Chinese Journal of Tissue Engineering Research ›› 2016, Vol. 20 ›› Issue (1): 36-41.doi: 10.3969/j.issn.2095-4344.2016.01.007

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Extraction of prostate cancer stem cells using self-designed magnetic beads

Gong Rui1, Li Sheng-ying2, Huo Zhi-xia3, Ding Hao4, Sun Er-lin4   

  1. 1Pharmaceutical Department, the Second Hospital of Tianjin Medical University, Tianjin 300211, China; 2Clinical Laboratory, Tianjin Children’s Hospital, Tianjin 300070, China; 3School of Pharmacology Science and Technology, Tianjin University, Tianjin 300050, China; 4Department of Urology, the Second Hospital of Tianjin Medical University, Tianjin Institute of Urology, Tianjin 300211, China
  • Received:2015-10-26 Online:2016-01-01 Published:2016-01-01
  • About author:Gong Rui, Master, Pharmacist in charge, Pharmaceutical Department, the Second Hospital of Tianjin Medical University, Tianjin 300211, China
  • Supported by:

    the Science and Technology Fund of Tianjin Public Health Bureau, No. 2014KZ093

Abstract:

BACKGROUND: Effective sorting of prostate cancer stem cells is the basis of experimental studies in prostate cancer developing. The most common sorting method is magnetic-activated cell sorting.
OBJECTIVE: To separate CD133+/CD44+ cells in prostate cancer tissues using self-designed magnetic beads followed by culture, passage and immunological identification.
METHODS: Self-designed magnetic microspheres were applied to establish immunomagnetic beads to sort CD133+/CD44+ cells in prostate cancer tissues. The sorted cells were cultured in serum-free medium. The sphere formation, cell morphology, and proliferation ability after cell passage were statistically compared between the sorted cells and the normal tumor cell lines. Immunofluorescence detection was performed to detect the expression of specific antibodies.
RESULTS AND CONCLUSION: Self-designed immunomagnetic beads had small diameter and a high-sorting effect. The sorted cells possessed a high capacity of microsphere formation. After cell culture and passage, the cells highly expressed CD133 and CD44 antigens. The sorted cells with no induction had varying shapes and grew vigorously. After induction with transforming growth factor-β, the cultured cells were noted to have a single shape and grow slowly. The cell proliferation ability of sorted cells in these two groups differed significantly from that of the normal cancer cell lines (both P < 0.05). In conclusion, the CD133+/CD44+ cells sorted from prostate tumor cells possessed cell morphology and function characteristics of stem cells which can provide a basis for extraction and culture of prostate cancer stem cells.

 

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