Yang Jing, Xie Qi-Yang, Zhang Yi, Xiang Hong-Xia, Guo Zan
Department of Physiology, Hebei Medical University, Shijiazhuang, China.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2007 Apr;32(2):268-75.
To explore the ability of QY1 bone marrow mesenchymal stem cell (MSCs) line cells to differentiate into adipocytes, chondrocytes, osteoblasts, cardiac myocytes,vascular endothelial cells, and neural cells in vitro.
The QY1 cells at passage 5 were treated with the adipogenic medium, the chondrogenic medium and the osteogenic medium, 5-azacytidine, vascular endothelial growth factor and neural cell medium (revulsant 1 was 10 mmol/L beta-mercaptoethanol; revulsant 2 was 2%dimethylsulfoxide and 10(-8)mol/L dexamethasone) in culture respectively in vitro. The differentiated cells were identified by staining, immunohistochemistry and RT-PCR.
The differentiated cells induced by the adipogenic medium formed adipocytes and contained fat lipid droplets, which were stained positively with Sudan III after 21 days of culture. The differentiated cells induced by the chondrogenic medium formed chondrogenic nodules, which were stained positively by Alcian blue at pH 1.0 after 21 days of culture. The differentiated cells induced by the osteogenic medium formed osteogenic nodules, which were stained positively by Von Kossa staining after 35 days of culture, and the secretion of a calcified extracellular matrix as black nodules was observed. The differentiated cells treated with 10 micromol/L 5-azacytidine could beat spontaneously and formed myotube structures,which were identified by the positive immunohistochemistry staining with anti-alpha-sarcomeric antibody and anti-Cx-43 antibody. The expression of alpha-myosin heavy chain was also observed by RT-PCR. The differentiated cells treated with 50 ng/mL vascular endothelial growth factor could form vascular endothelial cells and vascular endothelial web like structure, which were identified by the positive immunohistochemistry staining with CD31 and Factor VIII. The differentiated cells induced by revulsant 1 were positive in the immunohistochemistry staining with neuron-specific nuclear protein, while the expression of glial fibrillary acidic protein was negative. The differentiated cells induced by revulsant 2 were positive in the immunohistochemistry staining with glial fibrillary acidic protein, while the expression of neuron-specific nuclear protein was negative.
QY1 bone marrow mesenchymal stem cell line has the ability to differentiate into adipocytes, chondrocytes, osteocytes, cardiomyocytes, vascular endothelial cells, neurons and neural glial cells in vitro. A bone marrow mesenchymal stem cell line cell can at least differentiate into 7 types of cells, which come from mesoderm and ectoderm.
探讨QY1骨髓间充质干细胞系细胞在体外分化为脂肪细胞、软骨细胞、成骨细胞、心肌细胞、血管内皮细胞和神经细胞的能力。
将第5代的QY1细胞分别用成脂培养基、成软骨培养基、成骨培养基、5-氮杂胞苷、血管内皮生长因子和神经细胞培养基(诱导剂1为10 mmol/Lβ-巯基乙醇;诱导剂2为2%二甲基亚砜和10⁻⁸ mol/L地塞米松)在体外进行培养。通过染色、免疫组织化学和逆转录-聚合酶链反应(RT-PCR)对分化后的细胞进行鉴定。
成脂培养基诱导分化的细胞形成脂肪细胞并含有脂滴,培养21天后用苏丹Ⅲ染色呈阳性。成软骨培养基诱导分化的细胞形成软骨结节,培养21天后用pH 1.0的阿尔辛蓝染色呈阳性。成骨培养基诱导分化的细胞形成骨结节,培养35天后用冯库萨染色呈阳性,并观察到钙化细胞外基质分泌为黑色结节。用10 μmol/L 5-氮杂胞苷处理的分化细胞能自发搏动并形成肌管结构,用抗α-肌节抗体和抗Cx-43抗体免疫组织化学染色呈阳性鉴定。RT-PCR也观察到α-肌球蛋白重链的表达。用50 ng/mL血管内皮生长因子处理的分化细胞能形成血管内皮细胞和血管内皮网状结构,用CD31和因子Ⅷ免疫组织化学染色呈阳性鉴定。诱导剂1诱导分化的细胞用神经元特异性核蛋白免疫组织化学染色呈阳性,而胶质纤维酸性蛋白表达为阴性。诱导剂2诱导分化的细胞用胶质纤维酸性蛋白免疫组织化学染色呈阳性,而神经元特异性核蛋白表达为阴性。
QY1骨髓间充质干细胞系具有在体外分化为脂肪细胞、软骨细胞、骨细胞、心肌细胞、血管内皮细胞、神经元和神经胶质细胞的能力。一种骨髓间充质干细胞系细胞至少能分化为7种细胞,这些细胞来源于中胚层和外胚层。