Clinical Medical College of Yangzhou University, Yangzhou, China.
Department of Cardiology, Northern Jiangsu People's Hospital, Yangzhou, China.
Cell Death Dis. 2021 Jul 2;12(7):667. doi: 10.1038/s41419-021-03949-5.
Long non-coding RNA (lncRNA) is receiving increasing attention in embryonic stem cells (ESCs) research. However, the roles of lncRNA in the differentiation of ESCs into pacemaker-like cells are still unclear. Therefore, the present study aims to explore the roles and mechanisms of lncRNA in the differentiation of ESCs into pacemaker-like cells. ESCs were cultured and induced differentiation to pacemaker-like cells. RNA sequencing was used to identify the differential expression lncRNAs during the differentiation of ESCs into pacemaker-like cells. Cell morphology observation, flow cytometry, quantitative real-time polymerase chain reaction, western blot, and immunofluorescence were used to detect the differentiation of ESCs into pacemaker-like cells. LncRNA and genes overexpression or knockdown through transfected adenovirus in the differentiation process. The fluorescence in situ hybridization (FISH) detected the lncRNA location in the differentiated ESCs. Luciferase reporter gene assay, methylation-specific PCR, chromatin immunoprecipitation assay, and RNA immunoprecipitation assay were performed to reveal the mechanism of lncRNA-regulating HCN4 expression. Rescue experiments were used to confirm that lncRNA regulates the differentiation of ESCs into pacemaker-like cells through HCN4. We cultured the ESCs and induced the differentiation of ESCs into pacemaker-like cells successfully. The expression of lncRNA RCPCD was significantly decreased in the differentiation of ESCs into pacemaker-like cells. Overexpression of RCPCD inhibited the differentiation of ESCs into pacemaker-like cells. RCPCD inhibited the expression of HCN4 by increasing HCN4 methylation at the promoter region through DNMT1, DNMT2, and DNMT3. RCPCD inhibited the differentiation of ESCs into pacemaker-like cells by inhibiting the expression of HCN4. Our results confirm the roles and mechanism of lncRNA RCPCD in the differentiation of ESCs into pacemaker-like cells, which could pave the path for the development of a cell-based biological pacemaker.
长链非编码 RNA(lncRNA)在胚胎干细胞(ESC)研究中受到越来越多的关注。然而,lncRNA 在 ESC 分化为起搏样细胞中的作用尚不清楚。因此,本研究旨在探讨 lncRNA 在 ESC 分化为起搏样细胞中的作用和机制。培养 ESC 并诱导其分化为起搏样细胞。采用 RNA 测序技术鉴定 ESC 分化为起搏样细胞过程中差异表达的 lncRNA。通过转染腺病毒在分化过程中过表达或敲低 lncRNA 和基因。荧光原位杂交(FISH)检测分化后的 ESC 中 lncRNA 的位置。采用荧光素酶报告基因检测、甲基化特异性 PCR、染色质免疫沉淀检测和 RNA 免疫沉淀检测揭示 lncRNA 调节 HCN4 表达的机制。通过 rescue 实验证实 lncRNA 通过 HCN4 调节 ESC 分化为起搏样细胞。我们成功培养了 ESC 并诱导其分化为起搏样细胞。在 ESC 分化为起搏样细胞的过程中,lncRNA RCPCD 的表达显著降低。过表达 RCPCD 抑制 ESC 分化为起搏样细胞。RCPCD 通过增加启动子区域的 HCN4 甲基化(通过 DNMT1、DNMT2 和 DNMT3)抑制 HCN4 的表达。RCPCD 通过抑制 HCN4 的表达抑制 ESC 分化为起搏样细胞。我们的结果证实了 lncRNA RCPCD 在 ESC 分化为起搏样细胞中的作用和机制,这为开发基于细胞的生物起搏器铺平了道路。