Biomedical Engineering Research Center, Asan Institute for Life Sciences, Asan Medical Center, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea.
Department of Biomedical Engineering, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea.
Tissue Eng Regen Med. 2022 Apr;19(2):363-375. doi: 10.1007/s13770-021-00409-1. Epub 2021 Dec 6.
In vitro generation of three-dimensional vessel network is crucial to investigate and possibly improve vascularization after implantation in vivo. This work has the purpose of engineering complex tissue regeneration of a vascular network including multiple cell-type, an extracellular matrix, and perfusability for clinical application.
The two electrospun membranes bonded with the vascular network shape are cultured with endothelial cells and medium flow through the engineered vascular network. The flexible membranes are bonded by amine-epoxy reaction and examined the perfusability with fluorescent beads. Also, the perfusion culture for 7 days of the endothelial cells is compared with static culture on the engineered vascular network membrane.
The engineered membranes are showed perfusability through the vascular network, and the perfused network resulted in more cell proliferation and variation of the shear stress-related genes expression compared to the static culture. Also, for the generation of the complex vascularized network, pericytes are co-cultured with the engineered vascular network, which results in the Collagen I is expressed on the outer surface of the engineered structure.
This study is showing the perfusable in vitro engineered vascular network with electrospun membrane. In further, the 3D vascularized network module can be expected as a platform for drug screening and regenerative medicine.
体外生成三维血管网络对于研究和可能改善体内植入后的血管化至关重要。这项工作的目的是为包括多种细胞类型、细胞外基质和可灌注性的血管网络复杂组织再生工程提供服务,以满足临床应用的需求。
带有血管网络形状的两个静电纺丝膜与内皮细胞一起培养,介质通过工程化的血管网络流动。柔性膜通过胺-环氧反应结合,并通过荧光珠检查灌注能力。此外,还比较了内皮细胞在工程化血管网络膜上的灌注培养和静态培养 7 天的情况。
工程化的膜显示出通过血管网络的灌注能力,与静态培养相比,灌注网络导致更多的细胞增殖和与剪切应力相关基因表达的变化。此外,为了生成复杂的血管化网络,周细胞与工程化血管网络共培养,这导致胶原蛋白 I 在工程结构的外表面表达。
本研究展示了带有静电纺丝膜的可灌注体外工程化血管网络。进一步的,3D 血管化网络模块有望成为药物筛选和再生医学的平台。