Department of Thyroid Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Front Endocrinol (Lausanne). 2021 Feb 24;12:609308. doi: 10.3389/fendo.2021.609308. eCollection 2021.
Thyroid hormones mediate a remarkable range of functions in many tissues and organ systems through the thyroid hormone receptors-THRA and THRB. Tissues and organs are composed of heterogeneous cells of different cell types. These different cell types have varying receptor expression abilities, which lead to variable responses in thyroid hormone regulation. The tissue-specific Thra and Thrb gene expression patterns help us understand the action of thyroid hormones at the tissue level. However, the situation becomes complicated if we wish to focus on tissues more closely to trace the responsive cells, which is a vital step in the process of understanding the molecular mechanism of diseases related to thyroid hormone regulation. Single-cell RNA sequencing technology is a powerful tool used to profile gene expression programs in individual cells. The Tabula Muris Consortium generates a single-cell transcriptomic atlas across the life span of that includes data from 23 tissues and organs. It provides an unprecedented opportunity to understand thyroid hormone regulation at the cell type resolution. We demonstrated the approaches that allow application of the single-cell RNA-Seq data generated by the Tabula Muris Consortium to trace responsive cells in tissues. First, employing the single-cell RNA-Seq data, we calculated the ability of different cell types to express Thra and Thrb, which direct us to the cell types sensitive to thyroid hormone regulation in tissues and organs. Next, using a cell clustering algorithm, we explored the subtypes with low Thra or Thrb expression within the different cell types and identified the potentially responsive cell subtypes. Finally, in the liver tissue treated with thyroid hormones, using the single-cell RNA-Seq data, we successfully traced the responsive cell types. We acknowledge that the computational predictions reported here need to be further validated using wet-lab experiments. However, we believe our results provide powerful information and will be beneficial for wet lab researchers.
甲状腺激素通过甲状腺激素受体-THRA 和 THRB 在许多组织和器官系统中介导广泛的功能。组织和器官由不同细胞类型的异质细胞组成。这些不同的细胞类型具有不同的受体表达能力,这导致甲状腺激素调节的反应不同。组织特异性的 Thra 和 Thrb 基因表达模式有助于我们了解甲状腺激素在组织水平上的作用。然而,如果我们希望更密切地关注组织以追踪反应性细胞,情况就会变得复杂,这是理解与甲状腺激素调节相关疾病的分子机制的重要步骤。单细胞 RNA 测序技术是一种用于分析单个细胞中基因表达程序的强大工具。Tabula Muris 联盟在整个生命周期内生成了横跨 23 个组织和器官的单细胞转录组图谱,它提供了一个前所未有的机会,使我们能够在细胞类型分辨率上理解甲状腺激素的调节。我们展示了将 Tabula Muris 联盟生成的单细胞 RNA-Seq 数据应用于追踪组织中反应性细胞的方法。首先,我们利用单细胞 RNA-Seq 数据计算了不同细胞类型表达 Thra 和 Thrb 的能力,这使我们能够确定组织和器官中对甲状腺激素调节敏感的细胞类型。接下来,我们使用细胞聚类算法探索了不同细胞类型中低表达 Thra 或 Thrb 的亚群,并鉴定了潜在的反应性细胞亚群。最后,在经甲状腺激素处理的肝组织中,我们利用单细胞 RNA-Seq 数据成功追踪了反应性细胞类型。我们承认,这里报告的计算预测需要进一步通过湿实验室实验进行验证。然而,我们相信我们的结果提供了有力的信息,将对湿实验室研究人员有益。