Document Detail


The regenerative potential of the kidney: what can we learn from developmental biology?
MedLine Citation:
PMID:  20714827     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Cell turnover in the healthy adult kidney is very slow but the kidney has a strong capacity for regeneration after acute injury. Although many molecular aspects of this process have been clarified, the source of the newly-formed renal epithelial cells is still being debated. Several studies have shown, moreover, that the repair of injured renal epithelium starts from mature tubular cells, which enter into an activated proliferative state characterized by the reappearance of mesenchymal markers detectable during nephrogenesis, thus pointing to a marked plasticity of renal epithelial cells. The regenerative potential of mature epithelial cells might stem from their almost unique morphogenetic process. Unlike other tubular organs, all epithelial and mesenchymal cells in the kidney derive from the same germ layer, the mesoderm. In a fascinating view of vertebrate embryogenesis, the mesoderm might be seen as a cell layer capable of oscillating between epithelial and mesenchymal states, thus acquiring a remarkable plasticity that lends it an extended potential for innovation and a better control of three-dimensional body organization. The renal papilla contains a population of cells with the characteristic of adult stem cells. Mesenchymal stromal stem cells (MSC) have been found to reside in the connective tissue of most organs, including the kidney. Recent studies indicate that the MSC compartment extends throughout the body postnatally as a result of its perivascular location. Developmental biology suggests that this might be particularly true of the kidney and that the papilla might represent the perivascular renal stem cell niche. The perivascular niche hypothesis fits well with the evolving concept of the stem cell niche as an entity of action. It is its dynamic capability that makes the niche concept so important and essential to the feasibility of regenerative medicine.
Authors:
Franca Anglani; Federica Mezzabotta; Monica Ceol; Rosalba Cristofaro; Dorella Del Prete; Angela D'Angelo
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Stem cell reviews     Volume:  6     ISSN:  1558-6804     ISO Abbreviation:  Stem Cell Rev     Publication Date:  2010 Dec 
Date Detail:
Created Date:  2010-10-04     Completed Date:  2011-01-20     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101255952     Medline TA:  Stem Cell Rev     Country:  United States    
Other Details:
Languages:  eng     Pagination:  650-7     Citation Subset:  IM    
Affiliation:
Laboratory of Kidney Histomorphology and Molecular Biology, Department of Medical and Surgical Sciences, University of Padua, Padua, Italy. franca.anglani@unipd.it
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MeSH Terms
Descriptor/Qualifier:
Animals
Developmental Biology
Humans
Kidney / cytology*,  growth & development
Models, Biological
Pericytes / cytology
Regeneration / physiology*
Stem Cells / cytology

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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