[Correlation of Nucleostemin with Programmed Death-ligand-1 in Multiple Myeloma U266 Cells]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019 Dec;27(6):1894-1900. doi: 10.19746/j.cnki.issn.1009-2137.2019.06.030.
[Article in Chinese]

Abstract

Objective: To investigate the correlation of nucleostemin (NS) gene with programmed death ligand-1 (PD-L1) in myeloma cells and the effect of NS expression down-regulation on the apoptosis of multiple myeloma cells, and to evaluate the associations among NS, PD-L1 and biological behavior of MM cells, and the feasibility of both NS and PD-1 as markers reflecting the status of MM cells.

Methods: The NS gene expression in U266 cells was down-regulated by NS-RNAi-GV248 recombinant lentivirus, the real-time PCR was used to detect the mRNA expression of NS, PD-L1 and PI3K/AKT/mTOR. The Western blot and flow cytometry were used to detect the expression of NS and PD-L1. The Annexin V-APC/7-AAD staining method was used to detect the apoptosis of U266 cells before and after knocking out the NS gene.

Results: Under the condition of MOI=10, the transfection efficiency was more than 75% by means of the fluorescent microscopy; real-time PCR showed that compared with the negative control group (1.002±0.026), the mRNA expression of NS, PD-L1 and PI3K/AKT/mTOR gene in the transfection group (0.415±0.089) was significantly reduced (P<0.05). The results of flow cytometry and Western blot showed that the protein expression of PD-L1 was significantly down-regulated after transfection. After down-regulation of NS gene expression, the apoptosis of U266 cells increased (P<0.05).

Conclusion: The abnormal high expression of NS and PD-L1 genes exists in U266 cells, moreover, the down-regulation of PD-L1 and the related PISK/AKT/mTOR pathway gene expression appears after down-regulation of NS gene expression, which suggest that the cell biological changes resulted from above-mentioned results, show a synergestic effect on U266 cells.

题目: 骨髓瘤U266细胞中核干细胞因子NS与程序性细胞死亡配体PD-L1关联性的研究.

目的: 探讨骨髓瘤U266细胞内Nucleostemin(NS)基因和程序性死亡配体-1(programmed death-ligand-1,PD-L1)的关联性以及NS表达下调对骨髓瘤细胞的凋亡影响,评价NS、PD-L1关联性与MM细胞生物学行为改变的关系以及二者联合作为反映MM肿瘤细胞状态标志物的可行性.

方法: 通过NS-RNAi-GV248重组慢病毒下调U266细胞的NS基因表达;采用real-time PCR检测转染后NS、 PD-L1及相关PI3K/AKT/mTOR通路基因变化;应用Western blot、流式细胞术检测NS及PD-L1蛋白表达;采用Annexin V-APC /7-AAD 双染法检测敲除NS基因前后的U266细胞的凋亡变化.

结果: 在MOI=10条件下,NS-RNAi-GV248重组慢病毒转染U266细胞后,荧光显微镜下观察显示,转染效率达到75%以上;real-time PCR显示,与阴性对照组(1.002±0.026)相比,转染组(0.415±0.089)的NS、PD-L1及PI3K/AKT/mTOR基因的mRNA相对表达量明显减低(P<0.05);流式细胞术和Western blot结果表明,慢病毒转染后PD-L1蛋白表达量明显下调,U266细胞凋亡增加(P<0.05).

结论: 骨髓瘤细胞U266中存在NS及PD-L1基因的异常高表达。下调NS基因表达后出现PD-L1基因及相关PI3K/AKT/mTOR通路基因表达的下调,说明二者引起的细胞生物学改变存在联动效应.

MeSH terms

  • Apoptosis
  • B7-H1 Antigen
  • Cell Line, Tumor
  • Humans
  • Multiple Myeloma*
  • Phosphatidylinositol 3-Kinases

Substances

  • B7-H1 Antigen
  • CD274 protein, human