학술논문

Vacuolar-type H+-ATPases at the plasma membrane regulate pH and cell migration in microvascular endothelial cells.
Document Type
Article
Source
American Journal of Physiology: Heart & Circulatory Physiology. Sep2006, Vol. 291 Issue 3, pH1147-H1157. 11p. 1 Color Photograph, 5 Graphs.
Subject
*ADENOSINE triphosphatase
*CELL membranes
*ENDOTHELIUM
*HYDROGEN-ion concentration
*CELL migration
*CELLULAR control mechanisms
*NEOVASCULARIZATION
*CYTOLOGY
Language
ISSN
0363-6135
Abstract
Microvascular endothelial cells involved in angiogenesis are exposed to an acidic environment that is not conducive for growth and survival. These cells must exhibit a dynamic intracellular (cytosolic) pH (pHcyt) regulatory mechanism to cope with acidosis, in addition to the ubiquitous Na+/H+ exchanger and HCO3-based H+-transporting systems. We hypothesize that the presence of plasmalemmal vacuolar-type proton ATPases (pmV-ATPases) allows microvascular endothelial cells to better cope with this acidic environment and that pmV-ATPases are required for cell migration. This study indicates that microvascular endothelial cells, which are more migratory than macrovascular endothelial cells, express pmV-ATPases. Spectral imaging microscopy indicates a more alkaline pHcyt at the leading than at the lagging edge of microvascular endothelial cells. Treatment of microvascular endothelial cells with V-ATPase inhibitors decreases the proton fluxes via pmV-ATPases and ceil migration. These data suggest that pmV-ATPases are essential for pHcyt regulation and cell migration in microvascalar endothelial cells. [ABSTRACT FROM AUTHOR]