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包埋有明胶的微图案化聚(d,l-丙交酯-共-己内酯)薄膜用于促进雪旺细胞的排列和定向迁移。

Micropatterned poly(d,l-lactide-co-caprolactone) films entrapped with gelatin for promoting the alignment and directional migration of Schwann cells.

作者信息

Zhang Deteng, Xu Shengjun, Wu Sai, Gao Changyou

机构信息

MOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, China.

出版信息

J Mater Chem B. 2018 Feb 28;6(8):1226-1237. doi: 10.1039/c7tb03073h. Epub 2018 Feb 7.

DOI:10.1039/c7tb03073h
PMID:32254183
Abstract

Engineering microstructures with bioactive molecules critically influences Schwann cell (SC) behaviors in terms of cellular spatial arrangement and directional migration, which are advantageous for expediting the repair of peripheral nerve defects. In this study, stripe micropatterns were fabricated on poly(d,l-lactide-co-caprolactone) (PLCL) films by thermo-pressing using polydimethylsiloxane (PDMS) stamps with ridges/grooves of 3/3 and 10/10 μm in width. Their surfaces were further entrapped with 0.7 μg cm and 1.9 μg cm gelatin by a facile swelling-shrinking entrapment technique using lower and higher concentrations of gelatin solutions, respectively. The surfaces entrapped with gelatin became more hydrophilic. On the micropatterned surfaces, the water droplet had an ellipse shape and exhibited an orientation along the stripes. The gelatin-entrapped and micropatterned PLCL surfaces could guide the adhered SCs to form an elongated shape with a higher length to width ratio along the stripes. The migration rate of the SCs was significantly enhanced parallel to the stripe direction, and was fastest on the 3/3 μm PLCL films entrapped with 1.9 μg cm gelatin. The vinculin expression, adhesion force and expression of adhesion and migration-related genes such as integrin β1, Rac1, RhoA and Cdc42 revealed a stronger affinity of the SCs to the 3/3 μm PLCL films with a higher gelatin density.

摘要

利用生物活性分子构建微观结构,在细胞空间排列和定向迁移方面对雪旺细胞(SC)的行为有至关重要的影响,这有利于加快周围神经缺损的修复。在本研究中,通过热压法,使用宽度为3/3和10/10μm的脊/槽的聚二甲基硅氧烷(PDMS)印章,在聚(d,l-丙交酯-共-己内酯)(PLCL)薄膜上制备条纹微图案。通过分别使用较低和较高浓度的明胶溶液的简便溶胀-收缩包埋技术,在其表面进一步包埋0.7μg/cm和1.9μg/cm的明胶。包埋明胶的表面变得更亲水。在微图案化表面上,水滴呈椭圆形,并沿条纹方向取向。包埋明胶且有微图案的PLCL表面可引导粘附的雪旺细胞沿条纹形成长宽比更高的细长形状。雪旺细胞平行于条纹方向的迁移速率显著提高,在包埋1.9μg/cm明胶的3/3μm PLCL薄膜上迁移速率最快。纽蛋白表达、粘附力以及粘附和迁移相关基因如整合素β1、Rac1、RhoA和Cdc42的表达表明,雪旺细胞对具有更高明胶密度的3/3μm PLCL薄膜具有更强的亲和力。

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