The Microscopy and Flow Cytometry Core (MFCC) of the COBRE Center for Targeted Therapeutics (CTT) provides services to all four CTT research projects and other investigators supported by the CTT and other IDeA programs at the University of South Carolina (USC). These services include training in microscopy and flow cytometry, advice on study design, with an emphasis on the analysis of cellular drug effects, and assistance with the instrumentation usage, both at the Core and at other USC facilities (in particular at the USC School of Medicine), as well as expert assistance in anatomic pathology of human and animal tissues. The available equipment includes: Carl Zeiss LSM700 Laser scanning confocal microscope with 4 lasers functioning from 405 to 633 nm, equipped for live cell imaging (with environmental chamber), standard point scanning, 3D reconstruction, FRAP, FRET, time lapse and tile/stitching; a Leica Microsystems AS MDW fluorescence microscope optimized for live cell imaging with temperature and CO2 control; two Leica Microsystems DM IRE2 fluorescent microscopes, which are motorized for z-stack acquisition and one of which has an environmental chamber. Olympus IX81 fluorescence microscope with workstation running Metamorph software is used for fluorescence imaging and deconvolution of wide field fluorescence images; it also has a Sutter Instruments Smartshutter and rapid filter changing wheels for ratiometric measurement of intracellular ion changes. There are 3 Carl Zeiss Axiovert 200 microscopes and an Olympus upright BX41 microscope, each with a color camera. All microscopes are in dedicated rooms and on vibration isolation tables. Flow cytometric equipment includes the BD FACS ARIA III for cell sorting, BD LSR II Flow Cytometer with high-throughput option and a 96-well plate loader, and Beckman Coulter FC500 flow cytometer. Users may operate the microscopes and one of the flow cytometers independently, after training by the co-directors. Many standard protocols have been established for immunohistochemistry and immunofluorescence analysis of cells and tissues, and for the analysis of cell growth, cell death and cell cycle progression. The core also provides services of an experienced anatomic pathologist, with a broad experience in gross pathology and histopathology in human and animal studies. The pathology core services include advice on study design and specimen processing including paraffin and cryosectioning, routine H&E staining, histochemical stains, and immunohistochemical analysis. Pathology reports will include macroscopic and microscopic findings, diagnosis of lesions, discussion of significant findings, and biological significance of the pathological effects of genetic modifications and experimental compounds in different animal organs, as well as tumor morphology in animal models and in human tissue samples. The core personnel offer advice on the choice of instruments and experimental protocols, provide training and assist with preparation of manuscripts and grant proposals.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
5P20GM109091-07
Application #
9978922
Study Section
Special Emphasis Panel (ZGM1)
Project Start
Project End
Budget Start
2020-05-01
Budget End
2021-04-30
Support Year
7
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of South Carolina at Columbia
Department
Type
DUNS #
041387846
City
Columbia
State
SC
Country
United States
Zip Code
29208
Varadaraj, Archana; Magdaleno, Carina; Mythreye, Karthikeyan (2018) Deoxycholate Fractionation of Fibronectin (FN) and Biotinylation Assay to Measure Recycled FN Fibrils in Epithelial Cells. Bio Protoc 8:
Liu, Changlong; Banister, Carolyn E; Weige, Charles C et al. (2018) PRDM1 silences stem cell-related genes and inhibits proliferation of human colon tumor organoids. Proc Natl Acad Sci U S A 115:E5066-E5075
Yu, Jin; Zhu, Hong; Taheri, Saeid et al. (2018) Impact of nutrition on inflammation, tauopathy, and behavioral outcomes from chronic traumatic encephalopathy. J Neuroinflammation 15:277
Jenkins, Laura M; Horst, Ben; Lancaster, Carly L et al. (2018) Dually modified transmembrane proteoglycans in development and disease. Cytokine Growth Factor Rev 39:124-136
Alam, Amer; Küng, Raphael; Kowal, Julia et al. (2018) Structure of a zosuquidar and UIC2-bound human-mouse chimeric ABCB1. Proc Natl Acad Sci U S A 115:E1973-E1982
Liang, Jiaxin; Chen, Mengqian; Hughes, Daniel et al. (2018) CDK8 Selectively Promotes the Growth of Colon Cancer Metastases in the Liver by Regulating Gene Expression of TIMP3 and Matrix Metalloproteinases. Cancer Res 78:6594-6606
Chukwurah, Evelyn; Patel, Rekha C (2018) Stress-induced TRBP phosphorylation enhances its interaction with PKR to regulate cellular survival. Sci Rep 8:1020
Singh, Priyanka; Jenkins, Laura M; Horst, Ben et al. (2018) Inhibin Is a Novel Paracrine Factor for Tumor Angiogenesis and Metastasis. Cancer Res 78:2978-2989
Wyatt, Michael D; Reilly, Nicole M; Patel, Shikha et al. (2018) Thiopurine-induced mitotic catastrophe in Rad51d-deficient mammalian cells. Environ Mol Mutagen 59:38-48
Serrao, Anne; Jenkins, Laura M; Chumanevich, Alexander A et al. (2018) Mediator kinase CDK8/CDK19 drives YAP1-dependent BMP4-induced EMT in cancer. Oncogene 37:4792-4808

Showing the most recent 10 out of 49 publications