Section on Cellular Differentiation, Division of Translational Medicine, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20802, USA.
Section on Developmental Genetics, Division of Translational Medicine, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20802, USA.
Biochim Biophys Acta Mol Basis Dis. 2024 Jan;1870(1):166874. doi: 10.1016/j.bbadis.2023.166874. Epub 2023 Sep 4.
Glycogen storage disease type Ia (GSD-Ia) is caused by a deficiency in the enzyme glucose-6-phosphatase-α (G6Pase-α or G6PC) that is expressed primarily in the gluconeogenic organs, namely liver, kidney cortex, and intestine. Renal G6Pase-α deficiency in GSD-Ia is characterized by impaired gluconeogenesis, nephromegaly due to elevated glycogen accumulation, and nephropathy caused, in part, by renal fibrosis, mediated by activation of the renin-angiotensin system (RAS). The Wnt/β-catenin signaling regulates the expression of a variety of downstream mediators implicated in renal fibrosis, including multiple genes in the RAS. Sustained activation of Wnt/β-catenin signaling is associated with the development and progression of renal fibrotic lesions that can lead to chronic kidney disease. In this study, we examined the molecular mechanism underlying GSD-Ia nephropathy. Damage to the kidney proximal tubules is known to trigger acute kidney injury (AKI) that can, in turn, activate Wnt/β-catenin signaling. We show that GSD-Ia mice have AKI that leads to activation of the Wnt/β-catenin/RAS axis. Renal fibrosis was demonstrated by increased renal levels of Snail1, α-smooth muscle actin (α-SMA), and extracellular matrix proteins, including collagen-Iα1 and collagen-IV. Treating GSD-Ia mice with a CBP/β-catenin inhibitor, ICG-001, significantly decreased nuclear translocated active β-catenin and reduced renal levels of renin, Snail1, α-SMA, and collagen-IV. The results suggest that inhibition of Wnt/β-catenin signaling may be a promising therapeutic strategy for GSD-Ia nephropathy.
糖原贮积病 Ia 型(GSD-Ia)是由葡萄糖-6-磷酸酶-α(G6Pase-α 或 G6PC)缺乏引起的,该酶主要在生糖器官中表达,即肝脏、肾皮质和肠道。GSD-Ia 中的肾脏 G6Pase-α 缺乏的特征是糖异生受损、由于糖原积累而导致的肾肿大、以及部分由肾纤维化引起的肾病,这部分由肾素-血管紧张素系统(RAS)的激活介导。Wnt/β-连环蛋白信号通路调节多种与肾纤维化相关的下游介质的表达,包括 RAS 中的多种基因。Wnt/β-连环蛋白信号通路的持续激活与肾纤维化病变的发展和进展有关,这些病变可能导致慢性肾病。在这项研究中,我们研究了 GSD-Ia 肾病的分子机制。已知肾脏近端小管的损伤会引发急性肾损伤(AKI),进而激活 Wnt/β-连环蛋白信号通路。我们表明,GSD-Ia 小鼠发生 AKI 会导致 Wnt/β-连环蛋白/RAS 轴的激活。肾纤维化通过增加肾脏中 Snail1、α-平滑肌肌动蛋白(α-SMA)和细胞外基质蛋白(包括胶原-Iα1 和胶原-IV)的水平来证明。用 CBP/β-连环蛋白抑制剂 ICG-001 治疗 GSD-Ia 小鼠可显著减少核转位的活性 β-连环蛋白,并降低肾脏中的肾素、Snail1、α-SMA 和胶原-IV 水平。这些结果表明,抑制 Wnt/β-连环蛋白信号通路可能是治疗 GSD-Ia 肾病的一种有前途的治疗策略。