Expression of the soluble lectin L-14 gene is induced by TSH in thyroid cells and suppressed by retinoic acid in transformed neural cells

Biochem Biophys Res Commun. 1994 Mar 15;199(2):540-6. doi: 10.1006/bbrc.1994.1262.

Abstract

Expression of the soluble lectin L-14 is low in normal and very high in transformed thyroid cells. We show that L-14 gene expression is transiently induced upon thyrotropin stimulation of normal quiescent FRTL-5 rat thyroid cells. Permanent activation of L-14 gene expression is obtained in the same cells infected with a wild-type and a temperature sensitive mutant of Kirsten murine sarcoma virus, both at the permissive and non permissive temperature for transformation. We also find that L-14 mRNA is undetectable in rat brain but is abundant in rat oligodendrocytes precursors transformed by polyoma middle T oncogene. Retinoic acid treatment of these transformed cells leads to acquisition of a differentiated phenotype accompanied by a 30-fold decrease of L-14 mRNA levels. Removal of retinoic acid restores both the transformed undifferentiated phenotype and high L-14 expression. Taken together these results indicate that growth stimulation and induction of cell differentiation are accompanied by strong modulation of L-14 gene expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Carrier Proteins / biosynthesis
  • Cell Division / drug effects
  • Cell Line
  • Cell Transformation, Neoplastic*
  • DNA / biosynthesis
  • Fibroblasts / metabolism
  • Galectins
  • Gene Expression / drug effects*
  • Hemagglutinins / biosynthesis*
  • Kinetics
  • Kirsten murine sarcoma virus / genetics*
  • Molecular Sequence Data
  • Oligodendroglia / drug effects
  • Oligodendroglia / metabolism*
  • Oligonucleotide Probes
  • RNA, Messenger / biosynthesis
  • Rats
  • Thymidine / metabolism
  • Thyroid Gland / cytology
  • Thyroid Gland / drug effects
  • Thyroid Gland / metabolism*
  • Thyrotropin / pharmacology*
  • Tretinoin / pharmacology*

Substances

  • Carrier Proteins
  • Galectins
  • Hemagglutinins
  • Oligonucleotide Probes
  • RNA, Messenger
  • Tretinoin
  • Thyrotropin
  • DNA
  • Thymidine