The deiodinases and the control of intracellular thyroid hormone signaling during cellular differentiation

被引:101
作者
Dentice, Monica [1 ]
Marsili, Alessandro [2 ,3 ]
Zavacki, AnnMarie [2 ,3 ]
Larsen, P. Reed [2 ,3 ]
Salvatore, Domenico [1 ,4 ]
机构
[1] Univ Naples Federico II, Dept Mol & Clin Endocrinol & Oncol, I-80131 Naples, Italy
[2] Brigham & Womens Hosp, Thyroid Sect, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] CEINGE Biotecnol Avanzate Scarl, Naples, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2013年 / 1830卷 / 07期
关键词
Thyroid hormone; Deiodinase; Cellular differentiation; TYPE-2 IODOTHYRONINE DEIODINASE; MUSCLE SATELLITE CELLS; MOUSE SKELETAL-MUSCLE; FOXO TRANSCRIPTION FACTORS; KERATIN GENE-EXPRESSION; CENTRAL-NERVOUS-SYSTEM; RAT CEREBRAL-CORTEX; MOLECULAR-BIOLOGY; ATPASE ACTIVITY; RECEPTOR-BETA;
D O I
10.1016/j.bbagen.2012.05.007
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
Background: Thyroid hormone influences gene expression in virtually all vertebrates. Its action is initiated by the activation of T4 to T3, an outer ring deiodination reaction that is catalyzed by the type 1 or the type 2 iodothyronine selenodeiodinases (D1 or D2). Inactivation of T4 and T3 occurs via inner ring deiodination catalyzed by the type 3 iodothyronine selenodeiodinases (D3). The T4 concentration is generally quite stable in human plasma, with T3 levels also remaining constant. Deiodinase actions are tightly regulated in both pre- and post-natal life when they are required to make local adjustments of intracellular T3 concentrations in a precise spatio- and temporal manner. Although all the signals governing the dynamic expression of deiodinases in specific cell types are not known, many important regulatory factors have been deciphered. Scope of review: This review provides striking examples from the recent literature illustrating how the expression of D2 and D3 is finely tuned during maturation of different organs, and how their action play a critical role in different settings to control intracellular T3 availability. Major conclusions: Emerging evidence indicates that in various cell contexts, D2 and D3 are expressed in a dynamic balance, in which the expression of one enzyme is coordinately regulated with that of the other to tightly control intracellular T3 levels commensurate with cell requirements at that time. General significance: Deiodinases control TH action in a precise spatio-temporal fashion thereby providing a novel mechanism for the local paracrine and autocrine regulation of TH action. This remarkable tissue-specific regulation of intracellular thyroid status remains hidden due to the maintenance of constant circulating TH concentrations by the hypothalamic pituitary thyroid axis. This article is part of a Special Issue entitled Thyroid hormone signalling. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:3937 / 3945
页数:9
相关论文
共 92 条
[41]   Type 2 Iodothyronine Deiodinase in Human Skeletal Muscle: New Insights into Its Physiological Role and Regulation [J].
Larsen, P. Reed .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2009, 94 (06) :1893-1895
[42]  
LARSEN PR, 1981, ENDOCR REV, V2, P87, DOI 10.1210/edrv-2-1-87
[43]  
LARSEN PR, 1982, NEW ENGL J MED, V306, P23
[44]   ACUTE POSTTRANSCRIPTIONAL REGULATION OF CEREBROCORTICAL AND PITUITARY IODOTHYRONINE 5'-DEIODINASES BY THYROID-HORMONE [J].
LEONARD, JL ;
SILVA, JE ;
KAPLAN, MM ;
MELLEN, SA ;
VISSER, TJ ;
LARSEN, PR .
ENDOCRINOLOGY, 1984, 114 (03) :998-1004
[45]   Thyroid disease and the skin [J].
Leonhardt, JM ;
Heymann, WR .
DERMATOLOGIC CLINICS, 2002, 20 (03) :473-+
[46]   FoxO3 controls autophagy in skeletal muscle in vivo [J].
Mammucari, Cristina ;
Milan, Giulia ;
Romanello, Vanina ;
Masiero, Eva ;
Rudolf, Ruediger ;
Del Piccolo, Paola ;
Burden, Steven J. ;
Di Lisi, Raffaella ;
Sandri, Claudia ;
Zhao, Jinghui ;
Goldberg, Alfred L. ;
Schiaffino, Stefano ;
Sandri, Marco .
CELL METABOLISM, 2007, 6 (06) :458-471
[47]   Asymmetric growth and development of the Xenopus laevis retina during metamorphosis is controlled by type III deiodinase [J].
Marsh-Armstrong, N ;
Huang, HC ;
Remo, BF ;
Liu, TT ;
Brown, DD .
NEURON, 1999, 24 (04) :871-878
[48]   Type II iodothyronine deiodinase provides intracellular 3,5,3′-triiodothyronine to normal and regenerating mouse skeletal muscle [J].
Marsili, Alessandro ;
Tang, Dan ;
Harney, John W. ;
Singh, Prabhat ;
Zavacki, Ann Marie ;
Dentice, Monica ;
Salvatore, Domenico ;
Larsen, P. Reed .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2011, 301 (05) :E818-E824
[49]   Type 2 Iodothyronine Deiodinase Levels Are Higher in Slow-Twitch than Fast-Twitch Mouse Skeletal Muscle and Are Increased in Hypothyroidism [J].
Marsili, Alessandro ;
Ramadan, Waile ;
Harney, John W. ;
Mulcahey, Michelle ;
Castroneves, Luciana Audi ;
Goemann, Iuri Martin ;
Wajner, Simone Magagnin ;
Huang, Stephen A. ;
Zavacki, Ann Marie ;
Maia, Ana Luiza ;
Dentice, Monica ;
Salvatore, Domenico ;
Silva, J. Enrique ;
Larsen, P. Reed .
ENDOCRINOLOGY, 2010, 151 (12) :5952-5960
[50]   SATELLITE CELL OF SKELETAL MUSCLE FIBERS [J].
MAURO, A .
JOURNAL OF BIOPHYSICAL AND BIOCHEMICAL CYTOLOGY, 1961, 9 (02) :493-&