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Light-activated Frizzled7 reveals a permissive role of non-canonical wnt signaling in mesendoderm cell migration

Non-canonical Wnt signaling plays a central role for coordinated cell polarization and directed migration in metazoan development. While spatiotemporally restricted activation of non-canonical Wnt-signaling drives cell polarization in epithelial tissues, it remains unclear whether such instructive a...

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Autores principales: Čapek, Daniel, Smutny, Michael, Tichy, Alexandra-Madelaine, Morri, Maurizio, Janovjak, Harald, Heisenberg, Carl-Philipp
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365057/
https://www.ncbi.nlm.nih.gov/pubmed/30648973
http://dx.doi.org/10.7554/eLife.42093
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author Čapek, Daniel
Smutny, Michael
Tichy, Alexandra-Madelaine
Morri, Maurizio
Janovjak, Harald
Heisenberg, Carl-Philipp
author_facet Čapek, Daniel
Smutny, Michael
Tichy, Alexandra-Madelaine
Morri, Maurizio
Janovjak, Harald
Heisenberg, Carl-Philipp
author_sort Čapek, Daniel
collection PubMed
description Non-canonical Wnt signaling plays a central role for coordinated cell polarization and directed migration in metazoan development. While spatiotemporally restricted activation of non-canonical Wnt-signaling drives cell polarization in epithelial tissues, it remains unclear whether such instructive activity is also critical for directed mesenchymal cell migration. Here, we developed a light-activated version of the non-canonical Wnt receptor Frizzled 7 (Fz7) to analyze how restricted activation of non-canonical Wnt signaling affects directed anterior axial mesendoderm (prechordal plate, ppl) cell migration within the zebrafish gastrula. We found that Fz7 signaling is required for ppl cell protrusion formation and migration and that spatiotemporally restricted ectopic activation is capable of redirecting their migration. Finally, we show that uniform activation of Fz7 signaling in ppl cells fully rescues defective directed cell migration in fz7 mutant embryos. Together, our findings reveal that in contrast to the situation in epithelial cells, non-canonical Wnt signaling functions permissively rather than instructively in directed mesenchymal cell migration during gastrulation.
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spelling pubmed-63650572019-02-07 Light-activated Frizzled7 reveals a permissive role of non-canonical wnt signaling in mesendoderm cell migration Čapek, Daniel Smutny, Michael Tichy, Alexandra-Madelaine Morri, Maurizio Janovjak, Harald Heisenberg, Carl-Philipp eLife Cell Biology Non-canonical Wnt signaling plays a central role for coordinated cell polarization and directed migration in metazoan development. While spatiotemporally restricted activation of non-canonical Wnt-signaling drives cell polarization in epithelial tissues, it remains unclear whether such instructive activity is also critical for directed mesenchymal cell migration. Here, we developed a light-activated version of the non-canonical Wnt receptor Frizzled 7 (Fz7) to analyze how restricted activation of non-canonical Wnt signaling affects directed anterior axial mesendoderm (prechordal plate, ppl) cell migration within the zebrafish gastrula. We found that Fz7 signaling is required for ppl cell protrusion formation and migration and that spatiotemporally restricted ectopic activation is capable of redirecting their migration. Finally, we show that uniform activation of Fz7 signaling in ppl cells fully rescues defective directed cell migration in fz7 mutant embryos. Together, our findings reveal that in contrast to the situation in epithelial cells, non-canonical Wnt signaling functions permissively rather than instructively in directed mesenchymal cell migration during gastrulation. eLife Sciences Publications, Ltd 2019-01-16 /pmc/articles/PMC6365057/ /pubmed/30648973 http://dx.doi.org/10.7554/eLife.42093 Text en © 2019, Čapek et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Čapek, Daniel
Smutny, Michael
Tichy, Alexandra-Madelaine
Morri, Maurizio
Janovjak, Harald
Heisenberg, Carl-Philipp
Light-activated Frizzled7 reveals a permissive role of non-canonical wnt signaling in mesendoderm cell migration
title Light-activated Frizzled7 reveals a permissive role of non-canonical wnt signaling in mesendoderm cell migration
title_full Light-activated Frizzled7 reveals a permissive role of non-canonical wnt signaling in mesendoderm cell migration
title_fullStr Light-activated Frizzled7 reveals a permissive role of non-canonical wnt signaling in mesendoderm cell migration
title_full_unstemmed Light-activated Frizzled7 reveals a permissive role of non-canonical wnt signaling in mesendoderm cell migration
title_short Light-activated Frizzled7 reveals a permissive role of non-canonical wnt signaling in mesendoderm cell migration
title_sort light-activated frizzled7 reveals a permissive role of non-canonical wnt signaling in mesendoderm cell migration
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365057/
https://www.ncbi.nlm.nih.gov/pubmed/30648973
http://dx.doi.org/10.7554/eLife.42093
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