Endothelial cells require related transcription enhancer factor-1 for cell-cell connections through the induction of gap junction proteins

Arterioscler Thromb Vasc Biol. 2012 Aug;32(8):1951-9. doi: 10.1161/ATVBAHA.112.250159. Epub 2012 May 31.

Abstract

Objective: Capillary network formation represents a specialized endothelial cell function and is a prerequisite to establish a continuous vessel lumen. Formation of endothelial cell connections that form the vascular structure is regulated, at least in part, at the transcriptional level. We report here that related transcription enhancer factor-1 (RTEF-1) plays an important role in vascular structure formation.

Methods and results: Knockdown of RTEF-1 by small interfering RNA or blockage of RTEF-1 function by the transcription enhancer activators domain decreased endothelial connections in a Matrigel assay, whereas overexpression of RTEF-1 in endothelial cells resulted in a significant increase in cell connections and aggregation. In a model of oxygen-induced retinopathy, endothelial-specific RTEF-1 overexpressing mice had enhanced angiogenic sprouting and vascular structure remodeling, resulting in the formation of a denser and more highly interconnected superficial capillary plexus. Mechanistic studies revealed that RTEF-1 induced the expression of functional gap junction proteins including connexin 43, connexin 40, and connexin 37. Blocking connexin 43 function inhibited RTEF-1-induced endothelial cell connections and aggregation.

Conclusions: These findings provide novel insights into the transcriptional control of endothelial function in the coordination of cell-cell connections.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Aggregation
  • Cell Communication*
  • Cells, Cultured
  • Connexin 43 / genetics
  • Connexins / physiology*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • DNA-Binding Proteins / physiology*
  • Endothelial Cells / physiology*
  • Humans
  • Mice
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*
  • Muscle Proteins / physiology*
  • Neovascularization, Physiologic
  • TEA Domain Transcription Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transcription Factors / physiology*

Substances

  • Connexin 43
  • Connexins
  • DNA-Binding Proteins
  • Muscle Proteins
  • TEA Domain Transcription Factors
  • TEAD4 protein, human
  • Tead4 protein, mouse
  • Transcription Factors