Non-genomic actions of thyroid hormone in brain development

Steroids

Volumn 73, Issue 9-10, 2008, Pages 1008-1012

  Leonard, Jack L ^a  

^a UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

Author keywords

Actin; Development; Laminin; Thyroid hormone

Indexed keywords

ACTIN; LAMININ; LIOTHYRONINE; THYROID HORMONE; THYROXINE;

ACTIN FILAMENT; ACTIN POLYMERIZATION; ASTROCYTE; BRAIN DEVELOPMENT; CELL ANCHORAGE; CELL MIGRATION; CELL SURFACE; CYTOSKELETON; ENZYME REGULATION; EXTRACELLULAR MATRIX; GENOME; HORMONE ACTION; HUMAN; MEMBRANE POTENTIAL; MICROFILAMENT; NERVE CONDUCTION; NERVE FIBER GROWTH; NEURITE; NONHUMAN; POLYMERIZATION; REVIEW; SIGNAL TRANSDUCTION; SYNAPTOGENESIS; TRANSCRIPTION INITIATION;

ACTINS; ANIMALS; ASTROCYTES; BRAIN; CELL MOVEMENT; CEREBELLUM; HUMANS; MODELS, BIOLOGICAL; NEURONS; PROTEIN BINDING; RATS; THYROID HORMONES; TRANSCRIPTION, GENETIC; TRIIODOTHYRONINE;

EID: 44549086642     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2007.12.016     Document Type: Review

References (58)

1. Santisteban P., and Bernal J. Thyroid development and effect on the nervous system. Rev Endocr Metab Disord 6 (2005) 217-228
2. Bernal J. Thyroid hormones and brain development. Vitam Horm 71 (2005) 95-122
3. Legrand J., and Rabie A. Influence of thyroid hormones on the size of the synaptosomal fraction of the cerebellum of young rats. Comptes Rendus Hebdomadaires Des Seances de L Academie Des Sciences. D: Sciences Naturelles 274 (1972) 922-924
4. Rabie A., Favre C., Clavel M.C., and Legrand J. Sequential effects of thyroxine on the developing cerebellum of rats made hypothyroid by propylthiouracil. Brain Res 161 (1979) 469-479
5. Mareck A., Fellous A., Francon J., and Nunez J. Changes in composition and activity of microtubule-associated proteins during brain development. Nature 284 (1980) 353-355
6. Nunez J., Couchie D., Aniello F., and Bridoux A.M. Regulation by thyroid hormone of microtubule assembly and neuronal differentiation. Neurochem Res 16 (1991) 975-982
7. Oppenheimer J.H., Schwartz H.L., Surks M.I., Koerner D., and Dillmann W.H. Nuclear receptors and the initiation of thyroid hormone action. Recent Prog Horm Res 32 (1976) 529-565
8. Evans R.M. The steroid and thyroid hormone receptor superfamily. Science 241 (1988) 889-895
9. Clos J., Crepel F., Legrand C., Legrand J., Rabie A., and Vigouroux E. Thyroid physiology during the postnatal period in the rat: a study of the development of thyroid function and of the morphogenetic effects of thyroxine with special reference to cerebellar maturation. Gen Comp Endocrinol 23 (1974) 178-192
10. Vigouroux E. Dynamic study of post-natal thyroid function in the rat. Acta Endocrinol 83 (1976) 752-762
11. Koibuchi N., Jingu H., Iwasaki T., and Chin W.W. Current perspectives on the role of thyroid hormone in growth and development of cerebellum. Cerebellum 2 (2003) 279-289
12. Sotelo C. Cellular and genetic regulation of the development of the cerebellar system. Prog Neurobiol 72 (2004) 295-339
13. Rabie A., Patel A.J., Clavel M.C., and Legrand J. Effect of thyroid deficiency on the growth of the hippocampus in the rat. A combined biochemical and morphological study. Dev Neurosci 2 (1979) 183-194
14. Dubuis J.M., Sanchez-Menegay C., and Burger A.G. Effects of thyroxine, triiodothyronine and reverse triiodothyronine on the neonatal hypothyroid rat cerebellum. Acta Med Austriaca 19 Suppl 1 (1992) 106-109
15. Legrand J. Morphogenic actions of thyroid hormones. Trends Neurol Sci 2 (1979) 234-236
16. Vincent J., Legrand C., Rabie A., and Legrand J. Effects of thyroid hormone on synaptogenesis in the molecular layer of the developing rat cerebellum. J Physiol 78 (1982) 729-738
17. Leonard J.L., and Koehrle J. Intracellular pathways of iodothyronine metabolism. In: Braverman L.E., and Utiger R.D. (Eds). The thyroid (1996), Lippincott-Raven, Philadelphia 125-161
18. Chopra I.J., Sack J., and Fisher D.A. 3,3′,5′-Triiodothyronine (reverse T3) and 3,3′,5-triiodothyronine (T3) in fetal and adult sheep: studies of metabolic clearance rates, production rates, serum binding, and thyroidal content relative to thyroxine. Endocrinology 97 (1975) 1080-1088
19. Cooper E., and Burke C.W. Thyroxine, 3,5,3′-triiodothyronine and 3,3′,5′-triiodothyronine in human amniotic fluid: relationships between concentrations and turnover. Med Hypotheses 12 (1983) 113-124
20. Santini F., Chiovato L., Ghirri P., Lapi P., Mammoli C., Montanelli L., et al. Serum iodothyronines in the human fetus and the newborn: evidence for an important role of placenta in fetal thyroid hormone homeostasis. J Clin Endocrinol Metab 84 (1999) 493-498
21. Samuels H.H., Forman B.M., Horowitz Z.D., and Ye Z.-S. Regulation of gene expression by thyroid hormone. J Clin Invest 81 (1988) 957-967
22. Brent G. The molecular basis of thyroid hormone action. N Engl J Med 331 (1994) 847-853
23. Anderson G.W., Mariash C.N., and Oppenheimer J.H. Molecular actions of thyroid hormone. In: Braverman L.E., and Utiger R. (Eds). The thyroid (2000), Lippincott-Williams & Wilkins, Philadelphia 174-195
24. Flamant F., Baxter J.D., Forrest D., Refetoff S., Samuels H., Scanlan T.S., et al. International Union of Pharmacology. LIX. The pharmacology and classification of the nuclear receptor superfamily: thyroid hormone receptors. Pharmacol Rev 58 (2006) 705-711
25. Strait K.A., Schwartz H.L., Perez-Castillo A., and Oppenheimer J.H. Relationship of c-erbA mRNA content to tissue triiodothyronine nuclear binding capacity and function in developing and adult rats. J Biol Chem 265 (1990) 10514-10521
26. Oppenheimer J.H., and Schwartz H.L. Molecular basis of thyroid hormone-dependent brain development. Endocr Rev 18 (1997) 462-475
27. Bradley D.J., Young W.S., and Weinberger C. Differential expression of α and β thyroid hormone receptor genes in rat brain and pituitary. Proc Natl Acad Sci USA 86 (1989) 7250-7254
28. Strait K.A., Zou L., and Oppenheimer J.H. Beta 1 isoform-specific regulation of a triiodothyronine-induced gene during cerebellar development. Mol Endocrinol 6 (1992) 1874-1880
29. Mellstrom B., Naranjo J.R., Santos A., Gonzalez A.M., and Bernal J. Independent expression of the alpha and beta c-erbA genes in developing rat brain. Mol Endocrinol 5 (1991) 1339-1350
30. Bernal J., and Guadano-Ferraz A. Thyroid hormone and the development of the brain. Curr Opin Endocrinol Diab 5 (1998) 296-302
31. Forrest D., and Vennstrom B. Functions of thyroid hormone receptors in mice. Thyroid 10 (2000) 41-52
32. Flamant F., and Samarut J. Thyroid hormone receptors: lessons from knockout and knock-in mutant mice. Trends Endocrinol Metab 14 (2003) 85-90
33. Hsu J.-H., and Brent G.A. Thyroid hormone receptor knockouts. Trends Endocrinol Metab 9 (1998) 103-112
34. Morte B., Manzano J., Scanlan T., Vennstrom B., and Bernal J. Deletion of the thyroid hormone receptor alpha 1 prevents the structural alterations of the cerebellum induced by hypothyroidism. Proc Natl Acad Sci USA 99 (2002) 3985-3989
35. Gothe S., Wang Z., Ng L., Kindblom J.M., Barros A.C., Ohlsson C., et al. 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 (1999) 1329-1341
36. Gauthier K., Plateroti M., Harvey C.B., Williams G.R., Weiss R.E., Refetoff S., et al. Genetic analysis reveals different functions for the products of the thyroid hormone receptor alpha locus. Mol Cell Biol 21 (2001) 4748-4760
37. Brent G.A. Tissue-specific actions of thyroid hormone: insights from animal models. Rev Endocr Metab Disord 1 (2000) 27-33
38. Glass C.K., and Rosenfeld M.G. The coregulator exchange in transcriptional functions of nuclear receptors. Genes Dev 14 (2000) 121-141
39. Koenig R.J., Lazar M.A., Hodin R.A., Brent G.A., Larsen P.R., Chin W.W., et al. Inhibition of thyroid hormone action by a non-hormone binding c-erbA protein generated by alternative mRNA splicing. Nature 337 (1989) 659-661
40. Siegrist-Kaiser C.A., Juge-Aubry C., Tranter M.P., Ekenbarger D.M., and Leonard J.L. Thyroxine-dependent modulation of actin polymerization in cultured astrocytes. A novel, extranuclear action of thyroid hormone. J Biol Chem 265 (1990) 5296-5302
41. Farwell A.P., Lynch R.M., Okulicz W.C., Comi A.M., and Leonard J.L. The actin cytoskeleton mediates the hormonally regulated translocation of type II iodothyronine 5′-deiodinase in astrocytes. J Biol Chem 265 (1990) 18546-18553
42. Farwell A.P., Dubord-Tomasetti S.A., Pietrzykowski A.Z., and Leonard J.L. Dynamic nongenomic actions of thyroid hormone in the developing rat brain. Endocrinology 147 (2006) 2567-2574
43. Faivre-Sarrailh C., and Rabie A. A lower proportion of filamentous to monomeric actin in the developing cerebellum of thyroid-deficient rats. Dev Brain Res 41 (1988) 293-297
44. Hatten M.E., and Heinz N. Mechanisms of neural patterning and specification in the developing cerebellum. Annu Rev Neurosci 18 (1995) 385-408
45. Tessier-Lavigne M., and Goodman C.S. The molecular biology of axon guidance. Science 274 (1996) 1123-1133
46. Lockerbie R.O. The neuronal growth cone: a review of its locomotory, navigational and target recognition capabilities. Neuroscience 20 (1987) 719-729
47. Dodd J., and Jessell T.M. Axon guidance and the patterning of neuronal projections in vertebrates. Science 242 (1988) 692-699
48. Rivas R.J., and Hatten M.E. Motility and cytoskeletal organization of migrating cerebellar granule neurons. J Neurosci 15 (1995) 981-989
49. Forscher P., and Smith S.J. Actions of cytochalasins on the organization of the actin filaments and microtubules in a neuronal growth cone. J Cell Biol 107 (1988) 1505-1516
50. Farwell A.P., Dubord-Tomasetti S.A., Pietrzykowski A.Z., Stachelek S.J., and Leonard J.L. Regulation of cerebellar neuronal migration and neurite outgrowth by thyroxine and 3,3′,5′-triiodothyronine. Brain Res Dev Brain Res 154 (2005) 121-135
51. Liesi P., Seppala I., and Trenkner E. Neuronal migration in cerebellar microcultures is inhibited by antibodies against a neurite outgrowth domain of laminin. J Neurosci Res 33 (1992) 170-176
52. Liesi P., Narvanen A., Soos J., Sariola H., and Snounou G. Identification of a neurite outgrowth-promoting domain of laminin using synthetic peptides [published erratum appears in FEBS Lett 1989 July 17;251(1-2):283]. FEBS Lett 244 (1989) 141-148
53. Liesi P., Hager G., Dodt H.-U., Seppala I., and Zieglgansberger W. Domain-specific antibodies against the B2 chain of laminin inhibit neuronal migration in the neonatal rat cerebellum. J Neurosci Res 40 (1995) 199-206
54. Hynes R.O. Integrin: versitility, modulation, and signaling in cell adhesion. Cell 69 (1992) 11-25
55. Ruoslahti E. Integrins. J Clin Invest 87 (1991) 1-5
56. Farwell A.P., Tranter M.P., and Leonard J.L. Thyroxine-dependent regulation of integrin-laminin interactions in astrocytes. Endocrinology 136 (1995) 3909-3915
57. Farwell A.P., and Dubord-Tomasetti S.A. Thyroid hormone regulates the extracellular organization of laminin on astrocytes. Endocrinology 140 (1999) 5014-5021
58. Farwell A.P., and Dubord-Tomasetti S.A. Thyroid hormone regulates the expression of laminin in the developing rat cerebellum. Endocrinology 140 (1999) 4221-4227