Microscopy and Imaging - Susette C. Mueller, PhD The objective of the Microscopy and Imaging Shared Resource (MISR) is to provide a supportive environment with state-of-the-art instrumentation for investigators with emphasis on light microscopy and image analysis of tumor cells, including training and education. The MISR also provides a rich environment for interactive exchanges and referrals among Lombardi Comprehensive Cancer Center users. MISR provides instrumentation for bright field microscopy;routine fluorescence microscopy and more advanced applications, including confocal microscopy, microinjection, total internal reflection microscopy (TIRF), multispectral emission imaging, fluorescence lifetime imaging (FLIM), fluorescence resonance energy transfer (FRET), fluorescence recovery after photobleaching (FRAP), and multiphoton, deep tissue imaging. Live cell, time-lapse imaging is possible using five different wide field and confocal systems. Using Metamorph Offline image analysis, MISR develops automated routines for users carrying out common assays such as for cell tracking, proliferation, mitosis, apoptosis, and angiogenesis experiments. MISR also develops custom journals as requested by users and offers individualized training. The resource also supports cytogenetics and molecular cytogenetics services with expert collaborations directed by Dr. Jan Blancato. Periodic training sessions, open house forums, and seminars are held for users to enhance their expertise in microscopy and provide opportunities to discuss the interpretation of images. Faculty collaborations with MISR provide expertise to others in sophisticated imaging and image analysis approaches. Web-based information and instrument signup calendars enhance use of the shared resource. The MISR provides access to ten major, digital microscope workstations, one stand-alone image analysis workstation and oversees 20 other licenses in individual labs. Since the last submission, MISR added two new sophisticated microscopes: a total internal fluorescence reflection (TIRF) microscope and a confocal/ multiphoton microscope with spectral emission and single photon, fluorescence lifetime imaging capabilities and added a wide field spectral emission camera with software. We plan an upgrade of the fluorescence widefield sceening workstation to include fast, spinning disk confocal, 3D imaging in the spring of 2009. The Microscopy and Imaging Shared Resource (MISR) has been directed by Dr. Susette Mueller since 1991. Dr. Mueller, a tumor cell biologist, became a member of the Lombardi Comprehensive Cancer Center in 1985. Her research on mechanisms of tumor cell invasion and metastasis utilizes a number of microscopic techniques. Dr. Xuehua Xu joined MISR in 2006 with expertise in quantitative dynamic imaging including TIRF, multispectral FRET analysis, and single molecule imaging. Overall, 5 programs and 39 Cancer Center members unfilled this resource in 2008.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA051008-20
Application #
8739829
Study Section
Subcommittee G - Education (NCI)
Project Start
1997-08-15
Project End
2014-04-30
Budget Start
2013-05-01
Budget End
2014-04-30
Support Year
20
Fiscal Year
2013
Total Cost
$41,847
Indirect Cost
Name
Georgetown University
Department
Type
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
Lee, Yichien; Rodriguez, Olga C; Albanese, Chris et al. (2018) Divergent brain changes in two audiogenic rat strains: A voxel-based morphometry and diffusion tensor imaging comparison of the genetically epilepsy prone rat (GEPR-3) and the Wistar Audiogenic Rat (WAR). Neurobiol Dis 111:80-90
Coia, Heidi; Ma, Ning; Hou, Yanqi et al. (2018) Prevention of Lipid Peroxidation-derived Cyclic DNA Adduct and Mutation in High-Fat Diet-induced Hepatocarcinogenesis by Theaphenon E. Cancer Prev Res (Phila) 11:665-676
Ory, Virginie; Kietzman, William B; Boeckelman, Jacob et al. (2018) The PPAR? agonist efatutazone delays invasive progression and induces differentiation of ductal carcinoma in situ. Breast Cancer Res Treat 169:47-57
Ozawa, Patricia Midori Murobushi; Alkhilaiwi, Faris; Cavalli, Iglenir João et al. (2018) Extracellular vesicles from triple-negative breast cancer cells promote proliferation and drug resistance in non-tumorigenic breast cells. Breast Cancer Res Treat 172:713-723
Smith, Jill P; Wang, Shangzi; Nadella, Sandeep et al. (2018) Cholecystokinin receptor antagonist alters pancreatic cancer microenvironment and increases efficacy of immune checkpoint antibody therapy in mice. Cancer Immunol Immunother 67:195-207
Edwardson, Matthew A; Zhong, Xiaogang; Fiandaca, Massimo S et al. (2018) Plasma microRNA markers of upper limb recovery following human stroke. Sci Rep 8:12558
Kaat, Aaron J; Schalet, Benjamin D; Rutsohn, Joshua et al. (2018) Physical function metric over measure: An illustration with the Patient-Reported Outcomes Measurement Information System (PROMIS) and the Functional Assessment of Cancer Therapy (FACT). Cancer 124:153-160
Maximov, Philipp Y; Abderrahman, Balkees; Fanning, Sean W et al. (2018) Endoxifen, 4-Hydroxytamoxifen and an Estrogenic Derivative Modulate Estrogen Receptor Complex Mediated Apoptosis in Breast Cancer. Mol Pharmacol 94:812-822
Czarnecka, Magdalena; Lu, Congyi; Pons, Jennifer et al. (2018) Neuropeptide Y receptor interactions regulate its mitogenic activity. Neuropeptides :
Gonzalez, Thomas L; Moos, Rebecca K; Gersch, Christina L et al. (2018) Metabolites of n-Butylparaben and iso-Butylparaben Exhibit Estrogenic Properties in MCF-7 and T47D Human Breast Cancer Cell Lines. Toxicol Sci 164:50-59

Showing the most recent 10 out of 1120 publications