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Structural changes in mixed Col I/Col V collagen gels probed by SHG microscopy: implications for probing stromal alterations in human breast cancer

Second Harmonic Generation (SHG) microscopy has been previously used to describe the morphology of collagen in the extracellular matrix (ECM) in different stages of invasion in breast cancer. Here this concept is extended by using SHG to provide quantitative discrimination of self-assembled collagen...

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Autores principales: Ajeti, Visar, Nadiarnykh, Oleg, Ponik, Suzanne M., Keely, Patricia J., Eliceiri, Kevin W., Campagnola, Paul J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149528/
https://www.ncbi.nlm.nih.gov/pubmed/21833367
http://dx.doi.org/10.1364/BOE.2.002307
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author Ajeti, Visar
Nadiarnykh, Oleg
Ponik, Suzanne M.
Keely, Patricia J.
Eliceiri, Kevin W.
Campagnola, Paul J.
author_facet Ajeti, Visar
Nadiarnykh, Oleg
Ponik, Suzanne M.
Keely, Patricia J.
Eliceiri, Kevin W.
Campagnola, Paul J.
author_sort Ajeti, Visar
collection PubMed
description Second Harmonic Generation (SHG) microscopy has been previously used to describe the morphology of collagen in the extracellular matrix (ECM) in different stages of invasion in breast cancer. Here this concept is extended by using SHG to provide quantitative discrimination of self-assembled collagen gels, consisting of mixtures of type I (Col I) and type V (Col V) isoforms which serve as models of changes in the ECM during invasion in vivo. To investigate if SHG is sensitive to changes due to Col V incorporation into Col I fibrils, gels were prepared with 0-20% Col V with the balance consisting of Col I. Using the metrics of SHG intensity, fiber length, emission directionality, and depth-dependent intensities, we found similar responses for gels comprised of 100% Col I, and 95% Col I/5% Col V, where these metrics were all significantly different from those of the 80% Col I/20% Col V gels. Specifically, the gels of lower Col V content produce brighter SHG, are characterized by longer fibers, and have a higher forward/backward emission ratio. These attributes are all consistent with more highly organized collagen fibrils/fibers and are in agreement with previous TEM characterization as well as predictions based on phase matching considerations. These results suggest that SHG can be developed to discriminate Col I/Col V composition in tissues to characterize and follow breast cancer invasion.
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spelling pubmed-31495282011-08-10 Structural changes in mixed Col I/Col V collagen gels probed by SHG microscopy: implications for probing stromal alterations in human breast cancer Ajeti, Visar Nadiarnykh, Oleg Ponik, Suzanne M. Keely, Patricia J. Eliceiri, Kevin W. Campagnola, Paul J. Biomed Opt Express Microscopy Second Harmonic Generation (SHG) microscopy has been previously used to describe the morphology of collagen in the extracellular matrix (ECM) in different stages of invasion in breast cancer. Here this concept is extended by using SHG to provide quantitative discrimination of self-assembled collagen gels, consisting of mixtures of type I (Col I) and type V (Col V) isoforms which serve as models of changes in the ECM during invasion in vivo. To investigate if SHG is sensitive to changes due to Col V incorporation into Col I fibrils, gels were prepared with 0-20% Col V with the balance consisting of Col I. Using the metrics of SHG intensity, fiber length, emission directionality, and depth-dependent intensities, we found similar responses for gels comprised of 100% Col I, and 95% Col I/5% Col V, where these metrics were all significantly different from those of the 80% Col I/20% Col V gels. Specifically, the gels of lower Col V content produce brighter SHG, are characterized by longer fibers, and have a higher forward/backward emission ratio. These attributes are all consistent with more highly organized collagen fibrils/fibers and are in agreement with previous TEM characterization as well as predictions based on phase matching considerations. These results suggest that SHG can be developed to discriminate Col I/Col V composition in tissues to characterize and follow breast cancer invasion. Optical Society of America 2011-07-20 /pmc/articles/PMC3149528/ /pubmed/21833367 http://dx.doi.org/10.1364/BOE.2.002307 Text en ©2011 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
Ajeti, Visar
Nadiarnykh, Oleg
Ponik, Suzanne M.
Keely, Patricia J.
Eliceiri, Kevin W.
Campagnola, Paul J.
Structural changes in mixed Col I/Col V collagen gels probed by SHG microscopy: implications for probing stromal alterations in human breast cancer
title Structural changes in mixed Col I/Col V collagen gels probed by SHG microscopy: implications for probing stromal alterations in human breast cancer
title_full Structural changes in mixed Col I/Col V collagen gels probed by SHG microscopy: implications for probing stromal alterations in human breast cancer
title_fullStr Structural changes in mixed Col I/Col V collagen gels probed by SHG microscopy: implications for probing stromal alterations in human breast cancer
title_full_unstemmed Structural changes in mixed Col I/Col V collagen gels probed by SHG microscopy: implications for probing stromal alterations in human breast cancer
title_short Structural changes in mixed Col I/Col V collagen gels probed by SHG microscopy: implications for probing stromal alterations in human breast cancer
title_sort structural changes in mixed col i/col v collagen gels probed by shg microscopy: implications for probing stromal alterations in human breast cancer
topic Microscopy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149528/
https://www.ncbi.nlm.nih.gov/pubmed/21833367
http://dx.doi.org/10.1364/BOE.2.002307
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