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Myosin XV is a negative regulator of signaling filopodia during long-range lateral inhibition
The self-organization of cells during development is essential for the formation of healthy tissues, and requires the coordination of cell activities at local scales. Cytonemes, or signaling filopodia, are dynamic actin-based cellular protrusions that allow cells to engage in contact mediated signal...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350058/ https://www.ncbi.nlm.nih.gov/pubmed/37461640 http://dx.doi.org/10.1101/2023.07.07.547992 |
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author | Clements, Rhiannon Smith, Tyler Cowart, Luke Zhumi, Jennifer Sherrod, Alan Cahill, Aidan Hunter, Ginger L |
author_facet | Clements, Rhiannon Smith, Tyler Cowart, Luke Zhumi, Jennifer Sherrod, Alan Cahill, Aidan Hunter, Ginger L |
author_sort | Clements, Rhiannon |
collection | PubMed |
description | The self-organization of cells during development is essential for the formation of healthy tissues, and requires the coordination of cell activities at local scales. Cytonemes, or signaling filopodia, are dynamic actin-based cellular protrusions that allow cells to engage in contact mediated signaling at a distance. While signaling filopodia have been shown to support several signaling paradigms during development, less is understood about how these protrusions are regulated. We investigated the role of the plus-end directed, unconventional MyTH4-FERM myosins in regulating signaling filopodia during sensory bristle patterning on the dorsal thorax of the fruit fly Drosophila melanogaster. We found that Myosin XV is required for regulating signaling filopodia dynamics and, as a consequence, lateral inhibition more broadly throughout the patterning epithelium. We found that Myosin XV is required for limiting the length and number of signaling filopodia generated by bristle precursor cells. Cells with additional and longer signaling filopodia due to loss of Myosin XV are not signaling competent, due to altered levels of Delta ligand and Notch receptor along their lengths. We conclude that Myosin XV acts to negatively regulate signaling filopodia, as well as promote the ability of signaling filopodia to engage in long-range Notch signaling. Since Myosin XV is present across several vertebrate and invertebrate systems, this may have significance for other long-range signaling mechanisms. |
format | Online Article Text |
id | pubmed-10350058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-103500582023-07-17 Myosin XV is a negative regulator of signaling filopodia during long-range lateral inhibition Clements, Rhiannon Smith, Tyler Cowart, Luke Zhumi, Jennifer Sherrod, Alan Cahill, Aidan Hunter, Ginger L bioRxiv Article The self-organization of cells during development is essential for the formation of healthy tissues, and requires the coordination of cell activities at local scales. Cytonemes, or signaling filopodia, are dynamic actin-based cellular protrusions that allow cells to engage in contact mediated signaling at a distance. While signaling filopodia have been shown to support several signaling paradigms during development, less is understood about how these protrusions are regulated. We investigated the role of the plus-end directed, unconventional MyTH4-FERM myosins in regulating signaling filopodia during sensory bristle patterning on the dorsal thorax of the fruit fly Drosophila melanogaster. We found that Myosin XV is required for regulating signaling filopodia dynamics and, as a consequence, lateral inhibition more broadly throughout the patterning epithelium. We found that Myosin XV is required for limiting the length and number of signaling filopodia generated by bristle precursor cells. Cells with additional and longer signaling filopodia due to loss of Myosin XV are not signaling competent, due to altered levels of Delta ligand and Notch receptor along their lengths. We conclude that Myosin XV acts to negatively regulate signaling filopodia, as well as promote the ability of signaling filopodia to engage in long-range Notch signaling. Since Myosin XV is present across several vertebrate and invertebrate systems, this may have significance for other long-range signaling mechanisms. Cold Spring Harbor Laboratory 2023-07-07 /pmc/articles/PMC10350058/ /pubmed/37461640 http://dx.doi.org/10.1101/2023.07.07.547992 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Clements, Rhiannon Smith, Tyler Cowart, Luke Zhumi, Jennifer Sherrod, Alan Cahill, Aidan Hunter, Ginger L Myosin XV is a negative regulator of signaling filopodia during long-range lateral inhibition |
title | Myosin XV is a negative regulator of signaling filopodia during long-range lateral inhibition |
title_full | Myosin XV is a negative regulator of signaling filopodia during long-range lateral inhibition |
title_fullStr | Myosin XV is a negative regulator of signaling filopodia during long-range lateral inhibition |
title_full_unstemmed | Myosin XV is a negative regulator of signaling filopodia during long-range lateral inhibition |
title_short | Myosin XV is a negative regulator of signaling filopodia during long-range lateral inhibition |
title_sort | myosin xv is a negative regulator of signaling filopodia during long-range lateral inhibition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350058/ https://www.ncbi.nlm.nih.gov/pubmed/37461640 http://dx.doi.org/10.1101/2023.07.07.547992 |
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