A Conditionally Immortalized Human Podocyte Cell Line Demonstrating Nephrin and Podocin Expression
Author(s) -
Moin A. Saleem,
Michael J. O’Hare,
Jochen Reiser,
Richard J. Coward,
Carol Inward,
Timothy Farren,
Chang Ying Xing,
Lan Ni,
Peter W. Mathieson,
Peter Mündel
Publication year - 2002
Publication title -
journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.451
H-Index - 279
eISSN - 1533-3450
pISSN - 1046-6673
DOI - 10.1681/asn.v133630
Subject(s) - podocin , podocyte , nephrin , synaptopodin , microbiology and biotechnology , slit diaphragm , biology , cell growth , transfection , cell cycle , downregulation and upregulation , cyclin , cell culture , cancer research , cell , genetics , gene , kidney , proteinuria
. Recent molecular insights have established the podocyte as a key component of the glomerular filtration barrier, and hence an important common pathway in proteinuric diseases. A conditionally immortalized human podocyte cell line has been developed by transfection with the temperature-sensitive SV40-T gene. These cells proliferate at the “permissive” temperature (33°C). After transfer to the “nonpermissive” temperature (37°C), they entered growth arrest and expressed markers of differentiated in vivo podocytes, including the novel podocyte proteins, nephrin, podocin, CD2AP, and synaptopodin, and known molecules of the slit diaphragm ZO-1, α-, β-, and γ-catenin and P-cadherin. The differentiation was accompanied by a growth arrest and the upregulation of cyclin-dependent kinase inhibitors, p27 and p57, as well as cyclin D 1 , whereas cyclin A was downregulated. These data are consistent with cell cycle protein expression during podocyte maturation in vivo . In conclusion, the development of this cell line provides a new tool in the study of podocyte biology, which will enable accurate assessment of the behavior of these complex cells in health and disease.
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