Stem Cell Biology Department, National Institute for Research in Reproductive Health, J.M. Street, Parel, Mumbai, 400 012, India.
Symbiosis Centre for Stem Cell Research (SCSCR), Symbiosis International University (SIU), Lavale, Mulshi, Pune, 412 115, India.
Mol Biol Rep. 2021 Feb;48(2):1615-1623. doi: 10.1007/s11033-021-06147-w. Epub 2021 Jan 23.
Differentiation processes for generating pancreatic progenitors from pluripotent stem cells inhibit Sonic hedgehog signaling through synthetic antagonists. However, the effect of sonic hedgehog inhibition in differentiating human embryonic stem cells remains unclear. The primary aim of this study was to understand the effect of Sonic hedgehog inhibition on key pancreas-specific transcription factors during differentiation of human embryonic stem cells towards a pancreatic lineage. We differentiated human embryonic stem (ES) cells towards the pancreatic progenitor stage. To analyze the effect of Sonic hedgehog inhibition, we differentiated human ES cells in the presence or absence of pathway antagonist, cyclopamine, using the same concentration (0.25 µM) as reported earlier. Changes in gene expression between the groups were examined by quantitative reverse-transcription PCR and immunoblot analyses. Surprisingly, we found that expression of key transcription factors, PDX1 and SOX9, was not majorly affected by inhibition of Sonic hedgehog signals. Effects of inhibiting Hedgehog signals on pancreas-specific markers in differentiating human embryonic stem cells were analyzed in the study. We identified that the expression of pancreas-specific PDX1 and SOX9 was not affected by the Sonic hedgehog pathway in pancreatic progenitor populations from human ES cells. Thus, the restrictive nature of Hedgehog signaling during the early stages of pancreas formation could be facilitated through a transcriptional network beyond PDX1 and SOX9.
从多能干细胞生成胰腺祖细胞的分化过程通过合成拮抗剂抑制 Sonic hedgehog 信号通路。然而, Sonic hedgehog 抑制在分化人类胚胎干细胞中的作用尚不清楚。本研究的主要目的是了解 Sonic hedgehog 抑制在人类胚胎干细胞向胰腺谱系分化过程中对关键胰腺特异性转录因子的影响。我们将人类胚胎干细胞分化为胰腺祖细胞阶段。为了分析 Sonic hedgehog 抑制的影响,我们使用与之前报道相同的浓度(0.25µM),在存在或不存在通路拮抗剂环巴胺的情况下,将人类 ES 细胞分化为胰腺祖细胞。通过定量逆转录 PCR 和免疫印迹分析检查两组之间基因表达的变化。令人惊讶的是,我们发现关键转录因子 PDX1 和 SOX9 的表达并没有被 Sonic hedgehog 信号的抑制主要影响。本研究分析了抑制 Hedgehog 信号对分化中的人类胚胎干细胞中胰腺特异性标志物的影响。我们发现,在人 ES 细胞的胰腺祖细胞群体中,Sonic hedgehog 通路对胰腺特异性标志物 PDX1 和 SOX9 的表达没有影响。因此, Hedgehog 信号在胰腺形成的早期阶段的限制性质可能通过 PDX1 和 SOX9 之外的转录网络来促进。