Department of Hepatobiliary Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Department of Emergency Medicine, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
BMC Immunol. 2023 Dec 6;24(1):50. doi: 10.1186/s12865-023-00588-7.
Screening of lysosome-related genes in sepsis patients to provide direction for lysosome-targeted therapy.
Peripheral blood samples were obtained from 22 patients diagnosed with sepsis and 10 normal controls for the purpose of RNA sequencing and subsequent analysis of differential gene expression. Concurrently, lysosome-related genes were acquired from the Gene Ontology database. The intersecting genes between the differential genes and lysosome-related genes were then subjected to PPI, GO and KEGG analyses. Core genes were identified through survival analysis, and their expression trends in different groups were determined using meta-analysis. Single-cell RNA sequencing was used to clarify the cellular localization of core genes.
The intersection of 1328 sepsis-differential genes with 878 lysosome-related genes yielded 76 genes. PPI analysis showed that intersecting genes were mainly involved in Cellular process, Response to stimulus, Immune system process, Signal transduction, Lysosome. GO and KEGG analysis showed that intersecting genes were mainly involved in leukocyte mediated immunity, cell activation involved in immune response, lytic vacuole, lysosome. Survival analysis screened four genes positively correlated with sepsis prognosis, namely GNLY, GZMB, PRF1 and RASGRP1. The meta-analysis revealed that the expression levels of these four genes were significantly higher in the normal control group compared to the sepsis group, which aligns with the findings from RNA sequencing data. Furthermore, single-cell RNA sequencing demonstrated that T cells and NK cells exhibited high expression levels of GNLY, GZMB, PRF1, and RASGRP1.
GNLY, GZMB, PRF1, and RASGRP1, which are lysosome-related genes, are closely linked to the prognosis of sepsis and could potentially serve as novel research targets for sepsis, offering valuable insights for the development of lysosome-targeted therapy. The clinical trial registration number is ChiCTR1900021261, and the registration date is February 4, 2019.
筛选脓毒症患者的溶酶体相关基因,为溶酶体靶向治疗提供方向。
采集 22 例脓毒症患者和 10 例正常对照者的外周血样本,进行 RNA 测序和差异基因表达分析。同时,从基因本体数据库中获取溶酶体相关基因。对差异基因与溶酶体相关基因的交集基因进行 PPI、GO 和 KEGG 分析。通过生存分析确定核心基因,并通过荟萃分析确定不同组间的表达趋势。单细胞 RNA 测序用于阐明核心基因的细胞定位。
1328 个脓毒症差异基因与 878 个溶酶体相关基因的交集有 76 个基因。PPI 分析显示,交集基因主要参与细胞过程、对刺激的反应、免疫系统过程、信号转导、溶酶体。GO 和 KEGG 分析显示,交集基因主要参与白细胞介导的免疫、细胞激活参与免疫反应、裂解液泡、溶酶体。生存分析筛选出 4 个与脓毒症预后呈正相关的基因,即 GNLY、GZMB、PRF1 和 RASGRP1。荟萃分析显示,这 4 个基因在正常对照组中的表达水平明显高于脓毒症组,与 RNA 测序数据一致。此外,单细胞 RNA 测序显示,T 细胞和 NK 细胞中 GNLY、GZMB、PRF1 和 RASGRP1 的表达水平较高。
GNLY、GZMB、PRF1 和 RASGRP1 是与脓毒症预后密切相关的溶酶体相关基因,可能成为脓毒症的新研究靶点,为溶酶体靶向治疗的发展提供有价值的见解。临床试验注册号为 ChiCTR1900021261,注册日期为 2019 年 2 月 4 日。