Ding Yunfeng, Tamhankar Soniya, Du Feifan, Christopherson Tessa, Schlueter Nate, Cohen Jenna R, Shusta Eric V, Palecek Sean P
Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Department of Neurological Surgery, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Biotechnol Bioeng. 2025 Jul;122(7):1914-1928. doi: 10.1002/bit.28979. Epub 2025 Mar 25.
Differentiating endothelial cells (ECs) from human pluripotent stem cells (hPSCs) typically takes 2 weeks and requires parameter optimization. Overexpression of cell type-specific transcription factors in hPSCs has shown efficient differentiation into various cell types. ETV2, a crucial transcription factor for endothelial fate, can be overexpressed in hPSCs to induce rapid and facile EC differentiation (iETV2-ECs). We developed a two-stage strategy which involves differentiating inducible ETV2-overexpressing hPSCs in a basal induction medium during stage I and expanding them in an endothelial medium during stage II. By optimizing seeding density and medium composition, we achieved 99% pure CD31+ CD144+ iETV2-ECs without cell sorting in 5 days. iETV2-ECs demonstrated in vitro angiogenesis potential, LDL uptake, and cytokine response. Transcriptomic comparisons revealed similar gene expression profiles between iETV2-ECs and traditionally differentiated ECs. Additionally, iETV2-ECs responded to Wnt signaling agonist and TGFβ inhibitor to acquire brain EC phenotypes, making them a scalable EC source for applications including blood-brain barrier modeling.
从人类多能干细胞(hPSC)中分化出内皮细胞(EC)通常需要2周时间,并且需要优化参数。在hPSC中过表达细胞类型特异性转录因子已显示出可有效分化为各种细胞类型。ETV2是内皮细胞命运的关键转录因子,可在hPSC中过表达以诱导快速且简便的EC分化(iETV2-EC)。我们开发了一种两阶段策略,包括在第一阶段于基础诱导培养基中分化可诱导过表达ETV2的hPSC,并在第二阶段于内皮细胞培养基中进行扩增。通过优化接种密度和培养基组成,我们在5天内无需细胞分选即可获得纯度为99%的CD31+ CD144+ iETV2-EC。iETV2-EC表现出体外血管生成潜力、低密度脂蛋白摄取和细胞因子反应。转录组比较显示iETV2-EC与传统分化的EC之间具有相似的基因表达谱。此外,iETV2-EC对Wnt信号激动剂和TGFβ抑制剂有反应,从而获得脑内皮细胞表型,使其成为包括血脑屏障建模在内的各种应用的可扩展内皮细胞来源。