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Lattice light sheet imaging of membrane nanotubes between human breast cancer cells in culture and in brain metastases
Membrane nanotubes are cytosolic protrusions with diameters <1 µm that extend between cells separated by tens of µm. They mediate several forms of intercellular communication and are upregulated in diverse diseases. Difficulties in visualizing and studying nanotubes within intact tissues have, ho...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591308/ https://www.ncbi.nlm.nih.gov/pubmed/28887508 http://dx.doi.org/10.1038/s41598-017-11223-y |
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author | Parker, Ian Evans, Katrina T. Ellefsen, Kyle Lawson, Devon A. Smith, Ian F. |
author_facet | Parker, Ian Evans, Katrina T. Ellefsen, Kyle Lawson, Devon A. Smith, Ian F. |
author_sort | Parker, Ian |
collection | PubMed |
description | Membrane nanotubes are cytosolic protrusions with diameters <1 µm that extend between cells separated by tens of µm. They mediate several forms of intercellular communication and are upregulated in diverse diseases. Difficulties in visualizing and studying nanotubes within intact tissues have, however, prompted skepticism regarding their in vivo relevance, and most studies have been confined to cell culture systems. Here, we introduce lattice-light sheet imaging of MDA-MB-231 human breast cancer cells genetically engineered to brightly express membrane–targeted GFP as a promising approach to visualize membrane nanotubes in vitro and in situ. We demonstrate that cultured cells form multiple nanotubes that mediate intercellular communication of Ca(2+) signals and actively traffic GFP-tagged membrane vesicles along their length. Furthermore, we directly visualize nanotubes in situ, interconnecting breast cancer cells in live acute brain slices from an experimental mouse model of breast cancer brain metastasis. This amenable experimental system should facilitate the transition of the study of intercellular communication by membrane nanotubes from cell culture to the whole animal. |
format | Online Article Text |
id | pubmed-5591308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55913082017-09-13 Lattice light sheet imaging of membrane nanotubes between human breast cancer cells in culture and in brain metastases Parker, Ian Evans, Katrina T. Ellefsen, Kyle Lawson, Devon A. Smith, Ian F. Sci Rep Article Membrane nanotubes are cytosolic protrusions with diameters <1 µm that extend between cells separated by tens of µm. They mediate several forms of intercellular communication and are upregulated in diverse diseases. Difficulties in visualizing and studying nanotubes within intact tissues have, however, prompted skepticism regarding their in vivo relevance, and most studies have been confined to cell culture systems. Here, we introduce lattice-light sheet imaging of MDA-MB-231 human breast cancer cells genetically engineered to brightly express membrane–targeted GFP as a promising approach to visualize membrane nanotubes in vitro and in situ. We demonstrate that cultured cells form multiple nanotubes that mediate intercellular communication of Ca(2+) signals and actively traffic GFP-tagged membrane vesicles along their length. Furthermore, we directly visualize nanotubes in situ, interconnecting breast cancer cells in live acute brain slices from an experimental mouse model of breast cancer brain metastasis. This amenable experimental system should facilitate the transition of the study of intercellular communication by membrane nanotubes from cell culture to the whole animal. Nature Publishing Group UK 2017-09-08 /pmc/articles/PMC5591308/ /pubmed/28887508 http://dx.doi.org/10.1038/s41598-017-11223-y Text en © The Author(s) 2017 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 Parker, Ian Evans, Katrina T. Ellefsen, Kyle Lawson, Devon A. Smith, Ian F. Lattice light sheet imaging of membrane nanotubes between human breast cancer cells in culture and in brain metastases |
title | Lattice light sheet imaging of membrane nanotubes between human breast cancer cells in culture and in brain metastases |
title_full | Lattice light sheet imaging of membrane nanotubes between human breast cancer cells in culture and in brain metastases |
title_fullStr | Lattice light sheet imaging of membrane nanotubes between human breast cancer cells in culture and in brain metastases |
title_full_unstemmed | Lattice light sheet imaging of membrane nanotubes between human breast cancer cells in culture and in brain metastases |
title_short | Lattice light sheet imaging of membrane nanotubes between human breast cancer cells in culture and in brain metastases |
title_sort | lattice light sheet imaging of membrane nanotubes between human breast cancer cells in culture and in brain metastases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591308/ https://www.ncbi.nlm.nih.gov/pubmed/28887508 http://dx.doi.org/10.1038/s41598-017-11223-y |
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