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Regulation of T3 Availability in the Developing Brain: The Mouse Genetics Contribution
Alterations in maternal thyroid physiology may have deleterious consequences on the development of the fetal brain, but the underlying mechanisms remain elusive, hampering the development of appropriate therapeutic strategies. The present review sums up the contribution of genetically modified mouse...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985302/ https://www.ncbi.nlm.nih.gov/pubmed/29892264 http://dx.doi.org/10.3389/fendo.2018.00265 |
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author | Richard, Sabine Flamant, Frédéric |
author_facet | Richard, Sabine Flamant, Frédéric |
author_sort | Richard, Sabine |
collection | PubMed |
description | Alterations in maternal thyroid physiology may have deleterious consequences on the development of the fetal brain, but the underlying mechanisms remain elusive, hampering the development of appropriate therapeutic strategies. The present review sums up the contribution of genetically modified mouse models to this field. In particular, knocking out genes involved in thyroid hormone (TH) deiodination, transport, and storage has significantly improved the picture that we have of the economy of TH in the fetal brain and the underlying genetic program. These data pave the way for future studies to bridge the gap in knowledge between thyroid physiology and brain development. |
format | Online Article Text |
id | pubmed-5985302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59853022018-06-11 Regulation of T3 Availability in the Developing Brain: The Mouse Genetics Contribution Richard, Sabine Flamant, Frédéric Front Endocrinol (Lausanne) Endocrinology Alterations in maternal thyroid physiology may have deleterious consequences on the development of the fetal brain, but the underlying mechanisms remain elusive, hampering the development of appropriate therapeutic strategies. The present review sums up the contribution of genetically modified mouse models to this field. In particular, knocking out genes involved in thyroid hormone (TH) deiodination, transport, and storage has significantly improved the picture that we have of the economy of TH in the fetal brain and the underlying genetic program. These data pave the way for future studies to bridge the gap in knowledge between thyroid physiology and brain development. Frontiers Media S.A. 2018-05-28 /pmc/articles/PMC5985302/ /pubmed/29892264 http://dx.doi.org/10.3389/fendo.2018.00265 Text en Copyright © 2018 Richard and Flamant. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Richard, Sabine Flamant, Frédéric Regulation of T3 Availability in the Developing Brain: The Mouse Genetics Contribution |
title | Regulation of T3 Availability in the Developing Brain: The Mouse Genetics Contribution |
title_full | Regulation of T3 Availability in the Developing Brain: The Mouse Genetics Contribution |
title_fullStr | Regulation of T3 Availability in the Developing Brain: The Mouse Genetics Contribution |
title_full_unstemmed | Regulation of T3 Availability in the Developing Brain: The Mouse Genetics Contribution |
title_short | Regulation of T3 Availability in the Developing Brain: The Mouse Genetics Contribution |
title_sort | regulation of t3 availability in the developing brain: the mouse genetics contribution |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985302/ https://www.ncbi.nlm.nih.gov/pubmed/29892264 http://dx.doi.org/10.3389/fendo.2018.00265 |
work_keys_str_mv | AT richardsabine regulationoft3availabilityinthedevelopingbrainthemousegeneticscontribution AT flamantfrederic regulationoft3availabilityinthedevelopingbrainthemousegeneticscontribution |