Podocyte Pathogenic Bone Morphogenetic Protein-2 Pathway and Immune Cell Behaviors in Primary Membranous Nephropathy.
Anxiang CaiYiwei MengHang ZhouHong CaiXinghua ShaoQin WangYao XuYin ZhouWenyan ZhouLuo-Nan ChenShan MouPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
Primary membranous nephropathy (PMN) is one of the leading causes of end-stage renal disease, and the most frequent cause of massive proteinuria in nondiabetic adults, resulting in fatal complications. However, the underlying pathomechanisms of PMN remain largely unclear. Here, single-cell RNA sequencing is employed to analyze kidney biopsies from eleven PMN patients and seven healthy subjects. Profiling 44 060 cells from patients allowed us to characterize the cellular composition and cell-type-specific gene expression in the PMN kidney. The complement-induced BMP2/pSMAD1/COL4 pathway is identified as the pathogenic pathway in podocytes, bridging two key events, i.e., complement system activation and glomerular basement membrane thickening in PMN. Augmented infiltration and activation of myeloid leukocytes and B lymphocytes are found, profiling delicate crosstalk of immune cells in PMN kidneys. Overall, these results provide valuable insights into the roles of podocytes and immune cells in PMN, and comprehensive resources toward the complete understanding of PMN pathophysiology.
Keyphrases
- end stage renal disease
- chronic kidney disease
- peritoneal dialysis
- single cell
- gene expression
- high glucose
- ejection fraction
- newly diagnosed
- rna seq
- dna methylation
- bone marrow
- peripheral blood
- acute myeloid leukemia
- immune response
- risk factors
- mesenchymal stem cells
- high throughput
- endothelial cells
- oxidative stress
- patient reported