Notch signaling is required for normal prostatic epithelial cell proliferation and differentiation.

Détails

ID Serval
serval:BIB_370A35956A4C
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Notch signaling is required for normal prostatic epithelial cell proliferation and differentiation.
Périodique
Developmental Biology
Auteur(s)
Wang X.D., Leow C.C., Zha J., Tang Z., Modrusan Z., Radtke F., Aguet M., de Sauvage F.J., Gao W.Q.
ISSN
0012-1606 (Print)
ISSN-L
0012-1606
Statut éditorial
Publié
Date de publication
2006
Volume
290
Numéro
1
Pages
66-80
Langue
anglais
Résumé
Notch pathway is crucial for stem/progenitor cell maintenance, growth and differentiation in a variety of tissues. Using a transgenic cell ablation approach, we found in our previous study that cells expressing Notch1 are crucial for prostate early development and re-growth. Here, we further define the role of Notch signaling in regulating prostatic epithelial cell growth and differentiation using biochemical and genetic approaches in ex vivo or in vivo systems. Treatment of developing prostate grown in culture with inhibitors of gamma-secretase/presenilin, which is required for Notch cleavage and activation, caused a robust increase in proliferation of epithelial cells co-expressing cytokeratin 8 and 14, lack of luminal/basal layer segregation and dramatically reduced branching morphogenesis. Using conditional Notch1 gene deletion mouse models, we found that inactivation of Notch1 signaling resulted in profound prostatic alterations, including increased tufting, bridging and enhanced epithelial proliferation. Cells within these lesions co-expressed both luminal and basal cell markers, a feature of prostatic epithelial cells in predifferentiation developmental stages. Microarray analysis revealed that the gene expression in a number of genetic networks was altered following Notch1 gene deletion in prostate. Furthermore, expression of Notch1 and its effector Hey-1 gene in human prostate adenocarcinomas were found significantly down-regulated compared to normal control tissues. Taken together, these data suggest that Notch signaling is critical for normal cell proliferation and differentiation in the prostate, and deregulation of this pathway may facilitate prostatic tumorigenesis.
Mots-clé
Amyloid Precursor Protein Secretases, Animals, Animals, Newborn, Aspartic Acid Endopeptidases, Basic Helix-Loop-Helix Transcription Factors/metabolism, Cell Cycle Proteins/metabolism, Cell Differentiation, Cell Proliferation, Cell Transformation, Neoplastic, Cells, Cultured, Down-Regulation, Endopeptidases/metabolism, Epithelial Cells/cytology, Epithelial Cells/metabolism, Humans, Keratins/metabolism, Male, Mice, Mice, Knockout, Morphogenesis, Oligonucleotide Array Sequence Analysis, Prostate/growth &amp, development, Prostate/metabolism, Protease Inhibitors/pharmacology, Receptor, Notch1/genetics, Receptor, Notch1/metabolism, Stem Cells/cytology, Stem Cells/metabolism
Pubmed
Web of science
Open Access
Oui
Création de la notice
28/01/2008 12:39
Dernière modification de la notice
08/05/2019 17:03
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