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rebuff regulates apical luminal matrix to control tube size in Drosophila trachea
The Drosophila embryonic tracheal network is an excellent model to study tube size. The chitin-based apical luminal matrix and cell polarity are well known to regulate tube size in Drosophila trachea. Defects in luminal matrix and cell polarity lead to tube overexpansion. Here, we address the novel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176944/ https://www.ncbi.nlm.nih.gov/pubmed/30185423 http://dx.doi.org/10.1242/bio.036848 |
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author | Chandran, Rachana R. Scholl, Aaron Yang, Yuyang Jiang, Lan |
author_facet | Chandran, Rachana R. Scholl, Aaron Yang, Yuyang Jiang, Lan |
author_sort | Chandran, Rachana R. |
collection | PubMed |
description | The Drosophila embryonic tracheal network is an excellent model to study tube size. The chitin-based apical luminal matrix and cell polarity are well known to regulate tube size in Drosophila trachea. Defects in luminal matrix and cell polarity lead to tube overexpansion. Here, we address the novel function of the rebuff (reb) gene, which encodes an evolutionarily conserved Smad-like protein. In reb mutants, tracheal tubes are moderately over-elongated. Despite the establishment of normal cell polarity, we observed significantly reduced apical luminal matrix in reb mutants. Among various luminal components, luminal Obstructor-A (ObstA) is drastically reduced. Interestingly, ObstA is localized in vesicle-like structures that are apically concentrated in reb mutants. To investigate the possibility that reb is involved in the endocytosis of ObstA, we analyzed the co-localization of ObstA and endocytic markers in reb mutants. We observed that ObstA is localized in late endosomes and recycling endosomes. This suggests that in reb mutant trachea, endocytosed ObstA is degraded or recycled back to the apical region. However, ObstA vesicles are retained in the apical region and are failed to be secreted to the lumen. Taken together, these results suggest one function of reb is regulating the endocytosis of luminal matrix components. |
format | Online Article Text |
id | pubmed-6176944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61769442018-10-11 rebuff regulates apical luminal matrix to control tube size in Drosophila trachea Chandran, Rachana R. Scholl, Aaron Yang, Yuyang Jiang, Lan Biol Open Research Article The Drosophila embryonic tracheal network is an excellent model to study tube size. The chitin-based apical luminal matrix and cell polarity are well known to regulate tube size in Drosophila trachea. Defects in luminal matrix and cell polarity lead to tube overexpansion. Here, we address the novel function of the rebuff (reb) gene, which encodes an evolutionarily conserved Smad-like protein. In reb mutants, tracheal tubes are moderately over-elongated. Despite the establishment of normal cell polarity, we observed significantly reduced apical luminal matrix in reb mutants. Among various luminal components, luminal Obstructor-A (ObstA) is drastically reduced. Interestingly, ObstA is localized in vesicle-like structures that are apically concentrated in reb mutants. To investigate the possibility that reb is involved in the endocytosis of ObstA, we analyzed the co-localization of ObstA and endocytic markers in reb mutants. We observed that ObstA is localized in late endosomes and recycling endosomes. This suggests that in reb mutant trachea, endocytosed ObstA is degraded or recycled back to the apical region. However, ObstA vesicles are retained in the apical region and are failed to be secreted to the lumen. Taken together, these results suggest one function of reb is regulating the endocytosis of luminal matrix components. The Company of Biologists Ltd 2018-09-15 /pmc/articles/PMC6176944/ /pubmed/30185423 http://dx.doi.org/10.1242/bio.036848 Text en © 2018. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Chandran, Rachana R. Scholl, Aaron Yang, Yuyang Jiang, Lan rebuff regulates apical luminal matrix to control tube size in Drosophila trachea |
title | rebuff regulates apical luminal matrix to control tube size in Drosophila trachea |
title_full | rebuff regulates apical luminal matrix to control tube size in Drosophila trachea |
title_fullStr | rebuff regulates apical luminal matrix to control tube size in Drosophila trachea |
title_full_unstemmed | rebuff regulates apical luminal matrix to control tube size in Drosophila trachea |
title_short | rebuff regulates apical luminal matrix to control tube size in Drosophila trachea |
title_sort | rebuff regulates apical luminal matrix to control tube size in drosophila trachea |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176944/ https://www.ncbi.nlm.nih.gov/pubmed/30185423 http://dx.doi.org/10.1242/bio.036848 |
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