|本期目录/Table of Contents|

[1]黄凤,段行武,董建勋,等.益气活血方含药血清对大鼠骨髓间充质干细胞体外增殖的影响[J].环球中医药,2014,7(05):327-332.
 HUANG Feng,DUAN Xing wu,DONG Jian xun,et al.Effect of qitonifying and bloodactivating Chinese herb serum on proliferation of SD rat bone marrow mesenchymal stem cells in vitro[J].,2014,7(05):327-332.
点击复制

益气活血方含药血清对大鼠骨髓间充质干细胞体外增殖的影响()
     
分享到:

《环球中医药》[ISSN:1006-6977/CN:61-1281/TN]

卷:
第7卷
期数:
2014年05期
页码:
327-332
栏目:
论著
出版日期:
2014-05-06

文章信息/Info

Title:
Effect of qitonifying and bloodactivating Chinese herb serum on proliferation of SD rat bone marrow mesenchymal stem cells in vitro
作者:
黄凤;段行武;董建勋;李健;荣培晶;徐旭英;
Author(s):
HUANG Feng DUAN Xingwu DONG Jianxunet al.
Department of dermatology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, China
关键词:
骨髓间充质干细胞细胞培养体外培养益气活血中药
Keywords:
Mesenchymal stem cellsCell proliferationIn VirtoQitonifying and bloodactiviting Chinese herb serum
分类号:
R2855
DOI:
-
文献标志码:
A
摘要:
目的探讨益气与活血中药含药血清对骨髓间充质干细胞(bone marrow mesenchymal stem cells,BMSCs )增殖能力的影响。方法全细胞贴壁培养法获取、纯化BMSCs,体外培养,建立大鼠骨髓间充质干细胞的培养体系,采集空白对照大鼠、益气药、活血药、益气活血中药灌胃大鼠含药血清,用10%浓度以上不同含药血清培养第三代BMSCs,置于37℃,5% CO2 培养箱中孵育。用流式细胞术鉴定BMSCs。噻唑基四唑比色法(methyl thiazolyl tetrazolium,MTT)测细胞活性,绘制生长曲线,观察10%益气、活血、益气活血中药含药血清对大鼠骨髓间充质干细胞体外增殖的影响。结果采用全骨髓贴壁法获取的BMSCs,经流式细胞术检测,CD44、CD106呈阳性表达,基本不表达CD45、CD34;MTT法检测结果显示,培养第2、4、5天细胞快速增长,均较前一天增长明显(P<005),第6天时活血方血清组与益气活血方血清组细胞增长已呈下降趋势,而其它三组在第6天细胞增长达最大,与前一天比较仍有差异(P<005),到第7天呈下降趋势。BMSCs去除基线增殖率组间比较,培养第2天时,各组间比较虽无差异,但活血方血清组达最大(7139±498%);第4、6天时,益气活血方组达最大(6640±147%),与其它三组比较P<001,活血方血清组次之;培养第6天时,益气方血清组较其它三组大,益气活血方血清组次之,活血方血清组最低。结论全细胞贴壁培养的大鼠骨髓间充质干细胞在细胞形态与表形表达上均具备BMSCs特征; 益气活血中药含药血清对培养BMSCs增殖影响最大,活血方含药血清对细胞增殖影响出现最早、益气方含药血清对细胞增殖影响时间最长。
Abstract:
ObjectiveTo explore the qitonifying and bloodactivating Chinese herb serum on proliferation of SD rat bone marrow mesenchymal stem cells (BMSCs) in vitro. MethodsRat BMSCs were isolated from rat bone marrow and expanded by whole bone marrow adherent culture method in vitro, collected blank serum of rat as control group and serum from qitonifying Chinese herb, bloodactivating Chinese herb, qitonifying & bloodactivating Chinese herb gavaged rats. BMSCs of the third generation were cultured in vitro with 10% concentrations of these four kinds of medicated serum at 37 ℃ and 5% CO2 incubator respectively. Flow cytometry was used for the identification of BMSCs and the proliferation of BMSCs was observed by MTT method and drew the growth curve. ResultsThe BMSCs were obtained by whole bone marrow adherent culture method. The membranes of third generation of BMSCs were positive for CD44 and CD106 and negative for CD45 and CD34 detected by flow cytometry. The results showed that BMSCs grown rapidly compared to the day before it selves to the 2nd, 4th, and 5th days, the difference was significantly (P<005). The cell growth of the bloodactivating Chinese herb serum group and qitonifying & bloodactivating Chinese herb serum group showed a downward trend, while the cell growth of the other three groups reached peak on the 6th day, but still had differences compared to the 5th day (P<005), and declined on the 7th day. The removed baseline proliferation rate of BMSCs had no differences comparison among groups at 2nd day, but the removed baseline proliferation rate of BMSCs in bloodactivating Chinese herb serum group reached maximum (7139±498%), but no differences compared with the other three groups (P>005). Compared with the other three groups, the removed baseline proliferation rate of qitonifying & bloodactivating Chinese herb serum group was the largest (6640±147%) (P<001) on the 4th and 6th days, followed by bloodactivating Chinese herb serum group. The removed baseline proliferation rate of qitonifying Chinese herb serum group was the highest on the 6th day, followed by qitonifying & bloodactivating Chinese herb serum group and bloodactivating Chinese herb serum group. ConclusionBMSCs of SD rat isolation and cultivation by whole bone marrow adherent culture method could steadily express the bone mesenchymal stem cells surface markers and cells morphology. Qitonifying & bloodactivating Chinese herb serum has the greatest effect on the proliferation of cultured BMSCs; bloodactivating Chinese herb serum motivates cell proliferation earliest; qitonifying Chinese herb serum has the longest effects on cell proliferation.

参考文献/References:

[1]Evelien Schurgers, Hilde Kelchtermans, Tania Mitera, et al. Discrepancy between the in vitro and in vivo effects of murine mesenchymal stem cells on Tcell proliferation and collageninduced arthritis[J]. Arthritis Research & Therapy, 2010, 12: R31.
[2]Conget PA, Minguell JJ.Phenotypical and functional properties of human bone marrow mesenchymal progenitor cells[J].J Ceil Physiol, 1999, 181(1):67.
[3]Pittenger MF, Mackay AM, Beck SC,et a1.Multilineage potential of adult human mesenchymal stem cells[J].Science, 1999, 284(5411): 143.
[4]祝小玲, 祝彼得. 黄芪体外作用对贫血小鼠骨髓基质细胞分泌SCF的影响[J]. 细胞与分子免疫学杂志, 2002, 18(4): 396398.
[5]王晓玲, 汪涛, 汪雅妮, 等. 当归补血汤载药血清对骨髓基质细胞增殖及细胞因子表达的影响[J]. 辽宁中医杂志, 2011, 38(2): 363363.
[6]古今. 当归补血汤中黄芪对小鼠造血功能的影响[J]. 中国中医基础医学杂志, 2009, 15(3): 215217.
[7]孙汉英, 房明皓, 任天华, 等. 川芎嗪对骨髓移植小鼠骨髓造血的影响[J]. 中国中西医结合杂志, 2002, 22(5): 365368.

相似文献/References:

[1]王晓娟.丹参多酚酸盐对大鼠骨髓间充质干细胞增殖及血管内皮生长因子表达的影响[J].环球中医药,2013,6(07):492.
 Wang Xiao juan..Effect of salvianolate on cell proliferation and levels of VEGF of rat bone marrow mesenchymal stem cells[J].,2013,6(05):492.
[2]刘文兰 油红捷 车念聪等.一贯煎促进骨髓间充质干细胞逆转肝纤维化的实验研究[J].环球中医药,2014,7(06):401.
 LIU Wen lan,YOU Hong jie,CHE Nian cong,et al.The promotion of Yiguanjian on the recovery of liver fibrosis through mesenchymal stem cells:an experimental study[J].,2014,7(05):401.

备注/Memo

备注/Memo:
基金项目:北京市自然科学基金面上项目(7122084);北京市卫生系统高层次卫生技术人才培养计划(20133080);北京市科委首都临床特色应用研究(Z131107002213117);北京市中医药科技年度规划项目(WZF201202);国家中医药管理局中医外科重点学科
作者单位:100700 北京中医药大学附属东直门医院皮肤科[黄凤(博士研究生)、段行武]、基础医学院(李健);首都医科大学附属北京中医医院外二科(黄凤、董建勋、徐旭英);中国中医科学院针灸研究所(荣培晶)
作者简介:黄凤(1984),2011级在读博士研究生。研究方向:中医药治疗周围血管病临床与基础研究。Email:hf2061043@163.com通讯作者:徐旭英(1973),博士,副主任医师,中华中医药学会周围血管病分会秘书长。研究方向:中医外科疮疡与周围血管疾病。Email:xxying7341@126.com
更新日期/Last Update: 1900-01-01