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Updated: Oct 6, 2025

Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
Exploring the Differences in Molecular Mechanisms and Key Biomarkers Between Membranous Nephropathy and Lupus
Zhaocheng Dong1,2, Haoran Dai3, Wenbin Liu4
1Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
This study reveals key gene expression differences between membranous nephropathy (MN) and lupus nephritis (LN), identifying potential biomarkers and offering insights into their distinct molecular mechanisms for improved disease modeling.
Area of Science:
- Nephrology
- Immunology
- Genomics
Background:
- Membranous nephropathy (MN) and lupus nephritis (LN) are autoimmune kidney diseases with overlapping pathogenesis.
- Understanding the molecular distinctions between MN and LN is crucial for accurate diagnosis and treatment.
- Current knowledge on the interrelationship and specific molecular mechanisms differentiating MN and LN remains incomplete.
Purpose of the Study:
- To investigate the differences in molecular mechanisms between MN and LN.
- To identify key differentially expressed genes (DEGs) and potential biomarkers distinguishing MN from LN.
- To provide insights for developing more accurate animal models of MN.
Main Methods:
- Downloaded gene expression profiles from the GEO database (GSE99325, GSE99339, GSE104948, GSE104954).
- Identified differentially expressed genes (DEGs) in MN and LN kidney samples.
- Utilized Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis, protein-protein interaction (PPI) network construction (Metascape), DEG filtering (NetworkAnalyst), and receiver operating characteristic (ROC) analysis.
Main Results:
- Identified 14 up-regulated and 77 down-regulated DEGs in MN glomeruli compared to LN.
- Found 21 down-regulated DEGs in MN renal tubules compared to LN, with no up-regulated genes.
- Screened six key genes (IFI6, MX1, XAF1, HERC6, IFI44L, IFI44) and observed significantly higher NELL1 expression in MN glomeruli versus LN.
Conclusions:
- The study highlights significant differences in gene expression profiles between MN and LN.
- Identified potential key biomarkers that may aid in differentiating these autoimmune kidney diseases.
- Findings offer novel insights into the pathogenesis of MN and LN, supporting the development of improved MN animal models.
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