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Aquaporin-4 expression and modulation in a rat model of post-traumatic syringomyelia
Aquaporin-4 (AQP4) has been implicated in post-traumatic syringomyelia (PTS), a disease characterised by the formation of fluid-filled cysts in the spinal cord. This study investigated the expression of AQP4 around a mature cyst (syrinx) and the effect of pharmacomodulation of AQP4 on syrinx size. P...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267129/ https://www.ncbi.nlm.nih.gov/pubmed/37316571 http://dx.doi.org/10.1038/s41598-023-36538-x |
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author | Berliner, Joel A. Lam, Magdalena A. Najafi, Elmira Hemley, Sarah J. Bilston, Lynne E. Stoodley, Marcus A. |
author_facet | Berliner, Joel A. Lam, Magdalena A. Najafi, Elmira Hemley, Sarah J. Bilston, Lynne E. Stoodley, Marcus A. |
author_sort | Berliner, Joel A. |
collection | PubMed |
description | Aquaporin-4 (AQP4) has been implicated in post-traumatic syringomyelia (PTS), a disease characterised by the formation of fluid-filled cysts in the spinal cord. This study investigated the expression of AQP4 around a mature cyst (syrinx) and the effect of pharmacomodulation of AQP4 on syrinx size. PTS was induced in male Sprague–Dawley rats by computerized spinal cord impact and subarachnoid kaolin injection. Immunofluorescence of AQP4 was carried out on mature syrinx tissue 12 weeks post-surgery. Increased AQP4 expression corresponded to larger, multiloculated cysts (R(2) = 0.94), yet no localized changes to AQP4 expression in perivascular regions or the glia limitans were present. In a separate cohort of animals, at 6 weeks post-surgery, an AQP4 agonist (AqF026), antagonist (AqB050), or vehicle was administered daily over 4 days, with MRIs performed before and after the completion of treatment. Histological analysis was performed at 12 weeks post-surgery. Syrinx volume and length were not altered with AQP4 modulation. The correlation between increased AQP4 expression with syrinx area suggests that AQP4 or the glia expressing AQP4 are recruited to regulate water movement. Given this, further investigation should examine AQP4 modulation with dose regimens at earlier time-points after PTS induction, as these may alter the course of syrinx development. |
format | Online Article Text |
id | pubmed-10267129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102671292023-06-15 Aquaporin-4 expression and modulation in a rat model of post-traumatic syringomyelia Berliner, Joel A. Lam, Magdalena A. Najafi, Elmira Hemley, Sarah J. Bilston, Lynne E. Stoodley, Marcus A. Sci Rep Article Aquaporin-4 (AQP4) has been implicated in post-traumatic syringomyelia (PTS), a disease characterised by the formation of fluid-filled cysts in the spinal cord. This study investigated the expression of AQP4 around a mature cyst (syrinx) and the effect of pharmacomodulation of AQP4 on syrinx size. PTS was induced in male Sprague–Dawley rats by computerized spinal cord impact and subarachnoid kaolin injection. Immunofluorescence of AQP4 was carried out on mature syrinx tissue 12 weeks post-surgery. Increased AQP4 expression corresponded to larger, multiloculated cysts (R(2) = 0.94), yet no localized changes to AQP4 expression in perivascular regions or the glia limitans were present. In a separate cohort of animals, at 6 weeks post-surgery, an AQP4 agonist (AqF026), antagonist (AqB050), or vehicle was administered daily over 4 days, with MRIs performed before and after the completion of treatment. Histological analysis was performed at 12 weeks post-surgery. Syrinx volume and length were not altered with AQP4 modulation. The correlation between increased AQP4 expression with syrinx area suggests that AQP4 or the glia expressing AQP4 are recruited to regulate water movement. Given this, further investigation should examine AQP4 modulation with dose regimens at earlier time-points after PTS induction, as these may alter the course of syrinx development. Nature Publishing Group UK 2023-06-14 /pmc/articles/PMC10267129/ /pubmed/37316571 http://dx.doi.org/10.1038/s41598-023-36538-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Berliner, Joel A. Lam, Magdalena A. Najafi, Elmira Hemley, Sarah J. Bilston, Lynne E. Stoodley, Marcus A. Aquaporin-4 expression and modulation in a rat model of post-traumatic syringomyelia |
title | Aquaporin-4 expression and modulation in a rat model of post-traumatic syringomyelia |
title_full | Aquaporin-4 expression and modulation in a rat model of post-traumatic syringomyelia |
title_fullStr | Aquaporin-4 expression and modulation in a rat model of post-traumatic syringomyelia |
title_full_unstemmed | Aquaporin-4 expression and modulation in a rat model of post-traumatic syringomyelia |
title_short | Aquaporin-4 expression and modulation in a rat model of post-traumatic syringomyelia |
title_sort | aquaporin-4 expression and modulation in a rat model of post-traumatic syringomyelia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267129/ https://www.ncbi.nlm.nih.gov/pubmed/37316571 http://dx.doi.org/10.1038/s41598-023-36538-x |
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