Induction of uPA but not NF-IL3A by calcitonin is dependent on Erk1/2 phosphorylation in porcine renal cell line LLC-PK1

Biochem Biophys Res Commun. 2002 Feb 8;290(5):1483-8. doi: 10.1006/bbrc.2001.6260.

Abstract

Calcitonin (CT) is a polypeptide hormone and has a variety of functions including regulation of urinary calcium excretion. By using a cDNA subtraction hybridization method, we identified that NF-IL3A and urokinase-type plasminogen activator (uPA) genes were up-regulated by CT in porcine renal cell line LLC-PK1. CT-mediated induction of these genes was not inhibited by cycloheximide. These data suggest that these up-regulations are not induced by increased synthesis of regulating proteins; therefore, they are immediately response early (IE). We also found that CT treatment led to the phosphorylation of Erk1/2. We demonstrated that PD98059, a MEK1 inhibitor, inhibited CT-induced mRNA expressions of uPA, but had no obvious influence on the NF-IL3A induction. These results demonstrated the inductions of uPA by CT involve Erk1/2 phosphorylation. We provide the first evidence that NF-IL3A expression is up-regulated by CT. The present findings suggest that the transcriptions of the NF-IL3A and uPA could be induced by CT and might be important mediators of CT function in renal cells.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Calcitonin / pharmacology*
  • Enzyme Induction / drug effects
  • Enzyme Induction / genetics
  • Enzyme Inhibitors / pharmacology
  • Flavonoids / pharmacology
  • G-Box Binding Factors
  • Gene Expression Regulation / drug effects
  • Genes, Immediate-Early / drug effects
  • LLC-PK1 Cells / drug effects
  • LLC-PK1 Cells / enzymology*
  • LLC-PK1 Cells / metabolism
  • MAP Kinase Kinase 1
  • MAP Kinase Signaling System / drug effects
  • MAP Kinase Signaling System / genetics
  • Mitogen-Activated Protein Kinase 1 / metabolism*
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinase Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinases / metabolism*
  • Phosphorylation / drug effects
  • Protein Serine-Threonine Kinases / antagonists & inhibitors
  • RNA, Messenger / biosynthesis
  • Swine
  • Trans-Activators / biosynthesis*
  • Trans-Activators / genetics
  • Trans-Activators / isolation & purification
  • Urokinase-Type Plasminogen Activator / biosynthesis*
  • Urokinase-Type Plasminogen Activator / genetics
  • Urokinase-Type Plasminogen Activator / isolation & purification

Substances

  • Enzyme Inhibitors
  • Flavonoids
  • G-Box Binding Factors
  • RNA, Messenger
  • Trans-Activators
  • Calcitonin
  • Protein Serine-Threonine Kinases
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 1
  • MAP2K1 protein, human
  • Mitogen-Activated Protein Kinase Kinases
  • Urokinase-Type Plasminogen Activator
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one