gastrointestinal inflammation and hepatic metabolic reprogramming in a mouse model of Gulf War Illness. Toxicol Appl Pharmacol 350:64-77
Finnell, Julie E; Muniz, Brandon L; Padi, Akhila R et al. (2018) Essential Role of Ovarian Hormones in Susceptibility to the Consequences of Witnessing Social Defeat in Female Rats. Biol Psychiatry 84:372-382
Dubey, Seema; Yoon, Hyunho; Cohen, Mark Steven et al. (2018) Withaferin A Associated Differential Regulation of Inflammatory Cytokines. Front Immunol 9:195

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