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Stem Cells and Development
Accelerated Growth and Prolonged Lifespan of Adipose Tissue-derived Human Mesenchymal Stem Cells in a Medium Using Reduced Calcium and Antioxidants

To cite this article:
Tsai-Ming Lin, Jin-Lian Tsai, Sin-Daw Lin, Chung-Sheng Lai, Chia-Cheng Chang. Stem Cells and Development. February 2005, 14(1): 92-102. doi:10.1089/scd.2005.14.92.

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Tsai-Ming Lin
Department of Plastic Surgery, Kaohsiung Medical University, Taiwan.
Jin-Lian Tsai
Graduate Institute of Occupational Safety and Health, Kaohsiung Medical University, Taiwan.
Sin-Daw Lin
Department of Plastic Surgery, Kaohsiung Medical University, Taiwan.
Chung-Sheng Lai
Department of Plastic Surgery, Kaohsiung Medical University, Taiwan.
Dr. Chia-Cheng Chang
Department of Pediatrics and Human Development, Michigan State University, East Lansing, MI 48824.

Human mesenchymal stem cells (MSCs) have been isolated from bone marrow and other adult tissues and are potentially useful for tissue engineering. Adipose tissue has several clear advantages as a starting material for harvesting stem cells, as it is abundant and relatively easy to procure. However, existing methods to expand adipose-derived MSCs are less than optimal. Here we describe a new cell culture method that accelerates greatly the growth rate and prolongs the lifespan of adipose MSCs. This was accomplished by using a growth medium with low calcium and supplemented with N-acetyl-L-cysteine and L-ascorbic acid-2-phosphate. Cells produced early in these cultures displayed characteristics similar to those previously reported for multipotential stem cells, including a high frequency of anchorage- independent growth in soft agar, lack of gap junctional intercellular communication in a cell type with serpiginous morphology, and the expression of Oct-4. Furthermore, these cells could readily be induced to differentiate into adipocytes, osteoblasts, and chondrocytes. Thus, modification of growth medium by reduction of calcium and addition of antioxidants greatly enhanced the growth rate and extended the lifespan of adipose-derived multipotential human MSCs.

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