Department of Laboratory Sciences, Faculty of Paramedicine, Yasuj University of Medical Sciences, Yasuj, Iran.
Department of Biochemistry, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
J Endocrinol Invest. 2018 May;41(5):557-566. doi: 10.1007/s40618-017-0766-z. Epub 2017 Oct 22.
Previous reports have demonstrated that genetic variations in microRNAs regulome could affect microRNAs-mediated regulation. Therefore, in the present study we were aimed at (1) comparison of microRNA 146-a (miR-146a) peripheral blood mononuclear cells (PBMCs) and plasma levels between diabetic patients and controls, and (2) investigating the possible association of rs2910164 with miR-146a and its related target genes expression and also serum cytokine levels.
The study population consisted of 60 subjects including 30 type 2 diabetes (T2D) patients and 30 controls with determined genotypes for rs2910164. The RNA expression levels were determined by real-time PCR. Moreover, TNF-α, IL-6, IL-10 and IL-1β serum levels were measured using ELISA method.
Our results showed that the miR-146a expression levels were significantly decreased in PBMCs (P = 0.004) and plasma (P = 0.008) samples of patients with T2D compared to healthy participants. In addition, we observed that IRAK1 mRNA expression-but not TLR4, TRAF6 and NFĸB-was significantly increased in patients with T2D compared to controls (P = 0.028). The relative expression levels of miR-146a in plasma and PBMCs samples of diabetic patients with the rs2910164 GG genotypes were significantly higher than that in CC (P < 0.05). Moreover, no significant differences were found in miR-146a targets and cytokine levels between the rs2910164 different genotypes.
Our study demonstrated that miR-146a circulating levels were significantly elevated in controls compared with T2D patients. In addition, we identified that rs2910164-C allele is associated with reduced expression levels of the miR-146a but not its mRNAs targets and cytokine levels in diabetic patients.
先前的报告表明,miRNA 调控组中的遗传变异可能会影响 miRNA 介导的调节。因此,在本研究中,我们旨在:(1)比较糖尿病患者和对照组外周血单核细胞(PBMC)和血浆中 miRNA146-a(miR-146a)的水平,以及(2)研究 rs2910164 与 miR-146a 及其相关靶基因表达的可能关联,以及血清细胞因子水平。
研究人群包括 60 名受试者,包括 30 名 2 型糖尿病(T2D)患者和 30 名确定 rs2910164 基因型的对照。通过实时 PCR 测定 RNA 表达水平。此外,使用 ELISA 法测量 TNF-α、IL-6、IL-10 和 IL-1β 血清水平。
我们的结果表明,与健康参与者相比,T2D 患者的 PBMC(P=0.004)和血浆(P=0.008)样本中的 miR-146a 表达水平显著降低。此外,我们观察到与对照组相比,T2D 患者 IRAK1 mRNA 表达(但不是 TLR4、TRAF6 和 NFκB)显著增加(P=0.028)。与 CC 相比,糖尿病患者 rs2910164 GG 基因型的血浆和 PBMC 样本中的 miR-146a 相对表达水平显著升高(P<0.05)。此外,rs2910164 不同基因型之间的 miR-146a 靶标和细胞因子水平没有差异。
我们的研究表明,与 T2D 患者相比,miR-146a 的循环水平在对照组中显著升高。此外,我们发现 rs2910164-C 等位基因与糖尿病患者 miR-146a 的表达水平降低有关,但与 miR-146a 的 mRNAs 靶标和细胞因子水平无关。