Oswald Joachim, Boxberger Sabine, Jørgensen Birgitte, Feldmann Silvia, Ehninger Gerhard, Bornhäuser Martin, Werner Carsten
Institute of Polymer Research Dresden and The Max Bergmann Center of Biomaterials Dresden, Dresden, Germany.
Stem Cells. 2004;22(3):377-84. doi: 10.1634/stemcells.22-3-377.
Human bone marrow-derived mesenchymal stem cells (MSCs) have the potential to differentiate into mesenchymal tissues like osteocytes, chondrocytes, and adipocytes in vivo and in vitro. The aim of this study was to investigate the in vitro differentiation of MSCs into cells of the endothelial lineage. MSCs were generated out of mononuclear bone marrow cells from healthy donors separated by density gradient centrifugation. Cells were characterized by flow cytometry using a panel of monoclonal antibodies and were tested for their potential to differentiate along different mesenchymal lineages. Isolated MSCs were positive for the markers CD105, CD73, CD166, CD90, and CD44 and negative for typical hematopoietic and endothelial markers. They were able to differentiate into adipocytes and osteocytes after cultivation in respective media. Differentiation into endothelial-like cells was induced by cultivation of confluent cells in the presence of 2% fetal calf serum and 50 ng/ml vascular endothelial growth factor. Laser scanning cytometry analysis of the confluent cells in situ showed a strong increase of expression of endothelial-specific markers like KDR and FLT-1, and immunofluorescence analysis showed typical expression of the von Willebrand factor. The functional behavior of the differentiated cells was tested with an in vitro angiogenesis test kit where cells formed characteristic capillary-like structures. We could show the differentiation of expanded adult human MSCs into cells with phenotypic and functional features of endothelial cells. These predifferentiated cells provide new options for engineering of artificial tissues based on autologous MSCs and vascularized engineered tissues.
人骨髓间充质干细胞(MSCs)在体内和体外均有分化为间充质组织(如骨细胞、软骨细胞和脂肪细胞)的潜力。本研究的目的是探讨MSCs在体外向内皮谱系细胞的分化情况。通过密度梯度离心从健康供体的单核骨髓细胞中分离出MSCs。使用一组单克隆抗体通过流式细胞术对细胞进行表征,并测试它们沿不同间充质谱系分化的潜力。分离出的MSCs对标志物CD105、CD73、CD166、CD90和CD44呈阳性,而对典型的造血和内皮标志物呈阴性。在相应培养基中培养后,它们能够分化为脂肪细胞和骨细胞。通过在2%胎牛血清和50 ng/ml血管内皮生长因子存在的情况下培养汇合细胞来诱导其分化为内皮样细胞。对汇合细胞进行激光扫描细胞术原位分析显示,内皮特异性标志物如KDR和FLT-1的表达显著增加,免疫荧光分析显示血管性血友病因子的典型表达。用体外血管生成测试试剂盒测试分化细胞的功能行为,结果显示细胞形成了特征性的毛细血管样结构。我们能够证明扩增的成人MSCs可分化为具有内皮细胞表型和功能特征的细胞。这些预分化细胞为基于自体MSCs的人工组织工程和血管化工程组织提供了新的选择。