Interferon regulatory factors regulate interleukin-1beta-converting enzyme expression and apoptosis in vascular smooth muscle cells

Hypertension. 1999 Jan;33(1):162-6. doi: 10.1161/01.hyp.33.1.162.

Abstract

-Apoptosis has been reported to play a pivotal role in vascular remodeling. However, cellular mechanisms of apoptosis in vascular smooth muscle cells (VSMCs) have not been well defined. In this study, we focused on interleukin-1beta-converting enzyme (ICE), a key protease in the induction of apoptosis in lymphocytes and fibroblasts. We observed an increase in ICE mRNA expression in rat aortic VSMCs after serum depletion, with a peak at 12 hours and then a gradual decline. This was associated with DNA fragmentation, a hallmark of apoptosis and morphological changes of apoptosis. Treatment of these VSMCs with the ICE inhibitor N-(N-acetyl-tyrosinyl-valinyl-alaninyl)-3-amino-4-oxob utanoic acid (YVAD-CHO) attenuated DNA fragmentation. The increased ICE mRNA expression was preceded by an increase in the mRNA expression of interferon regulatory factor (IRF)-1, peaking at 6 hours after serum removal, and a rapid but transient decrease in IRF-2 mRNA expression, reaching a nadir at 3 hours after serum depletion. To demonstrate that these reciprocal changes in IRF-1 and IRF-2 regulated ICE expression and induced apoptosis, we transfected antisense oligonucleotides for IRF-1 and IRF-2 into VSMCs and examined ICE mRNA expression and apoptotic changes. IRF-1 antisense pretreatment attenuated the increase in ICE expression and reduced apoptotic changes, whereas IRF-2 antisense treatment increased ICE mRNA expression and enhanced apoptotic changes. Taken together, our results suggest that serum growth factor depletion in VSMCs upregulates IRF-1 and downregulates IRF-2, thereby increasing ICE expression and inducing apoptosis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Aorta / cytology
  • Apoptosis*
  • Base Sequence
  • Blotting, Northern
  • Caspase 1 / genetics*
  • Caspase Inhibitors
  • Cells, Cultured
  • DNA Fragmentation
  • DNA-Binding Proteins / physiology*
  • Down-Regulation
  • Growth Substances / blood
  • Immunoblotting
  • Interferon Regulatory Factor-1
  • Interferon-gamma / genetics
  • Interferon-gamma / physiology*
  • Molecular Sequence Data
  • Muscle, Smooth, Vascular / cytology
  • Muscle, Smooth, Vascular / metabolism
  • Oligonucleotides, Antisense / genetics
  • Phosphoproteins / physiology*
  • RNA, Messenger / analysis
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors
  • Transcription Factors / physiology*
  • Transfection / genetics
  • Up-Regulation

Substances

  • Caspase Inhibitors
  • DNA-Binding Proteins
  • Growth Substances
  • Interferon Regulatory Factor-1
  • Irf1 protein, rat
  • Oligonucleotides, Antisense
  • Phosphoproteins
  • RNA, Messenger
  • Transcription Factors
  • Interferon-gamma
  • Caspase 1