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Cytonemes with complex geometries and composition extend into invaginations of target cells
Cytonemes are specialized filopodia that mediate paracrine signaling in Drosophila and other animals. Studies using fluorescence confocal microscopy (CM) established their general paths, cell targets, and essential roles in signaling. To investigate details unresolvable by CM, we used high-pressure...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980254/ https://www.ncbi.nlm.nih.gov/pubmed/33734293 http://dx.doi.org/10.1083/jcb.202101116 |
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author | Wood, Brent M. Baena, Valentina Huang, Hai Jorgens, Danielle M. Terasaki, Mark Kornberg, Thomas B. |
author_facet | Wood, Brent M. Baena, Valentina Huang, Hai Jorgens, Danielle M. Terasaki, Mark Kornberg, Thomas B. |
author_sort | Wood, Brent M. |
collection | PubMed |
description | Cytonemes are specialized filopodia that mediate paracrine signaling in Drosophila and other animals. Studies using fluorescence confocal microscopy (CM) established their general paths, cell targets, and essential roles in signaling. To investigate details unresolvable by CM, we used high-pressure freezing and EM to visualize cytoneme structures, paths, contents, and contacts. We observed cytonemes previously seen by CM in the Drosophila wing imaginal disc system, including disc, tracheal air sac primordium (ASP), and myoblast cytonemes, and identified cytonemes extending into invaginations of target cells, and cytonemes connecting ASP cells and connecting myoblasts. Diameters of cytoneme shafts vary between repeating wide (206 ± 51.8 nm) and thin (55.9 ± 16.2 nm) segments. Actin, ribosomes, and membranous compartments are present throughout; rough ER and mitochondria are in wider proximal sections. These results reveal novel structural features of filopodia and provide a basis for understanding cytoneme cell biology and function. |
format | Online Article Text |
id | pubmed-7980254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79802542021-11-03 Cytonemes with complex geometries and composition extend into invaginations of target cells Wood, Brent M. Baena, Valentina Huang, Hai Jorgens, Danielle M. Terasaki, Mark Kornberg, Thomas B. J Cell Biol Article Cytonemes are specialized filopodia that mediate paracrine signaling in Drosophila and other animals. Studies using fluorescence confocal microscopy (CM) established their general paths, cell targets, and essential roles in signaling. To investigate details unresolvable by CM, we used high-pressure freezing and EM to visualize cytoneme structures, paths, contents, and contacts. We observed cytonemes previously seen by CM in the Drosophila wing imaginal disc system, including disc, tracheal air sac primordium (ASP), and myoblast cytonemes, and identified cytonemes extending into invaginations of target cells, and cytonemes connecting ASP cells and connecting myoblasts. Diameters of cytoneme shafts vary between repeating wide (206 ± 51.8 nm) and thin (55.9 ± 16.2 nm) segments. Actin, ribosomes, and membranous compartments are present throughout; rough ER and mitochondria are in wider proximal sections. These results reveal novel structural features of filopodia and provide a basis for understanding cytoneme cell biology and function. Rockefeller University Press 2021-03-18 /pmc/articles/PMC7980254/ /pubmed/33734293 http://dx.doi.org/10.1083/jcb.202101116 Text en © 2021 Wood et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Wood, Brent M. Baena, Valentina Huang, Hai Jorgens, Danielle M. Terasaki, Mark Kornberg, Thomas B. Cytonemes with complex geometries and composition extend into invaginations of target cells |
title | Cytonemes with complex geometries and composition extend into invaginations of target cells |
title_full | Cytonemes with complex geometries and composition extend into invaginations of target cells |
title_fullStr | Cytonemes with complex geometries and composition extend into invaginations of target cells |
title_full_unstemmed | Cytonemes with complex geometries and composition extend into invaginations of target cells |
title_short | Cytonemes with complex geometries and composition extend into invaginations of target cells |
title_sort | cytonemes with complex geometries and composition extend into invaginations of target cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980254/ https://www.ncbi.nlm.nih.gov/pubmed/33734293 http://dx.doi.org/10.1083/jcb.202101116 |
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