Suppr超能文献

母鼠甲状腺激素在胚胎-胎儿发育过程中具有转录活性:来自新型转基因小鼠模型的结果。

Maternal thyroid hormones are transcriptionally active during embryo-foetal development: results from a novel transgenic mouse model.

机构信息

Endocrinology Unit, Molecular Endocrinology and Endocrine Cancers laboratory, Department of Internal Medicine, Medical School A. Gemelli, Catholic University, Roma, Italy.

出版信息

J Cell Mol Med. 2010 Oct;14(10):2417-35. doi: 10.1111/j.1582-4934.2009.00947.x.

Abstract

Even though several studies highlighted the role of maternal thyroid hormones (THs) during embryo-foetal development, direct evidence of their interaction with embryonic thyroid receptors (TRs) is still lacking. We generated a transgenic mouse model ubiquitously expressing a reporter gene tracing TH action during development. We engineered a construct (TRE2×) containing two TH-responsive elements controlling the expression of the LacZ reporter gene, which encodes β-galactosidase (β-gal). The specificity of the TRE2× activation by TH was evaluated in NIH3T3 cells by cotransfecting TRE2× along with TRs, retinoic or oestrogen receptors in the presence of their specific ligands. TRE2× transgene was microinjected into the zygotes, implanted in pseudopregnant BDF1 (a first-generation (F1) hybrid from a cross of C57BL/6 female and a DBA/2 male) mice and transgenic mouse models were developed. β-gal expression was assayed in tissue sections of transgenic mouse embryos at different stages of development. In vitro, TRE2× transactivation was observed only following physiological T3 stimulation, mediated exclusively by TRs. In vivo, β-gal staining, absent until embryonic day 9.5-10.5 (E9.5-E10.5), was observed as early as E11.5-E12.5 in different primordia (i.e. central nervous system, sense organs, intestine, etc.) of the TRE2× transgenic embryos, while the foetal thyroid function (FTF) was still inactive. Immunohistochemistry for TRs essentially colocalized with β-gal staining. No β-gal staining was detected in embryos of hypothyroid transgenic mice. Importantly, treatment with T3 in hypothyroid TRE2× transgenic mice rescued β-gal expression. Our results provide in vivo direct evidence that during embryonic life and before the onset of FTF, maternal THs are transcriptionally active through the action of embryonic TRs. This model may have clinical relevance and may be employed to design end-point assays for new molecules affecting THs action.

摘要

尽管有几项研究强调了母体甲状腺激素 (THs) 在胚胎-胎儿发育过程中的作用,但仍缺乏它们与胚胎甲状腺受体 (TRs) 相互作用的直接证据。我们生成了一种转基因小鼠模型,该模型可普遍表达一种示踪基因,以追踪发育过程中 TH 的作用。我们设计了一种构建体 (TRE2×),其中包含两个受 TH 控制的反应元件,控制β-半乳糖苷酶 (β-gal) 报告基因的表达。通过在存在其特异性配体的情况下共转染 TRE2×和 TRs、视黄酸或雌激素受体,在 NIH3T3 细胞中评估了 TRE2×被 TH 激活的特异性。将 TRE2×转基因微注射到受精卵中,将其植入假孕 BDF1(C57BL/6 雌性和 DBA/2 雄性杂交的第一代 (F1) 杂种)小鼠中,并开发了转基因小鼠模型。在不同发育阶段的转基因小鼠胚胎的组织切片中检测β-gal 的表达。在体外,仅在生理 T3 刺激下观察到 TRE2×的转录激活,该激活完全由 TRs 介导。在体内,β-gal 染色在胚胎第 9.5-10.5 天 (E9.5-E10.5) 之前不存在,但在 TRE2×转基因胚胎的不同原基(即中枢神经系统、感觉器官、肠道等)中,早在 E11.5-E12.5 就可以观察到,而胎儿甲状腺功能 (FTF) 仍然不活跃。TRs 的免疫组织化学分析基本上与β-gal 染色共定位。在甲状腺功能减退的转基因小鼠胚胎中未检测到β-gal 染色。重要的是,在甲状腺功能减退的 TRE2×转基因小鼠中用 T3 处理可挽救β-gal 的表达。我们的结果提供了体内直接证据,表明在胚胎生命期间,并且在 FTF 开始之前,母体 THs 通过胚胎 TRs 的作用进行转录激活。该模型可能具有临床相关性,并可用于设计影响 THs 作用的新分子的终点测定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d196/3823160/348828a66db5/jcmm0014-2417-f1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验