Document Detail


Genetics of nephrotic syndrome: new insights into molecules acting at the glomerular filtration barrier.
MedLine Citation:
PMID:  19649571     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Nephrotic syndrome is caused by increased permeability of the glomerular filtration barrier for macromolecules. The identification of mutations of various podocyte-expressed proteins as causes of familial nephrotic syndrome has significantly contributed to shedding light into the molecular pathogenesis of nephrotic proteinuria and into the physiology of the glomerular sieve. More recent findings have changed our conception of the glomerular filtration barrier from a relatively static structure to a highly dynamic one. Both the multiprotein slit diaphragm complex around nephrin and the integrin receptor complex that mediates binding of the podocyte to the glomerular basement membrane, may translate outside-inside signaling and lead to podocyte actin cytoskeleton rearrangement. This may enable the podocyte network to adapt to environmental changes and respond to injury. Disturbance in these processes may not only be involved in the pathogenesis of hereditary nephrotic syndrome but also in that of more common acquired proteinuric diseases. Elucidation of the molecular mechanisms involved will possibly open the way to new therapeutic approaches.
Authors:
Martin Zenker; Eduardo Machuca; Corinne Antignac
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review     Date:  2009-08-01
Journal Detail:
Title:  Journal of molecular medicine (Berlin, Germany)     Volume:  87     ISSN:  1432-1440     ISO Abbreviation:  J. Mol. Med.     Publication Date:  2009 Sep 
Date Detail:
Created Date:  2009-08-17     Completed Date:  2009-11-16     Revised Date:  2011-07-08    
Medline Journal Info:
Nlm Unique ID:  9504370     Medline TA:  J Mol Med (Berl)     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  849-57     Citation Subset:  IM    
Affiliation:
Institute of Human Genetics, University Hospital Erlangen, University of Erlangen-Nuremberg, Schwabachanlage 10, 91054, Erlangen, Germany, mzenker@humgenet.uni-erlangen.de
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MeSH Terms
Descriptor/Qualifier:
Cytoskeleton
Humans
Kidney Glomerulus / physiology*
Nephrotic Syndrome / genetics*
Permeability
Podocytes / ultrastructure

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