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Decoupling from yolk sac is required for extraembryonic tissue spreading in the scuttle fly Megaselia abdita
Extraembryonic tissues contribute to animal development, which often entails spreading over embryo or yolk. Apart from changes in cell shape, the requirements for this tissue spreading are not well understood. Here, we analyze spreading of the extraembryonic serosa in the scuttle fly Megaselia abdit...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231767/ https://www.ncbi.nlm.nih.gov/pubmed/30375972 http://dx.doi.org/10.7554/eLife.34616 |
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author | Caroti, Francesca González Avalos, Everardo Noeske, Viola González Avalos, Paula Kromm, Dimitri Wosch, Maike Schütz, Lucas Hufnagel, Lars Lemke, Steffen |
author_facet | Caroti, Francesca González Avalos, Everardo Noeske, Viola González Avalos, Paula Kromm, Dimitri Wosch, Maike Schütz, Lucas Hufnagel, Lars Lemke, Steffen |
author_sort | Caroti, Francesca |
collection | PubMed |
description | Extraembryonic tissues contribute to animal development, which often entails spreading over embryo or yolk. Apart from changes in cell shape, the requirements for this tissue spreading are not well understood. Here, we analyze spreading of the extraembryonic serosa in the scuttle fly Megaselia abdita. The serosa forms from a columnar blastoderm anlage, becomes a squamous epithelium, and eventually spreads over the embryo proper. We describe the dynamics of this process in long-term, whole-embryo time-lapse recordings, demonstrating that free serosa spreading is preceded by a prolonged pause in tissue expansion. Closer examination of this pause reveals mechanical coupling to the underlying yolk sac, which is later released. We find mechanical coupling prolonged and serosa spreading impaired after knockdown of M. abdita Matrix metalloprotease 1. We conclude that tissue–tissue interactions provide a critical functional element to constrain spreading epithelia. |
format | Online Article Text |
id | pubmed-6231767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-62317672018-11-16 Decoupling from yolk sac is required for extraembryonic tissue spreading in the scuttle fly Megaselia abdita Caroti, Francesca González Avalos, Everardo Noeske, Viola González Avalos, Paula Kromm, Dimitri Wosch, Maike Schütz, Lucas Hufnagel, Lars Lemke, Steffen eLife Developmental Biology Extraembryonic tissues contribute to animal development, which often entails spreading over embryo or yolk. Apart from changes in cell shape, the requirements for this tissue spreading are not well understood. Here, we analyze spreading of the extraembryonic serosa in the scuttle fly Megaselia abdita. The serosa forms from a columnar blastoderm anlage, becomes a squamous epithelium, and eventually spreads over the embryo proper. We describe the dynamics of this process in long-term, whole-embryo time-lapse recordings, demonstrating that free serosa spreading is preceded by a prolonged pause in tissue expansion. Closer examination of this pause reveals mechanical coupling to the underlying yolk sac, which is later released. We find mechanical coupling prolonged and serosa spreading impaired after knockdown of M. abdita Matrix metalloprotease 1. We conclude that tissue–tissue interactions provide a critical functional element to constrain spreading epithelia. eLife Sciences Publications, Ltd 2018-10-30 /pmc/articles/PMC6231767/ /pubmed/30375972 http://dx.doi.org/10.7554/eLife.34616 Text en © 2018, Caroti 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 | Developmental Biology Caroti, Francesca González Avalos, Everardo Noeske, Viola González Avalos, Paula Kromm, Dimitri Wosch, Maike Schütz, Lucas Hufnagel, Lars Lemke, Steffen Decoupling from yolk sac is required for extraembryonic tissue spreading in the scuttle fly Megaselia abdita |
title | Decoupling from yolk sac is required for extraembryonic tissue spreading in the scuttle fly Megaselia abdita |
title_full | Decoupling from yolk sac is required for extraembryonic tissue spreading in the scuttle fly Megaselia abdita |
title_fullStr | Decoupling from yolk sac is required for extraembryonic tissue spreading in the scuttle fly Megaselia abdita |
title_full_unstemmed | Decoupling from yolk sac is required for extraembryonic tissue spreading in the scuttle fly Megaselia abdita |
title_short | Decoupling from yolk sac is required for extraembryonic tissue spreading in the scuttle fly Megaselia abdita |
title_sort | decoupling from yolk sac is required for extraembryonic tissue spreading in the scuttle fly megaselia abdita |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231767/ https://www.ncbi.nlm.nih.gov/pubmed/30375972 http://dx.doi.org/10.7554/eLife.34616 |
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