(Taken directly from the application) The Cell Culture Core is a critical component of the Interdisciplinary Center for Polycystic Kidney Disease Research. It will provide and maintain primary cells and cell lines from human and murine control and cystic kidneys for in vitro experimentation by the eight center investigators (Project Leaders and Co-Investigators of the-3 major and two Pilot and Feasibility studies proposed). It will be the central resource for distribution of normal and cystic renal epithelial cell (REC) lines from the relevant models. This Core will concentrate expertise in the isolation of primary and immortalized (REC), maintenance and characterization of these cell lines, preparation of culture medium and cryopreservation of the cells. The goal of the Cell Culture Core is to provide investigators with high quality, phenotypically consistent cell lines in a cost-effective and efficient manner. In addition, the Core will provide Center Investigators with expertise in the utilization of organ culture methodology for specific studies proposed. Center personnel will be responsible for quality control within the facility. They will closely monitor the REC lines for phenotypic drift and perform periodic screening for contamination (i.e., mycoplasma). The Cell Core centralizes the isolation and handling of the primary cells and REC lines thus ensuring consistent reagents and minimizing phenotypic drift of cells being studied under various experimental protocols. The Core concentrates expertise in commonly utilized techniques thereby maximizing quality, efficiency, and cost effectiveness.

Project Start
2001-09-01
Project End
2002-08-31
Budget Start
Budget End
Support Year
3
Fiscal Year
2001
Total Cost
$162,000
Indirect Cost
Name
Case Western Reserve University
Department
Type
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Cotton, Calvin U; Hobert, Michael E; Ryan, Sean et al. (2013) Basolateral EGF receptor sorting regulated by functionally distinct mechanisms in renal epithelial cells. Traffic 14:337-54
Stelloh, Cary; Allen, Kenneth P; Mattson, David L et al. (2012) Prematurity in mice leads to reduction in nephron number, hypertension, and proteinuria. Transl Res 159:80-9
Ryan, Sean; Verghese, Susamma; Cianciola, Nicholas L et al. (2010) Autosomal recessive polycystic kidney disease epithelial cell model reveals multiple basolateral epidermal growth factor receptor sorting pathways. Mol Biol Cell 21:2732-45
Park, Frank; Sweeney Jr, William E; Jia, Guangfu et al. (2009) Chronic blockade of 20-HETE synthesis reduces polycystic kidney disease in an orthologous rat model of ARPKD. Am J Physiol Renal Physiol 296:F575-82
Sweeney Jr, William E; von Vigier, Rodo O; Frost, Philip et al. (2008) Src inhibition ameliorates polycystic kidney disease. J Am Soc Nephrol 19:1331-41
Park, Frank; Sweeney, William E; Jia, Guangfu et al. (2008) 20-HETE mediates proliferation of renal epithelial cells in polycystic kidney disease. J Am Soc Nephrol 19:1929-39
Holland, Nolan B; Nishimiya, Yoshiyuki; Tsuda, Sakae et al. (2008) Two domains of RD3 antifreeze protein diffuse independently. Biochemistry 47:5935-41
Falin, Rebecca A; Cotton, Calvin U (2007) Acute downregulation of ENaC by EGF involves the PY motif and putative ERK phosphorylation site. J Gen Physiol 130:313-28
Holland, Nolan B; Nishimiya, Yoshiyuki; Tsuda, Sakae et al. (2007) Activity of a two-domain antifreeze protein is not dependent on linker sequence. Biophys J 92:541-6
Sweeney Jr, William E; Avner, Ellis D (2006) Molecular and cellular pathophysiology of autosomal recessive polycystic kidney disease (ARPKD). Cell Tissue Res 326:671-85

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