Osmotic regulation of cellular glucose uptake

Methods Enzymol. 2007:428:343-54. doi: 10.1016/S0076-6879(07)28020-6.

Abstract

This chapter describes various approaches allowing the study of hyperosmolarity in the functions of 3T3-L1 adipocytes. Hyperosmolarity mimics insulin responses, such as glucose uptake and membrane ruffling, but also antagonizes these insulin effects, which can be evaluated in 3T3-L1 adipocytes. The molecular mechanisms of these effects can be also investigated by measuring the activation of different signaling pathways: (i) the phosphorylation of docking proteins on tyrosine and serine residues (serines 307 and 632), (ii) the phosphorylation of serine/threonine kinases, and (iii) the activation of phosphatidylinositol 3-kinase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / metabolism
  • Animals
  • Cell Membrane / physiology
  • Cell Membrane / ultrastructure
  • Glucose / metabolism*
  • Glucose Transporter Type 4 / metabolism
  • Insulin Antagonists
  • Mice
  • Osmotic Pressure*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Signal Transduction / physiology

Substances

  • Glucose Transporter Type 4
  • Insulin Antagonists
  • Phosphatidylinositol 3-Kinases
  • Glucose