Department of Bioengineering, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.
J Biomed Mater Res A. 2012 Nov;100(11):2921-8. doi: 10.1002/jbm.a.34234. Epub 2012 Jun 14.
The major challenge for bone tissue engineering lies in the fabrication of scaffolds that can mimic the extracellular matrix and promote osteogenesis. Electrospun fibers are being widely researched for this application due to high porosity, interconnectivity, and mechanical strength of the fibrous scaffolds. Electrospun poly methyl methacrylate (PMMA, 2.416 ± 0.100 μm) fibers were fabricated and etched using a 60% propylene glycol methyl ether acetate (PGMEA)/limonene (vol/vol) solution to obtain fiber diameters ranging from 2.5 to 0.5 μm in a time-dependent manner. The morphology of the fibrous scaffolds was evaluated using scanning electron microscopy and cellular compatibility with etchant-treated scaffold was assessed using immunoflurescence. Mitogen-activated protein kinases (MAPK) activation in response to different fiber diameter was evaluated with western blot as well as quantitative in-cell western. We report that electrospun micro-fibers can be etched to 0.552 ± 0.047 μm diameter without producing beads. Osteoblasts adhered to the fibers and a change in fiber diameter played a major role in modulating the activation of extracellular signal-regulated kinase (ERK) and p38 kinases with 0.882 ± 0.091 μm diameter fibers producing an inverse effect on ERK and p38 phosphorylation. These results indicate that nanofibers produced by wet etching can be effectively utilized to produce diameters that can differentially modulate MAPK activation patterns.
骨组织工程的主要挑战在于制造能够模拟细胞外基质并促进成骨的支架。静电纺丝纤维由于其高孔隙率、连通性和纤维支架的机械强度,因此被广泛用于该应用。使用 60%丙二醇甲醚乙酸酯(PGMEA)/柠檬烯(体积/体积)溶液对聚甲基丙烯酸甲酯(PMMA,2.416±0.100μm)纤维进行纺丝和蚀刻,以时间依赖性的方式获得纤维直径从 2.5μm至 0.5μm 的纤维。使用扫描电子显微镜评估纤维支架的形态,并用免疫荧光法评估与蚀刻处理支架的细胞相容性。通过 Western blot 和定量细胞内 Western blot 评估了不同纤维直径下细胞丝裂原活化蛋白激酶(MAPK)的激活情况。我们报告说,静电纺微纤维可以被蚀刻到 0.552±0.047μm 的直径而不会产生珠状物。成骨细胞附着在纤维上,纤维直径的变化在调节细胞外信号调节激酶(ERK)和 p38 激酶的激活方面起着重要作用,0.882±0.091μm 的纤维直径对 ERK 和 p38 磷酸化产生相反的影响。这些结果表明,通过湿法刻蚀产生的纳米纤维可以有效地用于产生可以差异调节 MAPK 激活模式的直径。