High membrane resistance allows the endothelium to effectively conduct electrical signals, though activation of multiple neighboring cells is required to initiate physiologically relevant hyperpolarization.
High EC resistance enables mm-scale electrical conduction in animal microvessels; leaves open physiologic relevance and human translation.
Objective Electrical signaling along the endothelium underlies spreading vasodilation and blood flow control. We use mathematical modeling to determine the electrical properties of the endothelium and gain insight into the biophysical determinants of electrical conduction. Methods Electrical conduction data along endothelial tubes (40 μm wide, 2.5 mm long) isolated from mouse skeletal muscle resistance arteries were analyzed using cable equations and a multicellular computational model. Results Responses to intracellular current injection attenuate with an axial length constant (λ) of 1.2‐1.4 mm. Data were fitted to estimate the axial ( r a ; 10.7 MΩ/mm) and membrane ( r m ; 14.5 MΩ∙mm) resistivities, EC membrane resistance ( R m ; 12 GΩ), and EC ‐ EC coupling resistance ( R gj ; 4.5 MΩ) and predict that stimulation of ≥30 neighboring EC s is required to elicit 1 mV of hyperpolarization at distance = 2.5 mm. Opening Ca 2+ ‐activated K + channels ( K C a ) along the endothelium reduced λ by up to 55%. Conclusions High R m makes the endothelium sensitive to electrical stimuli and able to conduct these signals effectively. Whereas the activation of a group of EC s is required to initiate physiologically relevant hyperpolarization, this requirement is increased by myoendothelial coupling and K C a activation along the endothelium inhibits conduction by dissipating electrical signals.
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Kapela et al. (2017) studied this question.
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