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Fast and precise targeting of single tumor cells in vivo by multimodal correlative microscopy
Intravital microscopy provides dynamic understanding of multiple cell biological processes, but its limited resolution has so far precluded structural analysis. Because it is difficult to capture rare and transient events, only a few attempts have been made to observe specific developmental and path...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4732291/ https://www.ncbi.nlm.nih.gov/pubmed/26659665 http://dx.doi.org/10.1242/jcs.181842 |
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author | Karreman, Matthia A. Mercier, Luc Schieber, Nicole L. Solecki, Gergely Allio, Guillaume Winkler, Frank Ruthensteiner, Bernhard Goetz, Jacky G. Schwab, Yannick |
author_facet | Karreman, Matthia A. Mercier, Luc Schieber, Nicole L. Solecki, Gergely Allio, Guillaume Winkler, Frank Ruthensteiner, Bernhard Goetz, Jacky G. Schwab, Yannick |
author_sort | Karreman, Matthia A. |
collection | PubMed |
description | Intravital microscopy provides dynamic understanding of multiple cell biological processes, but its limited resolution has so far precluded structural analysis. Because it is difficult to capture rare and transient events, only a few attempts have been made to observe specific developmental and pathological processes in animal models using electron microscopy. The multimodal correlative approach that we propose here combines intravital microscopy, microscopic X-ray computed tomography and three-dimensional electron microscopy. It enables a rapid (c.a. 2 weeks) and accurate (<5 µm) correlation of functional imaging to ultrastructural analysis of single cells in a relevant context. We demonstrate the power of our approach by capturing single tumor cells in the vasculature of the cerebral cortex and in subcutaneous tumors, providing unique insights into metastatic events. Providing a significantly improved throughput, our workflow enables multiple sampling, a prerequisite for making correlative imaging a relevant tool to study cell biology in vivo. Owing to the versatility of this workflow, we envision broad applications in various fields of biological research, such as cancer or developmental biology. |
format | Online Article Text |
id | pubmed-4732291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47322912016-02-09 Fast and precise targeting of single tumor cells in vivo by multimodal correlative microscopy Karreman, Matthia A. Mercier, Luc Schieber, Nicole L. Solecki, Gergely Allio, Guillaume Winkler, Frank Ruthensteiner, Bernhard Goetz, Jacky G. Schwab, Yannick J Cell Sci Tools and Techniques Intravital microscopy provides dynamic understanding of multiple cell biological processes, but its limited resolution has so far precluded structural analysis. Because it is difficult to capture rare and transient events, only a few attempts have been made to observe specific developmental and pathological processes in animal models using electron microscopy. The multimodal correlative approach that we propose here combines intravital microscopy, microscopic X-ray computed tomography and three-dimensional electron microscopy. It enables a rapid (c.a. 2 weeks) and accurate (<5 µm) correlation of functional imaging to ultrastructural analysis of single cells in a relevant context. We demonstrate the power of our approach by capturing single tumor cells in the vasculature of the cerebral cortex and in subcutaneous tumors, providing unique insights into metastatic events. Providing a significantly improved throughput, our workflow enables multiple sampling, a prerequisite for making correlative imaging a relevant tool to study cell biology in vivo. Owing to the versatility of this workflow, we envision broad applications in various fields of biological research, such as cancer or developmental biology. The Company of Biologists Ltd 2016-01-15 /pmc/articles/PMC4732291/ /pubmed/26659665 http://dx.doi.org/10.1242/jcs.181842 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Tools and Techniques Karreman, Matthia A. Mercier, Luc Schieber, Nicole L. Solecki, Gergely Allio, Guillaume Winkler, Frank Ruthensteiner, Bernhard Goetz, Jacky G. Schwab, Yannick Fast and precise targeting of single tumor cells in vivo by multimodal correlative microscopy |
title | Fast and precise targeting of single tumor cells in vivo by multimodal correlative microscopy |
title_full | Fast and precise targeting of single tumor cells in vivo by multimodal correlative microscopy |
title_fullStr | Fast and precise targeting of single tumor cells in vivo by multimodal correlative microscopy |
title_full_unstemmed | Fast and precise targeting of single tumor cells in vivo by multimodal correlative microscopy |
title_short | Fast and precise targeting of single tumor cells in vivo by multimodal correlative microscopy |
title_sort | fast and precise targeting of single tumor cells in vivo by multimodal correlative microscopy |
topic | Tools and Techniques |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4732291/ https://www.ncbi.nlm.nih.gov/pubmed/26659665 http://dx.doi.org/10.1242/jcs.181842 |
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