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Thyroid hormone receptors in brain development and function

Abstract

Thyroid hormones are important during development of the mammalian brain, acting on migration and differentiation of neural cells, synaptogenesis, and myelination. The actions of thyroid hormones are mediated through nuclear thyroid hormone receptors (TRs) and regulation of gene expression. The purpose of this article is to review the role of TRs in brain maturation. In developing humans maternal and fetal thyroid glands provide thyroid hormones to the fetal brain, but the timing of receptor ontogeny agrees with clinical data on the importance of the maternal thyroid gland before midgestation. Several TR isoforms, which are encoded by the THRA and THRB genes, are expressed in the brain, with the most common being TRα1. Deletion of TRα1 in rodents is not, however, equivalent to hormone deprivation and, paradoxically, even prevents the effects of hypothyroidism. Unliganded receptor activity is, therefore, probably an important factor in causing the harmful effects of hypothyroidism. Accordingly, expression of a mutant receptor with impaired triiodothyronine (T3) binding and dominant negative activity affected cerebellar development and motor performance. TRs are also involved in adult brain function. TRα1 deletion, or expression of a dominant negative mutant receptor, induces consistent behavioral changes in adult mice, leading to severe anxiety and morphological changes in the hippocampus.

Key Points

  • Thyroid hormones are important in brain development by regulating cell migration and differentiation, synaptogenesis, and myelination

  • The early steps of embryonic neural development, such as neural induction, neurulation, and establishment of polarity and segmentation, are probably not influenced by thyroid hormones

  • Deficient production of maternal thyroid hormones during the first half of gestation may lead to neurological deficits and is a primary factor in the pathogenesis of neurological cretinism

  • Gene regulation by thyroid hormones in brain follows a strict temporal and regional specificity; most genes are sensitive only during a limited time period of postnatal development, and some genes are under thyroid hormone control only in certain brain regions

  • Some of the morphological alterations induced by profound hypothyroidism might actually be a consequence of the altered transcriptional activity of unliganded receptors; receptor deletion is therefore not equivalent to hormone deprivation

  • Unlike deletion of the thyroid hormone receptor, expression of dominant negative receptors produces a phenotype more similar to the hypothyroid phenotype

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Figure 1: Control of gene expression by the TR
Figure 2: A summary of human fetal and postnatal brain development in relation to thyroid hormones

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References

  1. Bernal J (2005) Thyroid hormones and brain development. Vitam Horm 71: 95–122

    Article  CAS  PubMed  Google Scholar 

  2. Joffe RT and Sokolov ST (1994) Thyroid hormones, the brain, and affective disorders. Crit Rev Neurobiol 8: 45–63

    CAS  PubMed  Google Scholar 

  3. Bauer M and Whybrow PC (2001) Thyroid hormone, neural tissue and mood modulation. World J Biol Psychiatry 2: 59–69

    Article  CAS  PubMed  Google Scholar 

  4. Yen PM (2001) Physiological and molecular basis of thyroid hormone action. Physiol Rev 81: 1097–1142

    Article  CAS  PubMed  Google Scholar 

  5. Nagy L and Schwabe JW (2004) Mechanism of the nuclear receptor molecular switch. Trends Biochem Sci 29: 317–324

    Article  CAS  PubMed  Google Scholar 

  6. McKenna NJ and O'Malley BW (2002) Combinatorial control of gene expression by nuclear receptors and coregulators. Cell 108: 465–474

    Article  CAS  PubMed  Google Scholar 

  7. Rosenfeld MG et al. (2006) Sensors and signals: a coactivator/corepressor/epigenetic code for integrating signal-dependent programs of transcriptional response. Genes Dev 20: 1405–1428

    Article  CAS  PubMed  Google Scholar 

  8. Davis PJ et al. (2005) Membrane receptors mediating thyroid hormone action. Trends Endocrinol Metab 16: 429–435

    Article  CAS  PubMed  Google Scholar 

  9. Cao X et al. (2005) Thyroid hormone induces rapid activation of Akt/protein kinase B-mammalian target of rapamycin-p70S6K cascade through phosphatidylinositol 3-kinase in human fibroblasts. Mol Endocrinol 19: 102–112

    Article  CAS  PubMed  Google Scholar 

  10. Storey NM et al. (2006) Rapid signaling at the plasma membrane by a nuclear receptor for thyroid hormone. Proc Natl Acad Sci USA 103: 5197–5201

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Scanlan TS et al. (2004) 3-Iodothyronamine is an endogenous and rapid-acting derivative of thyroid hormone. Nat Med 10: 638–642

    Article  CAS  PubMed  Google Scholar 

  12. Silva JE and Matthews PS (1984) Production rates and turnover of triiodothyronine in rat-developing cerebral cortex and cerebellum. Responses to hypothyroidism. J Clin Invest 74: 1035–1049

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Guadaño-Ferraz A et al. (1997) The type 2 iodothyronine deiodinase is expressed primarily in glial cells in the neonatal rat brain. Proc Natl Acad Sci USA 94: 10391–10396

    Article  PubMed  PubMed Central  Google Scholar 

  14. Tu HM et al. (1997) Regional distribution of type 2 thyroxine deiodinase messenger ribonucleic acid in rat hypothalamus and pituitary and its regulation by thyroid hormone. Endocrinology 138: 3359–3368

    Google Scholar 

  15. Tu HM et al. (1999) Regional expression of the type 3 iodothyronine deiodinase messenger ribonucleic acid in the rat central nervous system and its regulation by thyroid hormone. Endocrinology 140: 784–790

    Google Scholar 

  16. Dumitrescu AM et al. (2004) A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene. Am J Hum Genet 74: 168–175

    Article  CAS  PubMed  Google Scholar 

  17. Friesema EC et al. (2004) Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation. Lancet 364: 1435–1437

    Article  CAS  PubMed  Google Scholar 

  18. Bernal J and Pekonen F (1984) Ontogenesis of the nuclear 3,5,3′-triiodothyronine receptor in the human fetal brain. Endocrinology 114: 677–679

    Google Scholar 

  19. Morreale de Escobar G et al. (2004) Role of thyroid hormone during early brain development. Eur J Endocrinol 151 (Suppl 3): U25–U37

    Article  CAS  PubMed  Google Scholar 

  20. Haddow JE et al. (1999) Maternal thyroid deficiency during pregnancy and subsequent neuropsychological development of the child. N Engl J Med 341: 549–555

    Article  CAS  PubMed  Google Scholar 

  21. Vermiglio F et al. (2004) Attention deficit and hyperactivity disorders in the offspring of mothers exposed to mild-moderate iodine deficiency: a possible novel iodine deficiency disorder in developed countries. J Clin Endocrinol Metab 89: 6054–6060

    Article  CAS  PubMed  Google Scholar 

  22. Vermiglio F et al. (1995) Maternal hypothyroxinaemia during the first half of gestation in an iodine deficient area with endemic cretinism and related disorders. Clin Endocrinol Oxf 42: 409–415

    Article  CAS  PubMed  Google Scholar 

  23. Fierro Benitez R et al. (1974) The clinical pattern of cretinism as seen in Highland Ecuador. Am J Clin Nutr 27: 531–543

    Article  CAS  PubMed  Google Scholar 

  24. Delong GR et al. (1985) Neurological signs in congenital iodine-deficiency disorder (endemic cretinism). Develop Med Child Neurol 27: 317–324

    Article  CAS  PubMed  Google Scholar 

  25. Yasuda T et al. (1999) Outcome of a baby born from a mother with acquired juvenile hypothyroidism having undetectable thyroid hormone concentrations. J Clin Endocrinol Metab 84: 2630–2632

    CAS  PubMed  Google Scholar 

  26. Kester MH et al. (2004) Iodothyronine levels in the human developing brain: major regulatory roles of iodothyronine deiodinases in different areas. J Clin Endocrinol Metab 89: 3117–3128

    Article  CAS  PubMed  Google Scholar 

  27. Porterfield SP and Hendrich CE (1993) The role of thyroid hormones in prenatal and neonatal neurological development. Current perspectives. Endocrine Rev 14: 94–106

    CAS  Google Scholar 

  28. Legrand J (1984) Effects of thyroid hormones on central nervous system. In Neurobehavioral Teratology, 331–363 (Ed. Yanai J) Amsterdam: Elsevier Science Publishers

    Google Scholar 

  29. Koibuchi N et al. (2003) Current perspectives on the role of thyroid hormone in growth and development of cerebellum. Cerebellum 2: 279–289

    Article  CAS  PubMed  Google Scholar 

  30. Thompson CC and Potter GB (2000) Thyroid hormone action in neural development. Cereb Cortex 10: 939–945

    Article  CAS  PubMed  Google Scholar 

  31. Anderson GW et al. (2003) Control of thyroid hormone action in the developing rat brain. Thyroid 13: 1039–1056

    Article  CAS  PubMed  Google Scholar 

  32. Perez-Castillo A et al. (1985) The early ontogenesis of thyroid hormone receptor in the rat fetus. Endocrinology 117: 2457–2461

    Google Scholar 

  33. Bradley DJ et al. (1992) Spatial and temporal expression of α- and β-thyroid hormone receptor mRNAs, including the β2-subtype, in the developing mammalian nervous system. J Neurosci 12: 2288–2302

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Howdeshell KL (2002) A model of the development of the brain as a construct of the thyroid system. Environ Health Perspect 110 (Suppl 3): 337–348

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Morreale de Escobar G et al. (1990) Contribution of maternal thyroxine to fetal thyroxine pools in normal rats near term. Endocrinology 126: 2765–2767

    Article  CAS  PubMed  Google Scholar 

  36. Vulsma T et al. (1989) Maternal-fetal transfer of thyroxine in congenital hypothyroidism due to a total organification defect or thyroid agenesis. N Engl J Med 321: 13–16

    Article  CAS  PubMed  Google Scholar 

  37. Calvo RM et al. (2002) Fetal tissues are exposed to biologically relevant free thyroxine concentrations during early phases of development. J Clin Endocrinol Metab 87: 1768–1777

    Article  CAS  PubMed  Google Scholar 

  38. Galton VA et al. (1999) Pregnant rat uterus expresses high levels of the type 3 iodothyronine deiodinase. J Clin Invest 103: 979–987

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Lavado-Autric R et al. (2003) Early maternal hypothyroxinemia alters histogenesis and cerebral cortex cytoarchitecture of the progeny. J Clin Invest 111: 1073–1082

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Ausó E et al. (2004) A moderate and transient deficiency of maternal thyroid function at the beginning of fetal neocorticogenesis alters neuronal migration. Endocrinology 145: 4037–4047

    Article  PubMed  Google Scholar 

  41. Utiger RD (1999) Maternal hypothyroidism and fetal development. N Engl J Med 341: 601–602

    Article  CAS  PubMed  Google Scholar 

  42. Morreale de Escobar G et al. (2000) Is neuropsychological development related to maternal hypothyroidism, or to maternal hypothyroxinemia? J Clin Endocrinol Metab 85: 3975–3987

    CAS  PubMed  Google Scholar 

  43. Forrest D and Vennstrom B (2000) Functions of thyroid hormone receptors in mice. Thyroid 10: 41–52

    Article  CAS  PubMed  Google Scholar 

  44. O'Shea PJ and Williams GR (2002) Insight into the physiological actions of thyroid hormone receptors from genetically modified mice. J Endocrinol 175: 553–570

    Article  CAS  PubMed  Google Scholar 

  45. Ercan-Fang S et al. (1996) Isoform specific 3,5,3′-triiodothyronine receptor binding capacity and messenger ribonucleic acid content in rat adenohypophysis: effect of thyroidal state and comparison with extrapituitary tissues. Endocrinology 137: 3228–3233

    Google Scholar 

  46. Yoshihara HA et al. (2003) Design and synthesis of receptor ligands. Methods Enzymol 364: 71–91

    Article  CAS  PubMed  Google Scholar 

  47. Baxter JD et al. (2004) Selective activation of thyroid hormone signaling pathways by GC-1: a new approach to controlling cholesterol and body weight. Trends Endocrinol Metab 15: 154–157

    Article  CAS  PubMed  Google Scholar 

  48. Morte B et al. (2002) Deletion of the thyroid hormone receptor α 1 prevents the structural alterations of the cerebellum induced by hypothyroidism. Proc Natl Acad Sci USA 99: 3985–3989

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Manzano J et al. (2003) Differential effects of triiodothyronine and the thyroid hormone receptor β-specific agonist GC-1 on thyroid hormone target genes in the brain. Endocrinology 144: 5480–5487

    Google Scholar 

  50. Roberts MR et al. (2006) Making the gradient: thyroid hormone regulates cone opsin expression in the developing mouse retina. Proc Natl Acad Sci USA 103: 6218–6223

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Gothe S et al. (1999) Mice devoid of all known thyroid hormone receptors are viable but exhibit disorders of the pituitary-thyroid axis, growth, and bone maturation. Genes Dev 13: 1329–1341

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Wondisford FE (2003) Thyroid hormone action: insight from transgenic mouse models. J Investig Med 51: 215–220

    Article  CAS  PubMed  Google Scholar 

  53. Heuer H and Mason CA (2003) Thyroid hormone induces cerebellar Purkinje cell dendritic development via the thyroid hormone receptor α1. J Neurosci 23: 10604–10612

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. Flamant F et al. (2002) Congenital hypothyroid Pax8(−/−) mutant mice can be rescued by inactivating the TRα gene. Mol Endocrinol 16: 24–32

    CAS  PubMed  Google Scholar 

  55. Yacubova E and Komuro H (2002) Intrinsic program for migration of cerebellar granule cells in vitro . J Neurosci 22: 5966–5981

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  56. Mittag J et al. (2005) Athyroid Pax8−/− mice cannot be rescued by the inactivation of thyroid hormone receptor α1. Endocrinology 146: 3179–3184

    Google Scholar 

  57. Muñoz A et al. (1993) Thyroid hormone receptor/c-erbA: control of commitment and differentiation in the neuronal/chromaffin progenitor line PC12. J Cell Biol 121: 423–438

    Article  PubMed  Google Scholar 

  58. Chassande O (2003) Do unliganded thyroid hormone receptors have physiological functions? J Mol Endocrinol 31: 9–20

    Article  CAS  PubMed  Google Scholar 

  59. Mai W et al. (2004) Thyroid hormone receptor α is a molecular switch of cardiac function between fetal and postnatal life. Proc Natl Acad Sci USA 101: 10332–10337

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Hernandez A et al. (2006) Type 3 deiodinase is critical for the maturation and function of the thyroid axis. J Clin Invest 116: 476–484

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  61. Itoh Y et al. (2001) Brain glucose utilization in mice with a targeted mutation in the thyroid hormone α or β receptor gene. Proc Natl Acad Sci USA 98: 9913–9918

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  62. Weiss RE and Refetoff S (2000) Resistance to thyroid hormone. Rev Endocr Metab Disord 1: 97–108

    Article  CAS  PubMed  Google Scholar 

  63. Liu YY et al. (2003) A thyroid hormone receptor α gene mutation (P398H) is associated with visceral adiposity and impaired catecholamine-stimulated lipolysis in mice. J Biol Chem 278: 38913–38920

    Article  CAS  PubMed  Google Scholar 

  64. Liu YY et al. (2002) A targeted thyroid hormone receptor α gene dominant-negative mutation (P398H) selectively impairs gene expression in differentiated embryonic stem cells. Endocrinology 143: 2664–2672

    Article  CAS  PubMed  Google Scholar 

  65. Tinnikov A et al. (2002) Retardation of post-natal development caused by a negatively acting thyroid hormone receptor α1. EMBO J 21: 5079–5087

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  66. Venero C et al. (2005) Anxiety, memory impairment, and locomotor dysfunction caused by a mutant thyroid hormone receptor α1 can be ameliorated by T3 treatment. Genes Dev 19: 2152–2163

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  67. Guadaño-Ferraz A et al. (2003) Lack of thyroid hormone receptor α1 is associated with selective alterations in behavior and hippocampal circuits. Mol Psychiatry 8: 30–38

    Google Scholar 

  68. Gould E et al. (1990) Dendritic spine density of adult hippocampal pyramidal cells is sensitive to thyroid hormone. Brain Res 525: 327–329

    Article  CAS  PubMed  Google Scholar 

  69. Montero-Pedrazuela A et al. (2006) Modulation of adult hippocampal neurogenesis by thyroid hormones: implications in depressive-like behavior. Mol Psychiatry 11: 361–371

    Google Scholar 

  70. Ishizuka T and Lazar MA (2003) The N-CoR/histone deacetylase 3 complex is required for repression by thyroid hormone receptor. Mol Cell Biol 23: 5122–5131

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  71. de Graaf-Peters VB and Hadders-Algra M (2006) Ontogeny of the human central nervous system: what is happening when? Early Hum Dev 82: 257–266

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

I have been supported by grant BFU2005-01740 from the Ministry of Education and Science, Spain, and by the European Union Integrated Project LSHM-CT-2005-018652, CRESCENDO (Consortium for Research into Nuclear Receptors in Development and Aging).

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Bernal, J. Thyroid hormone receptors in brain development and function. Nat Rev Endocrinol 3, 249–259 (2007). https://doi.org/10.1038/ncpendmet0424

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