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.
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.
|Sneddon, W Bruce; Ruiz, Giovanni W; Gallo, Luciana I et al. (2016) Convergent Signaling Pathways Regulate Parathyroid Hormone and Fibroblast Growth Factor-23 Action on NPT2A-mediated Phosphate Transport. J Biol Chem 291:18632-42|
|Chiba, Takuto; Skrypnyk, Nataliya I; Skvarca, Lauren Brilli et al. (2016) Retinoic Acid Signaling Coordinates Macrophage-Dependent Injury and Repair after AKI. J Am Soc Nephrol 27:495-508|
|Al-Qusairi, Lama; Basquin, Denis; Roy, Ankita et al. (2016) Renal tubular SGK1 deficiency causes impaired K+ excretion via loss of regulation of NEDD4-2/WNK1 and ENaC. Am J Physiol Renal Physiol 311:F330-42|
|Shi, Shujie; Luke, Cliff J; Miedel, Mark T et al. (2016) Activation of the Caenorhabditis elegans Degenerin Channel by Shear Stress Requires the MEC-10 Subunit. J Biol Chem 291:14012-22|
|Sharma, Akhil; Yabes, Jonathan; Al Mawed, Saleem et al. (2016) Impact of Cognitive Function Change on Mortality in Renal Transplant and End-Stage Renal Disease Patients. Am J Nephrol 44:462-472|
|Al-Bataineh, Mohammad M; Kinlough, Carol L; Poland, Paul A et al. (2016) Muc1 enhances the Î²-catenin protective pathway during ischemia-reperfusion injury. Am J Physiol Renal Physiol 310:F569-79|
|Schaufelberger, Sara A; Rosselli, Marinella; Barchiesi, Federica et al. (2016) 2-Methoxyestradiol, an endogenous 17Î²-estradiol metabolite, inhibits microglial proliferation and activation via an estrogen receptor-independent mechanism. Am J Physiol Endocrinol Metab 310:E313-22|
|Zhou, Dong; Tan, Roderick J; Fu, Haiyan et al. (2016) Wnt/Î²-catenin signaling in kidney injury and repair: a double-edged sword. Lab Invest 96:156-67|
|Walker, Kenneth A; Sims-Lucas, Sunder; Bates, Carlton M (2016) Fibroblast growth factor receptor signaling in kidney and lower urinary tract development. Pediatr Nephrol 31:885-95|
|Manos-Turvey, Alexandra; Al-Ashtal, Hiba A; Needham, Patrick G et al. (2016) Dihydropyrimidinones and -thiones with improved activity against human polyomavirus family members. Bioorg Med Chem Lett 26:5087-5091|
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