Department of Cardiovascular Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Department of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Cell Reprogram. 2022 Oct;24(5):283-293. doi: 10.1089/cell.2022.0014. Epub 2022 Jun 28.
Reprogramming of human dermal fibroblasts (HDFs) into induced cardiomyocyte-like cells (iCMs) represents a promising strategy for human cardiac regeneration. Different cocktails of cardiac transcription factors can convert HDFs into iCMs, although with low efficiency and immature phenotype. Here, GATA4, MEF2C, TBX5, MESP1, and MYOCD (GMTMeMy for short) were used to reprogram HDFs by retrovirus infection. We found that the exogenous expression stoichiometry of GATA4 (GATA4 stoichiometry) significantly affected reprogramming efficiency. When 1/8 dosage of GATA4 virus (GATA4 dosage) plus MTMeMy was used, the reprogramming efficiency was obviously improved compared with average pooled virus encoding each factor, which measured, by the expression level of cardiac genes, the percentage of cardiac troponin T and alpha-cardiac myosin heavy-chain immunopositive cells and the numbers of iCMs showing calcium oscillation or beating synchronously in co-culture with mouse CMs. In addition, we prepared conditioned maintenance medium (CMM) by CM differentiation of H9 human embryonic stem cell line. We found that compared with traditional maintenance medium (TMM), CMM made iCMs show well-organized sarcomere formation and characteristic calcium oscillation wave earlier. These findings demonstrated that appropriate GATA4 stoichiometry was essential for cardiac reprogramming and some components in CMM were important for maturation of iCMs.
重编程人真皮成纤维细胞(HDFs)为诱导性心肌细胞样细胞(iCMs)代表了人类心脏再生的一种很有前途的策略。不同的心脏转录因子鸡尾酒可以将 HDF 转化为 iCMs,尽管效率低且表型不成熟。在这里,GATA4、MEF2C、TBX5、MESP1 和 MYOCD(简称 GMTMeMy)通过逆转录病毒感染来重编程 HDF。我们发现 GATA4 的外源表达化学计量(GATA4 化学计量)显著影响重编程效率。当使用 1/8 剂量的 GATA4 病毒(GATA4 剂量)加 MTMeMy 时,与平均 pooled 病毒(每个因子的编码病毒)相比,重编程效率明显提高,这通过心脏基因的表达水平来衡量,即心脏肌钙蛋白 T 和α-心脏肌球蛋白重链免疫阳性细胞的百分比以及与小鼠 CMs 共培养时表现出钙振荡或同步搏动的 iCM 数量。此外,我们通过 H9 人胚胎干细胞系的 CM 分化制备了条件维持培养基(CMM)。我们发现,与传统维持培养基(TMM)相比,CMM 使 iCMs 更早地表现出有组织的肌节形成和特征性钙振荡波。这些发现表明,适当的 GATA4 化学计量对于心脏重编程至关重要,CMM 中的一些成分对于 iCM 的成熟也很重要。