The Role of Wnt Signalling in Chronic Kidney Disease (CKD)

Genes (Basel). 2020 Apr 30;11(5):496. doi: 10.3390/genes11050496.

Abstract

Chronic kidney disease (CKD) encompasses a group of diverse diseases that are associated with accumulating kidney damage and a decline in glomerular filtration rate (GFR). These conditions can be of an acquired or genetic nature and, in many cases, interactions between genetics and the environment also play a role in disease manifestation and severity. In this review, we focus on genetically inherited chronic kidney diseases and dissect the links between canonical and non-canonical Wnt signalling, and this umbrella of conditions that result in kidney damage. Most of the current evidence on the role of Wnt signalling in CKD is gathered from studies in polycystic kidney disease (PKD) and nephronophthisis (NPHP) and reveals the involvement of beta-catenin. Nevertheless, recent findings have also linked planar cell polarity (PCP) signalling to CKD, with further studies being required to fully understand the links and molecular mechanisms.

Keywords: Wnt signalling; beta-catenin; nephronophthisis; planar cell polarity signalling; polycystic kidney disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cell Polarity / genetics
  • Glomerular Filtration Rate / genetics
  • Humans
  • Kidney / metabolism
  • Kidney / pathology
  • Polycystic Kidney Diseases / genetics*
  • Polycystic Kidney Diseases / pathology
  • Renal Insufficiency, Chronic / genetics*
  • Renal Insufficiency, Chronic / pathology
  • Wnt Proteins / genetics*
  • Wnt Signaling Pathway / genetics*
  • beta Catenin / genetics

Substances

  • CTNNB1 protein, human
  • Wnt Proteins
  • beta Catenin