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High-Speed Single-Molecule Tracking of CXCL13 in the B-Follicle

Soluble factors are an essential means of communication between cells and their environment. However, many molecules readily interact with extracellular matrix components, giving rise to multiple modes of diffusion. The molecular quantification of diffusion in situ is thus a challenging imaging fron...

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Autores principales: Miller, Helen, Cosgrove, Jason, Wollman, Adam J. M., Taylor, Emily, Zhou, Zhaokun, O’Toole, Peter J., Coles, Mark C., Leake, Mark C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972203/
https://www.ncbi.nlm.nih.gov/pubmed/29872430
http://dx.doi.org/10.3389/fimmu.2018.01073
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author Miller, Helen
Cosgrove, Jason
Wollman, Adam J. M.
Taylor, Emily
Zhou, Zhaokun
O’Toole, Peter J.
Coles, Mark C.
Leake, Mark C.
author_facet Miller, Helen
Cosgrove, Jason
Wollman, Adam J. M.
Taylor, Emily
Zhou, Zhaokun
O’Toole, Peter J.
Coles, Mark C.
Leake, Mark C.
author_sort Miller, Helen
collection PubMed
description Soluble factors are an essential means of communication between cells and their environment. However, many molecules readily interact with extracellular matrix components, giving rise to multiple modes of diffusion. The molecular quantification of diffusion in situ is thus a challenging imaging frontier, requiring very high spatial and temporal resolution. Overcoming this methodological barrier is key to understanding the precise spatial patterning of the extracellular factors that regulate immune function. To address this, we have developed a high-speed light microscopy system capable of millisecond sampling in ex vivo tissue samples and submillisecond sampling in controlled in vitro samples to characterize molecular diffusion in a range of complex microenvironments. We demonstrate that this method outperforms competing tools for determining molecular mobility of fluorescence correlation spectroscopy (FCS) and fluorescence recovery after photobleaching (FRAP) for evaluation of diffusion. We then apply this approach to study the chemokine CXCL13, a key determinant of lymphoid tissue architecture, and B-cell-mediated immunity. Super-resolution single-molecule tracking of fluorescently labeled CCL19 and CXCL13 in collagen matrix was used to assess the heterogeneity of chemokine mobility behaviors, with results indicating an immobile fraction and a mobile fraction for both molecules, with distinct diffusion rates of 8.4 ± 0.2 and 6.2 ± 0.3 µm(2)s(−1), respectively. To better understand mobility behaviors in situ, we analyzed CXCL13-AF647 diffusion in murine lymph node tissue sections and observed both an immobile fraction and a mobile fraction with an example diffusion coefficient of 6.6 ± 0.4 µm(2)s(−1), suggesting that mobility within the follicle is also multimodal. In quantitatively studying mobility behaviors at the molecular level, we have obtained an increased understanding of CXCL13 bioavailability within the follicle. Our high-speed single-molecule tracking approach affords a novel perspective from which to understand the mobility of soluble factors relevant to the immune system.
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spelling pubmed-59722032018-06-05 High-Speed Single-Molecule Tracking of CXCL13 in the B-Follicle Miller, Helen Cosgrove, Jason Wollman, Adam J. M. Taylor, Emily Zhou, Zhaokun O’Toole, Peter J. Coles, Mark C. Leake, Mark C. Front Immunol Immunology Soluble factors are an essential means of communication between cells and their environment. However, many molecules readily interact with extracellular matrix components, giving rise to multiple modes of diffusion. The molecular quantification of diffusion in situ is thus a challenging imaging frontier, requiring very high spatial and temporal resolution. Overcoming this methodological barrier is key to understanding the precise spatial patterning of the extracellular factors that regulate immune function. To address this, we have developed a high-speed light microscopy system capable of millisecond sampling in ex vivo tissue samples and submillisecond sampling in controlled in vitro samples to characterize molecular diffusion in a range of complex microenvironments. We demonstrate that this method outperforms competing tools for determining molecular mobility of fluorescence correlation spectroscopy (FCS) and fluorescence recovery after photobleaching (FRAP) for evaluation of diffusion. We then apply this approach to study the chemokine CXCL13, a key determinant of lymphoid tissue architecture, and B-cell-mediated immunity. Super-resolution single-molecule tracking of fluorescently labeled CCL19 and CXCL13 in collagen matrix was used to assess the heterogeneity of chemokine mobility behaviors, with results indicating an immobile fraction and a mobile fraction for both molecules, with distinct diffusion rates of 8.4 ± 0.2 and 6.2 ± 0.3 µm(2)s(−1), respectively. To better understand mobility behaviors in situ, we analyzed CXCL13-AF647 diffusion in murine lymph node tissue sections and observed both an immobile fraction and a mobile fraction with an example diffusion coefficient of 6.6 ± 0.4 µm(2)s(−1), suggesting that mobility within the follicle is also multimodal. In quantitatively studying mobility behaviors at the molecular level, we have obtained an increased understanding of CXCL13 bioavailability within the follicle. Our high-speed single-molecule tracking approach affords a novel perspective from which to understand the mobility of soluble factors relevant to the immune system. Frontiers Media S.A. 2018-05-22 /pmc/articles/PMC5972203/ /pubmed/29872430 http://dx.doi.org/10.3389/fimmu.2018.01073 Text en Copyright © 2018 Miller, Cosgrove, Wollman, Taylor, Zhou, O’Toole, Coles and Leake. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Miller, Helen
Cosgrove, Jason
Wollman, Adam J. M.
Taylor, Emily
Zhou, Zhaokun
O’Toole, Peter J.
Coles, Mark C.
Leake, Mark C.
High-Speed Single-Molecule Tracking of CXCL13 in the B-Follicle
title High-Speed Single-Molecule Tracking of CXCL13 in the B-Follicle
title_full High-Speed Single-Molecule Tracking of CXCL13 in the B-Follicle
title_fullStr High-Speed Single-Molecule Tracking of CXCL13 in the B-Follicle
title_full_unstemmed High-Speed Single-Molecule Tracking of CXCL13 in the B-Follicle
title_short High-Speed Single-Molecule Tracking of CXCL13 in the B-Follicle
title_sort high-speed single-molecule tracking of cxcl13 in the b-follicle
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972203/
https://www.ncbi.nlm.nih.gov/pubmed/29872430
http://dx.doi.org/10.3389/fimmu.2018.01073
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