共 125 条
The sodium/iodide symporter: State of the art of its molecular characterization
被引:72
作者:
Darrouzet, Elisabeth
[1
,2
,3
]
Lindenthal, Sabine
[2
,3
,4
]
Marcellin, Didier
[1
,2
,3
]
Pellequer, Jean-Luc
[5
]
Pourcher, Thierry
[2
,3
,4
]
机构:
[1] SBTN, Ctr Marcoule, F-30207 Bagnols Sur Ceze, France
[2] Univ Nice Sophia Antipolis, Fac Med, Lab TIRO, F-06107 Nice, France
[3] TIRO, CAL, F-06107 Nice, France
[4] CEA, iBEB, SBTN, TIRO, F-06107 Nice, France
[5] CEA, iBEB, SBTN, LIRM, F-30207 Bagnols Sur Ceze, France
来源:
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
|
2014年
/
1838卷
/
01期
关键词:
Sodium/iodide symporter;
NIS;
SLC5A5;
Thyroid Membrane protein;
Structure/function relationship;
SODIUM-IODIDE SYMPORTER;
THYROID NA+/I-SYMPORTER;
TRANSPORT DEFECT ITD;
AMINO-ACID-RESIDUES;
NA+/PROLINE TRANSPORTER;
CONGENITAL HYPOTHYROIDISM;
ANION SELECTIVITY;
MISSENSE MUTATION;
ESCHERICHIA-COLI;
GENE-EXPRESSION;
D O I:
10.1016/j.bbamem.2013.08.013
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The sodium/iodide symporter (NIS or SLC5A5) is an intrinsic membrane protein implicated in iodide uptake into thyroid follicular cells. It plays a crucial role in iodine metabolism and thyroid regulation and its function is widely exploited in the diagnosis and treatment of benign and malignant thyroid diseases. A great effort is currently being made to develop a NIS-based gene therapy also allowing the radiotreatment of nonthyroidal tumors. NIS is also expressed in other tissues, such as salivary gland, stomach and mammary gland during lactation, where its physiological role remains unclear. The molecular identity of the thyroid iodide transporter was elucidated approximately fifteen years ago. It belongs to the superfamily of sodium/solute symporters, SSS (and to the human transporter family, SLC5), and is composed of 13 transmembrane helices and 643 amino acid residues in humans. Knowledge concerning NIS structure/function relationship has been obtained by taking advantage of the high resolution structure of one member of the SSS family, the Vibrio parahaemolyticus sodium/galactose symporter (vSGLT), and from studies of gene mutations leading to congenital iodine transport defects (ITD). This review will summarize current knowledge regarding the molecular characterization of NIS. (C) 2013 Elsevier B.V. All rights reserved.
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页码:244 / 253
页数:10
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