The Sodium/Iodide Symporter (NIS): Molecular Physiology and Preclinical and Clinical Applications

被引:182
|
作者
Ravera, Silvia [1 ]
Reyna-Neyra, Andrea [1 ]
Ferrandino, Giuseppe [1 ]
Amzel, L. Mario [2 ]
Carrasco, Nancy [1 ]
机构
[1] Yale Sch Med, Dept Cellular & Mol Physiol, New Haven, CT 06510 USA
[2] Johns Hopkins Univ, Sch Med, Dept Biophys & Biophys Chem, Baltimore, MD 21205 USA
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 79 | 2017年 / 79卷
关键词
sodium/iodide symporter; thyroid hormones; NIS mutations; structure/function; gene transfer studies; imaging and radioiodide therapy; SODIUM-IODIDE SYMPORTER; ONCOLYTIC VACCINIA VIRUS; THYROID NA+/I-SYMPORTER; ADENOVIRUS-MEDIATED EXPRESSION; EPIDERMAL-GROWTH-FACTOR; PENDRED-SYNDROME GENE; BREAST-CANCER; IN-VIVO; TRANSPORT-DEFECT; MEASLES-VIRUS;
D O I
10.1146/annurev-physiol-022516-034125
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Active iodide (I-) transport in both the thyroid and some extrathyroidal tissues is mediated by the Na+/I- symporter (NIS). In the thyroid, NIS-mediated I- uptake plays a pivotal role in thyroid hormone (TH) biosynthesis. THs are key during embryonic and postembryonic development and critical for cell metabolism at all stages of life. The molecular characterization of NIS in 1996 and the use of radioactive I- isotopes have led to significant advances in the diagnosis and treatment of thyroid cancer and provide the molecular basis for studies aimed at extending the use of radioiodide treatment in extrathyroidal malignancies. This review focuses on the most recent findings on I- homeostasis and I- transport deficiency-causing NIS mutations, as well as current knowledge of the structure/function properties of NIS and NIS regulatory mechanisms. We also discuss employing NIS as a reporter gene using viral vectors and stem cells in imaging, diagnostic, and therapeutic procedures.
引用
收藏
页码:261 / 289
页数:29
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