Thyroid hormone rapidly stimulates alveolar Na,K-ATPase by activation of phosphatidylinositol 3-kinase

Curr Opin Endocrinol Diabetes Obes. 2007 Oct;14(5):416-20. doi: 10.1097/MED.0b013e3282f02ae8.

Abstract

Purpose of review: Nongenomic actions of 3,3',5-triiodo-L-thyronine (T3) occur quite rapidly usually via activation of signaling cascades. In this review, we focus on recent advances made in the understanding of activation of the phosphatidylinositol 3-kinase pathway by T3 in alveolar epithelial cells, resulting in upregulation of Na,K-ATPase hydrolytic activity and potential physiological significance of this finding.

Recent findings: T3 stimulates the Src family of kinases. Activation of Src-kinase and phosphatidylinositol 3-kinase/protein kinase B is required for the T3-induced stimulation of alveolar epithelial Na,K-ATPase activity in rat alveolar epithelial cells. The stimulation does not require transcription. This T3-sensitive Na,K-ATPase stimulation in rat alveolar epithelial cells is switched on late in gestation. In skin fibroblasts phosphatidylinositol 3-kinase is also involved in the nongenomic T3 stimulation of ZAK1-4alpha protein expression, an endogenous calcineurin inhibitor.

Summary: T3 plays an important role in cell survival and differentiation. Nongenomic regulation of phosphatidylinositol 3-kinase and downstream molecules by T3 is being recognized in different tissues. Upregulation of alveolar Na,K-ATPase is one such molecule, which plays an important role in removal of edema fluid from the alveolar space. These effects are rapid and do not require direct nuclear gene transcription.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Survival
  • Enzyme Activation / drug effects
  • Epithelial Cells / enzymology
  • Fibroblasts / enzymology
  • Organogenesis
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism
  • Pulmonary Alveoli / enzymology*
  • Rats
  • Signal Transduction
  • Skin / enzymology
  • Sodium-Potassium-Exchanging ATPase / metabolism*
  • Triiodothyronine / metabolism*
  • Triiodothyronine / pharmacology
  • src-Family Kinases / metabolism

Substances

  • Triiodothyronine
  • src-Family Kinases
  • Proto-Oncogene Proteins c-akt
  • Sodium-Potassium-Exchanging ATPase