AGH University of Science and Technology, International Centre of Electron Microscopy for Materials Science and Faculty of Metals Engineering and Industrial Computer Science, Al. A. Mickiewicza 30, 30-059 Kraków, Poland; School of Engineering and Materials Science, Queen Mary University of London, Mile End Road, London E1 4NS, United Kingdom.
AGH University of Science and Technology, International Centre of Electron Microscopy for Materials Science and Faculty of Metals Engineering and Industrial Computer Science, Al. A. Mickiewicza 30, 30-059 Kraków, Poland.
Mater Sci Eng C Mater Biol Appl. 2019 Feb 1;95:397-408. doi: 10.1016/j.msec.2017.08.076. Epub 2017 Aug 19.
Electrospun nanofibers have ability to boost cell proliferation in tissue engineered scaffolds as their structure remind cells extra cellular matrix of the native tissue. The complex architecture and network of nanofibrous scaffolds requires advanced characterization methods to understand interrelationship between cells and nanofibers. In our study, we used complementary 2D and 3D analyses of electrospun polylactide-co-glycolide acid (PLGA) scaffolds in two configurations: aligned and randomly oriented nanofibers. Sizes of pores and fibers, pores shapes and porosity, before and after cell culture, were verified by imaging with scanning electron microscopy (SEM) and combination of focus ion beam (FIB) and SEM to obtain 3D reconstructions of samples. Using FIB-SEM tomography for 3D reconstructions and 2D analyses, a unique set of data allowing understanding cell proliferation mechanism into the electrospun scaffolds, was delivered. Critically, the proliferation of cells into nanofibers network depends mainly on the pore shape and pores interconnections, which allow deep integration between cells and nanofibers. The proliferation of cells inside the network of fibers is much limited for aligned fibers comparing to randomly oriented fibers. For random fibers cells have easier way to integrate inside the scaffold as the circularity of pores and their sizes are larger than for aligned scaffolds. The complex architecture of electrospun scaffolds requires appropriate, for tissue engineering needs, cell seeding and culture methods, to maximize tissue growth in vitro environment.
静电纺纳米纤维能够促进组织工程支架中的细胞增殖,因为它们的结构类似于细胞外基质。纳米纤维支架的复杂结构和网络需要先进的特征分析方法来理解细胞与纳米纤维之间的相互关系。在我们的研究中,我们使用了二维和三维分析方法来研究两种配置的静电纺聚乳酸-共-乙醇酸(PLGA)支架:定向和随机取向的纳米纤维。通过扫描电子显微镜(SEM)成像以及聚焦离子束(FIB)和 SEM 的组合,验证了支架在细胞培养前后的孔径和纤维大小、孔形状和孔隙率。使用 FIB-SEM 断层扫描进行三维重建和二维分析,提供了一组独特的数据,有助于理解细胞在静电纺支架中的增殖机制。重要的是,细胞在纳米纤维网络中的增殖主要取决于孔的形状和孔的连通性,这允许细胞与纳米纤维之间的深度整合。与随机取向的纤维相比,定向纤维中纤维网络内的细胞增殖受到很大限制。对于随机纤维,由于孔的圆度和尺寸比定向支架大,细胞更容易整合到支架内。静电纺支架的复杂结构需要适当的细胞接种和培养方法,以满足组织工程的需要,从而最大限度地提高体外环境中的组织生长。