山东大学学报 (医学版) ›› 2023, Vol. 61 ›› Issue (2): 43-48.doi: 10.6040/j.issn.1671-7554.0.2022.0805
于瑞明,邴卫东,刘春晓,孟祥斌,毕研文
YU Ruiming, BING Weidong, LIU Chunxiao, MENG Xiangbin, BI Yanwen
摘要: 目的 改良人原代大隐静脉内皮细胞的提取方法,为冠状动脉旁路移植术后静脉移植物衰败的研究提供细胞模型。 方法 传统酶消法(酶消组)和刮取法(刮取组,刮取酶消法后的大隐静脉内皮并进一步酶消)从人大隐静脉中提取内皮细胞。获得的内皮细胞在含10%胎牛血清+1%内皮细胞生长补充剂+100 U/mL青霉素+100 mg/mL链霉素的内皮细胞培养基中传代培养。倒置显微镜观察内皮细胞形态和贴壁情况;血管性血友病因子(vWF)的免疫荧光实验鉴定内皮细胞特异性抗原;CD31流式细胞计数检测内皮细胞纯度;绘制不同观测日的内皮细胞生长曲线测定内皮细胞活性。 结果 显微镜下观察到两组大隐静脉内皮细胞贴壁汇合并且呈典型的鹅卵石样排列;免疫荧光实验证实培养的细胞vWF阳性表达;流式细胞计数结果显示,酶消组99.9%、刮取组89.2%的细胞阳性表达CD31;不同观测日的生长曲线结果显示,两组内皮细胞活性的主效应不显著(P=0.057)。两组内皮细胞均能够传至第7~8代。 结论 在传统酶消法的基础上增加刮取再消化的步骤,能够提取出数量更多且满足实验需要的原代人大隐静脉内皮细胞。
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