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缺氧预处理对骨髓来源内皮祖细胞生物学功能影响

薛奋龙   

  1. 天津市胸科医院
  • 收稿日期:2013-10-11 修回日期:2013-11-27 出版日期:2014-03-15 发布日期:2014-03-15
  • 通讯作者: 薛奋龙

Effect of Hypoxic Preconditioning on the Biological Function of Bone marrow-derived Endothelial Progenitor Cells

  • Received:2013-10-11 Revised:2013-11-27 Published:2014-03-15 Online:2014-03-15

摘要: 【摘要】 目的 研究缺氧条件对骨髓来源内皮祖细胞(BM-EPCs)生物学功能的影响。 方法 经密度梯度离心法获得大鼠骨髓来源单核细胞,接种在包被有大鼠玻连蛋白的培养皿中,加入内皮细胞生长培养基-2,于常规培养条件(37 ℃、5% CO2)下培养,第4天时,弃去未贴壁细胞,全量更换新鲜培养基,随机分为常规培养组和缺氧培养组,常规培养组于常规培养条件下继续培养至第7天;缺氧培养组分别于常规培养的第4天、第5天、第6天,于缺氧培养条件(1% O2+5% CO2+94% N2)下继续培养72小时、48小时、24小时;细胞表面标志物检测并Dil 标记的乙酰化低密度脂蛋白和FITC标记的荆豆凝集素- 1共同染色方法鉴定骨髓来源内皮祖细胞,分别对各组培养至第7天的细胞进行内皮分化功能检测(Matrigel Assay)、抗凋亡检测(Annexin V/PI),明确缺氧条件对BM-EPCs的功能影响,以求最佳缺氧培养时间。结果 随着缺氧时间的延长,骨髓来源内皮祖细胞早期凋亡率明显增加,缺氧培养24小时组早期凋亡率(1.33±0.07)与常规培养组(0.89±0.20)相比,差异无统计学意义(P>0.05),缺氧培养48小时组(3.25±0.12)、72小时组(7.48±1.53)与常规培养组相比,差异均具有统计学意义(P<0.05)。体外血管形成能力相比,缺氧培养24小时组较常规培养组相比,体外血管形成能力增强,差异具有统计学意义(P<0.01),缺氧培养48小时组、72h组与常规培养组相比,体外血管形成能力明显下降,差异具有统计学意义(P<0.01)。 结论 缺氧预处理BM-EPCs 24小时,BM-EPCs早期凋亡率增加不明显,细胞体外血管形成能力明显增强。

关键词: 缺氧诱导, 内皮细胞, 干细胞, 血管生成, 凋亡

Abstract: Objective To observe the effect of hypoxic preconditioning on the biological function of bone marrow-derived endothelial progenitor cells(BM-EPCs). Methods Mononuclear cells were collected by density gradient centfifugation from the bone marrow of rats. The isolated cells were cultivated in dishes coated with the vitronectin from rat plasma,filled with the endothelial cell basal medium-2. First,All of the cells were cultured under the conventional culture conditions (37 ℃ and 5% CO2) . After four days ,cultured cells were divided into control group and hypoxia training groups. Cells of the control group were cultured in previous conditions for another three days. However, cells of the hypoxia training groups were cultured in previous conditions for 0 days、1 days、2 days,then,under the hypoxic condition (1% O2+5% CO2+94% N2) for another 72 hours、48 hours、and 24 hours,respectively. In the seventh days,all of the groups were collected for the following study,immunofluorescence labeling and cell analyzer were used to indentify BM-EPCs. the tube formation of BM-EPCs were tested by matrigel assay. Apoptosis of BM-EPCs were assayed by Annexin V/PI antiapoptotic assay. So as to explore the hypoxic conditions on the function of BM-EPCs, for the best time to hypoxic. Results As the hypoxic time extended,The early apoptosis rate was significantly increased. There was no significantly difference between the control group(0.89±0.20) and the hypoxic 24 hours group(1.33±0.07)(P>0.05). Compare with the control group ,The tube formation of the hypoxic 24 hours group was stronged significantly (P<0.01). Conclusion After hypoxic preconditioning BM-EPCs for 24 hours, the rate of apoptosis was not obvious, but the tube formation ability was markedly increased.

Key words: hypoxic preconditioning, Endothelial cells, Stem Cells, Tube formation, Apoptosis