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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...

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Autores principales: Caroti, Francesca, González Avalos, Everardo, Noeske, Viola, González Avalos, Paula, Kromm, Dimitri, Wosch, Maike, Schütz, Lucas, Hufnagel, Lars, Lemke, Steffen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
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.
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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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