Total saponins of Panax ginseng (TSPG) promote erythroid differentiation of human CD34+ cells via EpoR-mediated JAK2/STAT5 signaling pathway

被引:24
作者
Chen, D. [1 ]
Zuo, G. [2 ]
Li, C. [3 ]
Hu, X. [1 ]
Guan, T. [4 ]
Jiang, R. [1 ]
Li, J. [1 ]
Lin, X. [1 ]
Li, F. [1 ]
Luo, C. [1 ]
Wang, H. [1 ]
Lei, C. [1 ]
Long, X. [1 ]
Wang, Y. [1 ]
Wang, J. [1 ]
机构
[1] Chongqing Med Univ, Dept Histol & Embryol, Lab Stem Cell & Tissue Engn, Chongqing, Peoples R China
[2] Chongqing Med Univ, Minist Educ, Key Lab, Lab Med Diagnost, Chongqing, Peoples R China
[3] Chongqing Med Univ, Inst Life Sci, Chongqing, Peoples R China
[4] Chongqing Med Univ, Dept Physiol, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
Total saponins of Panax ginseng (TSPG); CD34(+) cells; Differentiation; JAK(2); STAT(5); STAT5A(-/-)5B(-/-) MICE; ERYTHROPOIETIN; STAT5; PROGENITORS; JAK2;
D O I
10.1016/j.jep.2009.08.043
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Total saponins of Panax ginseng (TSPG), main constituents extracted from Panax ginseng, a highly valued traditional Chinese medicine, have been shown to be an effective agent on hematopoiesis. Objective: To investigate the effect and mechanism underlying in which TSPG promote human CD34(+) hematopoietic stem and progenitor cells to differentiate into erythroid-lineage cells. Materials and methods: The effect of TSPG on erythroid differentiation of purified CD34(+) cells derived from umbilical cord blood (UCB) was determined by methylcellulose assay system and colorimetry for hemoglobin content. The changes of EpoR expression in umbilical cord blood mononuclear cells (UCB-MNCs) and purified CD34(+) cells were detected with Western blotting and flow cytometry, respectively, and observed under laser scanning confocal microscope (LSCM). RT-PCR was performed to examine EpoR mRNA expression in CD34(+) cells. The effects of TSPG-pretreatment on Epo-induced JAK(2) and STAT(5) tyrosine phosphorylation were analyzed by immunoprecipitation. Results: The addition of TSPG (20-70 mg/L) increased the colony formation rate of BFU-E. TSPG (50 mg/L) alone used significantly increased the hemoglobin content, the addition of AG490 evidently reduced TSPG-induced elevation of hemoglobin content. TSPG increased the expression of EpoR on the surface membrane of CD34(+) cells but did not change the expression of EpoR in total UCB-MNCs. TSPG also increased the expression of EpoR mRNA in CD34(+) cells. TSPG markedly enhanced Epo-induced tyrosine phosphorylation of JAK(2) and STAT(5) in UCB-MNCs. Conclusion: These findings suggest that TSPG may enhance the erythroid differentiation of hematopoietic stem and progenitor cells via Epo/EpoR-mediated JAK(2)/STAT(5) signaling pathway. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:215 / 220
页数:6
相关论文
共 24 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]  
CHEN N, 2007, J MODERN ONCOLOGY, V15, P853
[3]  
Chen W, 2000, Se Pu, V18, P439
[4]  
[陈笛 Cheng Di], 2003, [免疫学杂志, Immunological Journal], V19, P411
[5]  
Chi Q, 1992, Zhongguo Zhong Yao Za Zhi, V17, P478
[6]  
DENG X, 2004, CHINESE J PRACTICAL, V17, P3061
[7]  
GAO RL, 1992, CHIN J INTEGR TRADIT, V12, P285
[8]  
HUANG G, 1990, CHIN J HEMATOL, V11, P66
[9]  
KRANTZ SB, 1991, BLOOD, V77, P419
[10]   Roles for an Epo receptor Tyr-343 Stat5 pathway in proliferative co-signaling with Kit [J].
Li, K ;
Miller, C ;
Hegde, S ;
Wojchowski, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (42) :40702-40709