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Phototrophic purple bacteria as optoacoustic in vivo reporters of macrophage activity
Τhe morphology, physiology and immunology, of solid tumors exhibit spatial heterogeneity which complicates our understanding of cancer progression and therapy response. Understanding spatial heterogeneity necessitates high resolution in vivo imaging of anatomical and pathophysiological tumor informa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416252/ https://www.ncbi.nlm.nih.gov/pubmed/30867430 http://dx.doi.org/10.1038/s41467-019-09081-5 |
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author | Peters, Lena Weidenfeld, Ina Klemm, Uwe Loeschcke, Anita Weihmann, Robin Jaeger, Karl-Erich Drepper, Thomas Ntziachristos, Vasilis Stiel, Andre C. |
author_facet | Peters, Lena Weidenfeld, Ina Klemm, Uwe Loeschcke, Anita Weihmann, Robin Jaeger, Karl-Erich Drepper, Thomas Ntziachristos, Vasilis Stiel, Andre C. |
author_sort | Peters, Lena |
collection | PubMed |
description | Τhe morphology, physiology and immunology, of solid tumors exhibit spatial heterogeneity which complicates our understanding of cancer progression and therapy response. Understanding spatial heterogeneity necessitates high resolution in vivo imaging of anatomical and pathophysiological tumor information. We introduce Rhodobacter as bacterial reporter for multispectral optoacoustic (photoacoustic) tomography (MSOT). We show that endogenous bacteriochlorophyll a in Rhodobacter gives rise to strong optoacoustic signals >800 nm away from interfering endogenous absorbers. Importantly, our results suggest that changes in the spectral signature of Rhodobacter which depend on macrophage activity inside the tumor can be used to reveal heterogeneity of the tumor microenvironment. Employing non-invasive high resolution MSOT in longitudinal studies we show spatiotemporal changes of Rhodobacter spectral profiles in mice bearing 4T1 and CT26.WT tumor models. Accessibility of Rhodobacter to genetic modification and thus to sensory and therapeutic functions suggests potential for a theranostic platform organism. |
format | Online Article Text |
id | pubmed-6416252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64162522019-03-15 Phototrophic purple bacteria as optoacoustic in vivo reporters of macrophage activity Peters, Lena Weidenfeld, Ina Klemm, Uwe Loeschcke, Anita Weihmann, Robin Jaeger, Karl-Erich Drepper, Thomas Ntziachristos, Vasilis Stiel, Andre C. Nat Commun Article Τhe morphology, physiology and immunology, of solid tumors exhibit spatial heterogeneity which complicates our understanding of cancer progression and therapy response. Understanding spatial heterogeneity necessitates high resolution in vivo imaging of anatomical and pathophysiological tumor information. We introduce Rhodobacter as bacterial reporter for multispectral optoacoustic (photoacoustic) tomography (MSOT). We show that endogenous bacteriochlorophyll a in Rhodobacter gives rise to strong optoacoustic signals >800 nm away from interfering endogenous absorbers. Importantly, our results suggest that changes in the spectral signature of Rhodobacter which depend on macrophage activity inside the tumor can be used to reveal heterogeneity of the tumor microenvironment. Employing non-invasive high resolution MSOT in longitudinal studies we show spatiotemporal changes of Rhodobacter spectral profiles in mice bearing 4T1 and CT26.WT tumor models. Accessibility of Rhodobacter to genetic modification and thus to sensory and therapeutic functions suggests potential for a theranostic platform organism. Nature Publishing Group UK 2019-03-13 /pmc/articles/PMC6416252/ /pubmed/30867430 http://dx.doi.org/10.1038/s41467-019-09081-5 Text en © The Author(s) 2019 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 Peters, Lena Weidenfeld, Ina Klemm, Uwe Loeschcke, Anita Weihmann, Robin Jaeger, Karl-Erich Drepper, Thomas Ntziachristos, Vasilis Stiel, Andre C. Phototrophic purple bacteria as optoacoustic in vivo reporters of macrophage activity |
title | Phototrophic purple bacteria as optoacoustic in vivo reporters of macrophage activity |
title_full | Phototrophic purple bacteria as optoacoustic in vivo reporters of macrophage activity |
title_fullStr | Phototrophic purple bacteria as optoacoustic in vivo reporters of macrophage activity |
title_full_unstemmed | Phototrophic purple bacteria as optoacoustic in vivo reporters of macrophage activity |
title_short | Phototrophic purple bacteria as optoacoustic in vivo reporters of macrophage activity |
title_sort | phototrophic purple bacteria as optoacoustic in vivo reporters of macrophage activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416252/ https://www.ncbi.nlm.nih.gov/pubmed/30867430 http://dx.doi.org/10.1038/s41467-019-09081-5 |
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