Prohibitin Signaling at the Kidney Filtration Barrier

Adv Exp Med Biol. 2017:982:563-575. doi: 10.1007/978-3-319-55330-6_29.

Abstract

The kidney filtration barrier consists of three well-defined anatomic layers comprising a fenestrated endothelium, the glomerular basement membrane (GBM) and glomerular epithelial cells, the podocytes. Podocytes are post-mitotic and terminally differentiated cells with primary and secondary processes. The latter are connected by a unique cell-cell contact, the slit diaphragm. Podocytes maintain the GBM and seal the kidney filtration barrier to prevent the onset of proteinuria. Loss of prohibitin-1/2 (PHB1/2) in podocytes results not only in a disturbed mitochondrial structure but also in an increased insulin/IGF-1 signaling leading to mTOR activation and a detrimental metabolic switch. As a consequence, PHB-knockout podocytes develop proteinuria and glomerulosclerosis and eventually loss of renal function. In addition, experimental evidence suggests that PHB1/2 confer additional, extra-mitochondrial functions in podocytes as they localize to the slit diaphragm and thereby stabilize the unique intercellular contact between podocytes required to maintain an effective filtration barrier.

Keywords: Insulin; Kidney filtration barrier; Podocyte; Slit diaphragm.

Publication types

  • Review

MeSH terms

  • Animals
  • Energy Metabolism*
  • Glomerular Filtration Barrier / metabolism*
  • Glomerular Filtration Barrier / pathology
  • Glomerular Filtration Barrier / physiopathology
  • Glomerular Filtration Rate*
  • Humans
  • Kidney Diseases / metabolism
  • Kidney Diseases / pathology
  • Kidney Diseases / physiopathology
  • Mitochondria / metabolism*
  • Mitochondria / pathology
  • Podocytes / metabolism
  • Podocytes / pathology
  • Prohibitins
  • Repressor Proteins / metabolism*
  • Signal Transduction*

Substances

  • PHB protein, human
  • Prohibitins
  • Repressor Proteins