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Expression and subcellular distribution of novel glomerulus-associated proteins dendrin, ehd3, sh2d4a, plekhh2, and 2310066E14Rik
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2007 (English)In: Journal of the American Society of Nephrology, ISSN 1046-6673, Vol. 18, no 3, 689-697 p.Article in journal (Refereed) Published
Abstract [en]

The glomerular capillary tuft is a highly specialized microcapillary that is dedicated to function as a sophisticated molecular sieve. The glomerulus filter has a unique molecular composition, and several essential glomerular proteins are expressed in the kidney exclusively by glomerular podocytes. A catalog of > 300 glomerulus-upregulated transcripts that were identified using expressed sequence tag profiling and microarray analysis was published recently. This study characterized the expression profile of five glomerulus-upregulated transcripts/proteins (ehd3, dendrin, sh2d4a, plekhh2, and 2310066E14Rik) in detail. The expression pattern of these novel glomerular transcripts in various mouse tissues was studied using reverse transcriptase-PCR, Northern blotting, and in situ hybridization. For studying the distribution of corresponding proteins, polyclonal antibodies were raised against the gene products, and Western blotting, immunofluorescence, and immunoelectron microscopic analyses were performed. Remarkably, it was discovered that all five transcripts/proteins were expressed in the kidney exclusively by glomerular cells. Ehd3 was expressed only by glomerular endothelial cells. Importantly, ehd3 is the first gene ever shown to be expressed exclusively by glomerular endothelial cells and not by other endothelial cells in the kidney. Dendrin, sh2d4a, plekhh2, and 2310066E14Rik, however, were transcribed solely by podocytes. With the use of polyclonal antibodies, dendrin, sh2d4a, and plekhh2 proteins were localized to the slit diaphragm and the foot process, whereas 2310066E14Rik protein was localized to the podocyte major processes and cell body. This study provides fresh insights into glomerular biology and uncovers new possibilities to explore the role of these novel proteins in the glomerular physiology and pathology.

Place, publisher, year, edition, pages
2007. Vol. 18, no 3, 689-697 p.
Keyword [en]
congenital nephrotic syndrome, pleckstrin homology domains, mice lacking, perinatal lethality, messenger-rna, nephrin, actin, podocytes, kidney, membrane
URN: urn:nbn:se:kth:diva-16572DOI: 10.1681/asn.2006060675ISI: 000245873400008ScopusID: 2-s2.0-33947232065OAI: diva2:334614
QC 20100525Available from: 2010-08-05 Created: 2010-08-05Bibliographically approved

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Al-Khalili Szigyarto, CristinaUhlén, Mathias
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