Institute of Biomedical & Health Engineering, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518035, China.
Department of Mechanical Engineering, The University of Hong Kong, Pokfulam Road, Hong Kong, China.
Acta Biomater. 2021 Mar 15;123:312-324. doi: 10.1016/j.actbio.2021.01.035. Epub 2021 Jan 27.
Nanofibrous scaffolds hold great promise in tissue engineering owing to their extracellular matrix (ECM)-mimicking architectures. Electrospinning, with its ease for producing nanofibrous scaffolds, has therefore been widely employed for various tissue engineering applications. However, electrospun nanofibrous scaffolds have faced the inherent challenge of three-dimensional (3D) cell distribution due to the small sizes of interconnected pores in these scaffolds when conventional approach of scaffold fabrication with subsequent cell seeding is adopted, which severely limits their applications in repairing/regenerating human body tissues with thick and vascularized structures. In this study, we demonstrate a method to directly place living endothelial cells within bioactive nanofibrous scaffolds in 3D through concurrent emulsion electrospinning and coaxial cell electrospraying. Using this concurrent manufacturing method, endothelial cells are encapsulated in hydrogel microspheres and deposited along with vascular endothelial growth factor (VEGF)-containing nanofibers in the scaffold fabrication process, resulting in nanofibrous scaffolds with 3D embedded cell-encapsulated microspheres. After selective disruption of the hydrogel microspheres, the encapsulated endothelial cells are released, yielding bioactive nanofibrous scaffolds with tissue-like 3D cell-incorporated nanofibrous structures. It is shown that cell viability is well preserved (>98%) during the concurrent manufacturing process and that a deep cell distribution (~100 μm) through the scaffold thickness has been achieved. With combined structural and biochemical cues via the 3D cell-incorporated architectures, endothelial cells can freely stretch, display enhanced intercellular connections, and maintain the phenotype in the bioactive nanofibrous scaffolds. Our investigations offer a promising platform technology for creating bioactive nanofibrous scaffolds with 3D cell incorporation and for overcoming inherent problems of electrospun nanofibrous scaffolds, which should open new avenues for biomanufacturing tissue-mimicking constructs with vascularized structures and complex anatomy. STATEMENT OF SIGNIFICANCE: Electrospun nanofibrous scaffolds face challenges in three-dimensional (3D) cell incorporation and vascularization. Enhancing cell penetration via enlarged interconnected pores is a common strategy to address that. However, there are conflicts between cell penetration and structural integrity for scaffolds formed using such strategy, as deep cell penetration, if possible, can only achieve in highly loose architectures. In this investigation, we demonstrate a concurrent emulsion electrospinning and coaxial cell electrospraying technique, realizing 3D endothelial cell incorporation in electrospun nanofibrous scaffolds independent of cell penetration. Our technology appropriately addresses the conflict between deep 3D cell incorporation and structural integrity. In the scaffolds, the 3D incorporated endothelial cells show well-preserved viability, phenotype and functions, implying improved vascularization potential.
纳米纤维支架因其类似细胞外基质 (ECM) 的结构而在组织工程中具有广阔的应用前景。因此,由于其易于制备纳米纤维支架,电纺技术已被广泛应用于各种组织工程应用中。然而,由于传统的支架制备方法结合后续细胞接种,电纺纳米纤维支架的互连孔尺寸较小,导致其在修复/再生具有厚壁和血管化结构的人体组织方面面临固有挑战。在这项研究中,我们通过乳液静电纺丝和同轴细胞静电喷涂的方法,展示了一种直接将活内皮细胞置于三维生物活性纳米纤维支架中的方法。使用这种共制造方法,内皮细胞被包裹在水凝胶微球中,并在支架制造过程中与含有血管内皮生长因子 (VEGF) 的纳米纤维一起沉积,从而在支架中形成具有三维嵌入式细胞包封微球的纳米纤维支架。选择性破坏水凝胶微球后,释放出包封的内皮细胞,得到具有组织状三维细胞结合纳米纤维结构的生物活性纳米纤维支架。结果表明,在共制造过程中细胞活力得到了很好的保持(>98%),并且通过支架厚度实现了深度为 100 μm 的细胞分布。通过三维细胞结合结构的结构和生化线索,内皮细胞可以自由伸展,显示出增强的细胞间连接,并在生物活性纳米纤维支架中保持表型。我们的研究为具有三维细胞结合的生物活性纳米纤维支架的制造提供了一种有前途的平台技术,并为克服电纺纳米纤维支架的固有问题提供了一种解决方案,这应该为制造具有血管化结构和复杂解剖结构的组织模拟构建体开辟新途径。
电纺纳米纤维支架在三维 (3D) 细胞结合和血管化方面面临挑战。通过扩大互连孔来增强细胞穿透是解决该问题的常用策略。然而,对于使用这种策略形成的支架,细胞穿透和结构完整性之间存在冲突,因为如果可能的话,深层细胞穿透只能在高度疏松的结构中实现。在这项研究中,我们展示了一种乳液静电纺丝和同轴细胞静电喷涂的技术,实现了电纺纳米纤维支架中内皮细胞的三维结合,而无需考虑细胞穿透性。我们的技术适当解决了深层 3D 细胞结合与结构完整性之间的冲突。在支架中,3D 结合的内皮细胞表现出良好的活力、表型和功能,表明其具有增强的血管化潜力。