Instituto de Investigaciones Biomédicas Sols-Morreale, Consejo Superior de Investigaciones Científicas (CSIC), Universidad Autónoma de Madrid (UAM), Madrid, Spain.
Facultad de Medicina, Universidad Alfonso X El Sabio, Madrid, Spain.
Methods Mol Biol. 2025;2876:117-130. doi: 10.1007/978-1-0716-4252-8_8.
Somatic cells can be transformed into induced pluripotent stem cells (iPSCs) using a technique called reprogramming. This process involves introducing Yamanaka factors (Oct4, Sox2, Klf4, and c-Myc) to the cells through retroviral supernatants. This chapter outlines a protocol for reprogramming mouse embryonic fibroblasts (MEFs) using the hormone triiodo-L-thyronine (T3) to enhance the generation of iPSCs. It also describes how to analyze these iPSCs by colony staining for alkaline phosphatase activity, a standard marker for identifying pluripotent embryonic stem cells. To further study iPSCs, individual colonies must be selected and expanded, and pluripotency is examined by analyzing gene expression profiles using quantitative real-time PCR to measure the endogenous expression of pluripotency genes. Integrating T3 into reprogramming methods may significantly improve the production of functional iPSCs. This advancement could open new avenues for research in cell plasticity, disease modeling, and regenerative therapies.
体细胞可以通过一种称为重编程的技术转化为诱导多能干细胞(iPSCs)。该过程涉及通过逆转录病毒上清液将 Yamanaka 因子(Oct4、Sox2、Klf4 和 c-Myc)引入细胞。本章概述了使用激素三碘甲状腺原氨酸(T3)重编程小鼠胚胎成纤维细胞(MEFs)以增强 iPSCs 生成的方案。它还描述了如何通过碱性磷酸酶活性的集落染色分析这些 iPSCs,碱性磷酸酶活性是鉴定多能胚胎干细胞的标准标志物。为了进一步研究 iPSCs,必须选择和扩增单个集落,并通过分析定量实时 PCR 测量多能性基因的内源性表达来检查基因表达谱来检查多能性。将 T3 整合到重编程方法中可能会显著提高功能性 iPSCs 的产量。这一进展可能为细胞可塑性、疾病建模和再生疗法的研究开辟新途径。