The signal transduction pathway that mediates the effect of interleukin-1 beta on the Na+-K+-ATPase in LLC-PK1 cells

Sawsan Ibrahim Kreydiyyeh, Rana Al-Sadi

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

IL-1β reduces the activity and protein expression of Na +-K+-ATPase in rat kidney cells. The aim of the present study was to elucidate the signalling pathway involved, using the LLC-PK 1 cell line. In these cells IL-1β caused a time and concentration-dependent decrease in the protein expression of the Na +-K+-ATPase. Inhibition of extracellular signal-regulated kinase (ERK), nuclear factor-κB (NF-κB) and cyclooxygenase (COX), but not p38 mitogen-activated kinase (MAPK), abolished the effect of the cytokine on the pump. The activation of NF-κB by IL-1β was maximal at 20 min and declined thereafter. Inhibition of the transcription factor by pyrrolidinediethyl-dithiocarbamate (PDTC) down-regulated the ATPase. The effects of IL-1β on the pump and NF-κB were prevented by the COX inhibitor indomethacin. Exogenous PGE2 reduced protein expression of the ATPase within 15 min, even in presence of an ERK inhibitor. It is concluded that IL-1β stimulates the mitogen and extracellular signal regulated protein kinase kinase/extracellular signal regulated protein kinase (MEK/ERK) pathway. This activates NF-κB, thus leading to increased COX-2 expression and PGE2 release. PGE2 in turn inhibits NF-κB and reduces the protein expression of Na+-K+-ATPase.

Original languageEnglish (US)
Pages (from-to)231-238
Number of pages8
JournalPflugers Archiv European Journal of Physiology
Volume448
Issue number2
DOIs
StatePublished - May 1 2004

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LLC-PK1 Cells
Signal transduction
Extracellular Signal-Regulated MAP Kinases
Interleukin-1beta
Interleukin-1
Adenosine Triphosphatases
Signal Transduction
Dinoprostone
Mitogen-Activated Protein Kinase Kinases
Mitogens
Protein Kinases
Proteins
Pumps
Cyclooxygenase Inhibitors
Cyclooxygenase 2
Prostaglandin-Endoperoxide Synthases
Indomethacin
Rats
Transcription Factors
Phosphotransferases

All Science Journal Classification (ASJC) codes

  • Physiology
  • Clinical Biochemistry
  • Physiology (medical)

Cite this

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abstract = "IL-1β reduces the activity and protein expression of Na +-K+-ATPase in rat kidney cells. The aim of the present study was to elucidate the signalling pathway involved, using the LLC-PK 1 cell line. In these cells IL-1β caused a time and concentration-dependent decrease in the protein expression of the Na +-K+-ATPase. Inhibition of extracellular signal-regulated kinase (ERK), nuclear factor-κB (NF-κB) and cyclooxygenase (COX), but not p38 mitogen-activated kinase (MAPK), abolished the effect of the cytokine on the pump. The activation of NF-κB by IL-1β was maximal at 20 min and declined thereafter. Inhibition of the transcription factor by pyrrolidinediethyl-dithiocarbamate (PDTC) down-regulated the ATPase. The effects of IL-1β on the pump and NF-κB were prevented by the COX inhibitor indomethacin. Exogenous PGE2 reduced protein expression of the ATPase within 15 min, even in presence of an ERK inhibitor. It is concluded that IL-1β stimulates the mitogen and extracellular signal regulated protein kinase kinase/extracellular signal regulated protein kinase (MEK/ERK) pathway. This activates NF-κB, thus leading to increased COX-2 expression and PGE2 release. PGE2 in turn inhibits NF-κB and reduces the protein expression of Na+-K+-ATPase.",
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The signal transduction pathway that mediates the effect of interleukin-1 beta on the Na+-K+-ATPase in LLC-PK1 cells. / Kreydiyyeh, Sawsan Ibrahim; Al-Sadi, Rana.

In: Pflugers Archiv European Journal of Physiology, Vol. 448, No. 2, 01.05.2004, p. 231-238.

Research output: Contribution to journalArticle

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