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三七总皂苷诱导人CD34+造血干/祖细胞的增殖与分化

[Proliferation and differentiation of human CD34+ hematopoietic stem/progenitor cells induced by Panax notoginosides].

作者信息

Qian Xu-Dai, Gao Rui-Lan, Ma Ke, Jin Jin-Mei

机构信息

Department of Hematology, Affiliated Hospital of Zhejiang College of Traditional Chinese Medicine, Hangzhou 310006, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2003 Apr;11(2):120-3.

Abstract

The object of this study was to explore the effects of Panax notoginosides (PNS) on proliferation and differentiation of human CD34(+) stem/progenitor cells. CD34(+) cells were isolated from human bone marrow by using immune beads of Dynal M- 450 system. The cells were exposed to PNS at different concentrations in both liquid and semi-solid culture for 14 days. The cells were marked with monoclonal antibodies and analyzed by flow cytometry after culture. The CFU-Mix colony formation from CD34(+) cells was assayed. The results showed that: (1) The yield of CD34(+) cells after being selected by immune beads were (1.03 +/- 0.74)% out of bone marrow nuclear cells with purity of 86% - 93%. (2) PNS (10 - 25 mg/L) stimulated the proliferation of CD34(+) cells, and raised the colony numbers of CFU-Mix obviously in vitro. PNS 25 mg/L was the optimal concentration to promote proliferation of CD34(+) cells, the increasing rate of CFU-Mix colony was (34.7 +/- 16.0)%. (3) The differentiation of CD34(+) cells was induced by exposure to PNS (25, 50 and 100 mg/L) in liquid culture for 14 days. The percentages of CD33(+) and CD15(+) cells were increased after PNS exposure, which were significantly higher than those of control (P < 0.01), however CD71(+) and G-A(+) cells were no obviously difference after PNS treatment. In conclusion, Panax notoginosides not only promote the proliferation of CD34(+) cells, but also induce the differentiation committed to granulocytes.

摘要

本研究的目的是探讨三七总皂苷(PNS)对人CD34(+)干/祖细胞增殖和分化的影响。采用Dynal M-450系统免疫磁珠从人骨髓中分离CD34(+)细胞。将细胞在液体和半固体培养中分别暴露于不同浓度的PNS中14天。培养后用单克隆抗体标记细胞并通过流式细胞术进行分析。检测CD34(+)细胞的CFU-Mix集落形成情况。结果显示:(1)经免疫磁珠筛选后,CD34(+)细胞产量占骨髓有核细胞的(1.03±0.74)%,纯度为86% - 93%。(2)PNS(10 - 25 mg/L)可刺激CD34(+)细胞增殖,并显著提高体外CFU-Mix集落数量。PNS 25 mg/L是促进CD34(+)细胞增殖的最佳浓度,CFU-Mix集落增加率为(34.7±16.0)%。(3)在液体培养中,将CD34(+)细胞暴露于PNS(25、50和100 mg/L)14天可诱导其分化。PNS处理后,CD33(+)和CD15(+)细胞百分比增加,显著高于对照组(P < 0.01),然而PNS处理后CD71(+)和G-A(+)细胞无明显差异。综上所述,三七总皂苷不仅促进CD34(+)细胞增殖,还诱导其向粒细胞方向分化。

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