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石墨烯增强纳米纤维支架在细胞行为方面展现出新特性。

Graphene-augmented nanofiber scaffolds demonstrate new features in cells behaviour.

作者信息

Kazantseva Jekaterina, Ivanov Roman, Gasik Michael, Neuman Toomas, Hussainova Irina

机构信息

Cellin Technologies LLC, Tallinn, Estonia.

Department of materials engineering, Tallinn University of Technology, Tallinn, Estonia.

出版信息

Sci Rep. 2016 Jul 22;6:30150. doi: 10.1038/srep30150.

Abstract

Three-dimensional (3D) customized scaffolds capable to mimic a native extracellular matrix open new frontiers in cells manipulation and advanced therapy. The major challenge is in a proper substrate for in vitro models on engineered scaffolds, capable to modulate cells differentiation. Here for the first time we demonstrate novel design and functionality of the 3D porous scaffolds of aligned, self-assembled ceramic nanofibers of ultra-high anisotropy ratio (~10(7)), augmented into graphene shells. This unique hybrid nano-network allows an exceptional combination of selective guidance stimuli of stem cells differentiation, immune reactions variations, and local immobilization of cancer cells, which was not available before. The scaffolds were shown to be able to direct human mesenchymal stem cells (important for stimulation of neuronal and muscle cells) preferential orientation, to suppress major inflammatory factors, and to localize cancer cells; all without additions of specific culture media. The selective downregulation of specific cytokines is anticipated as a new tool for understanding of human immune system and ways of treatment of associated diseases. The effects observed are self-regulated by cells only, without side effects, usually arising from use of external factors. New scaffolds may open new horizons for stem cells fate control such as towards axons and neurites regeneration (Alzheimer's disease) as well as cancer therapy development.

摘要

能够模拟天然细胞外基质的三维(3D)定制支架为细胞操控和先进治疗开辟了新领域。主要挑战在于为工程支架上的体外模型提供合适的基质,该基质能够调节细胞分化。在此,我们首次展示了具有超高各向异性比(约10⁷)的排列整齐、自组装陶瓷纳米纤维的3D多孔支架的新颖设计和功能,这些纳米纤维被增强到石墨烯壳中。这种独特的混合纳米网络实现了干细胞分化的选择性引导刺激、免疫反应变化以及癌细胞的局部固定等特殊组合,这是以前所没有的。研究表明,这些支架能够引导人间充质干细胞(对刺激神经元和肌肉细胞很重要)的优先取向,抑制主要炎症因子,并定位癌细胞;所有这些都无需添加特定的培养基。特定细胞因子的选择性下调有望成为理解人类免疫系统及相关疾病治疗方法的新工具。观察到的效果仅由细胞自我调节,没有通常因使用外部因素而产生的副作用。新型支架可能为干细胞命运控制开辟新视野,比如促进轴突和神经突再生(阿尔茨海默病)以及癌症治疗发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4511/4957128/77e75499efb0/srep30150-f1.jpg

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