Department of Nephrology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Eur Rev Med Pharmacol Sci. 2018 Aug;22(16):5082-5090. doi: 10.26355/eurrev_201808_15701.
The aim of this study was to elaborate the influence of changing energy metabolism pattern of renal tubular epithelial cells in the process of renal interstitial fibrosis on podocytes. Meanwhile, we also investigated the relationship between energy metabolism pattern and the development of renal interstitial fibrosis.
We established a model of renal interstitial fibrosis by unilateral ureteral obstruction (UUO). The protein and messenger RNA (mRNA) expression of fibrosis signs, such as α-smooth muscle actin (α-SMA) and fibronectin (FN) were detected. We also measured the protein and mRNA expression of key glycolytic enzymes, including pyruvate kinase muscle isozyme 2 (PKM2) and human glandular kallikrein 2 (HK2). The proliferation and differentiation of podocytes during fibrosis were observed by monitoring the expression of nephrin and myocardin. In vitro experiments, primary podocytes were extracted, cultured, and stimulated with lactate. Then the alterations during the process were observed. Finally, PKM2 expression was inhibited by intravenous infusion of the plasmid. The link between the expression of marker protein as well as differentiation protein in podocytes and renal interstitial fibrosis was analyzed.
During the process of renal interstitial fibrosis, phenotypic changes and enhanced expression of fibrosis and proliferation markers were found in fibroblasts. Meanwhile, in renal tubular epithelial cells, increased expression of key enzymes of glycolysis, the level of glycolysis as well as lactate metabolites cooperatively led to hypoxic and acidic environment, eventually inhibiting the proliferation and differentiation of podocytes and aggravating fibrosis. When the level of glycolysis in renal tubular epithelial cells was reduced, the number and function of podocytes were partially restored, and renal interstitial fibrosis was alleviated.
During renal interstitial fibrosis, glycolysis of renal tubular epithelial cell was increased, leading to the recodification of energy metabolism. This process affected the number and function of podocytes and aggravated renal interstitial fibrosis.
本研究旨在阐述肾小管上皮细胞能量代谢模式改变在肾间质纤维化过程中对足细胞的影响。同时,我们还研究了能量代谢模式与肾间质纤维化发展之间的关系。
通过单侧输尿管梗阻(UUO)建立肾间质纤维化模型。检测纤维化标志物如α-平滑肌肌动蛋白(α-SMA)和纤维连接蛋白(FN)的蛋白和信使 RNA(mRNA)表达。还测量了糖酵解关键酶,包括丙酮酸激酶肌肉同工酶 2(PKM2)和人腺激肽 2(HK2)的蛋白和 mRNA 表达。通过监测nephrin 和 myocardin 的表达来观察纤维化过程中足细胞的增殖和分化。在体外实验中,提取、培养原代足细胞,并通过乳酸刺激,观察其过程中的变化。最后,通过静脉输注质粒抑制 PKM2 表达。分析足细胞标志物蛋白和分化蛋白与肾间质纤维化之间的联系。
在肾间质纤维化过程中,成纤维细胞中观察到表型变化和纤维化及增殖标志物的表达增强。同时,在肾小管上皮细胞中,糖酵解关键酶的表达增加,糖酵解水平以及乳酸代谢物共同导致缺氧和酸性环境,最终抑制足细胞的增殖和分化,加重纤维化。当肾小管上皮细胞的糖酵解水平降低时,足细胞的数量和功能部分恢复,肾间质纤维化减轻。
在肾间质纤维化过程中,肾小管上皮细胞的糖酵解增加,导致能量代谢重新编码。这一过程影响了足细胞的数量和功能,加重了肾间质纤维化。