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The Role of Transthyretin in Oligodendrocyte Development
Transthyretin (TTR) is a protein that binds and distributes thyroid hormones (THs) in blood and cerebrospinal fluid. Previously, two reports identified TTR null mice as hypothyroid in the central nervous system (CNS). This prompted our investigations into developmentally regulated TH-dependent proce...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060235/ https://www.ncbi.nlm.nih.gov/pubmed/32144308 http://dx.doi.org/10.1038/s41598-020-60699-8 |
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author | Alshehri, Bandar Pagnin, Maurice Lee, Jae Young Petratos, Steven Richardson, Samantha J. |
author_facet | Alshehri, Bandar Pagnin, Maurice Lee, Jae Young Petratos, Steven Richardson, Samantha J. |
author_sort | Alshehri, Bandar |
collection | PubMed |
description | Transthyretin (TTR) is a protein that binds and distributes thyroid hormones (THs) in blood and cerebrospinal fluid. Previously, two reports identified TTR null mice as hypothyroid in the central nervous system (CNS). This prompted our investigations into developmentally regulated TH-dependent processes in brains of wildtype and TTR null mice. Despite logical expectations of a hypomyelinating phenotype in the CNS of TTR null mice, we observed a hypermyelination phenotype, synchronous with an increase in the density of oligodendrocytes in the corpus callosum and anterior commissure of TTR null mice during postnatal development. Furthermore, absence of TTR enhanced proliferation and migration of OPCs with decreased apoptosis. Neural stem cells (NSCs) isolated from the subventricular zone of TTR null mice at P21 revealed that the absence of TTR promoted NSC differentiation toward a glial lineage. Importantly, we identified TTR synthesis in OPCs, suggestive of an alternate biological function in these cells that may extend beyond an extracellular TH-distributor protein. The hypermyelination mechanism may involve increased pAKT (involved in oligodendrocyte maturation) in TTR null mice. Elucidating the regulatory role of TTR in NSC and OPC biology could lead to potential therapeutic strategies for the treatment of acquired demyelinating diseases. |
format | Online Article Text |
id | pubmed-7060235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70602352020-03-18 The Role of Transthyretin in Oligodendrocyte Development Alshehri, Bandar Pagnin, Maurice Lee, Jae Young Petratos, Steven Richardson, Samantha J. Sci Rep Article Transthyretin (TTR) is a protein that binds and distributes thyroid hormones (THs) in blood and cerebrospinal fluid. Previously, two reports identified TTR null mice as hypothyroid in the central nervous system (CNS). This prompted our investigations into developmentally regulated TH-dependent processes in brains of wildtype and TTR null mice. Despite logical expectations of a hypomyelinating phenotype in the CNS of TTR null mice, we observed a hypermyelination phenotype, synchronous with an increase in the density of oligodendrocytes in the corpus callosum and anterior commissure of TTR null mice during postnatal development. Furthermore, absence of TTR enhanced proliferation and migration of OPCs with decreased apoptosis. Neural stem cells (NSCs) isolated from the subventricular zone of TTR null mice at P21 revealed that the absence of TTR promoted NSC differentiation toward a glial lineage. Importantly, we identified TTR synthesis in OPCs, suggestive of an alternate biological function in these cells that may extend beyond an extracellular TH-distributor protein. The hypermyelination mechanism may involve increased pAKT (involved in oligodendrocyte maturation) in TTR null mice. Elucidating the regulatory role of TTR in NSC and OPC biology could lead to potential therapeutic strategies for the treatment of acquired demyelinating diseases. Nature Publishing Group UK 2020-03-06 /pmc/articles/PMC7060235/ /pubmed/32144308 http://dx.doi.org/10.1038/s41598-020-60699-8 Text en © The Author(s) 2020 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 Alshehri, Bandar Pagnin, Maurice Lee, Jae Young Petratos, Steven Richardson, Samantha J. The Role of Transthyretin in Oligodendrocyte Development |
title | The Role of Transthyretin in Oligodendrocyte Development |
title_full | The Role of Transthyretin in Oligodendrocyte Development |
title_fullStr | The Role of Transthyretin in Oligodendrocyte Development |
title_full_unstemmed | The Role of Transthyretin in Oligodendrocyte Development |
title_short | The Role of Transthyretin in Oligodendrocyte Development |
title_sort | role of transthyretin in oligodendrocyte development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060235/ https://www.ncbi.nlm.nih.gov/pubmed/32144308 http://dx.doi.org/10.1038/s41598-020-60699-8 |
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