Nerve growth factor induces transcription of transforming growth factor-beta 1 through a specific promoter element in PC12 cells

J Biol Chem. 1994 Feb 4;269(5):3739-44.

Abstract

Nerve growth factor (NGF) stimulates the differentiation of PC12 pheochromocytoma cells to those resembling sympathetic neurons. We have investigated whether NGF regulates transforming growth factor (TGF)-beta gene expression and protein secretion in PC12 cells. These cells constitutively express TGF-beta 1 mRNA, whereas TGF-beta 2 and -beta 3 mRNAs are expressed at very low levels. TGF-beta 1 gene expression was stimulated greater than 10-fold when PC12 cells were treated with NGF. Sequences between -119 and -98 in the TGF-beta 1 promoter, homologous to an Egr-1 binding site, were shown to be important for both basal and NGF-induced promoter activity. We also found that a factor(s) present in nuclear extracts from PC12 cells interacted with the sequences between -119 and -98 and that expression of this factor was induced by NGF treatment. Moreover, specific binding to TGF-beta 1 promoter fragments between -119 and -98 was seen using the bacterially expressed transcription factor Egr-1. These results indicate that activation of TGF-beta 1 expression is one of the cellular responses of PC12 cells to NGF and suggest that TGF-beta may play a role in the differentiation of sympathetic neurons.

MeSH terms

  • Adrenal Gland Neoplasms
  • Animals
  • Base Sequence
  • Binding Sites
  • Blotting, Northern
  • Cell Nucleus / metabolism
  • Chloramphenicol O-Acetyltransferase / biosynthesis
  • Chloramphenicol O-Acetyltransferase / metabolism
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / metabolism
  • Gene Expression / drug effects*
  • Kinetics
  • Molecular Sequence Data
  • Nerve Growth Factors / pharmacology*
  • Oligodeoxyribonucleotides
  • PC12 Cells
  • Pheochromocytoma
  • Plasmids
  • Promoter Regions, Genetic* / drug effects
  • RNA, Messenger / biosynthesis*
  • RNA, Messenger / metabolism
  • RNA, Neoplasm / analysis
  • Transcription Factors / biosynthesis
  • Transcription Factors / metabolism
  • Transcription, Genetic / drug effects*
  • Transfection
  • Transforming Growth Factor beta / biosynthesis*
  • Zinc Fingers

Substances

  • DNA-Binding Proteins
  • Nerve Growth Factors
  • Oligodeoxyribonucleotides
  • RNA, Messenger
  • RNA, Neoplasm
  • Transcription Factors
  • Transforming Growth Factor beta
  • Chloramphenicol O-Acetyltransferase