Chinese Journal of Tissue Engineering Research ›› 2010, Vol. 14 ›› Issue (45): 8531-8534.doi: 10.3969/j.issn.1673-8225.2010.45.040

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Effects of interleukin-15 on proliferation of children’s myelodysplastic syndrome hematopoietic stem/progenitor cells

Cheng Han-rong1, Ye Zhong-lü2, Chen Ming-zhen2   

  1. 1  Department of Pediatrics, Shenzhen People’s Hospital, Second Clinical Medical College of Jinan University, Shenzhen  518020, Guangdong Province, China; 2 Department of Pediatrics,  Affiliated Hospital of Guangdong Medical College, Zhanjiang 524023, Guangdong Province, China
  • Online:2010-11-05 Published:2010-11-05
  • Contact: Chen Ming-zhen, Proferssor, Chief physician, Department of Pediatrics, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524023, Guangdong Province, China.
  • About author:Cheng Han-rong★, Master, Attending physician, Department of Pediatrics, Shenzhen People’s Hospital, Second Clinical Medical College of Jinan University, Shenzhen 518020, Guangdong Province, China chr621@163.com
  • Supported by:

     the Science and Technology Key Program of Zhanjiang City, No. 020113* 

Abstract:

BACKGROUND: Interleukin (IL)-15 is a member of hematopoietic cytokine superfamily. It may stimulate the proliferation of the myelodysplastic syndrome (MDS) hematopoietic stem/progenitor cells.
OBJECTIVE: To investigate the effects of IL-15 on proliferation of hematopoietic cells in MDS child.
METHODS: Cell-counting, MTT-inhibitory test were used to examine the inhibitory effect of IL-15 (0, 10, 20, 50, 100, 200 µg/L) on the proliferation of MDS CD34+ cells in 18 children aged 1-14 years to find out the peak concentration of IL-15. IL-15 at peak concentration served as experimental group, whereas those without IL-15 as control group. 12-day culture was done to understand optimal proliferation time of cells.
RESULTS AND CONCLUSION: At day 8, CD34+cells cultured in vitro grew well. With increased IL-15 concentration, living cells number increased as well. When IL-15 was 100 µg/L, its proliferation status was the best, but when IL-15 was 200 µg/L, its proliferation status was below the mark. At day 8, the inhibitory rate of IL-15 on CD34+ cells was the lowest. When IL-15’s concentration was between 0 and 100 µg/L. With increased IL-15’s concentration, the inhibition decreased progressively. When IL-15 was above 100 µg/L, the inhibition reinforced on the contrary. These indicate that IL-15 can accelerate MDS bone marrow CD34+ hematopoietic stem/progenitor cell proliferation in a dose-and time-dependent manner

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