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改良成人大隐静脉平滑肌细胞培养方法
  • 期刊名称:武汉大学学报(医学版)
  • 时间:0
  • 页码:496-497+521+563
  • 语言:中文
  • 分类:R322.123[医药卫生—人体解剖和组织胚胎学;医药卫生—基础医学]
  • 作者机构:[1]武汉大学人民医院心血管外科,湖北武汉430060
  • 相关基金:课题来源:国家自然科学基金资助项目(编号:30872537)
  • 相关项目:Ras蛋白适配子对 VSMC 增殖、迁移及 CHD 术后再狭窄的作用及分子机制
中文摘要:

目的:研究提高成人大隐静脉平滑肌细胞(hVSMC)体外培养效率的方法。方法:无菌条件下取3 cm左右大隐静脉,去除内外膜后,切成1 mm×1 mm大小组织块,贴块法培养,高糖DMEM中加入血小板衍生生长因子(PDGF)10μg/L,免疫组织化学法鉴定平滑肌细胞。结果:大隐静脉平滑肌细胞沿组织块长出时间为8-12 d,原代培养(22±2)d传第1代,免疫组织化学染色细胞平均阳性率≥98%。结论:PDGF和高糖克服了hsVSMC体外培养休眠期过长的缺点。运用该方法,稳定获得hsVSMC原代细胞,且重复性好,细胞产量较大,简便而有效。

英文摘要:

Objective: To study on increasing the successful rate of in vitro culturing of the human saphenous vascular smooth muscle cells (hVSMCs). Methods: A group of 3-cm-long saphenous veins were harvested under sterile conditions. After the internal and external membrane were removed, the middle membranes were cut into 1 mm× 1 mm size pieces, and were cultured by tissue-piece inoculation method, added to DMEM medium with PDGF (10 μg/L) and high concentration of glucose. The smooth muscle cells were identified by immunohistochemistry. Results: The hVSMCs grew along the tissue pieces for 8-12 days, the original generation was cultured for (22±2)days, and the purity of the third passage SMCs was more than 98%. The cultured cells showed the typical peak and valley appearance under microscope. Immunohistochemistry staining with m-Ab against rabbit SM-α-actin identified the cells. Conclusion: Culturing with PDGF and high glucose in vitro overcomes the shortcoming of the long period of hsVSMC dormancy. And the method was reproducible, simple, stable, and effective.

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