Ischemic injury to kidney induces glomerular podocyte effacement and dissociation of slit diaphragm proteins Neph1 and ZO-1

J Biol Chem. 2008 Dec 19;283(51):35579-89. doi: 10.1074/jbc.M805507200. Epub 2008 Oct 14.

Abstract

Glomerular injury is often characterized by the effacement of podocytes, loss of slit diaphragms, and proteinuria. Renal ischemia or the loss of blood flow to the kidneys has been widely associated with tubular and endothelial injury but rarely has been shown to induce podocyte damage and disruption of the slit diaphragm. In this study, we have used an in vivo rat ischemic model to demonstrate that renal ischemia induces podocyte effacement with loss of slit diaphragm and proteinuria. Biochemical analysis of the ischemic glomerulus shows that ischemia induces rapid loss of interaction between slit diaphragm junctional proteins Neph1 and ZO-1. To further understand the effect of ischemia on molecular interactions between slit diaphragm proteins, a cell culture model was employed to study the binding between Neph1 and ZO-1. Under physiologic conditions, Neph1 co-localized with ZO-1 at cell-cell contacts in cultured human podocytes. Induction of injury by ATP depletion resulted in rapid loss of Neph1 and ZO-1 binding and redistribution of Neph1 and ZO-1 proteins from cell membrane to the cytoplasm. Recovery resulted in increased Neph1 tyrosine phosphorylation, restoring Neph1 and ZO-1 binding and their localization at the cell membrane. We further demonstrate that tyrosine phosphorylation of Neph1 mediated by Fyn results in significantly increased Neph1 and ZO-1 binding, suggesting a critical role for Neph1 tyrosine phosphorylation in reorganizing the Neph1-ZO-1 complex. This study documents that renal ischemia induces dynamic changes in the molecular interactions between slit diaphragm proteins, leading to podocyte damage and proteinuria.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Membrane / metabolism
  • Disease Models, Animal
  • Humans
  • Ischemia / metabolism*
  • Kidney Diseases / metabolism*
  • Male
  • Membrane Proteins / metabolism*
  • Multiprotein Complexes / metabolism*
  • Phosphoproteins / metabolism*
  • Phosphorylation
  • Podocytes / metabolism*
  • Podocytes / pathology
  • Protein Binding
  • Proteinuria / metabolism
  • Proto-Oncogene Proteins c-fyn / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Zonula Occludens-1 Protein

Substances

  • KIRREL1 protein, human
  • Kirrel1 protein, rat
  • Membrane Proteins
  • Multiprotein Complexes
  • Phosphoproteins
  • TJP1 protein, human
  • Tjp1 protein, rat
  • Zonula Occludens-1 Protein
  • FYN protein, human
  • Fyn protein, rat
  • Proto-Oncogene Proteins c-fyn