Zhang Kaiping, Fang Xiang, Zhang Ye, Zhang Yin, Chao Min
Department of Urology, Anhui Provincial Children's Hospital/Children's Hospital of Fudan University (Affiliated Anhui Branch), Hefei, 230000, PR China.
Cell Death Discov. 2024 Sep 6;10(1):397. doi: 10.1038/s41420-024-02117-w.
This study aims to uncover the molecular mechanisms underlying pediatric kidney stone formation induced by renal calcium deposition by utilizing high-throughput sequencing data to reveal the regulation of PINK1 by MyoD1. We performed transcriptome sequencing on peripheral blood samples from healthy children and children with kidney stones to obtain differentially expressed genes (DEGs). Genes related to mitochondrial oxidative stress were obtained from the Genecards website and intersected with DEGs to obtain candidate target genes. Additionally, we conducted protein-protein interaction (PPI) analysis using the STRING database to identify core genes involved in pediatric kidney stone disease (KSD) and predicted their transcription factors using the hTFtarget database. We assessed the impact of MyoD1 on the activity of the PINK1 promoter using dual-luciferase reporter assays and investigated the enrichment of MyoD1 on the PINK1 promoter through chromatin immunoprecipitation (ChIP) experiments. To validate our hypothesis, we selected HK-2 cells and established an in vitro kidney stone model induced by calcium oxalate monohydrate (COM). We evaluated the expression levels of various genes, cell viability, volume of adherent crystals in each group, as well as mitochondrial oxidative stress in cells by measuring mitochondrial membrane potential (Δψm), superoxide dismutase (SOD) activity, reactive oxygen species (ROS), and malondialdehyde (MDA) content. Mitochondrial autophagy was assessed using mtDNA fluorescence staining and Western blot analysis of PINK1-related proteins. Apoptosis-related proteins were evaluated using Western blot analysis, and cell apoptosis was measured using flow cytometry. Furthermore, we developed a rat model of KSD and assessed the expression levels of various genes, as well as the pathologic changes in rat renal tissues using H&E and von Kossa staining, transmission electron microscopy (TEM), and the expression of creatinine, blood urea nitrogen, neutrophil gelatinase-associated lipocalin (NGAL), and kidney injury molecule-1 (KIM-1) to evaluate the mitochondrial oxidative stress in vivo (through measurement of Δψm, SOD activity, ROS, and MDA content). Mitochondrial autophagy was evaluated by Western blot analysis of PINK1-associated proteins. Apoptosis-related proteins were detected using Western blot analysis, and cellular apoptosis was examined using cell flow cytometry and TUNEL staining. Bioinformatics analysis revealed that the PINK1 gene is upregulated and vital in pediatric kidney stone patients. Our in vitro and in vivo experiments demonstrated that silencing PINK1 could inhibit kidney stone formation by suppressing mitochondrial oxidative stress both in vitro and in vivo. We identified MyoD1 as an upstream transcription factor of PINK1 that contributes to the occurrence of pediatric kidney stones through the activation of PINK1. Our in vivo and in vitro experiments collectively confirmed that silencing MyoD1 could inhibit mitochondrial oxidative stress, mitochondrial autophagy, and cellular apoptosis in a rat model of kidney stones by downregulating PINK1 expression, consequently suppressing the formation of kidney stones. In this study, we discovered that MyoD1 may promote kidney stone formation and development in pediatric patients by transcriptionally activating PINK1 to induce mitochondrial oxidative stress.
本研究旨在利用高通量测序数据揭示MyoD1对PINK1的调控作用,以探究肾钙沉积诱导小儿肾结石形成的分子机制。我们对健康儿童和肾结石患儿的外周血样本进行转录组测序,以获得差异表达基因(DEG)。从Genecards网站获取与线粒体氧化应激相关的基因,并与DEG进行交集分析,以获得候选靶基因。此外,我们使用STRING数据库进行蛋白质-蛋白质相互作用(PPI)分析,以鉴定小儿肾结石疾病(KSD)中涉及的核心基因,并使用hTFtarget数据库预测其转录因子。我们使用双荧光素酶报告基因检测评估MyoD1对PINK1启动子活性的影响,并通过染色质免疫沉淀(ChIP)实验研究MyoD1在PINK1启动子上的富集情况。为了验证我们的假设,我们选择HK-2细胞并建立了一水合草酸钙(COM)诱导的体外肾结石模型。我们通过测量线粒体膜电位(Δψm)、超氧化物歧化酶(SOD)活性、活性氧(ROS)和丙二醛(MDA)含量,评估了每组中各种基因的表达水平、细胞活力、黏附晶体体积以及细胞中的线粒体氧化应激。使用mtDNA荧光染色和PINK1相关蛋白的蛋白质印迹分析评估线粒体自噬。使用蛋白质印迹分析评估凋亡相关蛋白,并使用流式细胞术测量细胞凋亡。此外,我们建立了KSD大鼠模型,并使用苏木精和伊红(H&E)染色、冯·科萨(von Kossa)染色、透射电子显微镜(TEM)评估各种基因的表达水平以及大鼠肾组织的病理变化,以及肌酐、血尿素氮、中性粒细胞明胶酶相关脂质运载蛋白(NGAL)和肾损伤分子-1(KIM-1)的表达,以评估体内线粒体氧化应激(通过测量Δψm、SOD活性、ROS和MDA含量)。通过PINK1相关蛋白的蛋白质印迹分析评估线粒体自噬。使用蛋白质印迹分析检测凋亡相关蛋白,并使用细胞流式细胞术和TUNEL染色检查细胞凋亡。生物信息学分析表明,PINK1基因在小儿肾结石患者中上调且至关重要。我们的体外和体内实验表明,沉默PINK1可通过抑制体外和体内的线粒体氧化应激来抑制肾结石形成。我们鉴定出MyoD1是PINK1的上游转录因子,其通过激活PINK1促进小儿肾结石的发生。我们的体内和体外实验共同证实,沉默MyoD1可通过下调PINK1表达来抑制肾结石大鼠模型中的线粒体氧化应激、线粒体自噬和细胞凋亡,从而抑制肾结石的形成。在本研究中,我们发现MyoD1可能通过转录激活PINK1诱导线粒体氧化应激,从而促进小儿患者肾结石的形成和发展。