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Spatial mapping of collagen content and structure in human intervertebral disk degeneration

Collagen plays a key structural role in both the annulus fibrosus (AF) and nucleus pulposus (NP) of intervertebral disks (IVDs). Changes in collagen content with degeneration suggest a shift from collagen type II to type I within the NP, and the activation of pro‐inflammatory factors is indicative o...

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Autores principales: Zeldin, Lawrence, Mosley, Grace E., Laudier, Damien, Gallate, Zachary S., Gansau, Jennifer, Hoy, Robert C., Poeran, Jashvant, Iatridis, James C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770200/
https://www.ncbi.nlm.nih.gov/pubmed/33392461
http://dx.doi.org/10.1002/jsp2.1129
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author Zeldin, Lawrence
Mosley, Grace E.
Laudier, Damien
Gallate, Zachary S.
Gansau, Jennifer
Hoy, Robert C.
Poeran, Jashvant
Iatridis, James C.
author_facet Zeldin, Lawrence
Mosley, Grace E.
Laudier, Damien
Gallate, Zachary S.
Gansau, Jennifer
Hoy, Robert C.
Poeran, Jashvant
Iatridis, James C.
author_sort Zeldin, Lawrence
collection PubMed
description Collagen plays a key structural role in both the annulus fibrosus (AF) and nucleus pulposus (NP) of intervertebral disks (IVDs). Changes in collagen content with degeneration suggest a shift from collagen type II to type I within the NP, and the activation of pro‐inflammatory factors is indicative of fibrosis throughout. While IVD degeneration is considered a fibrotic process, an increase in collagen content with degeneration, reflective of fibrosis, has not been demonstrated. Additionally, changes in collagen content and structure in human IVDs with degeneration have not been characterized with high spatial resolution. The collagen content of 23 human lumbar L2/3 or L3/4 IVDs was quantified using second harmonic generation imaging (SHG) and multiple image processing algorithms, and these parameters were correlated with the Rutges histological degeneration grade. In the NP, SHG intensity increased with degeneration grade, suggesting fibrotic collagen deposition. In the AF, the entropy of SHG intensity was reduced with degeneration indicating increased collagen uniformity and suggesting less‐organized lamellar structure. Collagen orientation entropy decreased throughout most IVD regions with increasing degeneration grade, further supporting a loss in collagen structural complexity. Overall, SHG imaging enabled visualization and quantification of IVD collagen content and organization with degeneration. There was an observed shift from an initially complex structure to more uniform structure with loss of microstructural elements and increased NP collagen polarity, suggesting fibrotic remodeling.
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spelling pubmed-77702002020-12-31 Spatial mapping of collagen content and structure in human intervertebral disk degeneration Zeldin, Lawrence Mosley, Grace E. Laudier, Damien Gallate, Zachary S. Gansau, Jennifer Hoy, Robert C. Poeran, Jashvant Iatridis, James C. JOR Spine Special Issue PSRS Conference 2019 Collagen plays a key structural role in both the annulus fibrosus (AF) and nucleus pulposus (NP) of intervertebral disks (IVDs). Changes in collagen content with degeneration suggest a shift from collagen type II to type I within the NP, and the activation of pro‐inflammatory factors is indicative of fibrosis throughout. While IVD degeneration is considered a fibrotic process, an increase in collagen content with degeneration, reflective of fibrosis, has not been demonstrated. Additionally, changes in collagen content and structure in human IVDs with degeneration have not been characterized with high spatial resolution. The collagen content of 23 human lumbar L2/3 or L3/4 IVDs was quantified using second harmonic generation imaging (SHG) and multiple image processing algorithms, and these parameters were correlated with the Rutges histological degeneration grade. In the NP, SHG intensity increased with degeneration grade, suggesting fibrotic collagen deposition. In the AF, the entropy of SHG intensity was reduced with degeneration indicating increased collagen uniformity and suggesting less‐organized lamellar structure. Collagen orientation entropy decreased throughout most IVD regions with increasing degeneration grade, further supporting a loss in collagen structural complexity. Overall, SHG imaging enabled visualization and quantification of IVD collagen content and organization with degeneration. There was an observed shift from an initially complex structure to more uniform structure with loss of microstructural elements and increased NP collagen polarity, suggesting fibrotic remodeling. John Wiley & Sons, Inc. 2020-11-02 /pmc/articles/PMC7770200/ /pubmed/33392461 http://dx.doi.org/10.1002/jsp2.1129 Text en © 2020 The Authors. JOR Spine published by Wiley Periodicals LLC on behalf of Orthopaedic Research Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Special Issue PSRS Conference 2019
Zeldin, Lawrence
Mosley, Grace E.
Laudier, Damien
Gallate, Zachary S.
Gansau, Jennifer
Hoy, Robert C.
Poeran, Jashvant
Iatridis, James C.
Spatial mapping of collagen content and structure in human intervertebral disk degeneration
title Spatial mapping of collagen content and structure in human intervertebral disk degeneration
title_full Spatial mapping of collagen content and structure in human intervertebral disk degeneration
title_fullStr Spatial mapping of collagen content and structure in human intervertebral disk degeneration
title_full_unstemmed Spatial mapping of collagen content and structure in human intervertebral disk degeneration
title_short Spatial mapping of collagen content and structure in human intervertebral disk degeneration
title_sort spatial mapping of collagen content and structure in human intervertebral disk degeneration
topic Special Issue PSRS Conference 2019
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770200/
https://www.ncbi.nlm.nih.gov/pubmed/33392461
http://dx.doi.org/10.1002/jsp2.1129
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