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Tissue-Specific Thyroid Hormone Deprivation and Excess in Monocarboxylate Transporter (Mct) 8-Deficient Mice
Abstract
Mutations of the X-linked thyroid hormone (TH) transporter (monocarboxylate transporter, MCT8) produce in humans unusual abnormalities of thyroid function characterized by high serum T3 and low T4 and rT3. The mechanism of these changes remains obscure and raises questions regarding the regulation of intracellular availability and metabolism of TH. To study the pathophysiology of MCT8 deficiency, we generated Mct8 knockout mice. Male mice deficient in Mct8 (Mct8(-/y)) replicate the thyroid abnormalities observed in affected men. TH deprivation and replacement with L-T3 showed that suppression of TSH required higher serum levels T3 in Mct8(-/y) than wild-type (WT) littermates, indicating hypothalamus and/or thyrotroph resistance to T3. Furthermore, T4 is required to maintain the high serum T3 level because the latter was not different between the two genotypes during administration of T3. Mct8(-/y) mice have 2.3-fold higher T3 content in liver associated with 6.1- and 3.1-fold increase in deiodinase 1 mRNA and enzymatic activity, respectively. The relative T3 excess in liver of Mct8(-/y) mice produced a decrease in serum cholesterol (79 +/- 18 vs. 137 +/- 38 mg/dl in WT) and an increase in alkaline phosphatase (107 +/- 23 vs. 58 +/- 3 U/liter in WT) levels. In contrast, T3 content in cerebrum was 1.8-fold lower in Mct8(-/y) mice, associated with a 1.6- and 10.6-fold increase in D2 mRNA and enzymatic activity, respectively, as previously observed in TH-deprived WT mice. We conclude that cell-specific differences in intracellular TH content due to differences in contribution of the various TH transporters are responsible for the unusual clinical presentation of this defect, in contrast to TH deficiency.
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“two Mct8 knockout (KO) mouse strains closely recapitulate the thyroid phenotype, but they fail to display neurological or behavioral abnormalities (Dumitrescu et al., 2006; Trajkovic et al., 2007).”
From Modeling Psychomotor Retardation using iPSCs from MCT8-Deficient Patients Indicates a Prominent Role for the Blood-Brain Barrier (2017) · cites this paper as Dumitrescu et al., 2006
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Cites
Bianco, A. C., Salvatore, D., Gereben, B., Berry, M. J., & Larsen, P. R. (2002) · Endocrine Reviews · doi:10.1210/edrv.23.1.0455 · Cited by 1,853
Guideline to reference gene selection for quantitative real-time PCR
Radonić, A., Thulke, S., Mackay, I. M., Landt, O., Siegert, W., & Nitsche, A. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2003.11.177 · Cited by 1,645
Identification of monocarboxylate transporter 8 as a specific thyroid hormone transporter
Friesema, E. C. H., Ganguly, S., Abdalla, A., Fox, J. E. M., Halestrap, A. P., & Visser, T. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300909200 · Cited by 725
Friesema, E. C., Grueters, A., Biebermann, H., Krude, H., von Moers, A., Reeser, M., Barrett, T. G., Mancilla, E. E., Svensson, J., Kester, M. H., et al. (2004) · The Lancet · doi:10.1016/s0140-6736(04)17226-7 · Cited by 709
Dumitrescu, A. M., Liao, X.-H., Best, T. B., Brockmann, K., & Refetoff, S. (2004) · The American Journal of Human Genetics · doi:10.1086/380999 · Cited by 706
Self-citationSelenium, the Thyroid, and the Endocrine System
Köhrle, J., Jakob, F. J., Contempré, B., & Dumont, J. E. (2005) · Endocrine Reviews · doi:10.1210/er.2001-0034 · Cited by 535
Mutations in SECISBP2 result in abnormal thyroid hormone metabolism
Dumitrescu, A. M., Liao, X.-H., Abdullah, M. S. Y., Lado-Abeal, J., Majed, F. A., Moeller, L. C., Boran, G., Schomburg, L., Weiss, R. E., & Refetoff, S. (2005) · Nature Genetics · doi:10.1038/ng1654 · Cited by 412
Self-citationAllan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 (MCT8) Gene
Schwartz, C. E., May, M. M., Carpenter, N. J., Rogers, R. C., Martin, J. A., Bialer, M. G., Ward, J. C., Sanabria, J., Marsa, S., Lewis, J. A., et al. (2005) · The American Journal of Human Genetics · doi:10.1086/431313 · Cited by 377
Action of thyroid hormone in brain
Bernal, J. (2002) · Journal of Endocrinological Investigation · doi:10.1007/bf03344003 · Cited by 359
de Escobar, G. M., PASTOR, R., Obregón, M.-J., & del Rey, F. E. (1985) · Endocrinology · doi:10.1210/endo-117-5-1890 · Cited by 356
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Research works printed but not linked: 4
- Allan, 1944, Some examples of the inheritance of mental deficiency: apparently sex-linked idiocy and microcephaly, Am J Ment Defic, 48, 325
- Delange, 2000, Endemic cretinism, 743
- Refetoff, 2001, Thyroid disorders, 4029
- Dumitrescu, 2004, Abstract presented at the 76th ATA meeting on the mechanism producing the unusual thyroid phenotype in defects of the MCT8 gene, Thyroid, 14, 761
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Berbel, P. J., & Bernal, J. (2010) · Expert Review of Endocrinology & Metabolism · doi:10.1586/eem.10.37 · Cited by 19
Šošić‐Jurjević, B., Lütjohann, D., Jarić, I., Miler, M., Milutinović, D. V., Filipović, B. R., Ajdžanović, V. Z., Renko, K., Wirth, E. K., Janković, S., et al. (2017) · Experimental Gerontology · doi:10.1016/j.exger.2017.03.016 · Cited by 17
Mayerl, S. E., Alcaide, M. A., Bauer, R., Schwaninger, M., Heuer, H., & ffrench‐Constant, C. (2022) · Cells · doi:10.3390/cells11030524 · Cited by 17
Chen, J., Salveridou, E., Liebmann, L., Sundaram, S. M., Doycheva, D., Markova, B., Hübner, C. A., Boelen, A., Visser, W. E., Heuer, H., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043452 · Cited by 17
Lago‐Lestón, R. M., Iglesias, M., San‐José, E., Areal, C., Eiras, A., Araújo‐Vilar, D., Lado‐Abeal, J., & Domínguez‐Gerpe, L. (2008) · Clinical Endocrinology · doi:10.1111/j.1365-2265.2008.03377.x · Cited by 17
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Mayerl, S. E., & Heuer, H. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106195 · Cited by 15
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Mughal, B. B., Leemans, M., de Souza, E. C. L., Mével, S. L., Špirhanzlová, P., Visser, T. J., Fini, J., & DEMENEIX, B. A. (2017) · Endocrinology · doi:10.1210/en.2017-00108 · Cited by 17
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Bárez‐López, S., Grijota-Martínez, C., Liao, X.-H., Refetoff, S., & Guadaño‐Ferraz, A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0226017 · Cited by 16
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ters, A. G. U. (2007) · KARGER eBooks · doi:10.1159/000106823 · Cited by 14
Wirth, E. K., Rijntjes, E., Meyer, F. I., Köhrle, J., & Schweizer, U. (2015) · European Thyroid Journal · doi:10.1159/000381021 · Cited by 13
Vancamp, P., & Darras, V. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2017.01.045 · Cited by 13
Jones, R. S., Tu, C., Zhang, M., Qu, J., & Morris, M. E. (2019) · Molecular Pharmacology · doi:10.1124/mol.119.116731 · Cited by 13
Krude, H., Biebermann, H., Schuelke, M., Müller, T. D., & Tschöp, M. H. (2020) · Experimental and Clinical Endocrinology & Diabetes · doi:10.1055/a-1108-1456 · Cited by 12
Guzmán‐Gutiérrez, E., Veas, C., Leiva, A., Escudero, C., & Sobrevía, L. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00136 · Cited by 13
Mochizuki, K., Ishihara, A., Goda, T., & Yamauchi, K. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.12.097 · Cited by 13
Ohba, K., Sinha, R. A., Singh, B. K., Iannucci, L. F., Zhou, J., Kovalik, J., Liao, X.-H., Refetoff, S., Sng, J., Leow, M. K., et al. (2017) · Thyroid · doi:10.1089/thy.2016.0456 · Cited by 13
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Serrano, M., Moreno, M., Ortega, F. J., Xifra, G., Ricart, W., Moreno‐Navarrete, J. M., & Fernández‐Real, J. M. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-1327 · Cited by 12
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Ridgway, E. C., Tomer, Y., & McLachlan, S. M. (2007) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2007-1855 · Cited by 7
Germain, D. L. S. (2010) · Elsevier eBooks · doi:10.1016/b978-1-4160-5583-9.00075-7 · Cited by 7
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Zhang, Q., Yang, Q., Zhou, X., Qin, Z., Yi, S., & Luo, J. (2022) · Frontiers in Pediatrics · doi:10.3389/fped.2022.1050023 · Cited by 5
Richardson, S. J., Herck, S. V., Delbaere, J., McAllan, B. M., & Darras, V. (2017) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2017.09.012 · Cited by 5
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Self-citationLuis, E., Fernández, Y., Alvarado-Olivarez, M., Juárez-Santacruz, L., Garcı́a-Nieto, E., & Anaya‐Hernández, A. (2019) · Acta Histochemica · doi:10.1016/j.acthis.2019.151440 · Cited by 3
Chan, L. F., Albertsson-Wikland, K. G., Camacho‐Hübner, C., & Hochberg, Z. (2010) · Science Signaling · doi:10.1126/scisignal.3143mr3 · Cited by 3
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Azhan, A., Cumberland, A. L., Chincarini, G., Barresi, M., Hale, N., Rowitch, D. H., Wong, F., Walker, D. W., & Tolcos, M. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.12.068 · Cited by 1
Alcaide-Martin, A., Jaber, R., Boelen, A., Heuer, H., & Mayerl, S. E. (2026) · Frontiers in Endocrinology · doi:10.3389/fendo.2026.1781214 · Cited by 1
Dumitrescu, A. M., & Refetoff, S. (2009) · Elsevier eBooks · doi:10.1016/b978-1-4160-4745-2.00022-5 · Cited by 1
Self-citationRole of Thyrotropin-Releasing Hormone in the Regulation of the Thyroid Axis
Hollenberg, A. N. (2009) · Elsevier eBooks · doi:10.1016/b978-1-4160-4745-2.00006-7 · Cited by 1
In vitro blood–brain barrier model derived from human iPS cells and its applications
Zhang, H., Yamaguchi, T., & Kawabata, K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822231-7.00003-5 · Cited by 1
La resistenza e le altre sindromi da ridotta sensibilità agli ormoni tiroidei
Cosmo, C. D. (2022) · L Endocrinologo · doi:10.1007/s40619-021-01008-x · Cited by 1
Shcherbitskaia, A. D., Kovalenko, A. A., Milyutina, Y. P., & Vasilev, D. S. (2022) · Neurochemical Journal · doi:10.1134/s1819712422030102 · Cited by 1
Zhang, D., Guo, Z., Yang, Y., & Chang, J. (2022) · Journal of Holistic Integrative Pharmacy · doi:10.1016/s2707-3688(23)00061-4 · Cited by 2
Les hormones thyroïdiennes régulent le destin des cellules souches neurales
Remaud, S., & DEMENEIX, B. A. (2019) · Biologie Aujourd hui · doi:10.1051/jbio/2019007 · Cited by 1
Genetic Influences on Thyroid Function Tests
van der Deure, W. M., Medici, M., Peeters, R. P., & Visser, T. J. (2010) · Endocrine updates · doi:10.1007/978-1-4419-1485-9_2 · Cited by 1
Manifestazioni cliniche delle mutazioni del trasportatore degli ormoni tiroidei MCT8
Cosmo, C. D. (2013) · L Endocrinologo · doi:10.1007/bf03346046
Papel do TR na termogênese induzida pela dieta.
Amorim, B. S. (2010) · doi:10.11606/d.42.2010.tde-19052010-130712
Studien zum Transport von Schilddrüsenhormonen durch Membrantransporter der MCT- und LAT-Familie
Kinne, A. (2011) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-15773
Cho, S. W., & Park, Y. J. (2012) · Journal of Korean Thyroid Association · doi:10.11106/jkta.2012.5.2.83
Thyroid physiology becomes more complicated
Larsen, P. R. (2007) · Nature Clinical Practice Endocrinology & Metabolism · doi:10.1038/ncpendmet0551
Capelo, L. P. (2009) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2009.tde-06042009-160228
Genetic Defects in Thyroid Hormone Synthesis and Action∗
Macchia, P. E., & Fenzi, G. (2015) · Elsevier eBooks · doi:10.1016/b978-0-323-18907-1.00094-9
Mebis, L., Debaveye, Y. A., Ellger, B., Derde, S., Ververs, E.-J., Langouche, L., Darras, V., Fliers, E., Visser, T. J., & den Berghe, G. V. (2009)
Deficit in Thyroid Hormone Transporters and Brain Development
Suzuki, T., & Abe, T. (2016) · Contemporary clinical neuroscience · doi:10.1007/978-1-4939-3737-0_11
Metadata
- Authors
- Dumitrescu, A. M., Liao, X.-H., Weiss, R. E., Millen, K., & Refetoff, S.
- Affiliations
- University of Chicago (US)
- Corresponding author
- Refetoff, Samuel
- Venue
- Endocrinology
- Publisher
- The Endocrine Society
- Published
- 2006-09-01
- Volume
- 147
- Issue
- 9
- Pages
- 4036-4043
- ISSN
- 0013-7227 (ISSN-L)
- 1945-7170
- OpenAlex
- W2102611661
- Cited by
- 318
- References
- 30
- Citations by year
- 2026: 4 · 2025: 7 · 2024: 7 · 2023: 3 · 2022: 19 · 2021: 15 · 2020: 11 · 2019: 20 · 2018: 9 · 2017: 21 · 2016: 18 · 2015: 24 · 2014: 23 · 2013: 19 · 2012: 17
- FWCI
- 13.53
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Endocrinology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Chicago
- National Institutes of Health (DK 15070)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 15070, DK 58281, DK 20595, R01DK058281)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Thyroid Disorders and Treatments
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Chemical Analysis and Environmental Impact
- Keywords
- MCT8, thyroid hormone excess, deiodinase 2, T3, thyroxine, reverse T3, TSH suppression, liver, cerebrum, serum cholesterol, alkaline phosphatase, knockout mice
- MeSH terms
- Alkaline Phosphatase, Animals, Brain Chemistry, Cholesterol, Disease Models, Animal, Drug Resistance, Female, Humans, Hypothalamus, Kinetics, Liver, Male, Mice, Inbred C57BL, Mutation, Phenotype, Thyroid Hormones, Thyrotropin, Thyroxine, Triiodothyronine, Mice, Knockout, Membrane Transport Proteins, Monocarboxylic Acid Transporters, Symporters, Mice
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