Novel Insights on Thyroid-Stimulating Hormone Receptor Signal Transduction

被引:100
作者
Kleinau, Gunnar [1 ]
Neumann, Susanne [2 ]
Grueters, Annette [1 ]
Krude, Heiko [1 ]
Biebermann, Heike [1 ]
机构
[1] Charite, Inst Expt Pediat Endocrinol, D-13353 Berlin, Germany
[2] NIDDK, NIH, Lab Endocrinol & Receptor Biol, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
PROTEIN-COUPLED-RECEPTORS; HUMAN THYROTROPIN RECEPTOR; HUMAN CHORIONIC-GONADOTROPIN; SITE-DIRECTED MUTAGENESIS; ADENYLATE-CYCLASE ACTIVATION; FREE ALPHA-SUBUNIT; HUMAN TSH RECEPTOR; TERMINAL EXTRACELLULAR DOMAIN; BETA(2) ADRENERGIC-RECEPTOR; RESONANCE ENERGY-TRANSFER;
D O I
10.1210/er.2012-1072
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The TSH receptor (TSHR) is a member of the glycoprotein hormone receptors, a subfamily of family A G protein-coupled receptors. The TSHR is of great importance for the growth and function of the thyroid gland. The TSHR and its endogenous ligand TSH are pivotal proteins with respect to a variety of physiological functions and malfunctions. The molecular events of TSHR regulation can be summarized as a process of signal transduction, including signal reception, conversion, and amplification. The steps during signal transduction from the extra-to the intracellular sites of the cell are not yet comprehensively understood. However, essential new insights have been achieved in recent years on the interrelated mechanisms at the extracellular region, the transmembrane domain, and intracellular components. This review contains a critical summary of available knowledge of the molecular mechanisms of signal transduction at the TSHR, for example, the key amino acids involved in hormone binding or in the structural conformational changes that lead to G protein activation or signaling regulation. Aspects of TSHR oligomerization, signaling promiscuity, signaling selectivity, phenotypes of genetic variations, and potential extrathyroidal receptor activity are also considered, because these are relevant to an understanding of the overall function of the TSHR, including physiological, pathophysiological, and pharmacological perspectives. Directions for future research are discussed.
引用
收藏
页码:691 / 724
页数:34
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