猪miR-331-3p过表达载体的构建及其对细胞增殖的影响

Construction of miR-331-3p overexpression vector and its effect on cell proliferation

摘要:

本研究旨在阐明猪miR-331-3p对细胞增殖的影响，探讨其对细胞增殖的作用机制首先构建了miR-331-3p的过表达载体pcDNA 3.1 (+)-miR-331-3p，并将将PK15细胞分为4组，分别为实验组、实验组对照组、抑制剂组和抑制剂对照组。实验组和对照组分别转染pcDNA 3.1(+)-miR-331-3p和pcDNA 3.1(+)。抑制剂组和抑制剂对照组分别转染miR-331-3p Inhibitor和miR-331-3p阴性对照(miR-331-3p NC)。通过在各组添加CCK-8试剂绘制细胞增殖曲线，并使用PI染色检测细胞所处周期比例。同时，利用实时荧光定量PCR (Quantitative real-time PCR，qPCR) 检测生长抑制蛋白家族成员5 (Inhibitor of growth family member 5，ING5)、细胞周期蛋白依赖性激酶2 (Cyclin dependent kinase 2，CDK2)、细胞周期蛋白依赖性激酶3 (Cyclin dependent kinase 3，CDK3)、细胞周期蛋白依赖性激酶4 (Cyclin dependent kinase 4，CDK4)、细胞周期蛋白B (Cyclin B) 和细胞周期蛋白依赖性激酶抑制剂1A (Cyclin dependent kinase inhibitor 1A，CDKN1A) 的表达变化。结果表明，实验组miR-331-3p表达量显著升高，细胞增殖曲线表明48 h和72 h时细胞数目均呈现出实验组>实验对照组和抑制剂对照组>抑制剂组的趋势 (P<0.05)。与实验对照组相比，实验组处于G0/G1期的细胞比例下调，S期和G2/M细胞的比例上调，抑制剂对照组趋势与之相反；同时，实验组中与促进增殖的基因CDK2、CDK3、CDK4和Cyclin B的mRNA表达水平均显著升高，而抑制增殖的基因ING5和CDKN1A均表现出显著下降的趋势。本研究成功构建了miR-331-3p过表达载体，且发现miR-331-3p具有促进猪肾上皮细胞增殖的能力，研究结果为深入研究miR-331-3p在猪生长发育中的作用机制奠定了基础。

关键词:miR-331-3p，细胞增殖，过表达载体，PK15，猪

Abstract:

To investigate the effect of miR-331-3p on the proliferation of porcine renal epithelial cells (PK15) and its mechanism, the pcDNA 3.1(+) overexpression vector of miRNA-331-3p (pcDNA 3.1(+)-miR-331-3p) was constructed. PK15 cells were divided into four groups, including experimental group, experimental control group, inhibitor group and inhibitor control group. Experimental group and experimental control group were transfected with pcDNA 3.1(+)-miR-331-3p and pcDNA 3.1(+), respectively. Inhibitor group and inhibitor control group were transfected with miR-331-3p inhibitor and miR-331-3p negative control (miR-331-3p NC), respectively. Above all, CCK-8 reagent was used to plot the cell proliferation curve and Propidium (PI) staining was used to detect the proportion of cell stages. Secondly, its expression change were detected by quantitative real-time PCR that included the growth inhibitory protein family member 5 (ING5), cyclin-dependent kinase 2 (CDK2), cyclin-dependent kinase 3 (CDK3), cyclin-dependent kinase 4 (CDK4), Cyclin B and cyclin-dependent kinase inhibitor 1A (CDKN1A). The results showed that the expression of miRNA-331-3p was significantly increased in the experimental group. The cell proliferation curve showed that the number of cells in experimental group was significantly higher than that in experimental control group or inhibitor control group at 48 h and 72 h (P<0.05). Simultaneously, Inhibitor group was significantly lower than experimental control group or inhibitor control group in the number of cells at 48 h and 72 h (P<0.05), but there was no significant difference between the experimental group and the control group. Compared with the experimental control group, the proportion of cells of experimental group in G0/G1 phase decreased, the proportion of S phase and G2/M phase increased, and the inhibitor control group showed the opposite trend. Simultaneously, the expression levels of CDK2, CDK3, CDK4 and Cyclin B genes in the experimental group were significantly increased, while ING5 and CDKN1A genes inhibiting proliferation showed a significant downward trend. These results demonstrate that the miR-331-3p overexpression vector was successfully constructed, and miR-331-3p has the ability to promote the proliferation of PK15 cells. The study lays a solid foundation for further research for its role in pig growth and development.

Key words:miR-331-3p, cell proliferation, overexpression vector, PK15, pig