Division of Nephrology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Southern Medical University, Guangzhou, China.
Kidney Int. 2017 Jul;92(1):140-153. doi: 10.1016/j.kint.2017.01.010. Epub 2017 Mar 15.
The contribution of DNA methylation to diabetic nephropathy, especially the effect on podocyte integrity, is not clarified. Here we found that albuminuria in a db/db mouse model was markedly attenuated after treatment with a DNA methylation inhibitor. This was accompanied by alleviation of glomerular hypertrophy, mesangial matrix expansion, and podocyte injury. The expression of DNA methyltransferase 1 (Dnmt1), nuclear factor Sp1, and nuclear factor kappa B (NFκB)-p65 markedly increased in podocytes in vivo and in vitro under the diabetic state. The increased expression of Dnmt1 was attenuated after treatment with 5-azacytidine or 5-aza-2'-deoxycytidine or Dnmt1 knockdown, accompanied by restored decreased podocyte slit diaphragm proteins resulting from hypermethylation and improved podocyte motility. Further studies found that increased Sp1 and NFκB-p65 interacted in the nucleus of podocytes incubated with high glucose, and Sp1 bound to the Dnmt1 promoter region. The involvement of the Sp1/NFκB-p65 complex in Dnmt1 regulation was confirmed by the observation that Sp1 knockdown using mithramycin A or siRNA decreased Dnmt1 protein levels. The luciferase reporter assay further indicated that Dnmt1 was a direct target of Sp1. Thus, inhibition of DNA methylation may be a new therapeutic avenue for treating diabetic nephropathy. Hence, the Sp1/NFκB p65-Dnmt1 pathway may be exploited as a therapeutic target for protecting against podocyte injury in diabetic nephropathy.
DNA 甲基化对糖尿病肾病的作用,尤其是对足细胞完整性的影响,尚不清楚。在这里,我们发现,在 db/db 小鼠模型中,用 DNA 甲基化抑制剂治疗后,白蛋白尿明显减轻。这伴随着肾小球肥大、系膜基质扩张和足细胞损伤的缓解。在糖尿病状态下,体内和体外的足细胞中 DNA 甲基转移酶 1(Dnmt1)、核因子 Sp1 和核因子 kappa B(NFκB)-p65 的表达明显增加。在用 5-氮杂胞苷或 5-氮杂-2'-脱氧胞苷或 Dnmt1 敲低治疗后,Dnmt1 的表达增加减弱,伴随着由于过度甲基化而导致的足细胞裂孔蛋白的恢复性减少和足细胞运动性的改善。进一步的研究发现,在高葡萄糖孵育的足细胞中,Sp1 和 NFκB-p65 在核内相互作用,Sp1 结合到 Dnmt1 启动子区域。Sp1 下调使用米托蒽醌 A 或 siRNA 降低 Dnmt1 蛋白水平证实了 Sp1/NFκB-p65 复合物在 Dnmt1 调节中的参与。荧光素酶报告基因分析进一步表明,Dnmt1 是 Sp1 的直接靶标。因此,抑制 DNA 甲基化可能是治疗糖尿病肾病的一种新的治疗途径。因此,Sp1/NFκB p65-Dnmt1 途径可能被用作治疗糖尿病肾病中保护足细胞损伤的治疗靶点。