Vacuole formation in mast cells responding to osmotic stress and to F-actin disassembly

Cell Biol Int. 2002;26(10):885-92. doi: 10.1006/cbir.2002.0940.

Abstract

Fluorescent probes were used to visualize the morphology of membranes and of F-actin in rat peritoneal mast cells, exposed to hyperosmotic medium and consequently reversed to isotonicity. Hypertonicity induced cell shrinkage followed by a regulatory volume increase, and cell alkalinization that was sensitive to amiloride, an inhibitor of the Na(+)/H(+) exchanger (NHE), but not to Latrunculin B, an inhibitor of actin polymerization. Using Bodipy-Sphingomyelin, we have observed formation of vacuole-like dilations (VLDs), primarily at or close to the adhesion plane, following the reversal from hyper- to isotonic medium. VLD formation was not inhibited by Latrunculin B or by amiloride. Phalloidin staining has shown that actin filaments do not surround the vacuoles and latrunculin-induced depolymerization of actin has actually promoted vacuole formation, even in isotonic conditions. The results support the idea that a decrease in membrane tension promotes the internalization of the plasma membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / drug effects
  • Actins / metabolism*
  • Amiloride / pharmacology
  • Animals
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism*
  • Cell Membrane / ultrastructure
  • Cell Size / drug effects
  • Cell Size / physiology
  • Enzyme Inhibitors / pharmacology
  • Hypertonic Solutions / pharmacology
  • Male
  • Mast Cells / cytology
  • Mast Cells / drug effects
  • Mast Cells / metabolism*
  • Osmotic Pressure
  • Polymers / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Sodium-Hydrogen Exchangers / antagonists & inhibitors
  • Sodium-Hydrogen Exchangers / metabolism
  • Surface Tension / drug effects
  • Thiazoles / pharmacology
  • Thiazolidines
  • Vacuoles / drug effects
  • Vacuoles / metabolism*
  • Vacuoles / ultrastructure
  • Water-Electrolyte Balance / physiology*

Substances

  • Actins
  • Bridged Bicyclo Compounds, Heterocyclic
  • Enzyme Inhibitors
  • Hypertonic Solutions
  • Polymers
  • Sodium-Hydrogen Exchangers
  • Thiazoles
  • Thiazolidines
  • Amiloride
  • latrunculin B