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The structural origin of second harmonic generation in fascia
Fascia tissue is rich in collagen type I proteins and can be imaged by second harmonic generation (SHG) microscopy. While identifying the overall alignment of the collagen fibrils is evident from those images, the tridimensional structural origin for the observation of SHG signal is more complex tha...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Optical Society of America
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3028495/ https://www.ncbi.nlm.nih.gov/pubmed/21326632 http://dx.doi.org/10.1364/BOE.2.000026 |
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author | Rivard, Maxime Laliberté, Mathieu Bertrand-Grenier, Antony Harnagea, Catalin Pfeffer, Christian P. Vallières, Martin St-Pierre, Yves Pignolet, Alain El Khakani, My Ali Légaré, François |
author_facet | Rivard, Maxime Laliberté, Mathieu Bertrand-Grenier, Antony Harnagea, Catalin Pfeffer, Christian P. Vallières, Martin St-Pierre, Yves Pignolet, Alain El Khakani, My Ali Légaré, François |
author_sort | Rivard, Maxime |
collection | PubMed |
description | Fascia tissue is rich in collagen type I proteins and can be imaged by second harmonic generation (SHG) microscopy. While identifying the overall alignment of the collagen fibrils is evident from those images, the tridimensional structural origin for the observation of SHG signal is more complex than it apparently seems. Those images reveal that the noncentrosymmetric (piezoelectric) structures are distributed heterogeneously on spatial dimensions inferior to the resolution provided by the nonlinear optical microscope (sub-micron). Using piezoresponse force microscopy (PFM), we show that an individual collagen fibril has a noncentrosymmetric structural organization. Fibrils are found to be arranged in nano-domains where the anisotropic axis is preserved along the fibrillar axis, while across the collagen sheets, the phase of the second order nonlinear susceptibility is changing by 180 degrees between adjacent nano-domains. This complex architecture of noncentrosymmetric nano-domains governs the coherent addition of 2ω light within the focal volume and the observed features in the SHG images taken in fascia. |
format | Text |
id | pubmed-3028495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Optical Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-30284952011-02-16 The structural origin of second harmonic generation in fascia Rivard, Maxime Laliberté, Mathieu Bertrand-Grenier, Antony Harnagea, Catalin Pfeffer, Christian P. Vallières, Martin St-Pierre, Yves Pignolet, Alain El Khakani, My Ali Légaré, François Biomed Opt Express Microscopy Fascia tissue is rich in collagen type I proteins and can be imaged by second harmonic generation (SHG) microscopy. While identifying the overall alignment of the collagen fibrils is evident from those images, the tridimensional structural origin for the observation of SHG signal is more complex than it apparently seems. Those images reveal that the noncentrosymmetric (piezoelectric) structures are distributed heterogeneously on spatial dimensions inferior to the resolution provided by the nonlinear optical microscope (sub-micron). Using piezoresponse force microscopy (PFM), we show that an individual collagen fibril has a noncentrosymmetric structural organization. Fibrils are found to be arranged in nano-domains where the anisotropic axis is preserved along the fibrillar axis, while across the collagen sheets, the phase of the second order nonlinear susceptibility is changing by 180 degrees between adjacent nano-domains. This complex architecture of noncentrosymmetric nano-domains governs the coherent addition of 2ω light within the focal volume and the observed features in the SHG images taken in fascia. Optical Society of America 2010-12-01 /pmc/articles/PMC3028495/ /pubmed/21326632 http://dx.doi.org/10.1364/BOE.2.000026 Text en ©2010 Optical Society of America http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially. |
spellingShingle | Microscopy Rivard, Maxime Laliberté, Mathieu Bertrand-Grenier, Antony Harnagea, Catalin Pfeffer, Christian P. Vallières, Martin St-Pierre, Yves Pignolet, Alain El Khakani, My Ali Légaré, François The structural origin of second harmonic generation in fascia |
title | The structural origin of second harmonic generation in fascia |
title_full | The structural origin of second harmonic generation in fascia |
title_fullStr | The structural origin of second harmonic generation in fascia |
title_full_unstemmed | The structural origin of second harmonic generation in fascia |
title_short | The structural origin of second harmonic generation in fascia |
title_sort | structural origin of second harmonic generation in fascia |
topic | Microscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3028495/ https://www.ncbi.nlm.nih.gov/pubmed/21326632 http://dx.doi.org/10.1364/BOE.2.000026 |
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