We request a Zeiss LSM 510MP microscope for the multiphoton-excited fluorescence imaging of a variety of cells, tissues and organisms. The Zeiss 510MP is a dedicated multiphoton-excitation system, thus complementing four confocal microscopes, including two Zeiss 510-Meta confocals, already in the School of Medicine Microscope Facility. As the largest core microscope facility on campus, our well-trained staff and established resources already serves over 250 users annually. However, there is no multiphoton microscope available for regular, general use by NIH-funded investigators. Existing instruments are inaccessible for a number of reasons. Furthermore, recent advances in laser technologies (Spectra-Physics MaiTai DeepSee) greatly facilitate state-of-the-art multiphoton fluorescence microscopy in a multi-user core facility. Initially, the system will serve 5 major users and potentially 60 minor users from multiple departments throughout Johns Hopkins. Because multiphoton fluorescent imaging provides unprecedented depth and sensitivity of imaging in living samples, we expect that minor users will slowly become major users. Supported by a broad base of interest, need, and financial support by the University, and will serve a large NIH-funded scientific community. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10RR024550-01
Application #
7388421
Study Section
Special Emphasis Panel (ZRG1-CB-B (30))
Program Officer
Levy, Abraham
Project Start
2008-05-01
Project End
2009-04-30
Budget Start
2008-05-01
Budget End
2009-04-30
Support Year
1
Fiscal Year
2008
Total Cost
$500,000
Indirect Cost
Name
Johns Hopkins University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Oh, Min-Hee; Collins, Samuel L; Sun, Im-Hong et al. (2017) mTORC2 Signaling Selectively Regulates the Generation and Function of Tissue-Resident Peritoneal Macrophages. Cell Rep 20:2439-2454
Head, Sarah A; Shi, Wei Q; Yang, Eun Ju et al. (2017) Simultaneous Targeting of NPC1 and VDAC1 by Itraconazole Leads to Synergistic Inhibition of mTOR Signaling and Angiogenesis. ACS Chem Biol 12:174-182
Rouf, Rosanne; MacFarlane, Elena Gallo; Takimoto, Eiki et al. (2017) Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice. JCI Insight 2:
Groves, Jennifer A; Maduka, Austin O; O'Meally, Robert N et al. (2017) Fatty acid synthase inhibits the O-GlcNAcase during oxidative stress. J Biol Chem 292:6493-6511
Pollizzi, Kristen N; Sun, Im-Hong; Patel, Chirag H et al. (2016) Asymmetric inheritance of mTORC1 kinase activity during division dictates CD8(+) T cell differentiation. Nat Immunol 17:704-11
Song, Chang; Nicholson, James D; Clark, Sarah M et al. (2016) Expansion of brain T cells in homeostatic conditions in lymphopenic Rag2(-/-) mice. Brain Behav Immun 57:161-172
Serbo, Janna V; Kuo, Scot; Lewis, Shawna et al. (2016) Patterning of Fibroblast and Matrix Anisotropy within 3D Confinement is Driven by the Cytoskeleton. Adv Healthc Mater 5:146-58
Savonenko, Alena V; Melnikova, Tatiana; Wang, Yuchuan et al. (2015) Cannabinoid CB2 Receptors in a Mouse Model of A? Amyloidosis: Immunohistochemical Analysis and Suitability as a PET Biomarker of Neuroinflammation. PLoS One 10:e0129618
Blazeski, Adriana; Kostecki, Geran M; Tung, Leslie (2015) Engineered heart slices for electrophysiological and contractile studies. Biomaterials 55:119-28
Gallo, Elena M; Loch, David C; Habashi, Jennifer P et al. (2014) Angiotensin II-dependent TGF-? signaling contributes to Loeys-Dietz syndrome vascular pathogenesis. J Clin Invest 124:448-60

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