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机构地区:[1]天津中医药大学,天津300193
出 处:《辽宁中医杂志》2017年第12期2486-2489,共4页Liaoning Journal of Traditional Chinese Medicine
基 金:国家自然科学基金(81673732;81503401;81273892);国家大学生创新创业计划项目(201510063006)
摘 要:目的:探讨在体外造血微环境中肌源性干细胞Wnt/β-catenin信号通路相关基因的表达情况及当归补血汤(DBD)载药血清的干预作用。方法:将分离纯化并经流式细胞仪鉴定的MDSCs与BMSCs体外培养,根据实验需要随机分为6组进行药物干预,即空白对照组、共培养Wnt激动剂组、共培养Wnt抑制剂组、DBD+共培养组、DBD+共培养激动剂组及DBD+共培养抑制剂组。Real-time PCR检测各实验组MDSCs Wnt通路上下游节点基因Wnt3、Wnt3a、β-catenin及MDSCs增殖分化相关基因Cyclin D1、C-myc、CD34 mRNA的表达变化。结果:流式细胞仪检测结果显示MDSCs CD34、Sca-1阳性。倒置显微镜下观察:共培养Wnt激动剂组、DBD+共培养组、DBD+共培养激动剂组MDSCs较空白对照组生长密集且生长速度快,激动剂组聚团明显,共培养Wnt抑制剂组MDSCs增殖明显受到抑制。Real-time PCR检测结果显示:DBD+共培养激动剂组的Wnt3、Cyclin D1、CD34 mRNA表达水平最高,共培养激动剂组与DBD共培养组其次,空白对照组最低。结论:当归补血汤载药血清作用于共培养体系下的肌源性干细胞,Wnt信号通路持续激活后,体外造血微环境中的MDSCs更易增殖并分化。Objective:To investigate the variation of gene expression of Wnt signaling pathway on muscle derived stem cells in- tervene by Danggui Buxue Decoction(DBD) in vitro hematopoietic microenvironment. Methods:MDSCs purified and detected by FACS and co - cultured with BMSCs in vitro were randomly divided into 6 groups. The expressions of Wnt3,Wnt3a, [3 - eatenin, CD34,C - mye and CyclinD1 mRNA in MDSCs were detected by RT - PCR and the expressions of CD34 and Sca- 1 in MDSCs were detected by FACS. Results :The FACS showed that CD34 and Sca - 1 were positive in MDSCs. Observed under the inverted microscope, MDSCs in co - cultured Wnt agitated group, DBD + co - cultured group, DBD + co - cultured Wnt agitated group mat- ted growth faster than those in blank control group. MDSCs in DBD + Wnt agitated group was clustered obviously. The proliferation of MDSCs was significantly suppressed in co - cultured Wnt inhibited group. RT - PCR analysis showed that the expressions of Wnt3, CyclinD1, CD34 mRNA in DBD + co - cultured Wnt agitated group were the highest and that in co - cultured Wnt agitated group were higher than those in blank control group. Conclusion:The sustained activation of Wnt signaling pathway can promote the proliferation and differentiation of MDSCs intervened by Danggui Buxue Decoction in vitro hematopoietic microenvironment.
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