Helmholtz Gemeinschaft


Podocyte-specific deletion of murine CXADR does not impair podocyte development, function or stress response

[img] PDF - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader

Item Type:Article
Title:Podocyte-specific deletion of murine CXADR does not impair podocyte development, function or stress response
Creators Name:Schell, C. and Kretz, O. and Bregenzer, A. and Rogg, M. and Helmstädter, M. and Lisewski, U. and Gotthardt, M. and Tharaux, P.L. and Huber, T.B. and Grahammer, F.
Abstract:The coxsackie- and adenovirus receptor (CXADR) is a member of the immunoglobulin protein superfamily, present in various epithelial cells including glomerular epithelial cells. Beside its known function as a virus receptor, it also constitutes an integral part of cell-junctions. Previous studies in the zebrafish pronephros postulated a potential role of CXADR for the terminal differentiation of glomerular podocytes and correct patterning of the elaborated foot process architecture. However, due to early embryonic lethality of constitutive Cxadr knockout mice, mammalian data on kidney epithelial cells have been lacking. Interestingly, Cxadr is robustly expressed during podocyte development and in adulthood in response to glomerular injury. We therefore used a conditional transgenic approach to elucidate the function of Cxadr for podocyte development and stress response. Surprisingly, we could not discern a developmental phenotype in podocyte specific Cxadr knock-out mice. In addition, despite a significant up regulation of CXADR during toxic, genetic and immunologic podocyte injury, we could not detect any impact of Cxadr on these injury models. Thus these data indicate that in contrast to lower vertebrate models, mammalian podocytes have acquired molecular programs to compensate for the loss of Cxadr.
Keywords:Coxsackie and Adenovirus Receptor-Like Membrane Protein, Gene Deletion, Gene Expression, Gene Knockout Techniques, Kidney, Kidney Glomerulus, Knockout Mice, Physiological Stress, Podocytes, Animals, Mice
Source:PLoS ONE
Publisher:Public Library of Science
Page Range:e0129424
Date:15 June 2015
Official Publication:https://doi.org/10.1371/journal.pone.0129424
PubMed:View item in PubMed

Repository Staff Only: item control page


Downloads per month over past year

Open Access
MDC Library