Title of article
Thyroid hormone transport by monocarboxylate transporters
Author/Authors
W. Edward Visser، نويسنده , , Edith C.H. Friesema، نويسنده , , Jurgen Jansen، نويسنده , , Theo J. Visser، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2006
Pages
14
From page
223
To page
236
Abstract
Thyroid hormone (TH) is essential for the normal development and metabolism of different tissues. TH action and metabolism take place intracellularly, which requires cellular uptake via transporters. Several transporter families have been identified, of which the monocarboxylate transporter (MCT) family deserves special attention. So far, only MCT1, MCT2, MCT3, MCT4 and MCT6 have been demonstrated to transport monocarboxylates; MCT8 has been identified as a specific TH transporter. MCT8 mutations in humans are associated with severe psychomotor retardation and elevated 3,3′,5-triiodothyronine (T3) levels. Recently, MCT8 knockout mice have been shown to perfectly imitate the thyroid state in patients with MCT8 mutations; however, they lack the neurological defects. Although it was long hypothesized that a T-type amino acid transporter also transports iodothyronines, it only recently became clear that MCT10 is involved in the bidirectional transport of aromatic amino acids and iodothyronines. MCT10 preferentially transports T3 even more effectively than does MCT8. However, its precise function in the human body is poorly understood.
Keywords
MCT8 , MCT , MCT10 , monocarboxylate transporter , TAT1 , thyroid hormonetransporter.
Journal title
Best Practice and Research Clinical Endocrinology and Metabolism
Serial Year
2006
Journal title
Best Practice and Research Clinical Endocrinology and Metabolism
Record number
466062
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