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汉黄芩素上调小鼠骨髓Lin-细胞Pecam1基因表达
引用本文:李慧影,马亚珂,杨岳,王虹.汉黄芩素上调小鼠骨髓Lin-细胞Pecam1基因表达[J].天津中医药大学学报,2015,34(2):86-90.
作者姓名:李慧影  马亚珂  杨岳  王虹
作者单位:天津中医药大学中医药研究院, 天津市现代中药重点实验室-省部共建国家重点实验室培育基地, 天津 300193,天津中医药大学中医药研究院, 天津市现代中药重点实验室-省部共建国家重点实验室培育基地, 天津 300193,天津中医药大学中医药研究院, 天津市现代中药重点实验室-省部共建国家重点实验室培育基地, 天津 300193,天津中医药大学中医药研究院, 天津市现代中药重点实验室-省部共建国家重点实验室培育基地, 天津 300193
基金项目:国家自然科学基金面上项目(81173592);新世纪优秀人才支持计划(NCET-13-0935);长江学者和创新团队发展计划资助(IRT0973).
摘    要:目的]探讨汉黄芩素对小鼠骨髓Lin-细胞增殖、分化、迁移、黏附关键功能基因表达的影响。方法]采用免疫磁珠法分离小鼠骨髓Lin-细胞,采用CD117作为标志进行细胞鉴定。应用实时定量聚合酶链式反应(RT-PCR)芯片技术研究汉黄芩素对小鼠骨髓Lin-细胞功能基因表达的影响。采用黏附能力测定实验观察Lin-细胞的黏附能力。结果]流式细胞技术结果显示,小鼠骨髓源性单个核细胞免疫磁珠分选后CD117的阳性率为93.7%;芯片结果发现汉黄芩素明显上调Lin-细胞血小板内皮细胞黏附分子-1(Pecam1)基因表达;黏附能力测定实验结果可见汉黄芩素增强Lin-细胞的黏附能力。结论]免疫磁珠法分离小鼠骨髓Lin-细胞是一种较为理想的分离方法;汉黄芩素可能通过上调小鼠骨髓Lin-细胞Pecam1基因表达,从而增加Lin-细胞的黏附能力。

关 键 词:小鼠骨髓Lin-细胞  汉黄芩素  关键功能基因  黏附能力
收稿时间:2014/11/14 0:00:00

Regulated Pecam1 gene expression in bone marrow-derived Lin- cells by wogonin
LI Hui-ying,MA Ya-ke,YANG Yue and WANG Hong.Regulated Pecam1 gene expression in bone marrow-derived Lin- cells by wogonin[J].Journal of Tianjin University of Traditonal Chinese Medicine,2015,34(2):86-90.
Authors:LI Hui-ying  MA Ya-ke  YANG Yue and WANG Hong
Institution:Research Institute of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin 300193, China,Research Institute of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin 300193, China,Research Institute of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin 300193, China and Research Institute of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin 300193, China
Abstract:Objective] To explore the effects of wogonin on the proliferation, differentiation, migration, adhesion gene expression of bone Marrow-derived Lin- cells. Method] Using magnetic activated cell sorting (MACS) to separate Lin- cells from bone marrow and using CD117 as a marker for cell identification. To investigate the effect of wogonin on functional gene expression of bone marrow-derived Lin- cells by real-time-RT-PCR array technology. Adhesion method was used to detect the effect of wogonin on the adhesion of Lin- cells. Result] Flow cytometry results showed that, mononuclear cells derived from bone marrow of mice after MACS, the separation rate of CD117 was 93.7%. The PCR chip results showed that the gene expression of platelet endothelial cell adhesion molecule -1 (Pecam1) of Lin-cell was significantly up-regulation by wogonin. The adhesion ability experimental result showed that wogonin could enhance the adhesion ability of Lin- cells. Conclusion] It is an ideal separation method by using MACS to separate Lin- cells from bone marrow. Wogonin may up regulate Lin- cells in bone marrow of mice Pecam1 gene expression, thereby increasing the adhesion ability of Lin- cells.
Keywords:bone marrow-derived Lin- cells  wogonin  key functional gene  adhesion ability
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