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1 Biomedical Engineering Laboratory, Swiss Federal Institute of Technology, 1015 Lausanne; and 2 Department of Zoology and Animal Biology, University of Geneva, 1211 Geneva, Switzerland
The goal of the
present study was to analyze the intercellular calcium communication
between smooth muscle cells (SMCs) and endothelial cells (ECs) by
simultaneously monitoring artery diameter and intracellular calcium
concentration in a rat mesenteric arterial segment in vitro under
physiological pressure (50 mmHg) and flow (50 µl/min) in a specially
developed system. Intracellular calcium was expressed as the fura 2 ratio. The diameter was measured using a digital image acquisition
system. Stimulation of SMCs with the
1-agonist
phenylephrine (PE) caused not only an increase in the free
intracellular calcium concentration of the SMCs as expected but also in
the ECs, suggesting a calcium flux from the SMCs to the ECs. The gap
junction uncoupler palmitoleic acid greatly reduced this increase in
calcium in the ECs on stimulation of the SMCs with PE. This indicates
that the signaling pathway passes through the gap junctions. Similarly,
although vasomotion originates in the SMCs, calcium oscillates in both
SMCs and ECs during vasomotion, suggesting again a calcium flux from
the SMCs to the ECs.
smooth muscle cells; endothelial cells; calcium imaging; gap junctions; rat mesenteric artery
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