The Type 3 Deiodinase: Epigenetic Control of Brain Thyroid Hormone Action and Neurological Function

Thyroid hormones (THs) influence multiple processes in the developing and adult central nervous system, and their local availability needs to be maintained at levels that are tailored to the requirements of their biological targets. The local complement of TH transporters, deiodinase enzymes, and re...

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Main Authors: Arturo Hernandez, J. Patrizia Stohn
Format: Article
Language:English
Published: MDPI AG 2018-06-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/19/6/1804
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spelling doaj-4d81e04a3a7248338b3092a52c5d7f3a2020-11-25T00:55:59ZengMDPI AGInternational Journal of Molecular Sciences1422-00672018-06-01196180410.3390/ijms19061804ijms19061804The Type 3 Deiodinase: Epigenetic Control of Brain Thyroid Hormone Action and Neurological FunctionArturo Hernandez0J. Patrizia Stohn1Center for Molecular Medicine, Maine Medical Center Research Institute, Maine Medical Center, Scarborough, ME 04074, USACenter for Molecular Medicine, Maine Medical Center Research Institute, Maine Medical Center, Scarborough, ME 04074, USAThyroid hormones (THs) influence multiple processes in the developing and adult central nervous system, and their local availability needs to be maintained at levels that are tailored to the requirements of their biological targets. The local complement of TH transporters, deiodinase enzymes, and receptors is critical to ensure specific levels of TH action in neural cells. The type 3 iodothyronine deiodinase (DIO3) inactivates THs and is highly present in the developing and adult brain, where it limits their availability and action. DIO3 deficiency in mice results in a host of neurodevelopmental and behavioral abnormalities, demonstrating the deleterious effects of TH excess, and revealing the critical role of DIO3 in the regulation of TH action in the brain. The fact the Dio3 is an imprinted gene and that its allelic expression pattern varies across brain regions and during development introduces an additional level of control to deliver specific levels of hormone action in the central nervous system (CNS). The sensitive epigenetic nature of the mechanisms controlling the genomic imprinting of Dio3 renders brain TH action particularly susceptible to disruption due to exogenous treatments and environmental exposures, with potential implications for the etiology of human neurodevelopmental disorders.http://www.mdpi.com/1422-0067/19/6/1804thyroid hormonetype 3 deiodinaseDio3environmental factorsDlk1-Dio3 genomic imprintingbehaviorbrain developmentsensory functionneuroendocrine functionbrain morphology
collection DOAJ
language English
format Article
sources DOAJ
author Arturo Hernandez
J. Patrizia Stohn
spellingShingle Arturo Hernandez
J. Patrizia Stohn
The Type 3 Deiodinase: Epigenetic Control of Brain Thyroid Hormone Action and Neurological Function
International Journal of Molecular Sciences
thyroid hormone
type 3 deiodinase
Dio3
environmental factors
Dlk1-Dio3 genomic imprinting
behavior
brain development
sensory function
neuroendocrine function
brain morphology
author_facet Arturo Hernandez
J. Patrizia Stohn
author_sort Arturo Hernandez
title The Type 3 Deiodinase: Epigenetic Control of Brain Thyroid Hormone Action and Neurological Function
title_short The Type 3 Deiodinase: Epigenetic Control of Brain Thyroid Hormone Action and Neurological Function
title_full The Type 3 Deiodinase: Epigenetic Control of Brain Thyroid Hormone Action and Neurological Function
title_fullStr The Type 3 Deiodinase: Epigenetic Control of Brain Thyroid Hormone Action and Neurological Function
title_full_unstemmed The Type 3 Deiodinase: Epigenetic Control of Brain Thyroid Hormone Action and Neurological Function
title_sort type 3 deiodinase: epigenetic control of brain thyroid hormone action and neurological function
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2018-06-01
description Thyroid hormones (THs) influence multiple processes in the developing and adult central nervous system, and their local availability needs to be maintained at levels that are tailored to the requirements of their biological targets. The local complement of TH transporters, deiodinase enzymes, and receptors is critical to ensure specific levels of TH action in neural cells. The type 3 iodothyronine deiodinase (DIO3) inactivates THs and is highly present in the developing and adult brain, where it limits their availability and action. DIO3 deficiency in mice results in a host of neurodevelopmental and behavioral abnormalities, demonstrating the deleterious effects of TH excess, and revealing the critical role of DIO3 in the regulation of TH action in the brain. The fact the Dio3 is an imprinted gene and that its allelic expression pattern varies across brain regions and during development introduces an additional level of control to deliver specific levels of hormone action in the central nervous system (CNS). The sensitive epigenetic nature of the mechanisms controlling the genomic imprinting of Dio3 renders brain TH action particularly susceptible to disruption due to exogenous treatments and environmental exposures, with potential implications for the etiology of human neurodevelopmental disorders.
topic thyroid hormone
type 3 deiodinase
Dio3
environmental factors
Dlk1-Dio3 genomic imprinting
behavior
brain development
sensory function
neuroendocrine function
brain morphology
url http://www.mdpi.com/1422-0067/19/6/1804
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