Cargando…
Deciphering the roles of cell shape and Fat and Dachsous planar polarity in arranging the Drosophila apical microtubule network through quantitative image analysis
In epithelial cells, planar polarization of subapical microtubule networks is thought to be important for both breaking cellular symmetry and maintaining the resulting cellular polarity. Studies in the Drosophila pupal wing and other tissues have suggested two alternative mechanisms for specifying n...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10208094/ https://www.ncbi.nlm.nih.gov/pubmed/36735484 http://dx.doi.org/10.1091/mbc.E22-09-0442 |
_version_ | 1785046598696304640 |
---|---|
author | Ramírez-Moreno, Miguel Hunton, Robert Strutt, David Bulgakova, Natalia A. |
author_facet | Ramírez-Moreno, Miguel Hunton, Robert Strutt, David Bulgakova, Natalia A. |
author_sort | Ramírez-Moreno, Miguel |
collection | PubMed |
description | In epithelial cells, planar polarization of subapical microtubule networks is thought to be important for both breaking cellular symmetry and maintaining the resulting cellular polarity. Studies in the Drosophila pupal wing and other tissues have suggested two alternative mechanisms for specifying network polarity. On one hand, mechanical strain and/or cell shape have been implicated as key determinants; on the other hand, the Fat-Dachsous planar polarity pathway has been suggested to be the primary polarizing cue. Using quantitative image analysis in the pupal wing, we reassess these models. We found that cell shape was a strong predictor of microtubule organization in the developing wing epithelium. Conversely, Fat-Dachsous polarity cues do not play any direct role in the organization of the subapical microtubule network, despite being able to weakly recruit the microtubule minus-end capping protein Patronin to cell boundaries. We conclude that any effect of Fat-Dachsous on microtubule polarity is likely to be indirect, via their known ability to regulate cell shape. |
format | Online Article Text |
id | pubmed-10208094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-102080942023-07-20 Deciphering the roles of cell shape and Fat and Dachsous planar polarity in arranging the Drosophila apical microtubule network through quantitative image analysis Ramírez-Moreno, Miguel Hunton, Robert Strutt, David Bulgakova, Natalia A. Mol Biol Cell Articles In epithelial cells, planar polarization of subapical microtubule networks is thought to be important for both breaking cellular symmetry and maintaining the resulting cellular polarity. Studies in the Drosophila pupal wing and other tissues have suggested two alternative mechanisms for specifying network polarity. On one hand, mechanical strain and/or cell shape have been implicated as key determinants; on the other hand, the Fat-Dachsous planar polarity pathway has been suggested to be the primary polarizing cue. Using quantitative image analysis in the pupal wing, we reassess these models. We found that cell shape was a strong predictor of microtubule organization in the developing wing epithelium. Conversely, Fat-Dachsous polarity cues do not play any direct role in the organization of the subapical microtubule network, despite being able to weakly recruit the microtubule minus-end capping protein Patronin to cell boundaries. We conclude that any effect of Fat-Dachsous on microtubule polarity is likely to be indirect, via their known ability to regulate cell shape. The American Society for Cell Biology 2023-05-05 /pmc/articles/PMC10208094/ /pubmed/36735484 http://dx.doi.org/10.1091/mbc.E22-09-0442 Text en © 2023 Ramirez-Moreno et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial-Share Alike 4.0 International Creative Commons License. |
spellingShingle | Articles Ramírez-Moreno, Miguel Hunton, Robert Strutt, David Bulgakova, Natalia A. Deciphering the roles of cell shape and Fat and Dachsous planar polarity in arranging the Drosophila apical microtubule network through quantitative image analysis |
title | Deciphering the roles of cell shape and Fat and Dachsous planar polarity in arranging the Drosophila apical microtubule network through quantitative image analysis |
title_full | Deciphering the roles of cell shape and Fat and Dachsous planar polarity in arranging the Drosophila apical microtubule network through quantitative image analysis |
title_fullStr | Deciphering the roles of cell shape and Fat and Dachsous planar polarity in arranging the Drosophila apical microtubule network through quantitative image analysis |
title_full_unstemmed | Deciphering the roles of cell shape and Fat and Dachsous planar polarity in arranging the Drosophila apical microtubule network through quantitative image analysis |
title_short | Deciphering the roles of cell shape and Fat and Dachsous planar polarity in arranging the Drosophila apical microtubule network through quantitative image analysis |
title_sort | deciphering the roles of cell shape and fat and dachsous planar polarity in arranging the drosophila apical microtubule network through quantitative image analysis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10208094/ https://www.ncbi.nlm.nih.gov/pubmed/36735484 http://dx.doi.org/10.1091/mbc.E22-09-0442 |
work_keys_str_mv | AT ramirezmorenomiguel decipheringtherolesofcellshapeandfatanddachsousplanarpolarityinarrangingthedrosophilaapicalmicrotubulenetworkthroughquantitativeimageanalysis AT huntonrobert decipheringtherolesofcellshapeandfatanddachsousplanarpolarityinarrangingthedrosophilaapicalmicrotubulenetworkthroughquantitativeimageanalysis AT struttdavid decipheringtherolesofcellshapeandfatanddachsousplanarpolarityinarrangingthedrosophilaapicalmicrotubulenetworkthroughquantitativeimageanalysis AT bulgakovanataliaa decipheringtherolesofcellshapeandfatanddachsousplanarpolarityinarrangingthedrosophilaapicalmicrotubulenetworkthroughquantitativeimageanalysis |