Subscribe to RSS
DOI: 10.1055/a-1080-2969
Auto-Regulation of the Thyroid Gland Beyond Classical Pathways

Abstract
This mini-review asks how self-regulation of the thyroid gland is realized at the cellular and molecular levels by canonical and non-canonical means. Canonical pathways of thyroid regulation comprise thyroid stimulating hormone-triggered receptor signaling. As part of non-canonical regulation, we hypothesized an interplay between protease-mediated thyroglobulin processing and thyroid hormone release into the circulation by means of thyroid hormone transporters like Mct8. We proposed a sensing mechanism by different thyroid hormone transporters, present in specific subcellular locations of thyroid epithelial cells, selectively monitoring individual steps of thyroglobulin processing, and thus, the cellular thyroid hormone status. Indeed, we found that proteases and thyroid hormone transporters are functionally inter-connected, however, in a counter-intuitive manner fostering self-thyrotoxicity in particular in Mct8- and/or Mct10-deficient mice. Furthermore, the possible role of the G protein-coupled receptor Taar1 is discussed, because we detected Taar1 at cilia of the apical plasma membrane of thyrocytes in vitro and in situ. Eventually, through pheno-typing Taar1-deficient mice, we identified a co-regulatory role of Taar1 and the thyroid stimulating hormone receptors. Recently, we showed that inhibition of thyroglobulin-processing enzymes results in disappearance of cilia from the apical pole of thyrocytes, while Taar1 is re-located to the endoplasmic reticulum. This pathway features a connection between thyrotropin-stimulated secretion of proteases into the thyroid follicle lumen and substrate-mediated self-assisted control of initially peri-cellular thyroglobulin processing, before its reinternalization by endocytosis, followed by extensive endo-lysosomal liberation of thyroid hormones, which are then released from thyroid follicles by means of thyroid hormone transporters.
Key words
G-protein coupled receptor Taar1 - Mct8 - cysteine cathepsins - primary cilia - thyroglobulin - thyroid epithelial cellsPublication History
Received: 30 August 2019
Received: 05 December 2019
Accepted: 10 December 2019
Article published online:
19 February 2020
© Georg Thieme Verlag KG
Stuttgart · New York
-
References
- 1 Dumont JE, Lamy F, Roger P. et al. Physiological and pathological regulation of thyroid cell proliferation and differentiation by thyrotropin and other factors. Physiol Rev 1992; 72: 667-697
- 2 Fekete C, Lechan RM. Central regulation of hypothalamic-pituitary-thyroid axis under physiological and pathophysiological conditions. Endocr Rev 2014; 35: 159-194
- 3 Fliers E, Kalsbeek A, Boelen A. Beyond the fixed setpoint of the hypothalamus-pituitary-thyroid axis. Eur J Endocrinol 2014; 171: R197-R208
- 4 Cooper DS. Hyperthyroidism. Lancet 2003; 362: 459-468
- 5 Biondi B, Palmieri EA, Fazio S. et al. Endogenous subclinical hyperthyroidism affects quality of life and cardiac morphology and function in young and middle-aged patients. J Clin Endocrinol Metab 2000; 85: 4701-4705
- 6 Fuhrer D, Brix K, Biebermann H. Understanding the Healthy Thyroid State in 2015. Eur Thyroid J 2015; 4: 1-8
- 7 Colin IM, Denef JF, Lengele B. et al. Recent insights into the cell biology of thyroid angiofollicular units. Endocr Rev 2013; 34: 209-238
- 8 Nilsson M, Fagman H. Mechanisms of thyroid development and dysgenesis: an analysis based on developmental stages and concurrent embryonic anatomy. Curr Top Dev Biol 2013; 106: 123-170.
- 9 Brix K, Qatato M, Szumska J et al. “Thyroglobulin Storage, Processing and Degradation for Thyroid Hormone Liberation”. “In” Luster M, Duntas LH, Wartofsky L, Hrsg. The Thyroid and Its Diseases: A Comprehensive Guide for the Clinician. Cham: Springer International Publishing; 2019: 25–48. doi:10.1007/978-3-319-72102-6_3
- 10 Rapoport B, McLachlan SM. TSH receptor cleavage into subunits and shedding of the A-subunit; A molecular and clinical perspective. Endocr Rev 2016; 37: 114-134.
- 11 Allgeier A, Offermanns S, Van Sande J. et al. The human thyrotropin receptor activates G-proteins Gs and Gq/11. J Biol Chem 1994; 269: 13733-13735
- 12 Kero J, Ahmed K, Wettschureck N. et al. Thyrocyte-specific Gq/G11 deficiency impairs thyroid function and prevents goiter development. J Clin Invest 2007; 117: 2399-2407.
- 13 Calebiro D, Rieken F, Wagner J. et al. Single-molecule analysis of fluorescently labeled G-protein-coupled receptors reveals complexes with distinct dynamics and organization. Proc Natl Acad Sci USA 2013; 110: 743-748.
- 14 Godbole A, Lyga S, Lohse MJ. et al. Internalized TSH receptors en route to the TGN induce local Gs-protein signaling and gene transcription. Nat Commun 2017; 8: 443.
- 15 Lof C, Patyra K, Kero A. et al. Genetically modified mouse models to investigate thyroid development, function and growth. Best Pract Res Clin Endocrinol Metab 2018; 32: 241-256.
- 16 Sellitti DF, Suzuki K. Intrinsic regulation of thyroid function by thyroglobulin. Thyroid 2014; 24: 625-638.
- 17 Citterio CE, Targovnik HM, Arvan P. The role of thyroglobulin in thyroid hormonogenesis. Nat Rev Endocrinol 2019; 15: 323-338.
- 18 Suzuki K, Lavaroni S, Mori A. et al. Autoregulation of thyroid-specific gene transcription by thyroglobulin. Proc Natl Acad Sci USA 1998; 95: 8251-8256.
- 19 Eng PH, Cardona GR, Fang SL. et al. Escape from the acute Wolff-Chaikoff effect is associated with a decrease in thyroid sodium/iodide symporter messenger ribonucleic acid and protein. Endocrinology 1999; 140: 3404-3410.
- 20 Cohen DPA, Lebsir D, Benderitter M. et al. A systems biology approach to propose a new mechanism of regulation of repetitive prophylaxis of stable iodide on sodium/iodide symporter (NIS). Biochimie 2019; 162: 208-215.
- 21 Gerber H, Peter HJ, Studer H. Diffusion of thyroglobulin in the follicular colloid. (Minireview). Endocrinol Exp 1986; 20: 23-33
- 22 Friedrichs B, Tepel C, Reinheckel T. et al. Thyroid functions of mouse cathepsins B, K, and L. J Clin Invest 2003; 111: 1733-1745
- 23 Heuer H, Visser TJ. Minireview: Pathophysiological importance of thyroid hormone transporters. Endocrinology 2009; 150: 1078-1083.
- 24 Weber J, McInnes J, Kizilirmak C. et al. Interdependence of thyroglobulin processing and thyroid hormone export in the mouse thyroid gland. Eur J Cell Biol 2017; 96: 440-456.
- 25 Qatato M, Szumska J, Skripnik V. et al. Canonical TSH regulation of cathepsin-mediated thyroglobulin processing in the thyroid gland of male mice requires Taar1 expression. Front Pharmacol 2018; 9: 221
- 26 Dauth S, Rakov H, Sîrbulescu RF. et al. Function of Cathepsin K in the central nervous system of male mice is independent of its role in the thyroid gland. Cell Mol Neurobiol
- 27 Bianco AC, Anderson G, Forrest D. et al. American Thyroid Association Guide to investigating thyroid hormone economy and action in rodent and cell models. Thyroid 2014; 24: 88-168
- 28 Engels K, Rakov H, Zwanziger D. et al. Differences in mouse hepatic thyroid hormone transporter expression with age and hyperthyroidism.. Eur Thyroid J 2015; 4: 81-86
- 29 Engels K, Rakov H, Zwanziger D. et al. Efficacy of protocols for induction of chronic hyperthyroidism in male and female mice. Endocrine 2016; 54: 47-54
- 30 Rakov H, Engels K, Hones GS. et al. Sex-specific phenotypes of hyperthyroidism and hypothyroidism in aged mice. Biol Sex Differ 2017; 8: 38.
- 31 Engels K, Rakov H, Hones GS. et al. Aging alters phenotypic traits of thyroid dysfunction in male mice with divergent effects on complex systems but preserved thyroid hormone action in target organs. J Gerontol A Biol Sci Med Sci 2019;
- 32 Vassart G, Dumont JE. The thyrotropin receptor and the regulation of thyrocyte function and growth. Endocr Rev 1992; 13: 596-611
- 33 Szumska J, Qatato M, Rehders M. et al. Trace amine-associated receptor 1 localization at the apical plasma membrane domain of fisher rat thyroid epithelial cells is confined to cilia. Eur Thyroid J 2015; 4: 30-41
- 34 Szumska J, Batool Z, Al-Hashimi A. et al. Treatment of rat thyrocytes in vitro with cathepsin B and L inhibitors results in disruption of primary cilia leading to redistribution of the trace amine associated receptor 1 to the endoplasmic reticulum. Biochimie 2019; 166: 270-285.
- 35 Fischer J, Kleinau G, Rutz C. et al. Evidence of G-protein-coupled receptor and substrate transporter heteromerization at a single molecule level. Cell Mol Life Sci 2018; 75: 2227-2239.
- 36 Studer H, von Grunigen C, Haeberli A. et al. Iodination of thyroglobulin molecules depends on their diffusion velocity in follicular colloid. Mol Cell Endocrinol 1986; 45: 91-103
- 37 Herzog V, Berndorfer U, Saber Y. Isolation of insoluble secretory product from bovine thyroid: Extracellular storage of thyroglobulin in covalently cross-linked form. J Cell Biol 1992; 118: 1071-1083.
- 38 Berndorfer U, Wilms H, Herzog V. Multimerization of thyroglobulin (TG) during extracellular storage: isolation of highly cross-linked TG from human thyroids. J Clin Endocrinol Metab 1996; 81: 1918-1926.
- 39 Saber-Lichtenberg Y, Brix K, Schmitz A. et al. Covalent cross-linking of secreted bovine thyroglobulin by transglutaminase. Faseb J 2000; 14: 1005-1014.
- 40 Brix K, Linke M, Tepel C. et al. Cysteine proteinases mediate extracellular prohormone processing in the thyroid. Biol Chem 2001; 382: 717-725.
- 41 Brix K, Lemansky P, Herzog V. Evidence for extracellularly acting cathepsins mediating thyroid hormone liberation in thyroid epithelial cells. Endocrinology 1996; 137: 1963-1974.
- 42 Jordans S, Jenko-Kokalj S, Kuhl NM. et al. Monitoring compartment-specific substrate cleavage by cathepsins B, K, L, and S at physiological pH and redox conditions. BMC Biochem 2009; 10: 23.
- 43 Tepel C, Bromme D, Herzog V. et al. Cathepsin K in thyroid epithelial cells: sequence, localization and possible function in extracellular proteolysis of thyroglobulin. J Cell Sci 2000; 113 Pt 24: 4487-4498
- 44 Dunn AD, Crutchfield HE, Dunn JT. Thyroglobulin processing by thyroidal proteases. Major sites of cleavage by cathepsins B, D, and L. J Biol Chem 1991; 266: 20198-20204
- 45 Scanlan TS, Suchland KL, Hart ME. et al. 3-Iodothyronamine is an endogenous and rapid-acting derivative of thyroid hormone. Nat Med 2004; 10: 638-642
- 46 Zucchi R, Chiellini G, Scanlan TS. et al. Trace amine-associated receptors and their ligands. Br J Pharmacol 2006; 149: 967-978
- 47 Grandy DK. Trace amine-associated receptor 1-Family archetype or iconoclast?. Pharmacol Ther 2007; 116: 355-390
- 48 Hoefig CS, Wuensch T, Rijntjes E. et al. Biosynthesis of 3-Iodothyronamine From T4 in Murine Intestinal Tissue. Endocrinology 2015; 156: 4356-4364.
- 49 Schanze N, Jacobi SF, Rijntjes E. et al. 3-Iodothyronamine decreases expression of genes involved in iodide metabolism in mouse thyroids and inhibits iodide uptake in PCCL3 thyrocytes. Thyroid 2017; 27: 11-22.
- 50 Kohrle J, Biebermann H. 3-Iodothyronamine-A thyroid hormone metabolite with distinct target profiles and mode of action. Endocr Rev 2019; 40: 602-630
- 51 Abrahamson M, Alvarez-Fernandez M, Nathanson C-M. Cystatins. Biochem Soc Symp 2003; 70: 179-199
- 52 Brix K, Dunkhorst A, Mayer K. et al. Cysteine cathepsins: Cellular roadmap to different functions. Biochimie 2008; 90: 194-207
- 53 Lenarcic B, Turk V. Thyroglobulin type-1 domains in equistatin inhibit both papain-like cysteine proteinases and cathepsin D. J Biol Chem 1999; 274: 563-566
- 54 Lenarcic B, Krishnan G, Borukhovich R. et al. Saxiphilin, a saxitoxin-binding protein with two thyroglobulin type 1 domains, is an inhibitor of papain-like cysteine proteinases. J Biol Chem 2000; 275: 15572-15577
- 55 Mihelic M, Turk D. Two decades of thyroglobulin type-1 domain research. Biol Chem 2007; 388: 1123-1130
- 56 Novinec M, Grass RN, Stark WJ. et al. Interaction between human cathepsins K, L, and S and elastins: mechanism of elastinolysis and inhibition by macromolecular inhibitors. J Biol Chem 2007; 282: 7893-7902.
- 57 Fernandez-Santos JM, Utrilla JC, Vazquez-Roman V. et al. Primary cilium in the human thyrocyte: changes in frequency and length in relation to the functional pathology of the thyroid gland. Thyroid 2019; 29: 595-606
- 58 Kleinau G, Neumann S, Gruters A. et al. Novel insights on thyroid-stimulating hormone receptor signal transduction. Endocr Rev 2013; 34: 691-724.
- 59 Linke M, Jordans S, Mach L. et al. Thyroid stimulating hormone upregulates secretion of cathepsin B from thyroid epithelial cells. Biol Chem 2002; 383: 773-784.
- 60 Linke M, Herzog V, Brix K. Trafficking of lysosomal cathepsin B-green fluorescent protein to the surface of thyroid epithelial cells involves the endosomal/lysosomal compartment. J Cell Sci 2002; 115: 4877-4889
- 61 Biebermann H, Ambrugger P, Tarnow P. et al. Extended clinical phenotype, endocrine investigations and functional studies of a loss-of-function mutation A150V in the thyroid hormone specific transporter MCT8. Eur J Endocrinol 2005; 153: 359-366
- 62 Fischer J, Kleinau G, Muller A. et al. Modulation of monocarboxylate transporter 8 oligomerization by specific pathogenic mutations. J Mol Endocrinol 2015; 54: 39-50
- 63 Di Cosmo C, Liao XH, Dumitrescu AM. et al. Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion. J Clin Invest 2010; 120: 3377-3388
- 64 Wirth EK, Sheu SY, Chiu-Ugalde J. et al. Monocarboxylate transporter 8 deficiency: Altered thyroid morphology and persistent high triiodothyronine/thyroxine ratio after thyroidectomy. Eur J Endocrinol 2011; 165: 555-561.
- 65 Muller J, Mayerl S, Visser TJ. et al. Tissue-specific alterations in thyroid hormone homeostasis in combined Mct10 and Mct8 deficiency. Endocrinology 2014; 155: 315-325
- 66 Trajkovic-Arsic M, Muller J, Darras VM. et al. Impact of monocarboxylate transporter-8 deficiency on the hypothalamus-pituitary-thyroid axis in mice. Endocrinology 2010; 151: 5053-5062