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Matrix metalloproteinase 1 modulates invasive behavior of tracheal branches during entry into Drosophila flight muscles
Tubular networks like the vasculature extend branches throughout animal bodies, but how developing vessels interact with and invade tissues is not well understood. We investigated the underlying mechanisms using the developing tracheal tube network of Drosophila indirect flight muscles (IFMs) as a m...
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/PMC6795481/ https://www.ncbi.nlm.nih.gov/pubmed/31577228 http://dx.doi.org/10.7554/eLife.48857 |
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author | Sauerwald, Julia Backer, Wilko Matzat, Till Schnorrer, Frank Luschnig, Stefan |
author_facet | Sauerwald, Julia Backer, Wilko Matzat, Till Schnorrer, Frank Luschnig, Stefan |
author_sort | Sauerwald, Julia |
collection | PubMed |
description | Tubular networks like the vasculature extend branches throughout animal bodies, but how developing vessels interact with and invade tissues is not well understood. We investigated the underlying mechanisms using the developing tracheal tube network of Drosophila indirect flight muscles (IFMs) as a model. Live imaging revealed that tracheal sprouts invade IFMs directionally with growth-cone-like structures at branch tips. Ramification inside IFMs proceeds until tracheal branches fill the myotube. However, individual tracheal cells occupy largely separate territories, possibly mediated by cell-cell repulsion. Matrix metalloproteinase 1 (MMP1) is required in tracheal cells for normal invasion speed and for the dynamic organization of growth-cone-like branch tips. MMP1 remodels the CollagenIV-containing matrix around branch tips, which show differential matrix composition with low CollagenIV levels, while Laminin is present along tracheal branches. Thus, tracheal-derived MMP1 sustains branch invasion by modulating the dynamic behavior of sprouting branches as well as properties of the surrounding matrix. |
format | Online Article Text |
id | pubmed-6795481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-67954812019-10-17 Matrix metalloproteinase 1 modulates invasive behavior of tracheal branches during entry into Drosophila flight muscles Sauerwald, Julia Backer, Wilko Matzat, Till Schnorrer, Frank Luschnig, Stefan eLife Cell Biology Tubular networks like the vasculature extend branches throughout animal bodies, but how developing vessels interact with and invade tissues is not well understood. We investigated the underlying mechanisms using the developing tracheal tube network of Drosophila indirect flight muscles (IFMs) as a model. Live imaging revealed that tracheal sprouts invade IFMs directionally with growth-cone-like structures at branch tips. Ramification inside IFMs proceeds until tracheal branches fill the myotube. However, individual tracheal cells occupy largely separate territories, possibly mediated by cell-cell repulsion. Matrix metalloproteinase 1 (MMP1) is required in tracheal cells for normal invasion speed and for the dynamic organization of growth-cone-like branch tips. MMP1 remodels the CollagenIV-containing matrix around branch tips, which show differential matrix composition with low CollagenIV levels, while Laminin is present along tracheal branches. Thus, tracheal-derived MMP1 sustains branch invasion by modulating the dynamic behavior of sprouting branches as well as properties of the surrounding matrix. eLife Sciences Publications, Ltd 2019-10-02 /pmc/articles/PMC6795481/ /pubmed/31577228 http://dx.doi.org/10.7554/eLife.48857 Text en © 2019, Sauerwald 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 Sauerwald, Julia Backer, Wilko Matzat, Till Schnorrer, Frank Luschnig, Stefan Matrix metalloproteinase 1 modulates invasive behavior of tracheal branches during entry into Drosophila flight muscles |
title | Matrix metalloproteinase 1 modulates invasive behavior of tracheal branches during entry into Drosophila flight muscles |
title_full | Matrix metalloproteinase 1 modulates invasive behavior of tracheal branches during entry into Drosophila flight muscles |
title_fullStr | Matrix metalloproteinase 1 modulates invasive behavior of tracheal branches during entry into Drosophila flight muscles |
title_full_unstemmed | Matrix metalloproteinase 1 modulates invasive behavior of tracheal branches during entry into Drosophila flight muscles |
title_short | Matrix metalloproteinase 1 modulates invasive behavior of tracheal branches during entry into Drosophila flight muscles |
title_sort | matrix metalloproteinase 1 modulates invasive behavior of tracheal branches during entry into drosophila flight muscles |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795481/ https://www.ncbi.nlm.nih.gov/pubmed/31577228 http://dx.doi.org/10.7554/eLife.48857 |
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