Astrocyte differentiation of fetal neuroepithelial cells involving cardiotrophin-1-induced activation of STAT3

Cytokine. 2001 Jun 7;14(5):264-71. doi: 10.1006/cyto.2001.0883.

Abstract

Cardiotrophin-1 (CT-1) belongs to the interleukin (IL-)6 family of cytokines that share membrane glycoprotein 130 (gp130) as a receptor component critical for signal transduction. We here observed that CT-1 was expressed in mouse fetal neuroepithelial cells, and was capable of inducing astrocyte differentiation from these cells in a synergistic manner with bone morphogenetic protein (BMP)-2, whose expression was also found in the fetal brain. CT-1-induced astrocyte differentiation was solely gp130-dependent. CT-1-stimulation led to promoter activation of the gene for an astrocyte marker, glial fibrillary acidic protein (GFAP), which was clearly inhibited by expression of a dominant negative form of a gp130-downstream transcription factor, signal transducer and activator of transcription 3(STAT3), or by introduction of a mutation in a single STAT3-binding site in the promoter, suggesting a critical role of STAT3 in the CT-1-induced GFAP transcription. These results suggest that astrocyte differentiation in the developing brain involves CT-1-signaling which cooperates with BMP2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / cytology*
  • Astrocytes / metabolism
  • Binding Sites
  • Bone Morphogenetic Protein 2
  • Bone Morphogenetic Proteins / pharmacology
  • Brain / embryology*
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Cytokines / pharmacology*
  • DNA-Binding Proteins / metabolism*
  • DNA-Binding Proteins / physiology
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Glial Fibrillary Acidic Protein / genetics
  • Mice
  • Mice, Inbred ICR
  • Phosphotyrosine / metabolism
  • Promoter Regions, Genetic
  • RNA, Messenger / biosynthesis
  • STAT3 Transcription Factor
  • Trans-Activators / metabolism*
  • Trans-Activators / physiology
  • Transcriptional Activation
  • Transforming Growth Factor beta*

Substances

  • Bmp2 protein, mouse
  • Bone Morphogenetic Protein 2
  • Bone Morphogenetic Proteins
  • Cytokines
  • DNA-Binding Proteins
  • Glial Fibrillary Acidic Protein
  • RNA, Messenger
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • Trans-Activators
  • Transforming Growth Factor beta
  • Phosphotyrosine
  • cardiotrophin 1