Yen Jonathan, Yin Lichen, Cheng Jianjun
Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801, USA.
Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801, USA.
J Mater Chem B. 2014;2(46):8098-8105. doi: 10.1039/C4TB00750F.
Non-viral gene delivery into human embryonic stem cells (hESCs)is an important tool for controlling cell fate. However, the delivery efficiency remains low due in part to the tight colony structure of the cells which prevents effective exposure towards delivery vectors. We herein report a novel approach to enhance non-viral gene delivery to hESCs by transiently altering the cell and colony structure. ()-(+)--4-(1-aminoethyl)--(4-pyridyl)cyclohexanecarboxamide (Y-27632), a small molecule that inhibits the rho-associated protein kinase pathway, is utilized to induce transient colony spreading which leads to increased transfection efficiency by 1.5 to 2 folds in a spectrum of non-viral transfection reagents including Lipofectamine 2000 and Fugene HD. After removal of Y-27632 post-transfection, cells can revert back to its normal state and do not show alteration of pluripotency. This approach provides a simple, effective tool to enhance non-viral gene delivery into adherent hESCs for genetic manipulation.
非病毒基因导入人胚胎干细胞(hESCs)是控制细胞命运的重要工具。然而,由于细胞紧密的集落结构部分阻碍了对递送载体的有效暴露,递送效率仍然较低。我们在此报告一种通过瞬时改变细胞和集落结构来增强非病毒基因向hESCs递送的新方法。()-(+)-4-(1-氨基乙基)-2-(4-吡啶基)环己烷甲酰胺(Y-27632),一种抑制rho相关蛋白激酶途径的小分子,被用于诱导集落瞬时扩散,这使得在包括Lipofectamine 2000和Fugene HD在内的一系列非病毒转染试剂中,转染效率提高了1.5至2倍。转染后去除Y-27632,细胞可恢复到正常状态,且未显示多能性改变。该方法为增强非病毒基因导入贴壁hESCs进行基因操作提供了一种简单有效的工具。