The Confocal and Specialized Microscopy Shared Resource is a fully Cancer Center-managed facility.Subcellular imaging is an essential tool in cancer biology. However, although the ideal specimen forconventional optical microscopy is two-dimensional, biological material is organized in three dimensions.Several technologies, notably confocal microscopy, are available to collect 3D images of biologicalsamples, with a spatial resolution superior to conventional microscopy. These essential imaging systemsare expensive and difficult for inexperienced users to operate and maintain, and are not routinely availablein individual research laboratory. The services provided by the Confocal and Specialized MicroscopyShared Resource are: one-photon laser scanning confocal microscopy multiphoton excitation confocal microscopy spinning-disk confocal microscopy digital deconvolution microscopyAll of these 3-dimensional fluorescence imaging technologies are made conveniently and affordablyavailable to HICCC members and other Columbia University researchers in a centralized facility, withtraining, assisted use, and consultation on data analysis and presentation provided by a full-time employeeand a manager. Since 1996, the facility has been used by more than 154 principal investigators from over30 basic science and clinical departments at Columbia University, and has contributed images for more200 publications. The facility is currently used at 75% of its maximal capacity during peak hours. InJanuary 2007, the facility moved into newly renovated space in the Irving Cancer Research Center. Thefacility continually seeks to add new imaging technologies to meet the scientific needs of our users. Inconjunction with the HICCC, we will introduce a new confocal microscope in the next year.During the last period of the CCSG, 37% of the users have been Cancer Center members with peerreviewedfunding, with those members representing 26% of the hours used in the facilty. The totaloperating budget of the facility is $273,025, of which we are requesting $79,749 from the CCSG.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA013696-35
Application #
7669912
Study Section
Subcommittee G - Education (NCI)
Project Start
2008-08-01
Project End
2013-06-30
Budget Start
2008-08-01
Budget End
2009-06-30
Support Year
35
Fiscal Year
2008
Total Cost
$70,104
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Proto, Jonathan D; Doran, Amanda C; Gusarova, Galina et al. (2018) Regulatory T Cells Promote Macrophage Efferocytosis during Inflammation Resolution. Immunity 49:666-677.e6
Hernandez, Celine; Huebener, Peter; Pradere, Jean-Philippe et al. (2018) HMGB1 links chronic liver injury to progenitor responses and hepatocarcinogenesis. J Clin Invest 128:2436-2451
Lee, Younghyun; Pujol Canadell, Monica; Shuryak, Igor et al. (2018) Candidate protein markers for radiation biodosimetry in the hematopoietically humanized mouse model. Sci Rep 8:13557
Kraakman, Michael J; Liu, Qiongming; Postigo-Fernandez, Jorge et al. (2018) PPAR? deacetylation dissociates thiazolidinedione's metabolic benefits from its adverse effects. J Clin Invest 128:2600-2612
Cui, Xuan; Jauregui, Ruben; Park, Karen Sophia et al. (2018) Multimodal characterization of a novel mutation causing vitamin B6-responsive gyrate atrophy. Ophthalmic Genet 39:512-516
Evans, Lucy P; Newell, Elizabeth A; Mahajan, MaryAnn et al. (2018) Acute vitreoretinal trauma and inflammation after traumatic brain injury in mice. Ann Clin Transl Neurol 5:240-251
Dieck, Chelsea L; Tzoneva, Gannie; Forouhar, Farhad et al. (2018) Structure and Mechanisms of NT5C2 Mutations Driving Thiopurine Resistance in Relapsed Lymphoblastic Leukemia. Cancer Cell 34:136-147.e6
Nathan, J; Ruscitto, A; Pylawka, S et al. (2018) Fibrocartilage Stem Cells Engraft and Self-Organize into Vascularized Bone. J Dent Res 97:329-337
Kratchmarov, Radomir; Viragova, Sara; Kim, Min Jung et al. (2018) Metabolic control of cell fate bifurcations in a hematopoietic progenitor population. Immunol Cell Biol 96:863-871
Sengillo, Jesse D; Lee, Winston; Bakhoum, Mathieu F et al. (2018) CHOROIDEREMIA ASSOCIATED WITH A NOVEL SYNONYMOUS MUTATION IN GENE ENCODING REP-1. Retin Cases Brief Rep 12 Suppl 1:S67-S71

Showing the most recent 10 out of 331 publications