Cargando…

Stem Cell Factor Expression after Renal Ischemia Promotes Tubular Epithelial Survival

BACKGROUND: Renal ischemia leads to apoptosis of tubular epithelial cells and results in decreased renal function. Tissue repair involves re-epithelialization of the tubular basement membrane. Survival of the tubular epithelium following ischemia is therefore important in the successful regeneration...

Descripción completa

Detalles Bibliográficos
Autores principales: Stokman, Geurt, Stroo, Ingrid, Claessen, Nike, Teske, Gwendoline J. D., Weening, Jan J., Leemans, Jaklien C., Florquin, Sandrine
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006174/
https://www.ncbi.nlm.nih.gov/pubmed/21200435
http://dx.doi.org/10.1371/journal.pone.0014386
_version_ 1782194168350638080
author Stokman, Geurt
Stroo, Ingrid
Claessen, Nike
Teske, Gwendoline J. D.
Weening, Jan J.
Leemans, Jaklien C.
Florquin, Sandrine
author_facet Stokman, Geurt
Stroo, Ingrid
Claessen, Nike
Teske, Gwendoline J. D.
Weening, Jan J.
Leemans, Jaklien C.
Florquin, Sandrine
author_sort Stokman, Geurt
collection PubMed
description BACKGROUND: Renal ischemia leads to apoptosis of tubular epithelial cells and results in decreased renal function. Tissue repair involves re-epithelialization of the tubular basement membrane. Survival of the tubular epithelium following ischemia is therefore important in the successful regeneration of renal tissue. The cytokine stem cell factor (SCF) has been shown to protect the tubular epithelium against apoptosis. METHODOLOGY/PRINCIPAL FINDINGS: In a mouse model for renal ischemia/reperfusion injury, we studied how expression of c-KIT on tubular epithelium and its ligand SCF protect cells against apoptosis. Administration of SCF specific antisense oligonucleotides significantly decreased specific staining of SCF following ischemia. Reduced SCF expression resulted in impaired renal function, increased tubular damage and increased tubular epithelial apoptosis, independent of inflammation. In an in vitro hypoxia model, stimulation of tubular epithelial cells with SCF activated survival signaling and decreased apoptosis. CONCLUSIONS/SIGNIFICANCE: Our data indicate an important role for c-KIT and SCF in mediating tubular epithelial cell survival via an autocrine pathway.
format Text
id pubmed-3006174
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-30061742011-01-03 Stem Cell Factor Expression after Renal Ischemia Promotes Tubular Epithelial Survival Stokman, Geurt Stroo, Ingrid Claessen, Nike Teske, Gwendoline J. D. Weening, Jan J. Leemans, Jaklien C. Florquin, Sandrine PLoS One Research Article BACKGROUND: Renal ischemia leads to apoptosis of tubular epithelial cells and results in decreased renal function. Tissue repair involves re-epithelialization of the tubular basement membrane. Survival of the tubular epithelium following ischemia is therefore important in the successful regeneration of renal tissue. The cytokine stem cell factor (SCF) has been shown to protect the tubular epithelium against apoptosis. METHODOLOGY/PRINCIPAL FINDINGS: In a mouse model for renal ischemia/reperfusion injury, we studied how expression of c-KIT on tubular epithelium and its ligand SCF protect cells against apoptosis. Administration of SCF specific antisense oligonucleotides significantly decreased specific staining of SCF following ischemia. Reduced SCF expression resulted in impaired renal function, increased tubular damage and increased tubular epithelial apoptosis, independent of inflammation. In an in vitro hypoxia model, stimulation of tubular epithelial cells with SCF activated survival signaling and decreased apoptosis. CONCLUSIONS/SIGNIFICANCE: Our data indicate an important role for c-KIT and SCF in mediating tubular epithelial cell survival via an autocrine pathway. Public Library of Science 2010-12-21 /pmc/articles/PMC3006174/ /pubmed/21200435 http://dx.doi.org/10.1371/journal.pone.0014386 Text en Stokman et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Stokman, Geurt
Stroo, Ingrid
Claessen, Nike
Teske, Gwendoline J. D.
Weening, Jan J.
Leemans, Jaklien C.
Florquin, Sandrine
Stem Cell Factor Expression after Renal Ischemia Promotes Tubular Epithelial Survival
title Stem Cell Factor Expression after Renal Ischemia Promotes Tubular Epithelial Survival
title_full Stem Cell Factor Expression after Renal Ischemia Promotes Tubular Epithelial Survival
title_fullStr Stem Cell Factor Expression after Renal Ischemia Promotes Tubular Epithelial Survival
title_full_unstemmed Stem Cell Factor Expression after Renal Ischemia Promotes Tubular Epithelial Survival
title_short Stem Cell Factor Expression after Renal Ischemia Promotes Tubular Epithelial Survival
title_sort stem cell factor expression after renal ischemia promotes tubular epithelial survival
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006174/
https://www.ncbi.nlm.nih.gov/pubmed/21200435
http://dx.doi.org/10.1371/journal.pone.0014386
work_keys_str_mv AT stokmangeurt stemcellfactorexpressionafterrenalischemiapromotestubularepithelialsurvival
AT strooingrid stemcellfactorexpressionafterrenalischemiapromotestubularepithelialsurvival
AT claessennike stemcellfactorexpressionafterrenalischemiapromotestubularepithelialsurvival
AT teskegwendolinejd stemcellfactorexpressionafterrenalischemiapromotestubularepithelialsurvival
AT weeningjanj stemcellfactorexpressionafterrenalischemiapromotestubularepithelialsurvival
AT leemansjaklienc stemcellfactorexpressionafterrenalischemiapromotestubularepithelialsurvival
AT florquinsandrine stemcellfactorexpressionafterrenalischemiapromotestubularepithelialsurvival