Davodian Abdollah, Foroughi Kobra, Atashi Amir, Soleiman Masoud
Department of Hematology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Department of Medical Biotechnology, School of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran.
Rep Biochem Mol Biol. 2022 Oct;11(3):440-449. doi: 10.52547/rbmb.11.3.440.
MicroRNA is a form of non-coding RNAs that able to regulate gene expression. miR-424 is one of the members of the regulatory family, which plays an important role in the proliferation and differentiation of myeloid cells. Epigenetic changes can change the level of miR-424 under environmental factors. Therefore, the level of expression of miR-424 in U937 cells of the myeloid line was evaluated in this research under the influence of vitamin D3 (VitD3) and retinoic acid (RA).
In this study, U937 cells were cultured in the presence of VitD3, and RA to evaluate cell proliferation, viability via the trypan blue exclusion test, and expression level of miR-424 by real-time PCR at specific times.
Cell proliferation has shown a significant decrease in the RA group versus other groups during incubation times (P < 0.05). In VitD3 group, there was a significant increase in cell proliferation after 24- and 48-hours incubation periods versus other groups. In the VitD3 and RA groups, the increase of cell proliferation caused the downregulation of miR-424. In addition, the upregulation of VitD3 group and downregulation of the RA group were significant versus the control group (P < 0.05).
We concluded that the expression level of miR-424 was critically affected in the dose- and time-dependent of RA and VitD3 treatment in the U937 cell line. Treatment with VitD3 decreased the expression of miR-424 and RA treatment increase miR-424 expression level in physiological doses.
微小RNA是一种能够调节基因表达的非编码RNA形式。miR - 424是调控家族的成员之一,在髓系细胞的增殖和分化中起重要作用。表观遗传变化可在环境因素作用下改变miR - 424的水平。因此,本研究在维生素D3(VitD3)和视黄酸(RA)的影响下,评估了miR - 424在髓系U937细胞中的表达水平。
在本研究中,将U937细胞在VitD3和RA存在的情况下进行培养,通过台盼蓝排斥试验评估细胞增殖、活力,并在特定时间通过实时PCR评估miR - 424的表达水平。
在培养期间,RA组的细胞增殖与其他组相比显著降低(P < 0.05)。在VitD3组中,培养24小时和48小时后细胞增殖与其他组相比显著增加。在VitD3和RA组中,细胞增殖的增加导致miR - 424的下调。此外,VitD3组的上调和RA组的下调与对照组相比具有显著性(P < 0.05)。
我们得出结论,在U937细胞系中,miR - 424的表达水平在RA和VitD3治疗的剂量和时间依赖性方面受到严重影响。VitD3治疗降低了miR - 424的表达,而RA治疗在生理剂量下增加了miR - 424的表达水平。