Disruption of cell spreading by the activation of MEK/ERK pathway is dependent on AP-1 activity

Nagoya J Med Sci. 2010 Aug;72(3-4):139-44.

Abstract

We previously reported that the disruption of cell spreading by v-Crk was dependent on the activation of the MEK/ERK pathway. Here we demonstrate that the activation of that pathway is sufficient to suppress cell spreading. The MEK/ERK pathway regulates the activity of various proteins including AP-1, which is a transcriptional factor composed of heterodimeric proteins. To examine whether AP-1 activity is required for the suppression of cell spreading by the activation of the MEK/ERK pathway, we expressed BATF, which is a negative regulator of AP-1. The expression of BATF clearly restored cell spreading that was suppressed by the activation of MEK/ERK pathway. In addition, a disrupted formation of stress fibers and focal adhesions by such activation was restored by the suppression of AP-1. Our results define an essential role of the MEK/ERK/AP-1 pathway in the disruption of actin cytoskeleton and cell spreading.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / metabolism
  • Animals
  • Cell Line, Transformed
  • Cell Transformation, Neoplastic / metabolism*
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • MAP Kinase Kinase 1 / genetics
  • MAP Kinase Kinase 1 / metabolism*
  • MAP Kinase Signaling System / physiology*
  • Rabbits
  • Rats
  • Transcription Factor AP-1 / metabolism*

Substances

  • Transcription Factor AP-1
  • Extracellular Signal-Regulated MAP Kinases
  • MAP Kinase Kinase 1