Cumulated Ca2⁺ spike duration underlies Ca2⁺ oscillation frequency-regulated NFκB transcriptional activity

J Cell Sci. 2011 Aug 1;124(Pt 15):2591-601. doi: 10.1242/jcs.082727. Epub 2011 Jul 12.

Abstract

[Ca(2+)](i) oscillations drive downstream events, like transcription, in a frequency-dependent manner. Why [Ca(2+)](i) oscillation frequency regulates transcription has not been clearly revealed. A variation in [Ca(2+)](i) oscillation frequency apparently leads to a variation in the time duration of cumulated [Ca(2+)](i) elevations or cumulated [Ca(2+)](i) spike duration. By manipulating [Ca(2+)](i) spike duration, we generated a series of [Ca(2+)](i) oscillations with the same frequency but different cumulated [Ca(2+)](i) spike durations, as well as [Ca(2+)](i) oscillations with the different frequencies but the same cumulated [Ca(2+)](i) spike duration. Molecular assays demonstrated that, when generated in 'artificial' models alone, under physiologically simulated conditions or repetitive pulses of agonist exposure, [Ca(2+)](i) oscillation regulates NFκB transcriptional activity, phosphorylation of IκBα and Ca(2+)-dependent gene expression all in a way actually dependent on cumulated [Ca(2+)](i) spike duration whether or not frequency varies. This study underlines that [Ca(2+)](i) oscillation frequency regulates NFκB transcriptional activity through cumulated [Ca(2+)](i) spike-duration-mediated IκBα phosphorylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Calcium / metabolism*
  • Calcium Signaling / genetics
  • Calcium Signaling / physiology
  • Cell Line
  • Gene Expression Regulation / genetics
  • Gene Expression Regulation / physiology
  • Humans
  • Interleukin-8 / genetics
  • NF-kappa B / genetics
  • NF-kappa B / metabolism*
  • Phosphorylation
  • Reactive Oxygen Species / metabolism
  • Real-Time Polymerase Chain Reaction

Substances

  • Interleukin-8
  • NF-kappa B
  • Reactive Oxygen Species
  • Calcium