Abstract

See related article, pages 1026–1035 Coordination of cellular behavior is indispensable for vascular function. Because of the structural design of the vascular tree only an orchestrated diameter change along the vessel length increases conductance significantly and ensures optimal tissue perfusion. Mechanisms that suffice these needs include locally generated signals at upstream sites which reflect downstream requirements (flow-induced dilation)1 and longitudinal signal transmission through communication channels residing in the vessel wall itself which enable the synchronisation of cellular behavior. This latter is achieved by homocellular gap junctions which are composed of connexins that connect adjacent cells by intercellular low-resistance channels establishing a functional syncitium.2 Electrical communication through these channels is experimentally studied by locally initiated vasomotor responses which conduct along the vessel wall and promote synchronized dilations or constrictions of arteriolar segments reflecting the coordination of cellular behavior.3 Longitudinal communication through gap junctions is also required for the synchronisation of intracellular Ca2+ ([Ca2+]i) changes in smooth muscle and subsequent vasomotion, ie, rhythmic oscillations of vascular diameter. Although the physiological significance of vasomotion is still to be clearly defined it depends critically on Ca2+ release from intracellular stores which occurs in an oscillating fashion and the synchronization of [Ca2+]i transients through gap junctional communication.4,5 In addition, endothelial and smooth muscle cells are coupled heterocellularly (myoendothelial junctions) allowing the direct spread of current from the endothelium to the smooth muscle6 or other signaling molecules.7 The importance of gap junctional communication in vascular function contrasts with the poor knowledge of its regulation in vessels which is complicated by the existence of functional and structural different types of gap junctions. Moreover, longterm regulation because of degradation or upregulation of connexins has to be separated from shortterm effects which reflect an …

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