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Postnatal Development of the Murine Notochord Remnants Quantified by High-resolution Contrast-enhanced MicroCT
The notochord gives rise to spinal segments during development, and it becomes embedded within the nucleus pulposus of the intervertebral disc (IVD) during maturation. The disruption of the notochord band has been observed with IVD degeneration. Since the mechanical competence of the IVD relies on i...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645339/ https://www.ncbi.nlm.nih.gov/pubmed/29042621 http://dx.doi.org/10.1038/s41598-017-13446-5 |
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author | Bhalla, Sameer Lin, Kevin H. Tang, Simon Y. |
author_facet | Bhalla, Sameer Lin, Kevin H. Tang, Simon Y. |
author_sort | Bhalla, Sameer |
collection | PubMed |
description | The notochord gives rise to spinal segments during development, and it becomes embedded within the nucleus pulposus of the intervertebral disc (IVD) during maturation. The disruption of the notochord band has been observed with IVD degeneration. Since the mechanical competence of the IVD relies on its structural constituents, defining the structure of the notochord during aging is critical for investigations relating to IVD function and homeostasis. The assessment and imaging of the notochord has classically relied on histological techniques, which introduces sectioning artifacts during preparation and spatial biases. Magnetic resonance imaging (MRI) does not offer sufficient resolution to discriminate the notochord from the surrounding the nucleus pulposus, especially in murine models. Current X-ray based computed tomography systems provide imaging resolutions down to the single- and sub- micron scales, and when coupled with contrast-enhancing agents, enable the high-resolution three-dimensional imaging of relatively small features. Utilizing phosphomolybdic acid to preferentially bind to collagen cationic domains, we describe the structure of the notochord remnants with aging in the lumbar IVDs of BALB/c mice. These results provide a highly quantitative and sensitive approach to monitoring the IVD during postnatal development. |
format | Online Article Text |
id | pubmed-5645339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56453392017-10-26 Postnatal Development of the Murine Notochord Remnants Quantified by High-resolution Contrast-enhanced MicroCT Bhalla, Sameer Lin, Kevin H. Tang, Simon Y. Sci Rep Article The notochord gives rise to spinal segments during development, and it becomes embedded within the nucleus pulposus of the intervertebral disc (IVD) during maturation. The disruption of the notochord band has been observed with IVD degeneration. Since the mechanical competence of the IVD relies on its structural constituents, defining the structure of the notochord during aging is critical for investigations relating to IVD function and homeostasis. The assessment and imaging of the notochord has classically relied on histological techniques, which introduces sectioning artifacts during preparation and spatial biases. Magnetic resonance imaging (MRI) does not offer sufficient resolution to discriminate the notochord from the surrounding the nucleus pulposus, especially in murine models. Current X-ray based computed tomography systems provide imaging resolutions down to the single- and sub- micron scales, and when coupled with contrast-enhancing agents, enable the high-resolution three-dimensional imaging of relatively small features. Utilizing phosphomolybdic acid to preferentially bind to collagen cationic domains, we describe the structure of the notochord remnants with aging in the lumbar IVDs of BALB/c mice. These results provide a highly quantitative and sensitive approach to monitoring the IVD during postnatal development. Nature Publishing Group UK 2017-10-17 /pmc/articles/PMC5645339/ /pubmed/29042621 http://dx.doi.org/10.1038/s41598-017-13446-5 Text en © The Author(s) 2017 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 Bhalla, Sameer Lin, Kevin H. Tang, Simon Y. Postnatal Development of the Murine Notochord Remnants Quantified by High-resolution Contrast-enhanced MicroCT |
title | Postnatal Development of the Murine Notochord Remnants Quantified by High-resolution Contrast-enhanced MicroCT |
title_full | Postnatal Development of the Murine Notochord Remnants Quantified by High-resolution Contrast-enhanced MicroCT |
title_fullStr | Postnatal Development of the Murine Notochord Remnants Quantified by High-resolution Contrast-enhanced MicroCT |
title_full_unstemmed | Postnatal Development of the Murine Notochord Remnants Quantified by High-resolution Contrast-enhanced MicroCT |
title_short | Postnatal Development of the Murine Notochord Remnants Quantified by High-resolution Contrast-enhanced MicroCT |
title_sort | postnatal development of the murine notochord remnants quantified by high-resolution contrast-enhanced microct |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645339/ https://www.ncbi.nlm.nih.gov/pubmed/29042621 http://dx.doi.org/10.1038/s41598-017-13446-5 |
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