Cargando…
ADAM10 is expressed in human podocytes and found in urinary vesicles of patients with glomerular kidney diseases
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...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2843607/ https://www.ncbi.nlm.nih.gov/pubmed/20070888 http://dx.doi.org/10.1186/1423-0127-17-3 |
_version_ | 1782179234684338176 |
---|---|
author | Gutwein, Paul Schramme, Anja Abdel-Bakky, Mohamed Sadek Doberstein, Kai Hauser, Ingeborg A Ludwig, Andreas Altevogt, Peter Gauer, Stefan Hillmann, Anja Weide, Thomas Jespersen, Christine Eberhardt, Wolfgang Pfeilschifter, Josef |
author_facet | Gutwein, Paul Schramme, Anja Abdel-Bakky, Mohamed Sadek Doberstein, Kai Hauser, Ingeborg A Ludwig, Andreas Altevogt, Peter Gauer, Stefan Hillmann, Anja Weide, Thomas Jespersen, Christine Eberhardt, Wolfgang Pfeilschifter, Josef |
author_sort | Gutwein, Paul |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2843607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28436072010-03-23 ADAM10 is expressed in human podocytes and found in urinary vesicles of patients with glomerular kidney diseases Gutwein, Paul Schramme, Anja Abdel-Bakky, Mohamed Sadek Doberstein, Kai Hauser, Ingeborg A Ludwig, Andreas Altevogt, Peter Gauer, Stefan Hillmann, Anja Weide, Thomas Jespersen, Christine Eberhardt, Wolfgang Pfeilschifter, Josef J Biomed Sci Research 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. BioMed Central 2010-01-13 /pmc/articles/PMC2843607/ /pubmed/20070888 http://dx.doi.org/10.1186/1423-0127-17-3 Text en Copyright ©2010 Gutwein et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Gutwein, Paul Schramme, Anja Abdel-Bakky, Mohamed Sadek Doberstein, Kai Hauser, Ingeborg A Ludwig, Andreas Altevogt, Peter Gauer, Stefan Hillmann, Anja Weide, Thomas Jespersen, Christine Eberhardt, Wolfgang Pfeilschifter, Josef ADAM10 is expressed in human podocytes and found in urinary vesicles of patients with glomerular kidney diseases |
title | ADAM10 is expressed in human podocytes and found in urinary vesicles of patients with glomerular kidney diseases |
title_full | ADAM10 is expressed in human podocytes and found in urinary vesicles of patients with glomerular kidney diseases |
title_fullStr | ADAM10 is expressed in human podocytes and found in urinary vesicles of patients with glomerular kidney diseases |
title_full_unstemmed | ADAM10 is expressed in human podocytes and found in urinary vesicles of patients with glomerular kidney diseases |
title_short | ADAM10 is expressed in human podocytes and found in urinary vesicles of patients with glomerular kidney diseases |
title_sort | adam10 is expressed in human podocytes and found in urinary vesicles of patients with glomerular kidney diseases |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2843607/ https://www.ncbi.nlm.nih.gov/pubmed/20070888 http://dx.doi.org/10.1186/1423-0127-17-3 |
work_keys_str_mv | AT gutweinpaul adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases AT schrammeanja adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases AT abdelbakkymohamedsadek adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases AT dobersteinkai adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases AT hauseringeborga adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases AT ludwigandreas adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases AT altevogtpeter adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases AT gauerstefan adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases AT hillmannanja adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases AT weidethomas adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases AT jespersenchristine adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases AT eberhardtwolfgang adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases AT pfeilschifterjosef adam10isexpressedinhumanpodocytesandfoundinurinaryvesiclesofpatientswithglomerularkidneydiseases |