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      Ouabain, a steroid hormone that signals with slow calcium oscillations.

      Proceedings of the National Academy of Sciences of the United States of America
      Animals, Blotting, Western, Calcium, metabolism, physiology, Cells, Cultured, Immunohistochemistry, Kidney Tubules, Proximal, cytology, enzymology, Male, Microscopy, Confocal, NF-kappa B, Ouabain, Rats, Rats, Sprague-Dawley, Signal Transduction, Sodium-Potassium-Exchanging ATPase, antagonists & inhibitors, Subcellular Fractions

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          Abstract

          The plant-derived steroid, digoxin, a specific inhibitor of Na,K-ATPase, has been used for centuries in the treatment of heart disease. Recent studies demonstrate the presence of a digoxin analog, ouabain, in mammalian tissue, but its biological role has not been elucidated. Here, we show in renal epithelial cells that ouabain, in doses causing only partial Na,K-ATPase inhibition, acts as a biological inducer of regular, low-frequency intracellular calcium ([Ca(2+)](i)) oscillations that elicit activation of the transcription factor, NF-kappa B. Partial inhibition of Na,K-ATPase using low extracellular K(+) and depolarization of cells did not have these effects. Incubation of cells in Ca(2+)-free media, inhibition of voltage-gated calcium channels, inositol triphosphate receptor antagonism, and redistribution of actin to a thick layer adjacent to the plasma membrane abolished [Ca(2+)](i) oscillations, indicating that they were caused by a concerted action of inositol triphosphate receptors and capacitative calcium entry via plasma membrane channels. Blockade of ouabain-induced [Ca(2+)](i) oscillations prevented activation of NF-kappa B. The results demonstrate a new mechanism for steroid signaling via plasma membrane receptors and underline a novel role for the steroid hormone, ouabain, as a physiological inducer of [Ca(2+)](i) oscillations involved in transcriptional regulation in mammalian cells.

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