Trichostatin a prevents TGF-beta1-induced apoptosis by inhibiting ERK activation in human renal tubular epithelial cells

Eur J Pharmacol. 2010 Sep 10;642(1-3):28-36. doi: 10.1016/j.ejphar.2010.05.055. Epub 2010 Jun 8.

Abstract

Histone deacetylase (HDAC) inhibitors have recently been reported to have possible reno-protective effects in the last few years. In this study, we found that tricostatin A (TSA), an HDAC inhibitor, prevented transforming growth factor beta1 (TGF-beta1)-induced apoptosis in cultured human renal proximal tubular epithelial cells (RPTECs). TGF-beta1-induced apoptosis via the activation of both caspase-8 and caspase-9 but did not activate the Fas receptor and did not alter Bcl-2 or Bax protein expression. TSA prevented TGF-beta1-induced apoptosis and the activation of caspase-8 and caspase-9 in RPTECs but did not inhibit the TGF-beta1-induced phosphorylation of Smad3 and p38 mitogen-activated protein kinase (MAPK). However, TSA inhibited the TGF-beta1-induced phosphorylation of extracellular signal regulated kinase (ERK), and the MAPK/ERK kinase inhibitor U0126, which specifically inhibits ERK, also prevented TGF-beta1-induced apoptosis. Our results show, for the first time, that TSA inhibits TGF-beta1-induced ERK activation and overrides pro-apoptotic signals like Smad3 and p38 in human RPTECs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Caspase 8 / metabolism
  • Caspase 9 / metabolism
  • Enzyme Activation / drug effects
  • Epithelial Cells / cytology*
  • Epithelial Cells / drug effects*
  • Epithelial Cells / enzymology
  • Epithelial Cells / metabolism
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • Humans
  • Hydroxamic Acids / pharmacology*
  • Kidney Tubules / cytology*
  • MAP Kinase Signaling System / drug effects
  • Smad3 Protein / metabolism
  • Transforming Growth Factor beta1 / pharmacology*
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Hydroxamic Acids
  • Smad3 Protein
  • Transforming Growth Factor beta1
  • trichostatin A
  • Extracellular Signal-Regulated MAP Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Caspase 8
  • Caspase 9