天然产物研究与开发 ›› 2024, Vol. 36 ›› Issue (增刊2): 10-18.

• 研究论文 • 上一篇    下一篇

烟酰胺单核苷酸与二甲双胍对NK细胞增殖、脆性和杀瘤功能的影响

徐   哲1,刘志成2,戴晓宇1,赵莎莎1,戴依辰3,李   栋1,4*   

  1. 1济南万泉生物技术有限公司研发部;2银丰低温医学科技有限公司,济南 250100;3中国矿业大学人工智能学院,北京 100000;4山东大学齐鲁医院低温医学研究室,济南 250012
  • 出版日期:2024-12-09 发布日期:2024-12-09
  • 基金资助:
    山东省科技型中小企业创新能力提升工程(2022TSGC2001)

Effects of nicotinamide mononucleotide and metformin on proliferation,brittleness and tumor-killing function of NK cells

XU Zhe1,LIU Zhi-cheng2,DAI Xiao-yu1,ZHAO Sha-sha1,DAI Yi-chen3,LI Dong1,4*   

  1. 1Research and Development Department of Jinan Wanquan Biotechnology Co.,Ltd.;2Yinfeng Cryomedicine Technology 
    Co.,Ltd.,Jinan 250100,China;3School of Artificial Intelligence,China University of Mining and Technology,Beijing 100000,China;4Department of Cryomedicine,Qilu Hospital of Shandong University,Jinan 250012,China
  • Online:2024-12-09 Published:2024-12-09

摘要:

验证烟酰胺单核苷酸(nicotinamide mononucleotide,NMN)与二甲双胍(metformin,MET)是否可促进自然杀伤细胞(natural killer cell,NK细胞)增殖并提高杀瘤功能。本文采用在NK细胞扩增体系中添加不同浓度的NMN或MET,分析其对细胞增殖的影响,并利用流式细胞术检测其细胞表型、凋亡比率、细胞周期、细胞脆性和肿瘤杀伤能力。本文的研究得出的结果是通过预实验选择在NK细胞扩增体系中,添加终浓度为0.5 ng/mL NMN、10 mg/mL MET或0.5 ng/mL NMN+10 mg/mL MET。在第7 d,细胞计数显示各实验组均较对照组细胞数量显著增多(P<0.05),第7 d的CD3-CD56+CD16+细胞、细胞凋亡与细胞周期各组间没有显著差异(P>0.05);在第14 d,实验组细胞总数较对照组明显增多,与对照组相比,MET组与NMN+MET组的CD3-CD56+CD16+细胞总数显著提高(P<0.05),但两组间的细胞凋亡比率与细胞周期无显著差异(P>0.05)。第14 d的细胞脆性实验显示NMN组、MET组和NMN+MET组的存活细胞总数均显著高于对照组(P<0.05)。第14 d的肿瘤杀伤实验证明NMN与MET可明显抑制肿瘤细胞的生长(P<0.05)。研究发现,NMN与MET可有效促进NK细胞的增殖,同时降低细胞膜脆性;NMN与MET在促进增殖的同时,未引起凋亡增加和细胞周期的明显变化,并表现出显著增加的肿瘤杀伤活性。

关键词: 烟酰胺单核苷酸, 二甲双胍, 自然杀伤细胞, 细胞增殖, 细胞脆性

Abstract:

The purpose of this study was to verify whether nicotinamide mononucleotide (NMN) and metformin (MET) can promote the proliferation of natural killer cells (NK cells) and improve the anticidal function.The method used in this study was to add different concentrations of NMN or MET into the NK cell expansion system to analyze its effect on cell proliferation,and to detect its cell phenotype,apoptosis ratio,cell cycle,cell fragility and tumor killing ability by flow cytometry.The results of this study were that the final concentration of 0.5 ng/mL NMN,10 mg/mL MET or 0.5 ng/mL NMN+10 mg/mL MET was added to the NK cell expansion system through pre-experiment.On the 7th day,cell count showed that the number of cells in all experimental groups increased significantly compared with the control group (P<0.05),and there were no significant differences in CD3-CD56+CD16+ cells,apoptosis and cell cycle among all groups on the 7th day (P>0.05). On the 14th day,the total number of cells in the experimental group was significantly higher than that in the control group,and the total number of CD3-CD56+CD16+ cells in the MET group and the NMN+MET group was significantly higher than that in the control group (P<0.05),but there was no significant difference in apoptosis ratio and cell cycle between the two groups (P>0.05).The cell fragility test on the 14th day showed that the total number of surviving cells in NMN,MET and NMN+MET groups was significantly higher than that in control group (P<0.05).The tumor killing experiment on the 14th day showed that NMN and MET could significantly inhibit the growth of tumor cells (P<0.05).Research has found that NMN and MET can effectively promote the proliferation of NK cells,while reduce the brittleness of the cell membrane; NMN and MET can promote the proliferation, but do not cause the increase of apoptosis and the significant change of cell cycle,and show significantly increased tumor killing activity.

Key words: nicotinamide mononucleotide, metformin, natural killer cells, cell proliferation, cell fragility

中图分类号:  R932