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To further study the proliferation and multi-differentiation potentials of adipose-derived stem cells (ADSCs), the cells were isolated with improved methods and their growth curves were achieved with cck-8. Surface protein expression was analyzed by flow cytometry to characterize the cell phenotype. The multi-lineage potential of ADSCs was testified by differentiating cells with adipogenic, chondrogenic, osteogenic, and myogenic inducers. The results showed that about 5 x 10(5) stem cells could be obtained from 400 to 600 mg adipose tissue. The ADSCs can be continuously cultured in vitro for up to 1 month without passage and they have several logarithmic growth phases during the culture period. Also, the flow cytometry analysis showed that ADSCs expressed high levels of stem cell-related antigens (CD13, CD29, CD44, CD105, and CD166), while did not express hematopoiesis-related antigens CD34 and CD45, and human leukocyte antigen HLA-DR was also negative. Moreover, stem cell-related transcription factors, Nanog, Oct-4, Sox-2, and Rex-1 were positively expressed in ADSCs. The expression of alkaline phosphatase (ALP) was detected in the early osteogenic induction and the calcified nodules were observed by von Kossa staining. Intracellular lipid droplets could be observed by Oil Red staining. Differentiated cardiomyocytes were observed by connexin43 fluorescent staining. In order to obtain more stem cells, we can subculture ADSCs every 14 days instead of the normal 5 days. ADSCs still keep strong proliferation ability, maintain their phenotypes, and have stronger multi-differentiation potential after 25 passages.

Original publication

DOI

10.1002/cbf.1488

Type

Journal article

Journal

Cell Biochem Funct

Publication Date

08/2008

Volume

26

Pages

664 - 675

Keywords

Adipocytes, Adipose Tissue, White, Adult Stem Cells, Antigens, CD, Bone Marrow Cells, Calcification, Physiologic, Cell Differentiation, Cell Lineage, Cell Proliferation, Cell Separation, Cell Survival, Cells, Cultured, Chondrocytes, Connexin 43, Culture Media, Gene Expression, HLA-DR Antigens, Humans, Mesenchymal Stem Cells, Myocytes, Cardiac, Osteoblasts, Proteoglycans, Reverse Transcriptase Polymerase Chain Reaction, Transcription Factors