Shafiq Muhammad, Jung Youngmee, Kim Soo Hyun
Department of Biomedical Engineering, Korea University of Science and Technology (UST) (305-350), Gajeong-Ro, Yuseong-Gu, Daejeon, Korea.
Center for Biomaterials 5, Hwarang-Ro 14-Gil, Biomedical Research Institute, Korea Institute of Science and Technology (KIST), Seongbuk-Gu, Seoul, 136-791, Republic of Korea.
J Biomed Mater Res A. 2016 Jun;104(6):1352-71. doi: 10.1002/jbm.a.35666. Epub 2016 Feb 16.
The development of cell-free vascular grafts has tremendous potential for tissue engineering. However, thrombus formation, less-than-ideal cell infiltration, and a lack of growth potential limit the application of electrospun scaffolds for in situ tissue-engineered vasculature. To overcome these challenges, here we present development of an acellular tissue-engineered vessel based on electrospun poly(L-lactide-co-ɛ-caprolactone) scaffolds. Heparin was conjugated to suppress thrombogenic responses, and substance P (SP) was immobilized to recruit host cells. SP was released in a sustained manner from scaffolds and recruited human bone marrow-derived mesenchymal stem cells. The biocompatibility and biological performance of the grafts were evaluated by in vivo experiments involving subcutaneous scaffold implantation in Sprague-Dawley rats (n = 12) for up to 4 weeks. Histological analysis revealed a higher extent of accumulative host cell infiltration, neotissue formation, collagen deposition, and elastin deposition in scaffolds containing either SP or heparin/SP than in the control groups. We also observed the presence of a large number of laminin-positive blood vessels, von Willebrand factor (vWF(+) ) cells, and alpha smooth muscle actin-positive cells in the explants containing SP and heparin/SP. Additionally, SP and heparin/SP grafts showed the existence of CD90(+) and CD105(+) MSCs and induced a large number of M2 macrophages to infiltrate the graft wall compared with that observed with the control group. Our cell-free grafts could enhance vascular regeneration by endogenous cell recruitment and by mediating macrophage polarization into the M2 phenotype, suggesting that these constructs may be a promising cell-free graft candidate and are worthy of further in vivo evaluation. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 1352-1371, 2016.
无细胞血管移植物的发展在组织工程领域具有巨大潜力。然而,血栓形成、细胞浸润不理想以及生长潜力不足限制了电纺支架在原位组织工程血管中的应用。为了克服这些挑战,我们在此展示了一种基于电纺聚(L-丙交酯-共-ε-己内酯)支架的无细胞组织工程血管的研发。通过共轭肝素以抑制血栓形成反应,并固定P物质(SP)以募集宿主细胞。SP从支架中持续释放并募集人骨髓间充质干细胞。通过在Sprague-Dawley大鼠(n = 12)皮下植入支架长达4周的体内实验,评估了移植物的生物相容性和生物学性能。组织学分析显示,与对照组相比,含有SP或肝素/SP的支架中宿主细胞累积浸润、新组织形成、胶原蛋白沉积和弹性蛋白沉积的程度更高。我们还在含有SP和肝素/SP的外植体中观察到大量层粘连蛋白阳性血管、血管性血友病因子(vWF(+))细胞和α平滑肌肌动蛋白阳性细胞。此外,与对照组相比,SP和肝素/SP移植物显示存在CD90(+)和CD105(+)间充质干细胞,并诱导大量M2巨噬细胞浸润移植物壁。我们的无细胞移植物可以通过内源性细胞募集和介导巨噬细胞极化为M2表型来增强血管再生,这表明这些构建体可能是一种有前途的无细胞移植物候选物,值得进一步进行体内评估。© 2016 Wiley Periodicals, Inc.《生物医学材料研究杂志》A部分:第104A卷:1352 - 1371页,2016年。