Baicalin alleviates adriamycin-induced focal segmental glomerulosclerosis and proteinuria by inhibiting the Notch1-Snail axis mediated podocyte EMT

Life Sci. 2020 Sep 15:257:118010. doi: 10.1016/j.lfs.2020.118010. Epub 2020 Jun 26.

Abstract

Podocyte injury is an early event and core in the development of focal segmental glomerular sclerosis (FSGS) that induces poor prognosis. Epithelial-mesenchymal transition (EMT) as a response of podocyte to injury leads to podocyte depletion and proteinuria. The abnormally reactivated NOTCH pathway may be involved in podocyte EMT. Baicalin, as a natural flavonoid compound, had significant inhibitory activity on tissue fibrosis and tumor cell invasion. However, its potential role and molecular mechanisms to injured podocyte in FSGS are little known. Here we found that baicalin could inhibit podocyte EMT markers expression and cell migration induced by TGF-β1, accompanied by the up-regulated expression of slit diaphragm (SD) proteins and cell-cell adhesion molecule. Further investigation revealed that EMT inhibition of baicalin on injured podocyte is mainly mediated by the reduction of notch1 activation and its downstream Snail expression. Using the adriamycin-induced FSGS model, we determined that baicalin suppresses the Notch1-Snail axis activation in podocytes, relieves glomerulus structural disruption and dysfunction, and reduces proteinuria. Altogether, these findings suggest that baicalin is a novel renoprotective agent against podocyte EMT in FSGS and indicate its underlying mechanism that involves in negative regulation of the Notch1-Snail axis.

Keywords: Baicalin; EMT; FSGS; Notch1-Snail axis; Podocyte; Proteinuria.

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Cell Line
  • Cell Movement / drug effects
  • Doxorubicin / metabolism
  • Epithelial-Mesenchymal Transition / drug effects
  • Female
  • Flavonoids / metabolism
  • Flavonoids / pharmacology*
  • Glomerulosclerosis, Focal Segmental / drug therapy*
  • Glomerulosclerosis, Focal Segmental / metabolism
  • Kidney Glomerulus / metabolism
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Podocytes / metabolism
  • Proteinuria / drug therapy*
  • Proteinuria / metabolism
  • Receptor, Notch1 / metabolism
  • Snail Family Transcription Factors / metabolism
  • Transforming Growth Factor beta1 / metabolism

Substances

  • Biomarkers
  • Flavonoids
  • Receptor, Notch1
  • Snail Family Transcription Factors
  • Transforming Growth Factor beta1
  • baicalin
  • Doxorubicin