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Article

Isolation, culture and identification of human adipose-derived stem cells

  • Authors:
    • Jian‑Mei Wang
    • Yan Gu
    • Cai‑Jun Pan
    • Li‑Rong Yin
  • View Affiliations / Copyright

    Affiliations: Department of Gynaecology and Obstetrics, The Second Hospital of Tianjin Medical University, Tianjin 300211, P.R. China
  • Pages: 1039-1043
    |
    Published online on: January 20, 2017
       https://doi.org/10.3892/etm.2017.4069
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Abstract

The aim of the present study was to improve methods for the isolation and identification of adipose‑derived stem cells (ASCs). Human subcutaneous adipose tissue was collected during liposuction surgery, without ultrasound-assisted liposuction and other assisted techniques, and digested with 0.075% collagenase I. First (P1) and second (P2) passage ASCs were applied to the subsequent experiments. ASCs were observed under a microscope, the growth curves of the cells were assessed using a cell counting kit‑8 assay and the membrane expression of cell surface antigens, including cluster of differentiation (CD)44, CD105 and CD45, were detected by flow cytometry. In addition, ASCs were induced to differentiate into lipocytes and osteocytes. Oil red staining was applied to examine adipogenic induction, whereas alkaline phosphatase (ALP) staining was used to assess osteogenic induction. Primary ASCs adhered to the culture vessel wall after 72 h, were fusiform in appearance at 5 days and exhibited stable growth with active proliferation. In total, 1x105 stem cells were gained per 50 ml of lipo‑aspirate. ASCs were plated in a 25 cm2 culture flask at a density of 5x104/ml; the cells underwent the first logarithmic growth period after 72 h and grew to 90% confluence within 3 days. Flow cytometry demonstrated that the cells were highly positive for CD105 and CD44, and weakly positive for CD45; 18.6% of P1 cells and 90.7% of P2 cells were CD44+CD45‑CD105+. Oil red and ALP staining were positive. The results of the present study suggested that ASCs may be considered a promising cell type for tissue engineering. Furthermore, the present study established an effective method for the isolation and identification of ASCs, which reduced damage to the stem cells and simplified the identification procedure.
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Copy and paste a formatted citation
Spandidos Publications style
Wang JM, Gu Y, Pan CJ and Yin LR: Isolation, culture and identification of human adipose-derived stem cells. Exp Ther Med 13: 1039-1043, 2017.
APA
Wang, J., Gu, Y., Pan, C., & Yin, L. (2017). Isolation, culture and identification of human adipose-derived stem cells. Experimental and Therapeutic Medicine, 13, 1039-1043. https://doi.org/10.3892/etm.2017.4069
MLA
Wang, J., Gu, Y., Pan, C., Yin, L."Isolation, culture and identification of human adipose-derived stem cells". Experimental and Therapeutic Medicine 13.3 (2017): 1039-1043.
Chicago
Wang, J., Gu, Y., Pan, C., Yin, L."Isolation, culture and identification of human adipose-derived stem cells". Experimental and Therapeutic Medicine 13, no. 3 (2017): 1039-1043. https://doi.org/10.3892/etm.2017.4069
Copy and paste a formatted citation
x
Spandidos Publications style
Wang JM, Gu Y, Pan CJ and Yin LR: Isolation, culture and identification of human adipose-derived stem cells. Exp Ther Med 13: 1039-1043, 2017.
APA
Wang, J., Gu, Y., Pan, C., & Yin, L. (2017). Isolation, culture and identification of human adipose-derived stem cells. Experimental and Therapeutic Medicine, 13, 1039-1043. https://doi.org/10.3892/etm.2017.4069
MLA
Wang, J., Gu, Y., Pan, C., Yin, L."Isolation, culture and identification of human adipose-derived stem cells". Experimental and Therapeutic Medicine 13.3 (2017): 1039-1043.
Chicago
Wang, J., Gu, Y., Pan, C., Yin, L."Isolation, culture and identification of human adipose-derived stem cells". Experimental and Therapeutic Medicine 13, no. 3 (2017): 1039-1043. https://doi.org/10.3892/etm.2017.4069
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