Ischemia-responsive protein (irp94) is up-regulated by endoplasmic reticulum stress

Z Naturforsch C J Biosci. 2001 Nov-Dec;56(11-12):1169-71. doi: 10.1515/znc-2001-11-1241.

Abstract

The expression of the ischemia-responsive protein (irp94) was enhanced by endoplasmic reticulum (ER) stress inducing drugs such as brefeldin A (BFA), calcium ionophor A23187, dithiothreitol (DTT) and tunicamycin in fisher rat thyroid epithelial cell line (FRTL-5 cells). In particular, irp94 mRNA expression was increased dose dependently by tunicamycin, and there was increased irp94 expression when the cells were incubated with the thyroid-stimulating hormone (TSH) together.

MeSH terms

  • Animals
  • Cell Line
  • DNA Primers
  • Endoplasmic Reticulum / metabolism*
  • Gene Expression Regulation / physiology*
  • HSP110 Heat-Shock Proteins
  • HSP70 Heat-Shock Proteins / genetics*
  • Ischemia / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stress, Physiological / metabolism
  • Thyrotropin / pharmacology

Substances

  • DNA Primers
  • HSP110 Heat-Shock Proteins
  • HSP70 Heat-Shock Proteins
  • Thyrotropin