Marchionni C, Bonsi L, Alviano F, Lanzoni G, Di Tullio A, Costa R, Montanari M, Tazzari P L, Ricci F, Pasquinelli G, Orrico C, Grossi A, Prati C, Bagnara G P
Department of Histology, Embryology and Applied Biology, University of Bologna, and Transfusion Medicine Service, S. Orsola Hospital, Bologna, Italy.
Int J Immunopathol Pharmacol. 2009 Jul-Sep;22(3):699-706. doi: 10.1177/039463200902200315.
Dental pulp is a heterogeneous microenviroment where unipotent progenitor and pluripotent mesenchymal stem cells cohabit. In this study we investigated whether human dental pulp stromal (stem) cells (DP-SCs) committed to the angiogenic fate. DP-SCs showed the specific mesenchymal immunophenotypical profile positive for CD29, CD44, CD73, CD105, CD166 and negative for CD14, CD34, CD45, in accordance with that reported for bone marrow-derived SCs. The Oct-4 expression in DP-SCs, evaluated through RT-PCR analysis, increased in relation with the number of the passages in cell culture and decreased after angiogenic induction. In agreement with their multipotency, DP-SCs differentiated toward osteogenic and adipogenic commitments. In angiogenic experiments, differentiation of DP-SCs, through vascular endothelial growth factor (VEGF) induction, was evaluated by in vitro matrigel assay and by cytometric analysis. Accordingly, endothelial-specific markers like Flt-1 and KDR were basally expressed and they increased after exposure to VEGF together with the occurrence of ICAM-1 and von Willebrand factor positive cells. In addition, VEGF-induced DP-SCs maintained endothelial cell-like features when cultured in a 3-D fibrin mesh, displaying focal organization into capillary-like structures. The DP-SC angiogenic potential may prove a remarkable tool for novel approaches to developing tissue-engineered vascular grafts which are useful when vascularization of ischemic tissues is required.
牙髓是一个异质性的微环境,其中单能祖细胞和多能间充质干细胞共同存在。在本研究中,我们调查了人牙髓基质(干)细胞(DP-SCs)是否会向血管生成命运分化。与报道的骨髓来源的干细胞一致,DP-SCs表现出特定的间充质免疫表型特征,CD29、CD44、CD73、CD105、CD166呈阳性,CD14、CD34、CD45呈阴性。通过RT-PCR分析评估,DP-SCs中Oct-4的表达随着细胞培养传代次数的增加而增加,在血管生成诱导后降低。与它们的多能性一致,DP-SCs向成骨和成脂方向分化。在血管生成实验中,通过体外基质胶试验和细胞分析评估了DP-SCs在血管内皮生长因子(VEGF)诱导下的分化情况。因此,内皮特异性标志物如Flt-1和KDR在基础状态下表达,在暴露于VEGF后它们与ICAM-1和血管性血友病因子阳性细胞的出现一起增加。此外,VEGF诱导的DP-SCs在三维纤维蛋白网中培养时保持内皮细胞样特征,呈现出向毛细血管样结构的局部组织化。DP-SCs的血管生成潜力可能证明是一种用于开发组织工程血管移植物新方法的显著工具,在需要缺血组织血管化时很有用。