Reporter gene HEK 293 cells and WNT/Frizzled fusion proteins as tools to study WNT signaling pathways
| Autor: | Iris Peröbner, Peter Neth, Marianne Jochum, Larisa Ring, Marisa Karow, Alexander Faussner |
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| Rok vydání: | 2011 |
| Předmět: |
Reporter gene
Frizzled Base Sequence Recombinant Fusion Proteins Clinical Biochemistry HEK 293 cells Wnt signaling pathway LRP6 LRP5 Biology Biochemistry Frizzled Receptors Cell biology Wnt Proteins HEK293 Cells Genes Reporter Wnt3A Protein Cancer research Humans Signal transduction Wnt Signaling Pathway Molecular Biology WNT3A |
| Zdroj: | bchm. 392:1011-1020 |
| ISSN: | 1437-4315 1431-6730 |
| Popis: | WNT/Frizzled receptor (FZD) signaling pathways are pivotal for physiological and pathophysiological processes. In humans, the complexity of WNT/FZD signaling is based on 19 WNTs, 10 FZDs and at least two (co)receptors (LRP5/6) mediating supposably four different signaling cascades. The detailed investigation of the specific function of the different initiating components is primarily hampered by the lack of most WNT proteins in a purified form. Therefore, we constructed and examined a chimeric protein of WNT3a and FZD4 as a suitable approach to overcome this obstacle for future studies of the specificity of other WNT/FZD combinations. Furthermore, we produced four different reporter HEK 293 cell lines to quantify the induced activation of the proposed signaling cascades, the β-catenin-, the NFAT-, the AP-1- and the CRE-regulated pathways. The chimera WNT3aFZD4 efficiently induced β-catenin-mediated luciferase activity. This activity was increased 40-fold compared with basal when LRP6 was stably cotransfected, proving that the chimera WNT3aFZD4 can also interact efficiently with LRP6. Our results demonstrate that the approach of using reporter gene cell lines in combination with WNT/FZD chimeras is efficient to study the β-catenin-mediated pathway and should also allow clarifying the specificity of WNT/FZD combinations in the activation of the other pathways. |
| Databáze: | OpenAIRE |
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