Human mesenchymal stem cells isolated from the umbilical cord

• Published in: Cell biology international 2008, Vol.32 (1), p.8-15
• Main Authors: Qiao, Chun, Xu, Wenrong, Zhu, Wei, Hu, Jiabo, Qian, Hui, Yin, Qing, Jiang, Runqiu, Yan, Yongmin, Mao, Fei, Yang, Huan, Wang, Xingzhong, Chen, Yongchang
• Format: Article
• Language: English
• Subjects: Antigens, CD - analysis; Carrier Proteins - biosynthesis; Cell Culture Techniques - methods; Cell Differentiation; Cell Proliferation; Cell Separation - methods; Differentiation; DNA - metabolism; GTP-Binding Proteins; Humans; Karyotyping; Mesenchymal stem cells; Mesenchymal Stromal Cells - cytology; Mesenchymal Stromal Cells - metabolism; Nuclear Proteins - biosynthesis; Polycomb Repressive Complex 1; Proto-Oncogene Proteins - biosynthesis; Repressor Proteins - biosynthesis; Umbilical cord; Umbilical Cord - cytology
• ISSN: 1065-6995; 1095-8355
• DOI: 10.1016/j.cellbi.2007.08.002

Mesenchymal stem cells (MSCs) are known as a population of multi-potential cells able to proliferate and differentiate into multiple mesodermal tissues including bone, cartilage, muscle, ligament, tendon, fat and stroma. In this study human MSCs were successfully isolated from the umbilical cords. The research characteristics of these cells, e.g., morphologic appearance, surface antigens, growth curve, cytogenetic features, cell cycle, differentiation potential and gene expression were investigated. After 2 weeks of incubation, fibroblast-like cells appeared to be dominant. During the second passage the cells presented a homogeneous population of spindle fibroblast-like cells. After more than 4 months (approximately 26 passages), the cells continued to retain their characteristics. Flow cytometry analysis revealed that CD29, CD44, CD95, CD105 and HLA-I were expressed on the cell surface, but there was no expression of hematopoietic lineage markers, such as CD34, CD38, CD71 and HLA-DR. Chromosomal analysis showed the cells kept a normal karyotype. The cell cycle at the third passage showed the percentage of G 0/G 1, G 2/M and S phase were 88.86%, 5.69% and 5.45%, respectively. The assays in vitro demonstrated the cells exhibited multi-potential differentiation into osteogenic and adipogenic cells. Both BMI-1 and nucleostemin genes, expressed in adult MSCs from bone marrow, were also expressed in umbilical cord MSCs. Here we show that umbilical cords may be a novel alternative source of human MSCs for experimental and clinical applications.