您的位置:山东大学 -> 科技期刊社 -> 《山东大学学报(医学版)》

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

• 临床医学 • 上一篇    下一篇

刮取法改良人原代大隐静脉内皮细胞的提取方法

于瑞明,邴卫东,刘春晓,孟祥斌,毕研文   

  1. 山东大学齐鲁医院心脏外科, 山东 济南 250012
  • 发布日期:2023-02-17
  • 通讯作者: 毕研文. E-mail:yanwenbi1@126.com
  • 基金资助:
    山东省自然科学基金(26010111670901);山东大学科研发展基金(26010132007092)

Scraping method improves the extraction of primary endothelial cells from human saphenous vein

YU Ruiming, BING Weidong, LIU Chunxiao, MENG Xiangbin, BI Yanwen   

  1. Department of Cardiovascular Surgery, Qilu Hospital of Shandong University, Jinan 250012, Shandong, China
  • Published:2023-02-17

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。

关键词: 人大隐静脉, 内皮细胞, 提取方法, 血管性血友病因子, 静脉移植物衰败

Abstract: Objective To improve the extraction method of primary endothelial cells from human saphenous vein and to provide a cell model for the study of vein graft failure after coronary artery bypass grafting. Methods Endothelial cells were extracted from abandoned human saphenous vein by enzymatic digestion and scraping(scraping the vascular intima after enzymatic digestion for further enzymatic digestion). The extracted endothelial cells were cultured in the endothelial cell culture medium containing 10% fetal bovine serum +1% endothelial cell growth supplement +100 U/mL penicillin +100 mg/mL streptomycin. The morphology and adhesion of endothelial cells were observed under an inverted microscope. The specific antigen was identified with immune fluorescence assay of von Will brand Factor(vWF). The purity was detected with flow cytometry of CD31. The activity of endothelial cells was determined with the cell growth curve plotted on different observation days. Results Under the inverted microscope, endothelial cells converged on the wall and arrayed in a typical cobblestone shape. Immune fluorescence assay confirmed the positive expression of vWF. The results of flow cytometry showed that 99.9% and 89.2% of cultured cells in the enzymatic group and scraping group were positive for CD31. Data of the cell growth curve demonstrated that there was no significant difference in endothelial cell activity between the two groups(P=0.057). Endothelial cells from both groups were able to transmit to the 7th-8th generation. Conclusion Based on the traditional enzymatic digestion method, adding the scraping and re-digestion step can extract more primary human saphenous vein endothelial cells.

Key words: Human saphenous vein, Endothelial cell, Extraction method, von Willebrand factor, Vein graft failure

中图分类号: 

  • R574
[1] Head SJ, Milojevic M, Daemen J, et al. Mortality after coronary artery bypass grafting versus percutaneous coronary intervention with stenting for coronary artery disease: a pooled analysis of individual patient data[J].Lacent, 2018, 391(10124): 939-948.
[2] Caliskan E, Souza DR, Böning A, et al. Saphenous vein grafts in contemporary coronary artery bypass graft surgery[J]. Nat Rev Cardiol, 2020, 17(3): 155-169.
[3] Gaudino M, Benedetto U, Fremes S, et al. Association of radial artery graft vs saphenous vein graft with long-term cardiovascular outcomes among patients undergoing coronary artery bypass grafting: a systematic review and meta-analysis[J]. JAMA, 2020, 324(2): 179-187.
[4] Chiu JJ, Chien S. Effects of disturbedflow on vascular endothelium: pathophysiological basis and clinical perspectives[J]. Physiol Rev, 2011, 91(1): 327-387.
[5] Dobrin PB, Littooy FN, Endean ED. Mechanical factors predisposing to intimal hyperplasia and medial thickening in autogenous vein grafts[J]. Surgery, 1989, 105(3): 393-400.
[6] Khaleel MS, Dorheim TA, Duryee MJ, et al. High-pressure distentionof the saphenous vein during preparation results in increased markersof inflammation: a potential mechanism for graft failure[J]. Ann Thorac Surg, 2012, 93(2): 552-558.
[7] Ward AO, Caputo M, Angelini GD, et al. Activation and inflammation of the venous endothelium in vein graft disease[J]. Atherosclerosis, 2017, 265: 266-274. doi: 10.1016/j.atherosclerosis.2017.08.023.
[8] Guida G, Ward AO, Bruno VD, et al. Saphenous vein graft disease, pathophysiology, prevention, and treatment. A review of the literature[J]. J Card Surg, 2020, 35(6): 1314-1321.
[9] Mosquera DA, Goldman M. Endothelial cell seeding[J]. Br J Surg, 1991, 78: 656-660. doi: 10.1002/bjs.1800780608.
[10] Kent KC, Shindo S, Ikemoto T, et al. Species variation and the success of endothelial cell seeding[J]. J Vasc Surg, 1989, 9: 271-276. doi: 10.1016/0741-5214(89)90046-3.
[11] Belair DG, Khalil AS, Miller MJ, et al. Serum-dependence of affinity-mediated VEGF release from biomimetic microspheres[J]. Biomacromolecules, 2014, 15(6): 2038-2048.
[12] James SL, Abate D, Abate KH, et al. Global, regional, and national incidence, prevalence, and years lived with disability for 354 diseases and injuries for 195 countries and territories, 1990—2017: a systematic analysis for the Global Burden of Disease Study 2017[J]. Lancet, 2018, 392(10159): 1789-1858.
[13] Mohr FW, Morice MC, Kappetein AP, et al. Coronary artery bypass graft surgery versus percutaneous coronary intervention in patients with three-vessel disease and left main coronary disease: 5-year follow-up of the randomised, clinical SYNTAX trial[J]. Lancet, 2013, 381(9867): 629-638.
[14] Jaffe EA, Nachman RL, Becker CG, et al. Culture of human endothelial cells derived from umbilical veins. Identification by morphologic and immunologic criteria[J]. J Clin Invest, 1973, 52(11): 2745-2756.
[15] 白雪晶, 冯磊, 徐文波, 等. 人脐静脉内皮细胞培养技术的研究进展[J].吉林医学, 2018, 39(5): 960-962.
[16] 刘洋洋, 冉林武, 范学文, 等. 人原代脐静脉内皮细胞体外模型的建立及鉴定[J].宁夏医科大学学报, 2016, 38(2): 223-225.
[17] 肖紫春, 谭金海, 周益. 兔主动脉血管内皮细胞原代改良提取法[J].中国组织工程研究, 2016, 20(7):1019-1024. XIAO Zichun, TAN Jinhai, ZHOU Yi. Improved extraction of primary vascular endothelial cells from the rabbit aorta[J].Chinese Journal of Tissue Engineering Research, 2016, 20(7): 1019-1024.
[18] 陈小翠, 陈邦党, 杨毅宁, 等. 人脐静脉内皮细胞分离培养和鉴定[J].细胞与分子免疫学杂志, 2016, 32(3): 328-331. CHEN Xiaocui, CHEN Bangdang, YANG Yining, et al. Isolation, culture and identification of human umbilical vein endothelial cells[J]. Chinese Journal of Cellular and Molecular Immunology, 2016, 32(3): 328-331.
[19] Siow RC. Culture of human endothelial cells from umbilical veins[J]. Methods Mol Biol, 2012, 806:265-274. doi: 10.1007/978-1-61779-367-7_18.
[20] Jiménez N, Krouwer VJ, Post JA. A new, rapid and reproducible method to obtain high quality endothelium in vitro[J].Cytotechnology, 2013, 65(1): 1-14.
[21] 李刚,萧晗,唐军建,等. 胶原酶消化刮取再消化法分离培养犬静脉内皮细胞的实验研究[J].河北医科大学学报, 2021, 42(1): 7-11. LI Gang, XIAO Han, TANG Junjian, et al. Experimental study on isolation and culture of canine vascular endothelial cells by collagenase digestion scrape and repeat digestion techniques[J]. Journal of Hebei Medical University, 2021, 42(1): 7-11.
[22] Baudin B, Bruneel A, Bosselut N, et al. A protocol for isolation and culture of human umbilical vein endothelial cells[J]. Nat Protoc, 2007, 2(3): 481-485. doi: 10.1038/nprot.2007.54.
[23] Kadam SS, Tiwari S, Bhonde RR. Simultaneous isolation of vascular endothelial cells and mesenchymal stem cells from the human umbilical cord[J]. In Vitro Cell Dev Biol Anim, 2009, 45(1-2): 23-27.
[24] Hofbauer P, Riedl S, Witzeneder K, et al. Human platelet lysate is a feasible candidate to replace fetal calf serum as medium supplement for blood vascular and lymphatic endothelial cells[J]. Cytotherapy, 2014, 16(9): 1238-1244.
[25] 于世勇,黄岚,李丽,等. 人脐静脉内皮细胞分离培养及不同消化酶效力比较[J].华南国防医学杂志, 2007, 21(6): 1-3. YU Shiyong, HUANG Lan, LI Li, et al. Different enzyme Digestion in isolation and culture of Human umbilical vein endothelial cells[J]. Military Medical Journal of South China, 2007, 21(6): 1-3.
[26] 卞杰勇,周岱. 人脐静脉内皮细胞体外培养的影响因素[J].中国细胞生物学学报, 1997, 19(2): 66-69.
[1] 王晓磊 张海涛 张辉 郭成浩. 舒血宁注射液对高碘致培养血管内皮细胞损伤的保护作用[J]. 山东大学学报(医学版), 2209, 47(6): 38-.
[2] 顾金海,路宁,顾珈榕,文玉军,强媛媛,和祯泉,杨勇,王峰,孙涛,牛建国. 胶质瘤细胞与血管内皮细胞的信号Crosstalk对肿瘤细胞增殖和侵袭的影响[J]. 山东大学学报 (医学版), 2021, 59(2): 1-6.
[3] 崔锡铭,王霜,许顺江,张睿,谢冰,崔冬生,赵占胜. 白藜芦醇对高糖环境下人视网膜血管内皮细胞增殖的影响及分子机制[J]. 山东大学学报 (医学版), 2019, 57(3): 19-24.
[4] 谭琦,李娜,陶运明,唐浩,吴忠仕. 载血管内皮生长因子层层自组装提高异种去细胞血管生物相容性[J]. 山东大学学报(医学版), 2017, 55(5): 23-30.
[5] 李帅,王雅琳,孙忠文,朱梅佳. Nod样受体蛋白3炎性体在2型糖尿病脑微血管内皮细胞中的变化及变化机制[J]. 山东大学学报(医学版), 2017, 55(3): 6-11.
[6] 李冉冉,张鹏飞,袁冰,房菲菲, 韩明勇. 乳腺癌MCF-7细胞分泌的血管内皮生长因子诱导血管内皮细胞免疫功能抑制[J]. 山东大学学报(医学版), 2016, 54(2): 38-43.
[7] 李倩,戴桃李,韩炜,郭成浩. 血管内皮细胞活化在感染后肠易激综合征发病机制中的作用[J]. 山东大学学报(医学版), 2016, 54(12): 58-61.
[8] 曲立新,时兴华,杜怡峰. 急性缺血性脑卒中患者血浆PMP及EMP含量与预后的相关性[J]. 山东大学学报(医学版), 2016, 54(12): 32-36.
[9] 刘辉, 陈桐帅, 李娜, 王舒健, 李静媛, 卜培莉. Sirt3对人脐静脉内皮细胞衰老的影响[J]. 山东大学学报(医学版), 2015, 53(5): 41-45.
[10] 付海燕, 胡占升, 杜红阳. 白藜芦醇衍生物TMS对脂多糖诱导血管内皮细胞表达NO、ICAM-1和NF-κB的影响[J]. 山东大学学报(医学版), 2015, 53(11): 10-15.
[11] 肖芳, 蒋卫东, 王晓红, 秦爱琼, 韩敏, 陈丽. 小鼠胰岛微血管内皮细胞外泌体的提取和鉴定方法[J]. 山东大学学报(医学版), 2015, 53(1): 6-9.
[12] 赵仪云, 黄敬春, 王月莲, 邵山, 孙广平, 崔恩美, 卓绍杨, 刘少华. 平阳霉素联合透明质酸钠对人淋巴管畸形内皮细胞的作用[J]. 山东大学学报(医学版), 2015, 53(1): 41-46.
[13] 陈更越, 张静, 丁树艳, 马莉莉, 王伟, 田园. HO-1及MIF在子痫前期患者胎盘及脐组织的表达[J]. 山东大学学报(医学版), 2014, 52(S2): 1-2.
[14] 陈建华, 朱邦豪. 人参皂苷Re对人脐静脉内皮细胞PARP-1表达的抑制作用[J]. 山东大学学报(医学版), 2014, 52(9): 34-38.
[15] 付庆元, 戴桂强, 张松, 安洪春, 梁世民. 西洋参茎叶皂苷对脑梗死大鼠ET-1、VEGF及脑梗死面积的影响[J]. 山东大学学报(医学版), 2014, 52(9): 30-33.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!