Reduction of the Ca2+ transport systems in mouse young brown fat cells

Membr Cell Biol. 2000;13(4):503-10.

Abstract

Principal differences in the kinetics and amplitude of Ca2+ response to norepinephrine were found between freshly isolated young differentiated brown fat cells. An increase in the Ca2+ concentration in the cytoplasm ([Ca2+]i) in the young cells was unusually slow (A[Ca2+]i = 0.03 nM/s) in comparison with that in the differentiated cells, and the Ca2+ influx from the outside was not induced by Ca2+ mobilization agents, such as thapsigargin and ionomycin. Ionomycin increased [Ca2+]i up to 150 nM in a Ca2+-free medium and up to 270 nM in the normal medium. This results in that the intracellular Ca2+ stores in freshly isolated young cells are rather poor, and the mechanism of capacitive calcium entry does not virtually function. The data on chemical modification of Ca2+ channels in the plasma membrane by thimerosal suggest that the conductance of these channels is low and/or their number in young brown fat cells is insignificant.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / drug effects*
  • Adipocytes / metabolism*
  • Adipocytes / ultrastructure
  • Adipose Tissue, Brown / drug effects*
  • Adipose Tissue, Brown / metabolism*
  • Adipose Tissue, Brown / ultrastructure
  • Animals
  • Calcium / metabolism
  • Calcium Channels / drug effects
  • Calcium Channels / metabolism
  • Calcium Signaling / drug effects
  • Calcium Signaling / physiology
  • Calcium-Binding Proteins / drug effects*
  • Calcium-Binding Proteins / metabolism*
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cytosol / drug effects
  • Cytosol / metabolism
  • Endoplasmic Reticulum / drug effects
  • Endoplasmic Reticulum / metabolism
  • Endoplasmic Reticulum / ultrastructure
  • Kinetics
  • Male
  • Mice
  • Mice, Inbred Strains / metabolism
  • Norepinephrine / metabolism
  • Norepinephrine / pharmacology
  • Thapsigargin / pharmacology
  • Thimerosal / pharmacology

Substances

  • Calcium Channels
  • Calcium-Binding Proteins
  • Thimerosal
  • Thapsigargin
  • Calcium
  • Norepinephrine