Myocardin and Prx1 contribute to angiotensin II-induced expression of smooth muscle alpha-actin

Circ Res. 2004 Apr 30;94(8):1075-82. doi: 10.1161/01.RES.0000125622.46280.95. Epub 2004 Mar 11.

Abstract

Previous studies demonstrated that angiotensin II (Ang II)-induced hypertrophy of smooth muscle cells (SMCs) was associated with increased transcription of SM alpha-actin gene. The aim of the present study was to determine whether myocardin, a SMC-selective cofactor of serum response factor (SRF), contributed to Ang II-induced increases in SM alpha-actin transcription. Results showed that Ang II increased myocardin mRNA expression as well as SM alpha-actin mRNA expression via the Ang II type 1 receptor in cultured rat aortic SMCs. Cotransfection studies revealed that CArG elements were required for Ang II-induced transcription of SM alpha-actin gene, and a dominant-negative form of myocardin or a short interfering RNA (siRNA) specific for myocardin decreased Ang II-induced SM alpha-actin transcription. Prx1, a homeodomain protein whose expression was increased by Ang II, also increased SM alpha-actin gene transcription in part via CArG elements, and siRNA specific for Prx1 markedly decreased basal and Ang II-induced SM alpha-actin transcription. Electrophoretic mobility shift assay showed that myocardin and Ang II, respectively, increased formation of a SMC-specific CArG-SRF-myocardin higher order complex. However, Ang II had no effect on binding between myocardin and SRF as determined by a mammalian two-hybrid assay, suggesting that Ang II-induced increases in formation of CArG-SRF-myocardin complex was the result of increased SRF binding to CArG elements and increased myocardin expression. Taken together, these results support a model in which Ang II-induced increases in expression of SM alpha-actin are mediated through Prx1-dependent increases in SRF binding to CArG elements and subsequent recruitment of myocardin.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actins / biosynthesis*
  • Actins / genetics
  • Angiotensin II / pharmacology*
  • Animals
  • Aorta
  • Cells, Cultured / drug effects
  • Cells, Cultured / metabolism
  • Gene Expression Regulation / physiology*
  • Genes, Reporter
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / physiology*
  • Hypertrophy
  • Mice
  • Muscle, Smooth, Vascular / drug effects*
  • Muscle, Smooth, Vascular / metabolism
  • Mutagenesis, Site-Directed
  • Nuclear Proteins / genetics
  • Nuclear Proteins / physiology*
  • RNA, Messenger / biosynthesis
  • RNA, Small Interfering / pharmacology
  • Rats
  • Receptor, Angiotensin, Type 1 / drug effects
  • Recombinant Fusion Proteins / physiology
  • Regulatory Sequences, Nucleic Acid
  • Serum Response Factor / physiology
  • Trans-Activators / genetics
  • Trans-Activators / physiology*
  • Transcription, Genetic
  • Two-Hybrid System Techniques

Substances

  • Actins
  • Homeodomain Proteins
  • Nuclear Proteins
  • Prrx1 protein, mouse
  • RNA, Messenger
  • RNA, Small Interfering
  • Receptor, Angiotensin, Type 1
  • Recombinant Fusion Proteins
  • Serum Response Factor
  • Trans-Activators
  • myocardin
  • Angiotensin II