This shared instrumentation grant application is to acquire a state-of-the-art confocal microscopy imaging system (Zeiss LSM 510 core unit + critical upgrades) to replace our aging, limited-capability system (Nikon PCM 2000) and allow our user base to expand into critical and novel applications/techniques. Our present user base of 19 NIH-funded investigators with qualifying grants is comprised of faculty from several departments in the Schools of Medicine (Medicine, Pathology, Physiology and Biophysics, Biochemistry), Pharmaceutical Sciences and Dentistry. They have been using our existing system housed in the Confocal Microscopy Subcore of the Cell Biology Core of USC's Research Center for Liver Diseases (RCLD). This facility has been the sole and/or primary confocal microscopy resource they have access to. Although Nikon PCM 2000 is a workhorse instrument, it is capable of only simple 2-color imaging in fixed specimens and lacks advanced capabilities, such as live cell and time-lapse imaging, imaging specimens labeled with 3 or 4 fluorophores, fluorescence recovery after photobleaching, or fluorescence resonance energy transfer, which are sorely needed by our user base. The other four existing system on our campus are either dedicated to special uses or overloaded with their own user base. The new system will replace our old and be housed-operated in the same facility, with space/darkroom in place. RCLD is funded by NIH P30 DK 48522, Dr. Neil Kaplowitz, P.I., which is in its 3rd 5-yr cycle (3/1/05-2/28/10). It has an established track record in terms of all the necessary infrastructure, administrative, technical (full-time microscopy specialist) and financial (budget for warranty service-maintenance of microscope), to maintain and operate the new equipment. Drs. Murad Ookhtens and Sarah Hamm-Alvarez, the P.I. and co-P.I. on this application, serve as co-directors of the Cell Biology Core, a subcore of which houses the confocal microscopy equipment. They are highly experienced investigators, with extensive cumulative record and expertise in overseeing the use of a large base of sophisticated instrumentation and will share in technical oversight and management of the use of the new system, as they have done with the old. Relevance: The equipment will substantially advance the research of faculty involved in studying the normal and diseased states of the liver (hepatitis C, alcoholic/drug toxicity and injury), heart, lung, kidney, eye, teeth, as well as investigating various methods of drug delivery. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10RR022508-01A1
Application #
7220471
Study Section
Special Emphasis Panel (ZRG1-CB-F (30))
Program Officer
Levy, Abraham
Project Start
2007-04-15
Project End
2008-04-14
Budget Start
2007-04-15
Budget End
2008-04-14
Support Year
1
Fiscal Year
2007
Total Cost
$415,051
Indirect Cost
Name
University of Southern California
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
Zhou, Beiyun; Flodby, Per; Luo, Jiao et al. (2018) Claudin-18-mediated YAP activity regulates lung stem and progenitor cell homeostasis and tumorigenesis. J Clin Invest 128:970-984
Flodby, Per; Liebler, Janice M; Sunohara, Mitsuhiro et al. (2017) Region-specific role for Pten in maintenance of epithelial phenotype and integrity. Am J Physiol Lung Cell Mol Physiol 312:L131-L142
Carpenter, Philip M; Sivadas, Priyanka; Hua, Spencer S et al. (2017) Migration of breast cancer cell lines in response to pulmonary laminin 332. Cancer Med 6:220-234
Johnson, Sandra A S; Lin, Justin J; Walkey, Christopher J et al. (2017) Elevated TATA-binding protein expression drives vascular endothelial growth factor expression in colon cancer. Oncotarget 8:48832-48845
Flodby, Per; Kim, Yong Ho; Beard, LaMonta L et al. (2016) Knockout Mice Reveal a Major Role for Alveolar Epithelial Type I Cells in Alveolar Fluid Clearance. Am J Respir Cell Mol Biol 55:395-406
Gargus, Matthew; Niu, Chao; Vallone, John G et al. (2015) Human esophageal myofibroblasts secrete proinflammatory cytokines in response to acid and Toll-like receptor 4 ligands. Am J Physiol Gastrointest Liver Physiol 308:G904-23
Martin, Anthony; Xiong, Jian; Koromila, Theodora et al. (2015) Estrogens antagonize RUNX2-mediated osteoblast-driven osteoclastogenesis through regulating RANKL membrane association. Bone 75:96-104
Dara, Lily; Johnson, Heather; Suda, Jo et al. (2015) Receptor interacting protein kinase 1 mediates murine acetaminophen toxicity independent of the necrosome and not through necroptosis. Hepatology 62:1847-57
Siddique, Hifzur R; Feldman, Douglas E; Chen, Chia-Lin et al. (2015) NUMB phosphorylation destabilizes p53 and promotes self-renewal of tumor-initiating cells by a NANOG-dependent mechanism in liver cancer. Hepatology 62:1466-79
Rodgers, Mary A; Bowman, James W; Fujita, Hiroaki et al. (2014) The linear ubiquitin assembly complex (LUBAC) is essential for NLRP3 inflammasome activation. J Exp Med 211:1333-47

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