Spatial separation of endothelial small‐ and intermediate‐conductance calcium‐activated potassium channels (KCa) and connexins: possible relationship to vasodilator function?
Open Access
- 24 October 2006
- journal article
- Published by Wiley in Journal of Anatomy
- Vol. 209 (5) , 689-698
- https://doi.org/10.1111/j.1469-7580.2006.00647.x
Abstract
Activation of endothelial cell small‐ (S) and intermediate‐ (I) conductance calcium‐activated potassium channels (KCa) and current or molecular transfer via myoendothelial gap junctions underlies endothelium‐derived hyperpolarization leading to vasodilation. The mechanism underlying the KCa component of vasodilator activity and the characteristics of gap junctions are targets for the selective control of vascular function. In the rat mesenteric artery, where myoendothelial gap junctions and connexin (Cx) 40 are critical for the transmission of the endothelial cell hyperpolarization to the smooth muscle, SKCa and IKCa provide different facets of the endothelium‐derived hyperpolarization response, being critical for the hyperpolarization and repolarization phases, respectively. The present study addressed the question of whether this functional separation of responses may be related to the spatial localization of the associated channels? The distribution of endothelial SKCa and IKCa and Cx subtype(s) were examined in the rat mesenteric artery using conventional confocal and high‐resolution ultrastructural immunohistochemistry. At the internal elastic lamina–smooth muscle cell interface at internal elastic lamina holes (as potential myoendothelial gap junction sites), strong punctate IKCa, Cx37 and Cx40 expression was present. SKCa, Cx37, Cx40 and Cx43 were localized to adjacent endothelial cell gap junctions. High‐resolution immunohistochemistry demonstrated IKCa and Cx37‐conjugated gold to myoendothelial gap junction‐associated endothelial cell projections. Clear co‐localization of KCa and Cxs suggests a causal relationship between their activity and the previously described differential functional activation of SKCa and IKCa. Such precise localizations may represent a selective target for control of vasodilator function and vascular tone.Keywords
This publication has 34 references indexed in Scilit:
- Endothelium‐dependent Vasodilation in Myogenically Active Mouse Skeletal Muscle Arterioles: Role of EDH and K+ ChannelsMicrocirculation, 2009
- Endothelial coordination of cerebral vasomotion via myoendothelial gap junctions containing connexins 37 and 40American Journal of Physiology-Heart and Circulatory Physiology, 2006
- Evidence for Involvement of Both IK Ca and SK Ca Channels in Hyperpolarizing Responses of the Rat Middle Cerebral ArteryStroke, 2006
- Rapid Endothelial Cell–Selective Loading of Connexin 40 Antibody Blocks Endothelium-Derived Hyperpolarizing Factor Dilation in Rat Small Mesenteric ArteriesCirculation Research, 2005
- Endothelium‐dependent smooth muscle hyperpolarization: do gap junctions provide a unifying hypothesis?British Journal of Pharmacology, 2004
- Expression of intermediate conductance potassium channel immunoreactivity in neurons and epithelial cells of the rat gastrointestinal tractCell and tissue research, 2003
- Altered Expression of Small-Conductance Ca 2+ -Activated K + (SK3) Channels Modulates Arterial Tone and Blood PressureCirculation Research, 2003
- Structure, Function, and Endothelium-Derived Hyperpolarizing Factor in the Caudal Artery of the SHR and WKY RatArteriosclerosis, Thrombosis, and Vascular Biology, 2003
- What is new in endothelium-derived hyperpolarizing factors?Current Opinion in Nephrology and Hypertension, 2002
- Restricted expression of the gap junctional protein connexin 43 in the arterial system of the ratJournal of Anatomy, 1998