Cargando…

Fourier Transform Infrared Microscopy Enables Guidance of Automated Mass Spectrometry Imaging to Predefined Tissue Morphologies

Multimodal imaging combines complementary platforms for spatially resolved tissue analysis that are poised for application in life science and personalized medicine. Unlike established clinical in vivo multimodality imaging, automated workflows for in-depth multimodal molecular ex vivo tissue analys...

Descripción completa

Detalles Bibliográficos
Autores principales: Rabe, Jan-Hinrich, A. Sammour, Denis, Schulz, Sandra, Munteanu, Bogdan, Ott, Martina, Ochs, Katharina, Hohenberger, Peter, Marx, Alexander, Platten, Michael, Opitz, Christiane A., Ory, Daniel S., Hopf, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762902/
https://www.ncbi.nlm.nih.gov/pubmed/29321555
http://dx.doi.org/10.1038/s41598-017-18477-6
_version_ 1783291787653152768
author Rabe, Jan-Hinrich
A. Sammour, Denis
Schulz, Sandra
Munteanu, Bogdan
Ott, Martina
Ochs, Katharina
Hohenberger, Peter
Marx, Alexander
Platten, Michael
Opitz, Christiane A.
Ory, Daniel S.
Hopf, Carsten
author_facet Rabe, Jan-Hinrich
A. Sammour, Denis
Schulz, Sandra
Munteanu, Bogdan
Ott, Martina
Ochs, Katharina
Hohenberger, Peter
Marx, Alexander
Platten, Michael
Opitz, Christiane A.
Ory, Daniel S.
Hopf, Carsten
author_sort Rabe, Jan-Hinrich
collection PubMed
description Multimodal imaging combines complementary platforms for spatially resolved tissue analysis that are poised for application in life science and personalized medicine. Unlike established clinical in vivo multimodality imaging, automated workflows for in-depth multimodal molecular ex vivo tissue analysis that combine the speed and ease of spectroscopic imaging with molecular details provided by mass spectrometry imaging (MSI) are lagging behind. Here, we present an integrated approach that utilizes non-destructive Fourier transform infrared (FTIR) microscopy and matrix assisted laser desorption/ionization (MALDI) MSI for analysing single-slide tissue specimen. We show that FTIR microscopy can automatically guide high-resolution MSI data acquisition and interpretation without requiring prior histopathological tissue annotation, thus circumventing potential human-annotation-bias while achieving >90% reductions of data load and acquisition time. We apply FTIR imaging as an upstream modality to improve accuracy of tissue-morphology detection and to retrieve diagnostic molecular signatures in an automated, unbiased and spatially aware manner. We show the general applicability of multimodal FTIR-guided MALDI-MSI by demonstrating precise tumor localization in mouse brain bearing glioma xenografts and in human primary gastrointestinal stromal tumors. Finally, the presented multimodal tissue analysis method allows for morphology-sensitive lipid signature retrieval from brains of mice suffering from lipidosis caused by Niemann-Pick type C disease.
format Online
Article
Text
id pubmed-5762902
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-57629022018-01-17 Fourier Transform Infrared Microscopy Enables Guidance of Automated Mass Spectrometry Imaging to Predefined Tissue Morphologies Rabe, Jan-Hinrich A. Sammour, Denis Schulz, Sandra Munteanu, Bogdan Ott, Martina Ochs, Katharina Hohenberger, Peter Marx, Alexander Platten, Michael Opitz, Christiane A. Ory, Daniel S. Hopf, Carsten Sci Rep Article Multimodal imaging combines complementary platforms for spatially resolved tissue analysis that are poised for application in life science and personalized medicine. Unlike established clinical in vivo multimodality imaging, automated workflows for in-depth multimodal molecular ex vivo tissue analysis that combine the speed and ease of spectroscopic imaging with molecular details provided by mass spectrometry imaging (MSI) are lagging behind. Here, we present an integrated approach that utilizes non-destructive Fourier transform infrared (FTIR) microscopy and matrix assisted laser desorption/ionization (MALDI) MSI for analysing single-slide tissue specimen. We show that FTIR microscopy can automatically guide high-resolution MSI data acquisition and interpretation without requiring prior histopathological tissue annotation, thus circumventing potential human-annotation-bias while achieving >90% reductions of data load and acquisition time. We apply FTIR imaging as an upstream modality to improve accuracy of tissue-morphology detection and to retrieve diagnostic molecular signatures in an automated, unbiased and spatially aware manner. We show the general applicability of multimodal FTIR-guided MALDI-MSI by demonstrating precise tumor localization in mouse brain bearing glioma xenografts and in human primary gastrointestinal stromal tumors. Finally, the presented multimodal tissue analysis method allows for morphology-sensitive lipid signature retrieval from brains of mice suffering from lipidosis caused by Niemann-Pick type C disease. Nature Publishing Group UK 2018-01-10 /pmc/articles/PMC5762902/ /pubmed/29321555 http://dx.doi.org/10.1038/s41598-017-18477-6 Text en © The Author(s) 2018 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
Rabe, Jan-Hinrich
A. Sammour, Denis
Schulz, Sandra
Munteanu, Bogdan
Ott, Martina
Ochs, Katharina
Hohenberger, Peter
Marx, Alexander
Platten, Michael
Opitz, Christiane A.
Ory, Daniel S.
Hopf, Carsten
Fourier Transform Infrared Microscopy Enables Guidance of Automated Mass Spectrometry Imaging to Predefined Tissue Morphologies
title Fourier Transform Infrared Microscopy Enables Guidance of Automated Mass Spectrometry Imaging to Predefined Tissue Morphologies
title_full Fourier Transform Infrared Microscopy Enables Guidance of Automated Mass Spectrometry Imaging to Predefined Tissue Morphologies
title_fullStr Fourier Transform Infrared Microscopy Enables Guidance of Automated Mass Spectrometry Imaging to Predefined Tissue Morphologies
title_full_unstemmed Fourier Transform Infrared Microscopy Enables Guidance of Automated Mass Spectrometry Imaging to Predefined Tissue Morphologies
title_short Fourier Transform Infrared Microscopy Enables Guidance of Automated Mass Spectrometry Imaging to Predefined Tissue Morphologies
title_sort fourier transform infrared microscopy enables guidance of automated mass spectrometry imaging to predefined tissue morphologies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762902/
https://www.ncbi.nlm.nih.gov/pubmed/29321555
http://dx.doi.org/10.1038/s41598-017-18477-6
work_keys_str_mv AT rabejanhinrich fouriertransforminfraredmicroscopyenablesguidanceofautomatedmassspectrometryimagingtopredefinedtissuemorphologies
AT asammourdenis fouriertransforminfraredmicroscopyenablesguidanceofautomatedmassspectrometryimagingtopredefinedtissuemorphologies
AT schulzsandra fouriertransforminfraredmicroscopyenablesguidanceofautomatedmassspectrometryimagingtopredefinedtissuemorphologies
AT munteanubogdan fouriertransforminfraredmicroscopyenablesguidanceofautomatedmassspectrometryimagingtopredefinedtissuemorphologies
AT ottmartina fouriertransforminfraredmicroscopyenablesguidanceofautomatedmassspectrometryimagingtopredefinedtissuemorphologies
AT ochskatharina fouriertransforminfraredmicroscopyenablesguidanceofautomatedmassspectrometryimagingtopredefinedtissuemorphologies
AT hohenbergerpeter fouriertransforminfraredmicroscopyenablesguidanceofautomatedmassspectrometryimagingtopredefinedtissuemorphologies
AT marxalexander fouriertransforminfraredmicroscopyenablesguidanceofautomatedmassspectrometryimagingtopredefinedtissuemorphologies
AT plattenmichael fouriertransforminfraredmicroscopyenablesguidanceofautomatedmassspectrometryimagingtopredefinedtissuemorphologies
AT opitzchristianea fouriertransforminfraredmicroscopyenablesguidanceofautomatedmassspectrometryimagingtopredefinedtissuemorphologies
AT orydaniels fouriertransforminfraredmicroscopyenablesguidanceofautomatedmassspectrometryimagingtopredefinedtissuemorphologies
AT hopfcarsten fouriertransforminfraredmicroscopyenablesguidanceofautomatedmassspectrometryimagingtopredefinedtissuemorphologies