Literature DB >> 19641107

Neuronal 3',3,5-triiodothyronine (T3) uptake and behavioral phenotype of mice deficient in Mct8, the neuronal T3 transporter mutated in Allan-Herndon-Dudley syndrome.

Eva K Wirth1, Stephan Roth, Cristiane Blechschmidt, Sabine M Hölter, Lore Becker, Ildiko Racz, Andreas Zimmer, Thomas Klopstock, Valerie Gailus-Durner, Helmut Fuchs, Wolfgang Wurst, Thomas Naumann, Anja Bräuer, Martin Hrabé de Angelis, Josef Köhrle, Annette Grüters, Ulrich Schweizer.   

Abstract

Thyroid hormone transport into cells requires plasma membrane transport proteins. Mutations in one of these, monocarboxylate transporter 8 (MCT8), have been identified as underlying cause for the Allan-Herndon-Dudley syndrome, an X-linked mental retardation in which the patients also present with abnormally high 3',3,5-triiodothyronine (T(3)) plasma levels. Mice deficient in Mct8 replicate the thyroid hormone abnormalities observed in the human condition. However, no neurological deficits have been described in mice lacking Mct8. Therefore, we subjected Mct8-deficient mice to a comprehensive immunohistochemical, neurological, and behavioral screen. Several behavioral abnormalities were found in the mutants. Interestingly, some of these behavioral changes are compatible with hypothyroidism, whereas others rather indicate hyperthyroidism. We thus hypothesized that neurons exclusively dependent on Mct8 are in a hypothyroid state, whereas neurons expressing other T(3) transporters become hyperthyroid, if they are exposed directly to the high plasma T(3). The majority of T(3) uptake in primary cortical neurons is mediated by Mct8, but pharmacological inhibition suggested functional expression of additional T(3) transporter classes. mRNAs encoding six T(3) transporters, including L-type amino acid transporters (LATs), were coexpressed with Mct8 in isolated neurons. We then demonstrated Lat2 expression in cultured neurons and throughout murine brain development. In contrast, LAT2 is expressed in microglia in the developing human brain during gestation, but not in neurons. We suggest that lack of functional complementation by alternative thyroid hormone transporters in developing human neurons precipitates the devastating neurodevelopmental phenotype in MCT8-deficient patients, whereas Mct8-deficient mouse neurons are functionally complemented by other transporters, for possibly Lat2.

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Year:  2009        PMID: 19641107      PMCID: PMC6666526          DOI: 10.1523/JNEUROSCI.6055-08.2009

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  59 in total

Review 1.  Monocarboxylate Transporters: Therapeutic Targets and Prognostic Factors in Disease.

Authors:  R S Jones; M E Morris
Journal:  Clin Pharmacol Ther       Date:  2016-08-22       Impact factor: 6.875

2.  Structural insights into thyroid hormone transport mechanisms of the L-type amino acid transporter 2.

Authors:  Katrin M Hinz; Katja Meyer; Anita Kinne; Ralf Schülein; Josef Köhrle; Gerd Krause
Journal:  Mol Endocrinol       Date:  2015-05-06

Review 3.  Paradigms of Dynamic Control of Thyroid Hormone Signaling.

Authors:  Antonio C Bianco; Alexandra Dumitrescu; Balázs Gereben; Miriam O Ribeiro; Tatiana L Fonseca; Gustavo W Fernandes; Barbara M L C Bocco
Journal:  Endocr Rev       Date:  2019-08-01       Impact factor: 19.871

4.  Sobetirome and its Amide Prodrug Sob-AM2 Exert Thyromimetic Actions in Mct8-Deficient Brain.

Authors:  Soledad Bárez-López; Meredith D Hartley; Carmen Grijota-Martínez; Thomas S Scanlan; Ana Guadaño-Ferraz
Journal:  Thyroid       Date:  2018-06-29       Impact factor: 6.568

5.  Essential molecular determinants for thyroid hormone transport and first structural implications for monocarboxylate transporter 8.

Authors:  Anita Kinne; Gunnar Kleinau; Carolin S Hoefig; Annette Grüters; Josef Köhrle; Gerd Krause; Ulrich Schweizer
Journal:  J Biol Chem       Date:  2010-07-13       Impact factor: 5.157

Review 6.  Making sense with thyroid hormone--the role of T(3) in auditory development.

Authors:  Lily Ng; Matthew W Kelley; Douglas Forrest
Journal:  Nat Rev Endocrinol       Date:  2013-03-26       Impact factor: 43.330

7.  Thyroid hormone-regulated mouse cerebral cortex genes are differentially dependent on the source of the hormone: a study in monocarboxylate transporter-8- and deiodinase-2-deficient mice.

Authors:  Beatriz Morte; Ainhoa Ceballos; Diego Diez; Carmen Grijota-Martínez; Alexandra M Dumitrescu; Caterina Di Cosmo; Valerie Anne Galton; Samuel Refetoff; Juan Bernal
Journal:  Endocrinology       Date:  2010-03-08       Impact factor: 4.736

8.  Retinoic acid induces expression of the thyroid hormone transporter, monocarboxylate transporter 8 (Mct8).

Authors:  Takahiko Kogai; Yan-Yun Liu; Laura L Richter; Kaizeen Mody; Hiroyuki Kagechika; Gregory A Brent
Journal:  J Biol Chem       Date:  2010-06-23       Impact factor: 5.157

9.  Membrane-traversing mechanism of thyroid hormone transport by monocarboxylate transporter 8.

Authors:  Jonas Protze; Doreen Braun; Katrin Manuela Hinz; Dorothea Bayer-Kusch; Ulrich Schweizer; Gerd Krause
Journal:  Cell Mol Life Sci       Date:  2017-01-28       Impact factor: 9.261

Review 10.  Thyroid hormone transporters--functions and clinical implications.

Authors:  Juan Bernal; Ana Guadaño-Ferraz; Beatriz Morte
Journal:  Nat Rev Endocrinol       Date:  2015-05-05       Impact factor: 43.330

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