Department of Nephrology, The Second Hospital of Jilin University, Changchun, China.
Department of Gynaecology and Obstetrics, The Second Hospital of Jilin University, Changchun, China.
Nephrology (Carlton). 2021 May;26(5):432-441. doi: 10.1111/nep.13855. Epub 2021 Feb 11.
Immunoglobulin A nephropathy (IgAN) is the most common primary glomerular disease to cause end-stage kidney disease. This study investigated the difference in urinary exosomal circular RNA (circRNA) expression profiles between patients with IgAN and healthy controls (HCs), for better understanding of gene regulation in exosomes of IgAN patients.
A pairwise comparison of urinary circRNA expression profiles between IgAN patients and HCs was performed using methods, including high-throughput sequencing and quantitative polymerase chain reaction. Moreover, the potential functions of differentially expressed circRNAs (DECs) in IgAN were investigated by gene ontology (GO) enrichment analysis; Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis; and the circRNA-miRNA-mRNA network.
We identified 450 upregulated and 26 downregulated circRNAs in the IgAN patients. GO analysis showed that these enriched circRNAs might regulate primary miRNA processing, the ability of angiotensin receptor binding, and stress fibre function. KEGG analysis suggested these DECs may be closely associated with the phosphoinositide-3-kinase-protein kinase B/Akt (PI3K-Akt) signalling pathways. Network analysis revealed the relationship between circRNAs and their target genes.
The identified DECs may be useful for both researches on molecular aetiology of IgAN and development of potentially novel non-invasive biomarkers of IgAN.
免疫球蛋白 A 肾病(IgAN)是导致终末期肾病的最常见原发性肾小球疾病。本研究旨在探讨 IgAN 患者和健康对照(HCs)尿液外泌体环状 RNA(circRNA)表达谱的差异,以更好地了解 IgAN 患者外泌体中的基因调控。
采用高通量测序和实时定量聚合酶链反应等方法,对 IgAN 患者和 HCs 的尿液 circRNA 表达谱进行配对比较。此外,通过基因本体(GO)富集分析、京都基因与基因组百科全书(KEGG)分析和 circRNA-miRNA-mRNA 网络,探讨差异表达 circRNAs(DECs)在 IgAN 中的潜在功能。
我们在 IgAN 患者中鉴定出 450 个上调和 26 个下调的 circRNAs。GO 分析表明,这些富集的 circRNAs 可能调节初级 miRNA 加工、血管紧张素受体结合能力和应激纤维功能。KEGG 分析提示这些 DECs 可能与磷酸肌醇-3-激酶蛋白激酶 B/Akt(PI3K-Akt)信号通路密切相关。网络分析揭示了 circRNAs 与其靶基因之间的关系。
鉴定出的 DECs 可能有助于研究 IgAN 的分子发病机制,并开发潜在的新型 IgAN 非侵入性生物标志物。