Xydias Dionysios, Ziakas Georgios, Psilodimitrakopoulos Sotiris, Lemonis Andreas, Bagli Eleni, Fotsis Theodore, Gravanis Achille, Tzeranis Dimitrios S, Stratakis Emmanuel
Institute of Electronic Structure and Laser, Foundation for Research and Technology-Hellas, Greece.
Department of Materials Science and Technology, School of Sciences and Engineering, University of Crete, Greece.
Biomed Opt Express. 2021 Jan 28;12(2):1136-1153. doi: 10.1364/BOE.411501. eCollection 2021 Feb 1.
In this study, we use non-linear imaging microscopy to characterize the structural properties of porous collagen-GAG scaffolds (CGS) seeded with human umbilical vein endothelial cells (HUVECs), as well as human mesenchymal stem cells (hMSCs), a co-culture previously reported to form vessel-like structures inside CGS. The evolution of the resulting tissue construct was monitored over 10 days via simultaneous two- and three-photon excited fluorescence microscopy. Time-lapsed 2- and 3-photon excited fluorescence imaging was utilized to monitor the temporal evolution of the vascular-like structures up to 100 µm inside the scaffold up to 10 days post-seeding. 3D polarization-dependent second harmonic generation (PSHG) was utilized to monitor collagen-based scaffold remodeling and determine collagen fibril orientation up to 200 µm inside the scaffold. We demonstrate that polarization-dependent second harmonic generation can provide a novel way to quantify the reorganization of the collagen architecture in CGS simultaneously with key biomechanical interactions between seeded cells and CGS that regulate the formation of vessel-like structures inside 3D tissue constructs. A comparison between samples at different days in vitro revealed that gradually, the scaffolds developed an orthogonal net-like architecture, previously found in real skin.
在本研究中,我们使用非线性成像显微镜来表征接种了人脐静脉内皮细胞(HUVECs)以及人间充质干细胞(hMSCs)的多孔胶原-糖胺聚糖支架(CGS)的结构特性,此前有报道称这两种细胞共培养可在CGS内部形成血管样结构。通过双光子和三光子激发荧光显微镜同时监测所得组织构建体在10天内的演变。利用延时双光子和三光子激发荧光成像来监测接种后长达10天支架内深度达100 µm的血管样结构的时间演变。利用三维偏振相关二次谐波产生(PSHG)来监测基于胶原的支架重塑,并确定支架内深度达200 µm的胶原纤维取向。我们证明,偏振相关二次谐波产生能够提供一种新方法,可同时量化CGS中胶原结构的重组以及接种细胞与CGS之间调节三维组织构建体内血管样结构形成的关键生物力学相互作用。体外不同天数样本之间的比较表明,支架逐渐形成了一种先前在真实皮肤中发现的正交网状结构。