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Kolben, T.* ; Perobner, I.* ; Fernsebner, K. ; Lechner, F.* ; Geissler, C.* ; Ruiz-Heinrich, L.* ; Capovilla, S.* ; Jochum, M.* ; Neth, P.*

Dissecting the impact of Frizzled receptors in Wnt/β-catenin signaling of human mesenchymal stem cells.

Biol. Chem. 393, 1433-1447 (2012)
Verlagsversion Volltext DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Wnt/beta-catenin signaling is of fundamental importance in the regulation of self-renewal, migration/invasion, and differentiation of human mesenchymal stem cells (hMSCs). Because little information is available about the function of Frizzled receptors (Fzds) as the main receptors of Wnt proteins in hMSCs, we first performed comparative Fzd mRNA expression profiling. Fzd9 and Fzd10 were not expressed in hMSCs. While Fzd3 was expressed at low levels in hMSCs, the other Fzds exhibited high expression rates. Activation and repression of Wnt signaling in hMSCs revealed that the expression levels of Fzd1, Fzd6, and Fzd7 are positively correlated with the Wnt/beta-catenin activation status, whereas Fzd8 exhibited an inverse relation. For studying the functional relevance of Fzds in Wnt/beta-catenin signaling, RNA interference, ectopic expression studies, and rescue approaches were performed in hMSCs carrying a highly sensitive TCF/LEF reporter gene system (Gaussia luciferase). We found that, Fzd1, Fzd5, Fzd7, and Fzd8 are largely involved in Wnt/beta-catenin signaling of hMSCs. Moreover, the knockdown of Fzd5 can be compensated by the ectopic expression of Fzd7. Conversely, the ectopic expression of Fzd5 in Fzd7-knockdown hMSCs resulted in a rescue of Wnt/beta-catenin signaling, pointing to a functional redundancy of Fzd5 and Fzd7.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Frizzled Receptors (fzds) ; Human Mesenchymal Stem Cells (hmscs) ; Rna Interference ; Tcf/lef Reporter Gene System ; Wnt/beta-catenin Signaling; Protein-coupled Receptors ; Self-renewal ; Osteogenic Differentiation ; Functional-analysis ; Rna Interference ; Binding-sites ; Wnt Proteins ; Bone-marrow ; Expression ; Identification
ISSN (print) / ISBN 1431-6730
e-ISSN 1437-4315
Zeitschrift Biological Chemistry
Quellenangaben Band: 393, Heft: 12, Seiten: 1433-1447 Artikelnummer: , Supplement: ,
Verlag de Gruyter
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Research Unit Analytical BioGeoChemistry (BGC)