Abstract

Thyroid hormone acts virtually on every cell of the vertebrate body and regulates numerous cellular functions by binding to nuclear thyroid hormone receptors. Circulating concentration of thyroid hormone is under the control of thyroid-stimulating hormone (TSH) secreted from the pituitary gland. Thyroid hormone mainly secreted from the thyroid gland is thyroxine (T 4 ), while the nuclear thyroid hormone receptor prefers binding to triiodothyronine (T 3 ) about tenfold. Therefore, T 4 must be converted to T 3 mostly in extra-thyroidal tissues to exert its actions. Recently more researchers have paid attention to the fact that this conversion is carried out by members of iodothyronine deiodinases, enzymes that reside in the cellular membranes, thereby enabling cell-specific regulation of T 3 /T 4 balance largely independent of their circulating concentrations. Three different deiodinases (D1, D2 and D3) are characterized in vertebrate species, none of which is under the control of circulating TSH. D2 catalyzes deiodination of less active T 4 to produce active T 3 . D3 removes iodine from T 3 or T 4 to produce diiodothyronine (T 2 ) or reverse T3 (rT 3 ), respectively, both of which are inactive. On the contrary, D1 is an inefficient enzyme in that it is three orders of magnitude less efficient in catalyzing T 4 compared with D2 and D3. D1 may function like a futile enzyme, since it can both activate and inactivate T 4 with almost the same velocity. However, D1 catalyzes removal of iodine from rT 3 much more efficiently than from T 4 , and hence its possible importance in recycling iodine, especially in iodine deficiency such as in certain hypothyroid patients and avian embryos in the confined eggshells. In addition, deiodinase homologs of non-vertebrate chordates such as amphioxi and ascidians characterized recently have provided useful information to gain deep insight into thyroid hormone signaling system from evolutionary aspect. This review briefly summarizes the present status of research and perspectives of studying iodothyronine deiodinases, key enzymes behind the thyroid hormone action.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.