López-Fagundo Cristina, Livi Liane L, Ramchal Talisha, Darling Eric M, Hoffman-Kim Diane
Department of Molecular Pharmacology, Physiology and Biotechnology, Brown University, Providence, RI 02912, USA; Center for Biomedical Engineering, Brown University, Providence, RI 02912, USA.
Department of Molecular Pharmacology, Physiology and Biotechnology, Brown University, Providence, RI 02912, USA.
Acta Biomater. 2016 Jul 15;39:55-64. doi: 10.1016/j.actbio.2016.04.047. Epub 2016 Apr 30.
Successful realization of the enormous potential of pluripotent stem cells in regenerative medicine demands the development of well-defined culture conditions. Maintenance of embryonic stem cells (ESCs) typically requires co-culture with feeder layer cells, generally mouse embryonic fibroblasts (MEFs). Concerns about xenogeneic pathogen contamination and immune reaction to feeder cells underlie the need for ensuring the safety and efficacy of future stem cell-based products through the development of a controlled culture environment. To gain insight into the effectiveness of MEF layers, here we have developed a biomimetic synthetic feeder layer (BSFL) that is acellular and replicates the stiffness and topography of MEFs. The mechanical properties of MEFs were measured using atomic force microscopy. The average Young's modulus of the MEF monolayers was replicated using tunable polyacrylamide (PA) gels. BSFLs replicated topographical features of the MEFs, including cellular, subcellular, and cytoskeletal features. On BSFLs, mouse ESCs adhered and formed compact round colonies; similar to on MEF controls but not on Flat PA. ESCs on BSFLs maintained their pluripotency and self-renewal across passages, formed embryoid bodies and differentiated into progenitors of the three germ layers. This acellular biomimetic synthetic feeder layer supports stem cell culture without requiring co-culture of live xenogeneic feeder cells, and provides a versatile, tailorable platform for investigating stem cell growth.
Embryonic stem cells have enormous potential to aid therapeutics, because they can renew themselves and become different cell types. This study addresses a key challenge for ESC use - growing them safely for human patients. ESCs typically grow with a feeder layer of mouse fibroblasts. Since patients have a risk of immune response to feeder layer cells, we have developed a material to mimic the feeder layer and eliminate this risk. We investigated the influence of feeder layer topography and stiffness on mouse ESCs. While the biomimetic synthetic feeder layer contains no live cells, it replicates the stiffness and topography of feeder layer cells. Significantly, ESCs grown on BSFLs retain their abilities to grow and become multiple cell types.
要成功实现多能干细胞在再生医学中的巨大潜力,需要开发明确的培养条件。胚胎干细胞(ESC)的维持通常需要与饲养层细胞共培养,一般是小鼠胚胎成纤维细胞(MEF)。对异种病原体污染以及对饲养细胞的免疫反应的担忧,促使人们需要通过开发可控的培养环境来确保未来基于干细胞的产品的安全性和有效性。为了深入了解MEF层的有效性,我们在此开发了一种无细胞的仿生合成饲养层(BSFL),它能复制MEF的硬度和拓扑结构。使用原子力显微镜测量MEF的力学性能。使用可调聚丙烯酰胺(PA)凝胶复制MEF单层的平均杨氏模量。BSFL复制了MEF的拓扑特征,包括细胞、亚细胞和细胞骨架特征。在BSFL上,小鼠ESC粘附并形成紧密的圆形集落;类似于在MEF对照上,但在平坦的PA上则不然。在BSFL上的ESC在传代过程中保持其多能性和自我更新能力,形成胚状体并分化为三个胚层的祖细胞。这种无细胞的仿生合成饲养层支持干细胞培养,无需与活的异种饲养细胞共培养,并为研究干细胞生长提供了一个通用的、可定制的平台。
胚胎干细胞在辅助治疗方面具有巨大潜力,因为它们可以自我更新并成为不同的细胞类型。本研究解决了ESC应用中的一个关键挑战——为人类患者安全地培养它们。ESC通常在小鼠成纤维细胞的饲养层上生长。由于患者对饲养层细胞有免疫反应的风险,我们开发了一种材料来模拟饲养层并消除这种风险。我们研究了饲养层拓扑结构和硬度对小鼠ESC的影响。虽然仿生合成饲养层不包含活细胞,但它复制了饲养层细胞的硬度和拓扑结构。重要的是,在BSFL上生长的ESC保留了它们生长并成为多种细胞类型的能力。