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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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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. |
format | Online Article Text |
id | pubmed-6365057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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