Chinese Journal of Tissue Engineering Research ›› 2010, Vol. 14 ›› Issue (6): 1072-1077.doi: 10.3969/j.issn.1673-8225.2010.06.025

Previous Articles     Next Articles

Ligustrazine induces rat bone morrow mesenchymal stem cells to differentiate into neuron-like cells: Screening of the optimal inductive concentration

Chen Bing1, Yin Yan-qing1, Ke Jun-long2, Zou Xin-hui1, Peng Hao1, Tan Shan-feng1, Xu Zhi-en2   

  1. 1Department of Neurosurgery, 2Department of Neurology, Affiliated Hospital of Guangdong Medical College, Zhanjiang  524001, Guangdong Province, China
  • Online:2010-02-05 Published:2010-02-05
  • About author:Chen Bing, Doctor, Associate professor, Department of Neurosurgery, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong Province, China drcb@163.com

Abstract:

BACKGROUND: There are numerous inducers used in inducing bone marrow mesenchymal stem cells (BMMSCs) differentiate into neuron-like cells, however, due to poisonous, most chemical inducers can not be used in human.

OBJECTIVE: To investigate the effect of ligustrazine on differentiation of rat BMMSCs into neuron-like cells in vitro, and to search for the optimal inductive concentration.

METHODS: After SD rats were anesthetized, bone marrow was obtained from the femoral and tibial bones, centrifuged, and the supernatant was discarded. The extracted cells were cultured in L-DMEM supplemented with 15% fetal bovine serum. The expression of CD44 and CD45 of the 5th passage of BMMSCs were identified by immunocytochemical technique. Serum-free L-DMEM medium contains 1.00, 1.25 and 1.50 g/L ligustrazine concentrations were used to induce the 5th passage of BMMSCs in vitro. Morphology changes of BMMSCs were observed under an inverted phase microscope. Expression of nestin, neuron-specific enolase and glial fibrillary acidic protein were identified by immunocytochemical technique, and the expression ratio of neuron-like cells’ surface antigens induced by different concentrations of ligustrazine were compared. 

RESULTS AND CONCLUSION: ①Most primarily cultured BMMSCs adhered to the wall at 3 days after culture, which proliferated faster after passaged, and the 5th passage of cells were mostly purified into BMMSCs, spread radially or vortex-likely. ②The 5th passage of BMMSCs was positive expressed (98.02±0.81)% CD44, but negative for CD45. ③Neuron-like cells with prominence and bifurcation could be seen after induction. The immunocytochemical method showed that nestin and neuron-specific enolase in most induced cells were positive expressed, especially received a highest ration of neuron-specific enolase expressing in the induced group with 1.25 g/L concentration of ligustrazine. It revealed that ligustrazine can induce BMMSCs differentiated into neuron-like cells, and 1.25 g/L is the optimal inductive concentration.

CLC Number: