Literature DB >> 23529044

Making sense with thyroid hormone--the role of T(3) in auditory development.

Lily Ng1, Matthew W Kelley, Douglas Forrest.   

Abstract

The senses are our window to the world, our interface with the habitat in which we live in and the basis for our communication with each other. Although sensory systems are not generally viewed as major targets of endocrine regulation, sensory development is profoundly influenced by thyroid hormone (T(3)) signalling. In this article, we discuss this developmental role of T(3) and highlight the auditory system as the best-studied example of the interplay between systemic and local tissue mechanisms by which T(3) stimulates the onset of sensory function. Several genes that mediate the action of T(3) are known to promote sensory development in mice, including genes that encode T(3) receptors and deiodinase enzymes that amplify or deplete levels of T(3). We also discuss the current knowledge of sensory defects in human genetic disorders in which T(3) signalling is impaired. As sensory input provides the only means of acquiring information from the environment, the stimulation of sensory development is one of the most fundamental functions of T(3) signalling.

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Year:  2013        PMID: 23529044     DOI: 10.1038/nrendo.2013.58

Source DB:  PubMed          Journal:  Nat Rev Endocrinol        ISSN: 1759-5029            Impact factor:   43.330


  126 in total

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Authors:  Lutz Schomburg
Journal:  Nat Rev Endocrinol       Date:  2011-10-18       Impact factor: 43.330

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Journal:  Endocrinology       Date:  1999-02       Impact factor: 4.736

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5.  Complete activation of thyroid hormone receptor β by T3 is essential for normal cochlear function and morphology in mice.

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Journal:  Cell Physiol Biochem       Date:  2011-12-15

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Journal:  Eur J Endocrinol       Date:  2004-06       Impact factor: 6.664

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Journal:  Endocrinology       Date:  2003-09       Impact factor: 4.736

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Journal:  Diabetes       Date:  2018-04-06       Impact factor: 9.461

2.  A Novel Population of Inner Cortical Cells in the Adrenal Gland That Displays Sexually Dimorphic Expression of Thyroid Hormone Receptor-β1.

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3.  Genetic variation in thyroid folliculogenesis influences susceptibility to hypothyroidism-induced hearing impairment.

Authors:  Amanda H Mortensen; Qing Fang; Michelle T Fleming; Thomas J Jones; Alexandre Z Daly; Kenneth R Johnson; Sally A Camper
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4.  Effect of maternal care on hearing onset induced by developmental changes in the auditory periphery.

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Review 5.  Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing.

Authors:  Mei-ling A Joiner; Amy Lee
Journal:  Curr Mol Pharmacol       Date:  2015       Impact factor: 3.339

6.  The timecourse of apoptotic cell death during postnatal remodeling of the mouse cochlea and its premature onset by triiodothyronine (T3).

Authors:  R P Peeters; L Ng; M Ma; D Forrest
Journal:  Mol Cell Endocrinol       Date:  2015-02-28       Impact factor: 4.102

7.  Thyroid hormone is required for pruning, functioning and long-term maintenance of afferent inner hair cell synapses.

Authors:  Srividya Sundaresan; Jee-Hyun Kong; Qing Fang; Felipe T Salles; Felix Wangsawihardja; Anthony J Ricci; Mirna Mustapha
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8.  Developmental exposure to PCBs alters the activation of the auditory cortex in response to GABAA antagonism.

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9.  TBL1Y: a new gene involved in syndromic hearing loss.

Authors:  Mariateresa Di Stazio; Chiara Collesi; Diego Vozzi; Wei Liu; Mike Myers; Anna Morgan; Pio Adamo D Adamo; Giorgia Girotto; Elisa Rubinato; Mauro Giacca; Paolo Gasparini
Journal:  Eur J Hum Genet       Date:  2018-10-19       Impact factor: 4.246

10.  Age-Related Hearing Loss and Degeneration of Cochlear Hair Cells in Mice Lacking Thyroid Hormone Receptor β1.

Authors:  Lily Ng; Emily Cordas; Xuefeng Wu; Kristen R Vella; Anthony N Hollenberg; Douglas Forrest
Journal:  Endocrinology       Date:  2015-08-04       Impact factor: 4.736

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