Journal of Jilin University Medicine Edition ›› 2015, Vol. 41 ›› Issue (01): 105-109.doi: 10.13481/j.1671-587x.20150120

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Analysis on bioactivity for new-type FLT3 receptor interacting lectin from Astragalus root

DUAN Xiumei, WANG Yinping, BI Lirong, TIAN Zhang   

  1. Center of Clinical Pathological Diagnosis, First Hospital, Jilin University, Changchun 130021 China
  • Received:2014-07-18 Published:2015-01-30

Abstract:

Objective To extract and purify the Fms-like tyrosine kinase-3(FLT3) receptor interacting lectin (FRIL) from Astragalus root, and to analyze and identify its bioactivity. Methods Affinity chromatography was used to purify the crude extraction of Astragalus root;the concentration of FRIL was determined using BCA assay;the property of FRIL combined with sugar was verified using inhibition lectin reaction;the Raji cells were cultured and divided into control, 20 mg·L-1and 40 mg·L-1FRIL groups;the cultured HL-60 cells were grouped into 0, 2.5, 5.0, 10.0, 20.0, and 40.0 mg·L-1 FRIL groups;the proliferation effect of FRIL on human Raji cells and HL-60 cells were measured using flow cytometry and MTT method. Results The 27 mg of FRIL containing 4 subunits was obtained from Astragalus root, which had a high affinity for combining α-D-manoside.The apoptotic rate of Raji cells in 40 mg·L-1 FRIL group was lower than that in 20 mg·L-1 FRIL group(P<0.01).Compared with control group, the proliferation activities of the HL-60 cells expressing FLT3 receptors in 5.0-40.0 mg·L-1 FRIL groups were increased (P<0.05). Conclusion The FRIL protein possessing lectin activity is successfully isolated from Astragalus root, which has the promotion effect on the growth of the cells expressing FLT3 receptor.

Key words: astragalus root, FLT3 receptor interacting lectin, cell proliferation

CLC Number: 

  • R284.1