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Visualizing Osteogenesis In Vivo Within a Cell–Scaffold Construct for Bone Tissue Engineering Using Two-Photon Microscopy

机译:可视化的成骨细胞内脚手架构造内的骨组织工程使用双光子显微镜。

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摘要

Tissue-engineering therapies have shown early success in the clinic, however, the cell–biomaterial interactions that result in successful outcomes are not yet well understood and are difficult to observe. Here we describe a method for visualizing bone formation within a tissue-engineered construct in vivo, at a single-cell resolution, and in situ in three dimensions using two-photon microscopy. First, two-photon microscopy and histological perspectives were spatially linked using fluorescent reporters for cells in the skeletal lineage. In the process, the tissue microenvironment that precedes a repair-focused study was described. The distribution and organization of type I collagen in the calvarial microenvironment was also described using its second harmonic signal. Second, this platform was used to observe in vivo, for the first time, host cells, donor cells, scaffold, and new bone formation within cell-seeded constructs in a bone defect. We examined constructs during bone repair 4 and 6 weeks after implantation. New bone formed on scaffolds, primarily by donor cells. Host cells formed a new periosteal layer that covered the implant. Scaffold resorption appeared to be site specific, where areas near the top were removed and deeper areas were completely embedded in new mineral. Visualizing the in vivo progression of the cell and scaffold microenvironment will contribute to our understanding of tissue-engineered regeneration and should lead to the development of more streamlined and therapeutically powerful approaches.
机译:组织工程疗法在临床上已经显示出早期的成功,但是,导致成功结果的细胞-生物材料相互作用目前尚未得到很好的理解,也很难观察到。在这里,我们描述了一种用于可视化组织工程化构造体内的骨形成的方法,该方法以单细胞分辨率和使用双光子显微镜在三个维度上进行原位成像。首先,使用荧光报告基因在骨骼谱系中对细胞进行双光子显微镜观察和组织学观察。在此过程中,描述了修复重点研究之前的组织微环境。还使用颅骨微环境描述了I型胶原在颅盖微环境中的分布和组织。其次,该平台首次用于体内观察宿主细胞,供体细胞,支架和骨缺损的细胞播种构建物中新的骨形成。我们在植入后4周和6周的骨修复过程中检查了构建体。新骨主要由供体细胞在支架上形成。宿主细胞形成了覆盖植入物的新的骨膜层。支架吸收似乎是特定位置的,顶部附近的区域被去除,而更深的区域完全被新矿物包裹。可视化细胞和支架微环境的体内进程将有助于我们对组织工程再生的理解,并应导致开发更简化和治疗功能更强的方法。

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