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ADAM10 is expressed in human podocytes and found in urinary vesicles of patients with glomerular kidney diseases

Paul Gutwein email, Anja Schramme email, Mohamed SADEK Abdel-Bakky email, Kai Doberstein email, Ingeborg A Hauser email, Andreas Ludwig email, Peter Altevogt email, Stefan Gauer email, Anja Hillmann email, Thomas Weide email, Chrsitine Jespersen email, Wolfgang Eberhardt email and Josef Pfeilschifter email

Journal of Biomedical Science 2010, 17:3doi:10.1186/1423-0127-17-3

Published: 13 January 2010

Abstract (provisional)

Background

The importance of the Notch signaling in the development of glomerular diseases has been recently described. Therefore we analyzed in podocytes the expression and activity of ADAM10, one important component of the Notch signaling complex.

Methods

By Western blot, immunofluorescence and immunohistochemistry analysis we characterized the expression of ADAM10 in human podocytes, human urine and human renal tissue.

Results

We present evidence, that differentiated human podocytes possessed increased amounts of mature ADAM10 and released elevated levels of L1 adhesion molecule, one well known substrate of ADAM10. By using specific siRNA and metalloproteinase inhibitors we demonstrate that ADAM10 is involved in the cleavage of L1 in human podocytes. Injury of podocytes enhanced the ADAM10 mediated cleavage of L1. In addition, we detected ADAM10 in urinary podocytes from patients with kidney diseases and in tissue sections of normal human kidney. Finally, we found elevated levels of ADAM10 in urinary vesicles of patients with glomerular kidney diseases.

Conclusions

The activity of ADAM10 in human podocytes may play an important role in the development of glomerular kidney diseases.

The complete article is available as a provisional PDF. The fully formatted PDF and HTML versions are in production.


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