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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...

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Autores principales: Peters, Lena, Weidenfeld, Ina, Klemm, Uwe, Loeschcke, Anita, Weihmann, Robin, Jaeger, Karl-Erich, Drepper, Thomas, Ntziachristos, Vasilis, Stiel, Andre C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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