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长时间共递送山中因子进行细胞重编程。

Prolonged Three-Dimensional Co-Delivery of Yamanaka Factors for Cell Reprogramming.

机构信息

Department of Pharmaceutics, School of Pharmacy and Center for Drug/Gene Delivery and Tissue Engineering, Jiangsu University , Zhenjiang 212001, P.R. China.

Center for Drug/Gene Delivery and Tissue Engineering and School of Medicine, Jiangsu University , Zhenjiang 212001, P.R. China.

出版信息

ACS Appl Mater Interfaces. 2016 Aug 10;8(31):19916-27. doi: 10.1021/acsami.6b05825. Epub 2016 Jul 26.

Abstract

Reprogramming somatic cells into a pluripotent state has been widely investigated in two-dimensional (2D) systems but not described in the more biologically faithful three-dimensional (3D) scaffolds. Here, we devise a 3D porous tissue engineering scaffold that could achieve successful and efficient induction of pluripotency. To construct this 3D scaffold, nonviral hybrid nanoparticles were fabricated beforehand by employing calcium phosphate and cationized Pleurotus eryngii polysaccharide to codeliver plasmids OCT4, SOX2, KLF4 ,and C-MYC (pOSKM). These hybrid nanoparticles were then loaded into a 3D porous collagen scaffold to obtain the so-called pOSKM-activated 3D scaffold. This 3D scaffold could reprogram human umbilical cord mesenchymal stem cells (HUMSCs) into a pluripotent state, generating 3D cell spheres which showed positive expression of pluripotency markers in the 3D scaffolds and tightly packed colonies when transferred to 2D feeder layers. Besides sharing similar morphology, epigenetic modification, and expression of pluripotency genes with the embryonic stem cells, the 3D system-generated colonies could also be expanded on feeder layers for more than 20 passages, indicating the successful establishment of stable induced pluripotent stem cell (iPSC) lines. Our findings represent a first employment of porous 3D scaffolds to achieve successful reprogramming via a one-time transfection, offering a safe, simple, and effective alternative strategy for iPSC generation.

摘要

体细胞重编程为多能状态已在二维(2D)系统中得到广泛研究,但在更具生物真实性的三维(3D)支架中尚未描述。在这里,我们设计了一种 3D 多孔组织工程支架,可以成功有效地诱导多能性。为了构建这种 3D 支架,事先制备了非病毒杂化纳米粒子,方法是采用磷酸钙和阳离子化杏鲍菇多糖共递送质粒 OCT4、SOX2、KLF4 和 C-MYC(pOSKM)。然后将这些杂化纳米粒子载入 3D 多孔胶原支架中,得到所谓的 pOSKM 激活 3D 支架。这种 3D 支架可以将人脐带间充质干细胞(HUMSCs)重编程为多能状态,生成 3D 细胞球,在 3D 支架中显示出多能性标志物的阳性表达,当转移到 2D 饲养层时形成紧密堆积的集落。除了与胚胎干细胞具有相似的形态、表观遗传修饰和多能性基因表达外,3D 系统生成的集落还可以在饲养层上扩增 20 多代以上,表明稳定的诱导多能干细胞(iPSC)系已成功建立。我们的发现代表了首次使用多孔 3D 支架通过一次转染实现成功重编程,为 iPSC 生成提供了一种安全、简单、有效的替代策略。

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