北京大学学报(医学版) ›› 2018, Vol. 50 ›› Issue (4): 590-594. doi: 10.3969/j.issn.1671-167X.2018.04.002

• 论著 • 上一篇    下一篇

炎症因子预处理的脂肪干细胞可明显抑制外周血单个核细胞增殖

王子成1,程立1,吕同德1,苏黎2,林健1△,周利群1△   

  1. (1. 北京大学第一医院泌尿外科,北京大学泌尿外科研究所,国家泌尿、男性生殖系肿瘤研究中心, 北京100034; 2. 北京大学医药卫生分析中心, 北京100191)
  • 出版日期:2018-08-18 发布日期:2018-08-18
  • 通讯作者: 林健,周利群 E-mail:linjianbj@163.com, zhoulqmail@sina.com
  • 基金资助:
    国家自然科学基金(81670617、81672546)资助

Inflammatory priming adipose derived stem cells significantly inhibit the proliferation of peripheral blood mononuclear cells

WANG Zi-cheng1, CHENG Li1, LV Tong-de1, SU Li2, LIN Jian1△, ZHOU Li-qun1△   

  1. (1.Department of Urology, Peking University First Hospital; Institute of Urology, Peking University; National Urological Cancer Center, Beijing 100034, China; 2. Centre of Medical and Health Analysis, Peking University, Beijing 100191, China)
  • Online:2018-08-18 Published:2018-08-18
  • Contact: LIN Jian, ZHOU Li-qun E-mail:linjianbj@163.com, zhoulqmail@sina.com
  • Supported by:
    Supported by National Natural Science Foundation of China (81670617, 81672546)

摘要: 目的:观察炎症因子预处理脂肪干细胞(adipose derived stem cells,ASCs)模拟异常炎症环境能否增强ASCs抑制外周血单个核细胞(peripheral blood mononuclear cells,PBMCs)体外增殖的能力。方法:先用酶消化法对ASCs进行分离及体外培养,流式细胞仪检测其表面CD分子表达情况,用特定培养基诱导分化并鉴定其向脂肪组织和骨组织分化的能力。将PBMCs用CFSE标记后,与炎症因子预处理后的ASCs共培养,对照组无ASCs或使用未经炎症因子处理的ASCs,同时用CD3/CD28刺激PBMCs增殖,最后用流式细胞仪检测PBMC的母代细胞比例,从而判断其增殖情况。结果:ASCs形态为梭形,密集时可成鱼群状生长,可在诱导培养基培养下向脂肪组织和骨组织分化,表面CD分子表达情况与国际脂肪治疗联盟的关于ASCs的说明一致。PBMCs与ASCs体外共培养后,与无ASCs组相比,PBMCs的母代细胞比例有所增加,但效果并不显著,而将PBMCs与用炎症因子预处理后的ASCs共培养,PBMCs的母代细胞比例有明显增加(炎症因子处理后ASCs组 38.7%±10% vs. 无ASCs组28.4%±8.9%, P<0.05), 说明炎症因子预处理的ASCs可明显抑制PBMCs的增殖。结论:炎症因子可增强ASCs的抗炎能力,该发现有助于ASCs更好地在组织修复领域发挥治疗作用。

关键词: 脂肪组织, 干细胞, 组织工程, 白细胞, 单核, 细胞增殖

Abstract: Objective: To explored whether adipose derived stem cells (ASCs) could inhibit the pro-liferation of peripheral blood mononuclear cells (PBMCs) and whether inflammatory priming could enhance this property of ASCs. Methods: We isolated ASCs using collagenase from adipose tissue and expanded them in vitro. Cells were induced to differentiate into adipogenic and osteogenic lineages. The cells at passage 3 to passage 5 were used for the experiments. After carboxy fluoresce in succinimidyl ester (CFSE) staining, PBMCs were co-cultured with inflammatory priming ASCs. The PBMCs cultured without ASCs or with nontreated ASCs defined as control groups. Then we used flow cytometry to detect the proliferation of PBMCs. Results: ASCs had fibroblast-like phenotype and were spindle shaped. They were able to differentiate into cells of adipogenic and osteogenic lineages in specific induction media. ASCs had the CD expression profile consistant with the International Federation for Adipose Therapeutics statement. The percentage of parent cells in PBMC after co-cultured with ASCs increased, though there was no statistical significance. However, when co-cultured with inflammatory priming ASCs, the percentage of parent cells significantly increased (with inflammatory priming ASCs group vs. without ASCs group, 38.7%±10.0% vs. 28.4%±8.9%, P<0.05). This indicated that inflammatory priming ASCs could significantly inhibit the proliferation of PBMCs. Conclusion: Inflammatory cytokines can enhance the immunosuppressive ability of ASCs. Our findings may help the application of ASCs in tissue repairment with better results.

Key words: Adipose tissue, Stem cells, Tissue engineering, Leukocytes, mononuclear, Cell proliferation

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