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Fabrication of three-dimensional multi-protein microstructures for cell migration and adhesion enhancement

机译:三维多元蛋白质微结构的制造以促进细胞迁移和粘附

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摘要

In this study, three-dimensional (3D) multi-component microstructures were precisely fabricated via multiphoton excited photochemistry using a femtosecond laser direct-writing system with proposed repetition positioning and vector scanning techniques. Extracellular matrix (ECM) proteins, such as fibronectin (FN), are difficult to stack and form 3D structures larger than several-hundred microns in height due to the nature of their protein structure. Herein, to fabricate complex 3D microstructures with FN, a 3D scaffold was designed and formed from bovine serum albumin (BSA), after which human FN was inserted at specific locations on the BSA scaffold; in this manner, the fabricated ECM microstructure can guide cells in a 3D environment. A human breast cancer cell line, MDA-MB-231, was used to investigate the behavior of cell migration and adhesion on the fabricated human FN and BSA protein structures. Experimental results indicate that many cells are not able to attach or climb on a 3D structure’s inclined plane without FN support; hence, the influence of cell growth in a 3D context with FN should being taken into consideration. This 3D multi-protein fabrication technique holds potential for cell studies in designed complex 3D ECM scaffolds.
机译:在这项研究中,使用飞秒激光直接写入系统,并结合拟议的重复定位和矢量扫描技术,通过多光子激发光化学技术精确地制造了三维(3D)多组分微结构。细胞外基质(ECM)蛋白,例如纤连蛋白(FN),由于其蛋白质结构的性质,很难堆叠和形成高度大于数百微米的3D结构。在本文中,为了制造具有FN的复杂3D微结构,设计并由牛血清白蛋白(BSA)形成3D支架,然后将人FN插入BSA支架的特定位置。以这种方式,制造的ECM微观结构可以在3D环境中引导细胞。人类乳腺癌细胞系MDA-MB-231用于研究细胞在迁移的人FN和BSA蛋白结构上的迁移和粘附行为。实验结果表明,在没有FN支撑的情况下,许多单元格无法在3D结构的倾斜平面上附着或攀爬。因此,应考虑FN在3D环境中细胞生长的影响。这种3D多蛋白制造技术在设计的复杂3D ECM支架中具有进行细胞研究的潜力。

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