Fu Jiao, Fujisawa Haruki, Follman Benjamin, Liao Xiao-Hui, Dumitrescu Alexandra M
Department of Medicine, University of Chicago.
Department of Endocrinology, First Affiliated Hospital of Xi'an Jiaotong University, China.
Endocrinology. 2017 Dec 1;158(12):4317-4330. doi: 10.1210/en.2017-00618.
Selenocysteine insertion sequence binding protein 2 (SBP2) is an essential factor in selenoprotein synthesis. Patients with SBP2 defects have a characteristic thyroid phenotype and additional manifestations such as growth delay, male infertility, impaired motor coordination, and developmental delay. The thyroid phenotype has become pathognomonic for this defect, and putative deficiencies in the iodothyronine deiodinases selenoenzymes have been implicated. To investigate the role of SBP2 and selenoproteins in thyroid physiology and answer questions raised by the human syndrome, we generated a tamoxifen-inducible Sbp2 conditional knockout (iCKO) mouse model. These Sbp2-deficient mice have high serum thyroxine (T4), thyrotropin, and reverse triiodothyronine (T3), similar to the human phenotype of SBP2 deficiency, whereas serum T3 is normal. Their liver T4 and T3 content reflect the serum levels, and deiodinase 1 expression and enzymatic activity were decreased. In contrast, brain T3 content is decreased, indicative of local hypothyroidism, confirmed by the decreased expression of the thyroid hormone (TH) positively regulated gene hairless. Interestingly, the cerebrum T4 content did not parallel the high serum T4 levels, and the expression of TH transporters was decreased. Deiodinase 2 enzymatic activity and deiodinase 3 expression were decreased in cerebrum. The expression and/or activity of other selenoproteins were decreased in brain, liver, and serum, thus demonstrating a global deficiency in selenoprotein synthesis. Sbp2 iCKO mice replicate the thyroid phenotype of SBP2 deficiency and represent an important tool to advance our understanding of the role of SBP2 in thyroid homeostasis and for investigating selenoprotein biology relevant to human disease.
硒代半胱氨酸插入序列结合蛋白2(SBP2)是硒蛋白合成中的一个关键因子。患有SBP2缺陷的患者具有典型的甲状腺表型以及其他表现,如生长发育迟缓、男性不育、运动协调能力受损和发育迟缓。甲状腺表型已成为这种缺陷的特征性表现,并且推测碘甲状腺原氨酸脱碘酶硒酶存在缺陷。为了研究SBP2和硒蛋白在甲状腺生理学中的作用,并回答人类综合征引发的问题,我们构建了一种他莫昔芬诱导型Sbp2条件性敲除(iCKO)小鼠模型。这些Sbp2缺陷小鼠的血清甲状腺素(T4)、促甲状腺激素和反式三碘甲状腺原氨酸(T3)水平升高,类似于SBP2缺陷的人类表型,而血清T3水平正常。它们肝脏中的T4和T3含量反映了血清水平,脱碘酶1的表达和酶活性降低。相比之下,脑内T3含量降低,表明存在局部甲状腺功能减退,甲状腺激素(TH)正向调节基因无毛的表达降低证实了这一点。有趣的是,大脑中的T4含量与高血清T4水平并不平行,并且TH转运蛋白的表达降低。大脑中脱碘酶2的酶活性和脱碘酶3的表达降低。大脑、肝脏和血清中其他硒蛋白的表达和/或活性降低,从而表明硒蛋白合成存在整体缺陷。Sbp2 iCKO小鼠重现了SBP2缺陷的甲状腺表型,是增进我们对SBP2在甲状腺稳态中的作用的理解以及研究与人类疾病相关的硒蛋白生物学的重要工具。