Bu Lingyun, He Lingxiao, Wang Xiaoqing, Du Guoqiang, Wu Rongde, Liu Wei
Department of Pediatric Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, 324 Jingwu Road, Jinan, China.
Biochem Genet. 2024 Sep 19. doi: 10.1007/s10528-024-10913-3.
Hirschsprung's disease (HSCR) is the most common developmental disorder of the enteric nervous system and its etiology and pathogenesis remain largely unknown. This study aims to identify the differential proteomic patterns linked to the occurrence and development of Hirschsprung disease in colonic tissues. Biopsies were obtained from the aganglionic colon in human HSCR and the corresponding ganglionic colon segments for direct quantitative determination of the data-independent acquisition (DIA) followed by bioinformatics analysis. The differentially expressed main proteins were confirmed by Western blot and immunostaining. A total of 5832 proteins were identified in human colon tissues. Among them, 97 differentially expressed proteins (DEP) with fold change (FC) > 1.2 were screened, including 18 upregulated proteins and 79 downregulated proteins, and GO and KEGG enrichment analyses were performed on differential proteins. By comparing down-regulated proteins with highly connected protein nodes in the PPI network with those related to intracellular metabolic processes in the above analysis, we identified cellular retinoic acid binding protein 1(CRABP1). Its expression was verified in the aganglionic part of the colon by western blotting in an expanded sample set (P = 0.0031). The immunostaining results revealed that CRABP1 was highly expressed in the myenteric plexus ganglion in ganglionic colons compared to aganglionic segments (P = 0.0004). This study demonstrated the down-regulation of CRABP1 in the aganglionic hindgut of HSCR, which could provide potential markers or promising new candidate actors for the pathogenesis of HSCR.
先天性巨结肠症(HSCR)是最常见的肠道神经系统发育障碍疾病,其病因和发病机制在很大程度上仍不清楚。本研究旨在确定与先天性巨结肠症在结肠组织中的发生和发展相关的差异蛋白质组学模式。从人类HSCR患者的无神经节结肠和相应的有神经节结肠段获取活检组织,用于直接定量测定数据非依赖采集(DIA)数据,随后进行生物信息学分析。通过蛋白质免疫印迹法和免疫染色法对差异表达的主要蛋白质进行验证。在人类结肠组织中总共鉴定出5832种蛋白质。其中,筛选出97种差异表达蛋白(DEP),其变化倍数(FC)>1.2,包括18种上调蛋白和79种下调蛋白,并对差异蛋白进行了基因本体(GO)和京都基因与基因组百科全书(KEGG)富集分析。通过将下调蛋白与蛋白质-蛋白质相互作用(PPI)网络中高度连接的蛋白质节点以及上述分析中与细胞内代谢过程相关的蛋白质节点进行比较,我们鉴定出细胞视黄酸结合蛋白1(CRABP1)。在扩大的样本集中,通过蛋白质免疫印迹法在结肠的无神经节部分验证了其表达(P = 0.0031)。免疫染色结果显示,与无神经节段相比,CRABP1在有神经节结肠的肌间神经丛神经节中高表达(P = 0.0004)。本研究证明了CRABP1在HSCR患者无神经节后肠中的下调,这可能为HSCR的发病机制提供潜在的标志物或有前景的新候选因子。