The Kidney Imaging Core provides a national resource for Center users who require detailed and quantitative morphological analysis of kidney- and lower urinary tract-associated cells, tissues, and organs. The Imaging Core complements each of the other Center cores by providing critical information about the amounts, localization, and dynamics of molecules, cells, and tissues in normal and disease states. Thus, the Imaging Core is an integral part of the Center's mission to support multidisciplinary research in physiology, pathophysiology, and molecular biology of the kidney, as well as training and information transfer amongst Center users and cores. Users of the Imaging Core have access to state-of-the-art tools that allow for live cell and intravital microscopy, stimulated emission depletion (STED) super-resolution imaging, ultrastructural analysis, and novel magnetic resonance imaging modalities. Furthermore, the Imaging Core provides expertise that includes: detailed knowledge of kidney and lower urinary tract histology, pathology, and cytoarchitecture;sophisticated know-how in the proper techniques for culturing cells and tissues, as well as harvesting and fixing tissue obtained from research animals;familiarity with the specialized staining techniques needed to label these cells/tissues;expertise in the proper techniques to image and analyze live kidney and lower urinary tract tissues both ex vivo and in vivo;and knowledge of experimental design and image analysis, including interpretation of morphological data. The broad, long-range objectives and goals of the Core are multifold: (1) to serve as a national center for imaging of kidney- and lower urinary tractassociated cells, tissues, and organs;(2) to support the specialized techniques, methods, and procedures utilized by the investigators that comprise the Pittsburgh Center for Kidney Research;(3) to transfer Imaging Core expertise to Center investigators through training mechanisms including mini sabbaticals;(4) to provide for a higher standard of quality control through the Core's ability to conduct procedures on a routine and consistent basis.

Public Health Relevance

The Kidney Imaging Core is the component of the Pittsburgh Center for Kidney Research that examines the amounts, distribution, and dynamics of molecules and cells in the tissues and organs that comprise the urinary tract. These insights are important to understand the underlying reason for diseases that affect the kidneys and bladder.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK079307-07
Application #
8734389
Study Section
Special Emphasis Panel (ZDK1-GRB-6)
Project Start
Project End
Budget Start
2014-08-01
Budget End
2015-07-31
Support Year
7
Fiscal Year
2014
Total Cost
$246,400
Indirect Cost
$86,400
Name
University of Pittsburgh
Department
Type
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Joshi, Suhasini; Wang, Tai; Araujo, ThaĆ­s L S et al. (2018) Adapting to stress - chaperome networks in cancer. Nat Rev Cancer 18:562-575
Jackson, Edwin K; Gillespie, Delbert G; Mi, Zaichuan et al. (2018) Adenosine Receptors Influence Hypertension in Dahl Salt-Sensitive Rats: Dependence on Receptor Subtype, Salt Diet, and Sex. Hypertension 72:511-521
Wen, Xiaoyan; Cui, Liyan; Morrisroe, Seth et al. (2018) A zebrafish model of infection-associated acute kidney injury. Am J Physiol Renal Physiol 315:F291-F299
Kullmann, F Aura; Beckel, Jonathan M; McDonnell, Bronagh et al. (2018) Involvement of TRPM4 in detrusor overactivity following spinal cord transection in mice. Naunyn Schmiedebergs Arch Pharmacol 391:1191-1202
Kullmann, F A; Chang, H H; Gauthier, C et al. (2018) Serotonergic paraneurones in the female mouse urethral epithelium and their potential role in peripheral sensory information processing. Acta Physiol (Oxf) 222:
Espiritu, Eugenel B; Crunk, Amanda E; Bais, Abha et al. (2018) The Lhx1-Ldb1 complex interacts with Furry to regulate microRNA expression during pronephric kidney development. Sci Rep 8:16029
Preston, G Michael; Guerriero, Christopher J; Metzger, Meredith B et al. (2018) Substrate Insolubility Dictates Hsp104-Dependent Endoplasmic-Reticulum-Associated Degradation. Mol Cell 70:242-253.e6
Sannino, Sara; Guerriero, Christopher J; Sabnis, Amit J et al. (2018) Compensatory increases of select proteostasis networks after Hsp70 inhibition in cancer cells. J Cell Sci 131:
Gallo, Luciana I; Dalghi, Marianela G; Clayton, Dennis R et al. (2018) RAB27B requirement for stretch-induced exocytosis in bladder umbrella cells. Am J Physiol Cell Physiol 314:C349-C365
Kharade, Sujay V; Kurata, Haruto; Bender, Aaron M et al. (2018) Discovery, Characterization, and Effects on Renal Fluid and Electrolyte Excretion of the Kir4.1 Potassium Channel Pore Blocker, VU0134992. Mol Pharmacol 94:926-937

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