The trace element selenium and the thyroid gland

被引:115
作者
Köhrle, J
机构
[1] Univ Wurzburg, Abt Mol Innere Med, D-97070 Wurzburg, Germany
[2] Univ Wurzburg, Med Poliklin, Klin Forsch Grp, D-97070 Wurzburg, Germany
关键词
thyroid; selenium; iodine; selenoprotein; deiodinase; cell defence;
D O I
10.1016/S0300-9084(99)80105-9
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
Apart from the essential trace element iodine, which is the central constitutent of thyroid hormones, a second essential trace element, selenium, is required for appropriate thyroid hormone synthesis, activation and metabolism. The human thyroid gland has the highest selenium content per gram of tissue among all organs. Several selenocysteine-containing proteins respectively enzymes are functionally expressed in the thyroid, mainly in thyrocytes themselves: three forms of glutathione peroxidases (cGPx, pGPx, and PH-GPx), the type I 5-deiodinase, thioredoxin reductase and selenoprotein P. The thyroidal expression of type II 5-deiodinase still is controversial. As thyrocytes produce H2O2 continuously throughout life an effective cell defense system against H2O2 and reactive oxygen intermediates derived thereof is essential for maintenance of normal thyroid function and protection of the gland. In experimental animal models long-term and strong selenium deficiency leads to necrosis and fibrosis after high iodide loads. Combined iodide and selenium deficiency such as in central Zaire is thought to cause the myxedematous form of endemic cretinism. Inadequate selenium supply and prediagnostically low serum selenium levels are significantly correlated with the development of thyroid carcinoma and other tumors. Though selenium supply controls expression and translation of selenocysteine-containing proteins no direct correlation is found between selenium tissue content and expression of various thyroidal selenoproteins, indicating that other regulatory factors contribute to or override selenium-dependent expression control, e.g., in thyroid adenoma, carcinoma or autoimmune disease. As both trace elements, iodine and selenium, were washed out from the upper layers of the soil during and after the ice ages in many regions of the world adequate supply with these essential compounds needs to be provided either by a balanced diet or supplementation. (C) Societe francaise de biochimie et biologie moleculaire / Elsevier, Paris.
引用
收藏
页码:527 / 533
页数:7
相关论文
共 82 条
[1]  
AASETH J, 1996, THYR TRAC EL 6 THYR, P180
[2]  
[Anonymous], [No title captured]
[3]   HEPATIC IODOTHYRONINE 5'-DEIODINASE - THE ROLE OF SELENIUM [J].
ARTHUR, JR ;
NICOL, F ;
BECKETT, GJ .
BIOCHEMICAL JOURNAL, 1990, 272 (02) :537-540
[4]   The type 2 and type 3 iodothyronine deiodinases play important roles in coordinating development in Rana catesbeiana tadpoles [J].
Becker, KB ;
Stephens, KC ;
Davey, JC ;
Schneider, MJ ;
Galton, VA .
ENDOCRINOLOGY, 1997, 138 (07) :2989-2997
[5]   THE ROLE OF THYROIDAL TYPE-I IODOTHYRONINE DEIODINASE IN TRIIODOTHYRONINE PRODUCTION BY HUMAN AND SHEEP THYROCYTES IN PRIMARY CULTURE [J].
BEECH, SG ;
WALKER, SW ;
DORRANCE, AM ;
ARTHUR, JR ;
NICOL, F ;
LEE, D ;
BECKETT, GJ .
JOURNAL OF ENDOCRINOLOGY, 1993, 136 (03) :361-370
[6]   IDENTIFICATION OF TYPE-I IODOTHYRONINE 5'-DEIODINASE AS A SELENOENZYME [J].
BEHNE, D ;
KYRIAKOPOULOS, A ;
MEINHOLD, H ;
KOHRLE, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 173 (03) :1143-1149
[7]   EVIDENCE FOR SPECIFIC SELENIUM TARGET TISSUES AND NEW BIOLOGICALLY IMPORTANT SELENOPROTEINS [J].
BEHNE, D ;
HILMERT, H ;
SCHEID, S ;
GESSNER, H ;
ELGER, W .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 966 (01) :12-21
[8]   STUDIES ON THE DISTRIBUTION AND CHARACTERISTICS OF NEW MAMMALIAN SELENIUM-CONTAINING PROTEINS [J].
BEHNE, D ;
WEISSNOWAK, C ;
KALCKLOSCH, M ;
WESTPHAL, C ;
GESSNER, H ;
KYRIAKOPOULOS, A .
ANALYST, 1995, 120 (03) :823-825
[9]   TISSUE-SPECIFIC REGULATION OF SELENOENZYME GENE-EXPRESSION DURING SELENIUM DEFICIENCY IN RATS [J].
BERMANO, G ;
NICOL, F ;
DYER, JA ;
SUNDE, RA ;
BECKETT, GJ ;
ARTHUR, JR ;
HESKETH, JE .
BIOCHEMICAL JOURNAL, 1995, 311 :425-430
[10]   EVIDENCE THAT CYSTEINE, NOT SELENOCYSTEINE, IS IN THE CATALYTIC SITE OF TYPE-II IODOTHYRONINE DEIODINASE [J].
BERRY, MJ ;
KIEFFER, JD ;
LARSEN, PR .
ENDOCRINOLOGY, 1991, 129 (01) :550-552