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Nanotopography Promotes Pancreatic Differentiation of Human Embryonic Stem Cells and Induced Pluripotent Stem Cells

机译:纳米形貌促进人类胚胎干细胞和诱导多能干细胞的胰腺分化。

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Although previous studies suggest that nano topographical features influence properties and behaviors of stem cells, only a few studies have attempted to derive clinically useful somatic cells from human pluripotent stem cells using nanopatterned surfaces. In the present study, we report that polystyrene nanopore-patterned surfaces significantly promote the pancreatic differentiation of human embryonic and induced pluripotent stem cells. We compared different diameters of nanopores and showed that 200 nm nanopore-patterned surfaces highly upregulated the expression of PDX1, a critical transcription factor for pancreatic development, leading to an approximately 3-fold increase in the percentage of differentiating PDX1(+) pancreatic progenitors compared with control flat surfaces. Furthermore, in the presence of biochemical factors, 200 nm nanopore-patterned surfaces profoundly enhanced the derivation of pancreatic endocrine cells producing insulin, glucagon, or somatostatin. We also demonstrate that nanopore-patterned surface-induced upregulation of PDX1 is associated with downregulation of TAZ, suggesting the potential role of TAZ in nanopore-patterned surface-mediated mechano-transduction. Our study suggests that appropriate cytokine treatments combined with nanotopographical stimulation could be a powerful tool for deriving a high purity of desired cells from human pluripotent stem cells.
机译:尽管先前的研究表明纳米形貌特征会影响干细胞的特性和行为,但只有少数研究尝试使用纳米图案化表面从人多能干细胞中获得临床上有用的体细胞。在本研究中,我们报告说,聚苯乙烯纳米孔图案化的表面显着促进了人类胚胎和诱导多能干细胞的胰腺分化。我们比较了不同直径的纳米孔,发现200 nm纳米孔表面高度上调了PDX1的表达,PDX1是胰腺发育的关键转录因子,导致分化的PDX1(+)胰腺祖细胞的百分比增加了约3倍具有控制平面。此外,在存在生物化学因素的情况下,具有200 nm纳米孔图案的表面显着增强了产生胰岛素,胰高血糖素或生长抑素的胰腺内分泌细胞的衍生。我们还证明,PDX1的纳米孔表面诱导的上调与TAZ的下调相关,表明TAZ在纳米孔表面介导的机械转导中的潜在作用。我们的研究表明,适当的细胞因子治疗与纳米形貌刺激相结合可能是从人多能干细胞中获得高纯度所需细胞的强大工具。

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