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Cytokinetic bridge triggers de novo lumen formation in vivo
Multicellular rosettes are transient epithelial structures that serve as intermediates during diverse organ formation. We have identified a unique contributor to rosette formation in zebrafish Kupffer’s vesicle (KV) that requires cell division, specifically the final stage of mitosis termed abscissi...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062744/ https://www.ncbi.nlm.nih.gov/pubmed/32152267 http://dx.doi.org/10.1038/s41467-020-15002-8 |
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author | Rathbun, L. I. Colicino, E. G. Manikas, J. O’Connell, J. Krishnan, N. Reilly, N. S. Coyne, S. Erdemci-Tandogan, G. Garrastegui, A. Freshour, J. Santra, P. Manning, M. L. Amack, J. D. Hehnly, H. |
author_facet | Rathbun, L. I. Colicino, E. G. Manikas, J. O’Connell, J. Krishnan, N. Reilly, N. S. Coyne, S. Erdemci-Tandogan, G. Garrastegui, A. Freshour, J. Santra, P. Manning, M. L. Amack, J. D. Hehnly, H. |
author_sort | Rathbun, L. I. |
collection | PubMed |
description | Multicellular rosettes are transient epithelial structures that serve as intermediates during diverse organ formation. We have identified a unique contributor to rosette formation in zebrafish Kupffer’s vesicle (KV) that requires cell division, specifically the final stage of mitosis termed abscission. KV utilizes a rosette as a prerequisite before forming a lumen surrounded by ciliated epithelial cells. Our studies identify that KV-destined cells remain interconnected by cytokinetic bridges that position at the rosette’s center. These bridges act as a landmark for directed Rab11 vesicle motility to deliver an essential cargo for lumen formation, CFTR (cystic fibrosis transmembrane conductance regulator). Here we report that premature bridge cleavage through laser ablation or inhibiting abscission using optogenetic clustering of Rab11 result in disrupted lumen formation. We present a model in which KV mitotic cells strategically place their cytokinetic bridges at the rosette center, where Rab11-associated vesicles transport CFTR to aid in lumen establishment. |
format | Online Article Text |
id | pubmed-7062744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70627442020-03-18 Cytokinetic bridge triggers de novo lumen formation in vivo Rathbun, L. I. Colicino, E. G. Manikas, J. O’Connell, J. Krishnan, N. Reilly, N. S. Coyne, S. Erdemci-Tandogan, G. Garrastegui, A. Freshour, J. Santra, P. Manning, M. L. Amack, J. D. Hehnly, H. Nat Commun Article Multicellular rosettes are transient epithelial structures that serve as intermediates during diverse organ formation. We have identified a unique contributor to rosette formation in zebrafish Kupffer’s vesicle (KV) that requires cell division, specifically the final stage of mitosis termed abscission. KV utilizes a rosette as a prerequisite before forming a lumen surrounded by ciliated epithelial cells. Our studies identify that KV-destined cells remain interconnected by cytokinetic bridges that position at the rosette’s center. These bridges act as a landmark for directed Rab11 vesicle motility to deliver an essential cargo for lumen formation, CFTR (cystic fibrosis transmembrane conductance regulator). Here we report that premature bridge cleavage through laser ablation or inhibiting abscission using optogenetic clustering of Rab11 result in disrupted lumen formation. We present a model in which KV mitotic cells strategically place their cytokinetic bridges at the rosette center, where Rab11-associated vesicles transport CFTR to aid in lumen establishment. Nature Publishing Group UK 2020-03-09 /pmc/articles/PMC7062744/ /pubmed/32152267 http://dx.doi.org/10.1038/s41467-020-15002-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Rathbun, L. I. Colicino, E. G. Manikas, J. O’Connell, J. Krishnan, N. Reilly, N. S. Coyne, S. Erdemci-Tandogan, G. Garrastegui, A. Freshour, J. Santra, P. Manning, M. L. Amack, J. D. Hehnly, H. Cytokinetic bridge triggers de novo lumen formation in vivo |
title | Cytokinetic bridge triggers de novo lumen formation in vivo |
title_full | Cytokinetic bridge triggers de novo lumen formation in vivo |
title_fullStr | Cytokinetic bridge triggers de novo lumen formation in vivo |
title_full_unstemmed | Cytokinetic bridge triggers de novo lumen formation in vivo |
title_short | Cytokinetic bridge triggers de novo lumen formation in vivo |
title_sort | cytokinetic bridge triggers de novo lumen formation in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062744/ https://www.ncbi.nlm.nih.gov/pubmed/32152267 http://dx.doi.org/10.1038/s41467-020-15002-8 |
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