Center for Molecular Medicine, Maine Medical Center Research Institute, Maine Medical Center, Scarborough, Maine.
Graduate School for Biomedical Science and Engineering, University of Maine, Orono, Maine.
Endocrinology. 2019 Dec 1;160(12):2929-2945. doi: 10.1210/en.2019-00259.
Premature overexposure to thyroid hormone causes profound effects on testis growth, spermatogenesis, and male fertility. We used genetic mouse models of type 3 deiodinase (DIO3) deficiency to determine the genetic programs affected by premature thyroid hormone action and to define the role of DIO3 in regulating thyroid hormone economy in testicular cells. Gene expression profiling in the neonatal testis of DIO3-deficient mice identified 5699 differentially expressed genes. Upregulated and downregulated genes were, respectively, involved according to DAVID analysis with cell differentiation and proliferation. They included anti-Müllerian hormone and genes involved in the formation of the blood-testis barrier, which are specific to Sertoli cells (SCs). They also included steroidogenic genes, which are specific to Leydig cells. Comparison with published data sets of genes enriched in SCs and spermatogonia, and responsive to retinoic acid (RA), identified a subset of genes that were regulated similarly by RA and thyroid hormone. This subset of genes showed an expression bias, as they were downregulated when enriched in spermatogonia and upregulated when enriched in SCs. Furthermore, using a genetic approach, we found that DIO3 is not expressed in SCs, but spermatogonia-specific inactivation of DIO3 led to impaired testis growth, reduced SC number, decreased cell proliferation and, especially during neonatal development, altered gene expression specific to somatic cells. These findings indicate that spermatogonial DIO3 protects testicular cells from untimely thyroid hormone signaling and demonstrate a mechanism of cross-talk between somatic and germ cells in the neonatal testis that involves the regulation of thyroid hormone availability and action.
过早暴露于甲状腺激素会对睾丸生长、精子发生和男性生育力产生深远影响。我们使用 3 型脱碘酶(DIO3)缺乏的基因敲除小鼠模型,以确定受过早甲状腺激素作用影响的遗传程序,并定义 DIO3 在调节睾丸细胞中甲状腺激素代谢中的作用。DIO3 基因敲除小鼠新生睾丸的基因表达谱分析确定了 5699 个差异表达基因。根据 DAVID 分析,上调和下调的基因分别与细胞分化和增殖有关。它们包括抗苗勒管激素(AMH)和参与血睾屏障形成的基因,这些基因是睾丸支持细胞(SCs)特有的;它们还包括类固醇生成基因,这些基因是睾丸间质细胞(Leydig 细胞)特有的。与在SCs 和精原细胞中富集且对维甲酸(RA)有反应的基因的已发表数据集进行比较,确定了一组受 RA 和甲状腺激素相似调节的基因。这组基因表现出表达偏向,即当它们在精原细胞中富集时下调,在 SCs 中富集时上调。此外,我们通过遗传方法发现 DIO3 不在SCs 中表达,但在精原细胞中特异性敲除 DIO3 会导致睾丸生长受损、SCs 数量减少、细胞增殖减少,尤其是在新生儿发育期间,改变特定于体细胞的基因表达。这些发现表明,精原细胞 DIO3 可保护睾丸细胞免受过早的甲状腺激素信号转导,并证明了新生儿睾丸中体细胞和生殖细胞之间存在交叉对话的机制,该机制涉及甲状腺激素可用性和作用的调节。