Glomerular Endothelial Cell-Derived microRNA-192 Regulates Nephronectin Expression in Idiopathic Membranous Glomerulonephritis

J Am Soc Nephrol. 2021 Nov;32(11):2777-2794. doi: 10.1681/ASN.2020121699.

Abstract

Background: Autoantibodies binding to podocyte antigens cause idiopathic membranous glomerulonephritis (iMGN). However, it remains elusive how autoantibodies reach the subepithelial space because the glomerular filtration barrier (GFB) is size selective and almost impermeable for antibodies.

Methods: Kidney biopsies from patients with iMGN, cell culture, zebrafish, and mouse models were used to investigate the role of nephronectin (NPNT) regulating microRNAs (miRs) for the GFB.

Results: Glomerular endothelial cell (GEC)-derived miR-192-5p and podocyte-derived miR-378a-3p are upregulated in urine and glomeruli of patients with iMGN, whereas glomerular NPNT is reduced. Overexpression of miR-192-5p and morpholino-mediated npnt knockdown induced edema, proteinuria, and podocyte effacement similar to podocyte-derived miR-378a-3p in zebrafish. Structural changes of the glomerular basement membrane (GBM) with increased lucidity, splitting, and lamellation, especially of the lamina rara interna, similar to ultrastructural findings seen in advanced stages of iMGN, were found. IgG-size nanoparticles accumulated in lucidity areas of the lamina rara interna and lamina densa of the GBM in npnt-knockdown zebrafish models. Loss of slit diaphragm proteins and severe structural impairment of the GBM were further confirmed in podocyte-specific Npnt knockout mice. GECs downregulate podocyte NPNT by transfer of miR-192-5p-containing exosomes in a paracrine manner.

Conclusions: Podocyte NPNT is important for proper glomerular filter function and GBM structure and is regulated by GEC-derived miR-192-5p and podocyte-derived miR-378a-3p. We hypothesize that loss of NPNT in the GBM is an important part of the initial pathophysiology of iMGN and enables autoantigenicity of podocyte antigens and subepithelial immune complex deposition in iMGN.

Keywords: glomerular basement membrane; glomerular disease; glomerular endothelial cells; glomerular filtration barrier; membranous nephropathy; microRNAs; nephronectin; podocyte.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen-Antibody Complex / analysis
  • Autoantigens / genetics
  • Autoantigens / immunology
  • Cells, Cultured
  • Coculture Techniques
  • Endothelial Cells / metabolism*
  • Exosomes / metabolism
  • Extracellular Matrix Proteins / biosynthesis*
  • Extracellular Matrix Proteins / deficiency
  • Extracellular Matrix Proteins / physiology
  • Gene Expression Regulation
  • Gene Targeting
  • Glomerular Basement Membrane / immunology
  • Glomerular Basement Membrane / metabolism*
  • Glomerular Basement Membrane / physiopathology*
  • Glomerular Basement Membrane / ultrastructure
  • Glomerulonephritis, Membranous / genetics*
  • Glomerulonephritis, Membranous / immunology
  • Glomerulonephritis, Membranous / metabolism
  • Glomerulonephritis, Membranous / physiopathology
  • Gold Sodium Thiosulfate
  • Humans
  • Kidney Glomerulus / metabolism*
  • Metal Nanoparticles
  • Mice
  • MicroRNAs / biosynthesis
  • MicroRNAs / genetics
  • MicroRNAs / physiology*
  • MicroRNAs / urine
  • Paracrine Communication
  • Permeability
  • Podocytes / immunology
  • Podocytes / metabolism
  • Proteinuria / etiology
  • Transfection
  • Zebrafish
  • Zebrafish Proteins / deficiency
  • Zebrafish Proteins / genetics

Substances

  • Antigen-Antibody Complex
  • Autoantigens
  • Extracellular Matrix Proteins
  • MIRN192 microRNA, human
  • MIRN378 microRNA, human
  • MicroRNAs
  • Zebrafish Proteins
  • nephronectin
  • Gold Sodium Thiosulfate