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Optical coherence tomography complements confocal microscopy for investigation of multicellular tumour spheroids

Knowledge of optical properties, such as the refractive index (RI), of biological tissues is important in optical imaging, as they influence the distribution and propagation of light in tissue. To accurately study the response of cancerous cells to drugs, optimised imaging protocols are required. Th...

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Autores principales: Hari, Neelam, Patel, Priyanka, Ross, Jacqueline, Hicks, Kevin, Vanholsbeeck, Frédérique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646385/
https://www.ncbi.nlm.nih.gov/pubmed/31332221
http://dx.doi.org/10.1038/s41598-019-47000-2
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author Hari, Neelam
Patel, Priyanka
Ross, Jacqueline
Hicks, Kevin
Vanholsbeeck, Frédérique
author_facet Hari, Neelam
Patel, Priyanka
Ross, Jacqueline
Hicks, Kevin
Vanholsbeeck, Frédérique
author_sort Hari, Neelam
collection PubMed
description Knowledge of optical properties, such as the refractive index (RI), of biological tissues is important in optical imaging, as they influence the distribution and propagation of light in tissue. To accurately study the response of cancerous cells to drugs, optimised imaging protocols are required. This study uses a simple custom-built spectral domain optical coherence tomography (OCT) system to conduct RI measurements of multicellular spheroids, three-dimensional (3D) in-vitro culture systems, of the cell line HCT116. The spheroid RIs are compared to study the effect of growth over time. To improve confocal microscopy imaging protocols, two immersion media (glycerol and ScaleView-A2) matching the spheroid RIs were trialled, with the aim to reduce the RI mismatch between the spheroid and the immersion medium and thus improve imaging depth with confocal microscopy. ScaleView-A2 (n = 1.380) aided in achieving greater depths of imaging of the multicellular spheroids under confocal microscopy. This improvement in imaging depth confirmed the utility of our RI measurements, proving the promising outlook of OCT as a complementary tool to microscopy in cancer research.
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spelling pubmed-66463852019-07-29 Optical coherence tomography complements confocal microscopy for investigation of multicellular tumour spheroids Hari, Neelam Patel, Priyanka Ross, Jacqueline Hicks, Kevin Vanholsbeeck, Frédérique Sci Rep Article Knowledge of optical properties, such as the refractive index (RI), of biological tissues is important in optical imaging, as they influence the distribution and propagation of light in tissue. To accurately study the response of cancerous cells to drugs, optimised imaging protocols are required. This study uses a simple custom-built spectral domain optical coherence tomography (OCT) system to conduct RI measurements of multicellular spheroids, three-dimensional (3D) in-vitro culture systems, of the cell line HCT116. The spheroid RIs are compared to study the effect of growth over time. To improve confocal microscopy imaging protocols, two immersion media (glycerol and ScaleView-A2) matching the spheroid RIs were trialled, with the aim to reduce the RI mismatch between the spheroid and the immersion medium and thus improve imaging depth with confocal microscopy. ScaleView-A2 (n = 1.380) aided in achieving greater depths of imaging of the multicellular spheroids under confocal microscopy. This improvement in imaging depth confirmed the utility of our RI measurements, proving the promising outlook of OCT as a complementary tool to microscopy in cancer research. Nature Publishing Group UK 2019-07-22 /pmc/articles/PMC6646385/ /pubmed/31332221 http://dx.doi.org/10.1038/s41598-019-47000-2 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
Hari, Neelam
Patel, Priyanka
Ross, Jacqueline
Hicks, Kevin
Vanholsbeeck, Frédérique
Optical coherence tomography complements confocal microscopy for investigation of multicellular tumour spheroids
title Optical coherence tomography complements confocal microscopy for investigation of multicellular tumour spheroids
title_full Optical coherence tomography complements confocal microscopy for investigation of multicellular tumour spheroids
title_fullStr Optical coherence tomography complements confocal microscopy for investigation of multicellular tumour spheroids
title_full_unstemmed Optical coherence tomography complements confocal microscopy for investigation of multicellular tumour spheroids
title_short Optical coherence tomography complements confocal microscopy for investigation of multicellular tumour spheroids
title_sort optical coherence tomography complements confocal microscopy for investigation of multicellular tumour spheroids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646385/
https://www.ncbi.nlm.nih.gov/pubmed/31332221
http://dx.doi.org/10.1038/s41598-019-47000-2
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