间充质干细胞
体内
脐静脉
体外
脂肪组织
材料科学
碱性磷酸酶
细胞生物学
生物医学工程
生物
医学
生物化学
生物技术
酶
作者
Jinling Ma,Sanne K. Both,Wei Ji,Fang Yang,Henk‐Jan Prins,Marco N. Helder,Juli Pan,Fuzhai Cui,John A. Jansen,Jeroen J.J.P. van den Beucken
摘要
Abstract The aim of this study was to compare the osteogenic capacity between human adipose tissue‐derived mesenchymal stem cells (AT‐MSCs) and their cocultures with human umbilical vein endothelial cells (HUVECs) in vitro and their biological performance in vivo . First, the optimal cell ratio in cocultures for osteogenic differentiation was determined by seeding AT‐MSCs and HUVECs in ratios varying from 100:0 to 0:100 on tissue culture plates. Afterward, AT‐MSCs and AT‐MSCs/HUVECs (50:50) were seeded on porous titanium fiber mesh scaffolds (Ti) for both in vitro and in vivo osteogenic evaluation. For in vitro evaluation, cell osteogenic differentiation was assessed by alkaline phosphatase (ALP) activity and calcium assay. For in vivo evaluation, the scaffolds were implanted bilaterally into rat cranial defects (5 mm diameter) and bone formation was assessed histologically and histomorphometrically after 8 weeks. The ratio of 50:50 was chosen in the cocultures because this coculture condition retained similar amount of calcium deposition while using the least amount of AT‐MSCs. Moreover, AT‐MSCs showed higher osteogenic differentiation in comparison to AT‐MSCs/HUVECs on Ti in vitro . Furthermore, superior bone formation was observed in AT‐MSCs compared to AT‐MSCs/HUVECs in rat cranial defects. In conclusion, AT‐MSCs showed significantly higher osteogenic potential compared to AT‐MSCs/HUVECs both in vitro and in vivo . © 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 102A: 1026–1036, 2014.
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