Department of Nephrology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Biosci Rep. 2018 Nov 13;38(6). doi: 10.1042/BSR20181578. Print 2018 Dec 21.
Megalin is essential for proximal tubule reabsorption of filtered proteins, hormones, and vitamins, and its dysfunction has been reported in IgA nephropathy (IgAN). miR-148b has been shown to regulate renal megalin expression and in animal models of kidney disease. We examined a potential role of miR-148b and other miRNAs in regulating megalin expression in IgAN by analyzing the association between megalin and miR-148b, miR-21, miR-146a, and miR-192 expression. Quantitative PCR (qPCR) analysis identified a marked increase in renal levels of several miRNAs, including miR-148b, miR-21, miR-146a, and a significant decrease in mRNA levels in IgAN patients when compared with normal controls. By multiple linear regression analysis, however, only renal miR-148b was independently associated with megalin mRNA levels in IgAN. Proximal tubule megalin expression was further evaluated by immunofluorescence labeling of biopsies from the patients. The megalin expression was significantly lower in patients with highest levels of renal miR-148b compared with patients with lowest levels. To examine the direct effects of the miRNAs on megalin and other membrane proteins expression, proximal tubule LLC-PK1 cells were transfected with miR-148b, miR-21, miR-146a, or miR-192 mimics. Transfection with miR-148b mimic, but not the other three miRNA mimics inhibited endogenous megalin mRNA expression. No significant effect of any of the four miRNA mimics was observed on cubilin or aquaporin 1 (AQP1) mRNA expression. The findings suggest that miR-148b negatively regulates megalin expression in IgAN, which may affect renal uptake and metabolism of essential substances.
巨胞饮蛋白是近端肾小管重吸收滤过蛋白、激素和维生素所必需的,其功能障碍已在 IgA 肾病(IgAN)中报道。miR-148b 已被证明可调节肾脏巨胞饮蛋白的表达,并在肾脏病动物模型中发挥作用。我们通过分析巨胞饮蛋白与 miR-148b、miR-21、miR-146a 和 miR-192 表达之间的关联,研究了 miR-148b 和其他 miRNA 在调节 IgAN 中巨胞饮蛋白表达的潜在作用。定量 PCR(qPCR)分析确定了几种 miRNA(包括 miR-148b、miR-21、miR-146a 和 miR-192)在 IgAN 患者肾组织中的水平显著升高,而与正常对照组相比,这些 miRNA 的水平显著升高。然而,通过多元线性回归分析,只有肾组织中的 miR-148b 与 IgAN 患者的 megalin mRNA 水平独立相关。通过对患者活检标本的免疫荧光标记进一步评估近端肾小管 megalin 表达。与最低 miR-148b 水平的患者相比,最高 miR-148b 水平的患者的 megalin 表达显著降低。为了研究这些 miRNA 对 megalin 和其他膜蛋白表达的直接影响,用 miR-148b、miR-21、miR-146a 或 miR-192 模拟物转染近端肾小管 LLC-PK1 细胞。转染 miR-148b 模拟物,但不是其他三种 miRNA 模拟物,可抑制内源性 megalin mRNA 表达。这四种 miRNA 模拟物中的任何一种对 cubilin 或水通道蛋白 1(AQP1)mRNA 表达均无显著影响。这些发现表明,miR-148b 在 IgAN 中负调节 megalin 表达,这可能影响肾脏对必需物质的摄取和代谢。