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NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCESNIH · NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCESNIH

COBRE in Digestive and Liver Disease - Imaging Core

Lemasters, John J (Contact)·MEDICAL UNIVERSITY OF SOUTH CAROLINA, SC·2020–2030·ACTIVE
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INSTITUTION

MEDICAL UNIVERSITY OF SOUTH CAROLINA, SC

PRINCIPAL INVESTIGATOR

Lemasters, John J (Contact)

FUNDING

$210K

YEAR

2020

MOONBASE SCORE

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Abstract

Advanced Imaging Core – Project Summary The COBRE in Digestive & Liver Disease (CDLD) Advanced Imaging Core provides equipment, expertise, and training to CDLD investigators for state-of-the-art cell- and tissue-based imaging, including confocal, multiphoton and super-resolution microscopy of live and fixed cells and tissues, intravital imaging and automated imaging of histological slides. The Advanced Imaging Core houses the following major microscope systems: 1) Leica Stellaris 8 tauSTED Xtend Super-Resolution Microscope; 2) Andor BC43 Spinning Disk Confocal Microscope; 3) Zeiss LSM 880 NLO confocal/multiphoton microscope with Fast Airyscan super-resolution and Quasar spectral detectors; 4) Olympus FluoView 1200 MPE Intravital Microscope; 5) Olympus FluoView Fv10i confocal microscope; 6) Leica TCS SP8 laser scanning confocal microscope; and 7) BD Biosciences CARV II real-time spinning disk confocal microscope; 8) Zeiss LSM 510 META confocal; 9) Perkin-Elmer Vectra Polaris automated quantitative pathology imaging system; 10) Zeiss Axiovert 200M microscope; and 11) Agilent Cytation 5 Cell Imaging Multi-Mode Reader. Except for Vectra Polaris which is customized for histological slides, all microscopes are equipped with environmental chambers for temperature and gas phase control to allow non-destructive 3D imaging of living cells, tissues and organisms. Major applications include 1) live cell imaging of parameter- sensitive fluorophores to monitor ions, electrical potentials, radical generation, pyridine nucleotide reduction, membrane permeability, cell viability (apoptosis and necrosis), and the submicron distribution of fluorescent proteins and other fluorescent reporters; 2) high resolution imaging of tissue sections for immunocytochemistry and fluorescent protein distribution; 3) fluorescence resonance energy transfer (FRET) and DuoLink to characterize and quantify interactions between specific molecules; 4) intravital microscopy to monitor microcirculation, leukocyte margination, mitochondrial polarization and permeability, radical generation, gene expression and other parameters in living animals; and 5) high throughput, quantitative multiplexed imaging of conventionally and immunostained clinical and research specimens. Ancillary equipment required for specimen preparation is also provided. Consultation and services for TEM and SEM are available through the Department of Pathology & Laboratory Medicine. Computer workstations provide offline image processing/analysis (ImageJ FIJI, Metamorph, IPLab and other software). Advanced Imaging Core services provide training and assistance to promote the success of individual CDLD investigators.

NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCESP20Special Emphasis Panel[ZGM1 RCB-3 (C2)]throughincludelaboratorydepartmentfixedphasespinningworkstationsthroughputagilentolympussummarysfdmoleculesrequireddiseasenucleotideconfocalpolarizationpotentialsapoptosis

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