Transport of thyroid hormones via the choroid plexus into the brain: the roles of transthyretin and thyroid hormone transmembrane transporters

Thyroid hormones are key players in regulating brain development. Thus, transfer of appropriate quantities of thyroid hormones from the blood into the brain at specific stages of development is critical. The choroid plexus forms the blood-cerebrospinal fluid barrier. In reptiles, birds and mammals, the main protein synthesized and secreted by the choroid plexus is a thyroid hormone distributor protein: transthyretin. This transthyretin is secreted into the cerebrospinal fluid and moves thyroid hormones from the blood into the cerebrospinal fluid. Maximal transthyretin synthesis in the choroid plexus occurs just prior to the period of rapid brain growth, suggesting that choroid plexus-derived transthyretin moves thyroid hormones from blood into cerebrospinal fluid just prior to when thyroid hormones are required for rapid brain growth. The structure of transthyretin has been highly conserved, implying strong selection pressure and an important function. In mammals, transthyretin binds T4 (precursor form of thyroid hormone) with higher affinity than T3 (active form of thyroid hormone). In all other vertebrates, transthyretin binds T3 with higher affinity than T4. As mammals are the exception, we should not base our thinking about the role of transthyretin in the choroid plexus solely on mammalian data. Thyroid hormone transmembrane transporters are involved in moving thyroid hormones into and out of cells and have been identified in many tissues, including the choroid plexus. Thyroid hormones enter the choroid plexus via thyroid hormone transmembrane transporters and leave the choroid plexus to enter the cerebrospinal fluid via either thyroid hormone transmembrane transporters or via choroid plexus-derived transthyretin secreted into the cerebrospinal fluid. The quantitative contribution of each route during development remains to be elucidated. This is part of a review series on ontogeny and phylogeny of brain barrier mechanisms.

[1]  Sophie Papst,et al.  Comparative Anatomy Of The Vertebrates , 2016 .

[2]  V. Darras,et al.  Intracellular thyroid hormone metabolism as a local regulator of nuclear thyroid hormone receptor-mediated impact on vertebrate development. , 2015, Biochimica et biophysica acta.

[3]  J. Köhrle,et al.  Transport of Thyroid Hormone in Brain , 2014, Front. Endocrinol..

[4]  Julia Müller,et al.  Expression Pattern of Thyroid Hormone Transporters in the Postnatal Mouse Brain , 2014, Front. Endocrinol..

[5]  V. Darras,et al.  Transporters MCT8 and OATP1C1 maintain murine brain thyroid hormone homeostasis. , 2014, The Journal of clinical investigation.

[6]  G. Caridi,et al.  Congenital analbuminaemia: molecular defects and biochemical and clinical aspects. , 2013, Biochimica et Biophysica Acta.

[7]  J. Köhrle,et al.  Function of thyroid hormone transporters in the central nervous system. , 2013, Biochimica et biophysica acta.

[8]  R. Ramsay,et al.  Delayed development of specific thyroid hormone-regulated events in transthyretin null mice. , 2013, American journal of physiology. Endocrinology and metabolism.

[9]  F. B. Davis,et al.  Nongenomic regulation by thyroid hormone of plasma membrane ion and small molecule pumps. , 2012, Discovery medicine.

[10]  V. Darras,et al.  Impact of Oatp1c1 deficiency on thyroid hormone metabolism and action in the mouse brain. , 2012, Endocrinology.

[11]  J. Lechleiter,et al.  Fatty acid metabolism and thyroid hormones. , 2012, Current trends in endocrinology.

[12]  T. Visser,et al.  Tissue-specific effects of mutations in the thyroid hormone transporter MCT8. , 2011, Arquivos brasileiros de endocrinologia e metabologia.

[13]  F. B. Davis,et al.  Membrane receptor for thyroid hormone: physiologic and pharmacologic implications. , 2011, Annual review of pharmacology and toxicology.

[14]  H. Seo,et al.  Stanniocalcin 1 induction by thyroid hormone depends on thyroid hormone receptor β and phosphatidylinositol 3-kinase activation. , 2010, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

[15]  T. Visser,et al.  Minireview: thyroid hormone transporters: the knowns and the unknowns. , 2010, Molecular endocrinology.

[16]  A. Grüters,et al.  Essential Molecular Determinants for Thyroid Hormone Transport and First Structural Implications for Monocarboxylate Transporter 8* , 2010, The Journal of Biological Chemistry.

[17]  M. Benson Genetics: Clinical Implications of Transthyretin Amyloidosis , 2009 .

[18]  H. Fuchs,et al.  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 , 2009, The Journal of Neuroscience.

[19]  B. Demeneix,et al.  Cell division and apoptosis in the adult neural stem cell niche are differentially affected in transthyretin null mice , 2007, Neuroscience Letters.

[20]  S. Richardson Cell and molecular biology of transthyretin and thyroid hormones. , 2007, International review of cytology.

[21]  V. Likic,et al.  Structural and functional evolution of transthyretin and transthyretin‐like proteins , 2006, Proteins.

[22]  Alexandra M. Dumitrescu,et al.  Thyroid hormone mediated changes in gene expression can be initiated by cytosolic action of the thyroid hormone receptor β through the phosphatidylinositol 3-kinase pathway , 2006, Nuclear receptor signaling.

[23]  F. B. Davis,et al.  Membrane receptors mediating thyroid hormone action , 2005, Trends in Endocrinology & Metabolism.

[24]  G. Levi,et al.  Adult neural stem cell cycling in vivo requires thyroid hormone and its alpha receptor , 2005, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[25]  S. Davies,et al.  Ion Transporters and Channels Involved in CSF Formation , 2005 .

[26]  C. Ek,et al.  Development of the blood-cerebrospinal fluid barrier , 2005 .

[27]  J. Palha,et al.  Thyroid hormone distribution in the mouse brain: the role of transthyretin 1 1 Presented in part in the abstract form to the Society for Neuroscience meeting in San Diego, CA, USA, November 2001. , 2002, Neuroscience.

[28]  Joana Almeida Palha,et al.  Transthyretin as a Thyroid Hormone Carrier: Function Revisited , 2002, Clinical chemistry and laboratory medicine.

[29]  T. Visser,et al.  Plasma membrane transport of thyroid hormones and its role in thyroid hormone metabolism and bioavailability. , 2001, Endocrine reviews.

[30]  S. S. Stoffer,et al.  Werner and Ingbar's The Thyroid: A Fundamental and Clinical Text , 2001 .

[31]  G. D. de Escobar,et al.  Transthyretin regulates thyroid hormone levels in the choroid plexus, but not in the brain parenchyma: study in a transthyretin-null mouse model. , 2000, Endocrinology.

[32]  D. Power,et al.  Identification of Transthyretin in Fish (Sparus aurata): cDNA Cloning and Characterisation. , 1999, Endocrinology.

[33]  J. Palha,et al.  Transthyretin is not essential for thyroxine to reach the brain and other tissues in transthyretin-null mice. , 1997, The American journal of physiology.

[34]  S. Richardson,et al.  The evolution of gene expression, structure and function of transthyretin. , 1997, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.

[35]  M. Byrne,et al.  A new family with hyperthyroxinemia caused by transthyretin Val109 misdiagnosed as thyrotoxicosis and resistance to thyroid hormone--a clinical research center study. , 1996, The Journal of clinical endocrinology and metabolism.

[36]  R. Wettenhall,et al.  Protein synthesis at the blood-brain barrier: The major protein synthetized and secreted by the amphibian choroid plexus is a β-trace-like protein , 1996 .

[37]  J. Palha,et al.  Thyroid hormone metabolism in a transthyretin-null mouse strain. , 1994, The Journal of biological chemistry.

[38]  J. Köhrle,et al.  Thyroxine transport to the brain: role of protein synthesis by the choroid plexus. , 1993, Endocrinology.

[39]  J. Liepnieks,et al.  Thyroxine interactions with transthyretin: a comparison of 10 different naturally occurring human transthyretin variants. , 1993, The Journal of clinical endocrinology and metabolism.

[40]  S. Nishiguchi,et al.  Disruption of the transthyretin gene results in mice with depressed levels of plasma retinol and thyroid hormone. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[41]  R. Wettenhall,et al.  Protein synthesis at the blood-brain barrier. The major protein secreted by amphibian choroid plexus is a lipocalin. , 1992, The Journal of biological chemistry.

[42]  L. Braverman,et al.  Role of transthyretin in the transport of thyroxine from the blood to the choroid plexus, the cerebrospinal fluid, and the brain. , 1992, Endocrinology.

[43]  N. Saunders Ontogenetic Development of Brain Barrier Mechanisms , 1992 .

[44]  M. Lawrence,et al.  Isolation, characterization, cDNA cloning and gene expression of an avian transthyretin. Implications for the evolution of structure and function of transthyretin in vertebrates. , 1991, European journal of biochemistry.

[45]  A. Jaworowski,et al.  Transthyretin (prealbumin) gene expression in choroid plexus is strongly conserved during evolution of vertebrates. , 1991, Comparative biochemistry and physiology. B, Comparative biochemistry.

[46]  R. Weisiger,et al.  Thyroxine uptake by perfused rat liver. No evidence for facilitation by five different thyroxine-binding proteins. , 1990, The Journal of clinical investigation.

[47]  B. Southwell,et al.  Expression of the genes for transthyretin, cystatin C and beta A4 amyloid precursor protein in sheep choroid plexus during development. , 1990, Brain research. Developmental brain research.

[48]  C. Nilsson,et al.  Thyroxine transport from blood to brain via transthyretin synthesis in choroid plexus. , 1990, The American journal of physiology.

[49]  D. Fisher,et al.  Development of the thyroid. , 1989, Bailliere's clinical endocrinology and metabolism.

[50]  C. Mendel The free hormone hypothesis: a physiologically based mathematical model. , 1989, Endocrine reviews.

[51]  S. Refetoff Inherited thyroxine-binding globulin abnormalities in man. , 1989, Endocrine reviews.

[52]  R. Gregg,et al.  Binding of thyroxine to human plasma low density lipoprotein through specific interaction with apolipoprotein B (apoB-100). , 1989, Biochimie.

[53]  L. Gavin,et al.  Thyroxine transport and distribution in Nagase analbuminemic rats. , 1989, The Journal of clinical investigation.

[54]  P. Dickson,et al.  Structure and expression of the rat transthyretin (prealbumin) gene. , 1988, The Journal of biological chemistry.

[55]  J. Menting,et al.  Thyroxine transport in choroid plexus. , 1987, The Journal of biological chemistry.

[56]  A. Jones,et al.  Thyroid hormone-binding proteins in plasma facilitate uniform distribution of thyroxine within tissues: a perfused rat liver study. , 1987, Endocrinology.

[57]  M. Obregon,et al.  Fetal and maternal thyroid hormones. , 1987, Hormone research.

[58]  P. Dickson,et al.  Synthesis of transthyretin (pre-albumin) mRNA in choroid plexus epithelial cells, localized by in situ hybridization in rat brain. , 1986, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[59]  E. Schon,et al.  Demonstration of transthyretin mRNA in the brain and other extrahepatic tissues in the rat. , 1985, The Journal of biological chemistry.

[60]  F. Roelfsema,et al.  Concentrations of thyroxine and 3,5,3'-triiodothyronine at 34 different sites in euthyroid rats as determined by an isotopic equilibrium technique. , 1985, Endocrinology.

[61]  G. Howlett,et al.  High prealbumin and transferrin mRNA levels in the choroid plexus of rat brain. , 1985, Biochemical and biophysical research communications.

[62]  J. Haddow,et al.  Familial euthyroid hyperthyroxinemia resulting from increased thyroxine binding to thyroxine-binding prealbumin. , 1982, The New England journal of medicine.

[63]  G. Rao Mode of entry of steroid and thyroid hormones into cells , 1981, Molecular and Cellular Endocrinology.

[64]  Sturrock Rr A morphological study of the development of the mouse choroid plexus. , 1979, Journal of anatomy.

[65]  R. Sturrock A morphological study of the development of the mouse choroid plexus. , 1979, Journal of anatomy.

[66]  W. Börner,et al.  [Thyroid hormones]. , 1974, Die Medizinische Welt.

[67]  H. Cserr Physiology of the choroid plexus. , 1971, Physiological reviews.

[68]  J. Tata Transport of thyroid hormones. , 1960, British medical bulletin.

[69]  H. Christensen,et al.  Concentration of Taurine, β-Alanine, and Triiodothyronine by Ascites Carcinoma Cells , 1954 .

[70]  H. Christensen,et al.  Concentration of taurine, beta-alanine, and triiodothyronine by ascites carcinoma cells. , 1954, Cancer research.