Best Practice & Research Clinical Endocrinology & Metabolism
Volume 21, Issue 2 , Pages 237-251, June 2007

Tissue uptake of thyroid hormone by amino acid transporters

  • Peter M. Taylor (Principal Investigator)

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +44 (0) 1382 384961; Fax: +44 (0) 1382 385507.

Division of Molecular Physiology, College of Life Sciences, University of Dundee, Sir James Black Centre, Dundee DD1 5EH, UK

TopoTarget UK Ltd, Abingdon, Oxfordshire, UK

Thyroid hormones (THs) – thyroxine (T4) and tri-iodothyronine (T3) – are iodinated derivatives of the amino acid tyrosine, which regulates growth, development and critical metabolic functions. THs are taken up by target cells and act at the genomic level via nuclear thyroid receptors. Saturable transport mechanisms mediate the greater part of TH movement across the plasma membrane. System L1 permease is a transporter of THs and amino acids in mammalian adipose tissue, placenta and brain. T3 is also a substrate of a putative System T transporter, which is selective for aromatic amino acids. The activity and functional mechanisms of these transporters can be crucial to cells in determining both their hormone sensitivity and their responses to change in circulating hormone concentrations or availability of competing substrates (e.g. amino acids). TH transporters are potentially important pharmacological targets in the design of novel or improved therapies for thyroid-related disorders.

Key words: amino acid, membrane transport, nuclear hormone action, thyroid disease, thyroid hormone, tryptophan

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1521-690X(07)00023-1

doi:10.1016/j.beem.2007.03.002

Best Practice & Research Clinical Endocrinology & Metabolism
Volume 21, Issue 2 , Pages 237-251, June 2007