Multilineage Cells from Human Adipose Tissue: Implications for Cell-Based Therapies

干细胞移植修复关节软骨 脂肪组织 骨髓 干细胞 间充质干细胞的临床应用 细胞生物学 人口 羊膜干细胞 成体干细胞 多能干细胞 软骨发生 间充质干细胞 内皮干细胞 细胞疗法 组织工程 胚胎干细胞 生物 癌症研究 祖细胞 诱导多能干细胞 医学 间质细胞 免疫学 体外 内分泌学 生物化学 遗传学 基因 环境卫生
作者
Patricia A. Zuk,Min Zhu,Hiroshi Mizuno,Jerry I. Huang,J. William Futrell,Adam J. Katz,Prosper Benhaim,Helga Lorenz,Marc H. Hedrick
出处
期刊:Tissue Engineering [Mary Ann Liebert, Inc.]
卷期号:7 (2): 211-228 被引量:7942
标识
DOI:10.1089/107632701300062859
摘要

Future cell-based therapies such as tissue engineering will benefit from a source of autologous pluripotent stem cells. For mesodermal tissue engineering, one such source of cells is the bone marrow stroma. The bone marrow compartment contains several cell populations, including mesenchymal stem cells (MSCs) that are capable of differentiating into adipogenic, osteogenic, chondrogenic, and myogenic cells. However, autologous bone marrow procurement has potential limitations. An alternate source of autologous adult stem cells that is obtainable in large quantities, under local anesthesia, with minimal discomfort would be advantageous. In this study, we determined if a population of stem cells could be isolated from human adipose tissue. Human adipose tissue, obtained by suction-assisted lipectomy (i.e., liposuction), was processed to obtain a fibroblast-like population of cells or a processed lipoaspirate (PLA). These PLA cells can be maintained in vitro for extended periods with stable population doubling and low levels of senescence. Immunofluorescence and flow cytometry show that the majority of PLA cells are of mesodermal or mesenchymal origin with low levels of contaminating pericytes, endothelial cells, and smooth muscle cells. Finally, PLA cells differentiate in vitro into adipogenic, chondrogenic, myogenic, and osteogenic cells in the presence of lineage-specific induction factors. In conclusion, the data support the hypothesis that a human lipoaspirate contains multipotent cells and may represent an alternative stem cell source to bone marrow-derived MSCs.
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