3B's Research Group, I3Bs─Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, Barco, Guimarães 4805-017, Portugal.
ICVS/3B's─PT Government Associate Laboratory, Braga/Guimarães, Portugal.
ACS Biomater Sci Eng. 2022 Jul 11;8(7):2943-2953. doi: 10.1021/acsbiomaterials.2c00264. Epub 2022 Jun 15.
The promotion of angiogenesis is a fundamental step for efficient organ/tissue reconstitution and replacement. Thus, several strategies to promote vascularization of scaffolds were studied to satisfy this unsolved clinical need. The interface between cells and substrates is a determinant for the success of tissue engineering (TE) strategies. Substrate's topography is reported to play a key role in influencing endothelial cell behavior, namely, on its proliferation, metabolic activity, morphology, migration, and secretion of cytokines and chemokines. Therefore, surface topography of the biomaterial-based grafts is a crucial property that is considered in the development of a new TE approach. Herein, we hypothesize that the surface of leaf plays a crucial role in driving angiogenesis since its architecture resembles the vascular structures at a biologically relevant size scale. For this, we produced biomimetic polycaprolactone (PCL) membranes (BpMs) replicating the surface topography of a leaf by replica molding and nanoimprint lithography. Our results showed an enhanced performance in terms of proliferation of the human endothelial cell line on top of the BpM. Moreover, an asymmetric cellular spatial distribution among the surface of the BpM was observed. These cells seem to have higher density for longer time periods in the region that replicates the leaf veins. Finally, we assess the angiogenic capacity through a chick chorioallantoic membrane assay, revealing that BpMs are more prone to support angiogenesis than flat PCL membranes. We strongly believe that this strategy can bring new insights into developing TE strategies with an enhanced performance in terms of the vascular integration between the host and the scaffolds implanted.
促进血管生成是有效器官/组织重建和替代的基本步骤。因此,研究了几种促进支架血管化的策略来满足这一未解决的临床需求。细胞与基底之间的界面是组织工程(TE)策略成功的决定因素。据报道,基底的拓扑结构在影响内皮细胞行为方面起着关键作用,即影响其增殖、代谢活性、形态、迁移和细胞因子和趋化因子的分泌。因此,基于生物材料的移植物的表面拓扑结构是在开发新的 TE 方法时需要考虑的关键特性。在此,我们假设叶子的表面在驱动血管生成方面起着至关重要的作用,因为它的结构类似于在生物相关的大小尺度上的血管结构。为此,我们通过复制成型和纳米压印光刻生产了仿生聚己内酯(PCL)膜(BpM),复制了叶子表面的形貌。我们的结果表明,在 BpM 上,人内皮细胞系的增殖性能得到了提高。此外,在 BpM 的表面观察到细胞的不对称空间分布。这些细胞在复制叶脉的区域似乎具有更高的密度和更长的时间。最后,我们通过鸡胚尿囊膜试验评估了血管生成能力,结果表明 BpM 比平板 PCL 膜更有利于支持血管生成。我们坚信,这种策略可以为开发具有增强宿主与植入支架之间血管整合性能的 TE 策略带来新的见解。