Abstract

This study presents an investigation of pacemaker mechanisms underlying lymphatic vasomotion. We tested the hypothesis that active inositol 1,4,5-trisphosphate receptor (IP 3R)-operated Ca 2+ stores interact as coupled oscillators to produce near-synchronous Ca 2+ release events and associated pacemaker potentials, this driving action potentials and constrictions of lymphatic smooth muscle. Application of endothelin 1 (ET-1), an agonist known to enhance synthesis of IP 3, to quiescent lymphatic smooth muscle syncytia first enhanced spontaneous Ca 2+ transients and/or intracellular Ca 2+ waves. Larger near-synchronous Ca 2+ transients then occurred leading to global synchronous Ca 2+ transients associated with action potentials and resultant vasomotion. In contrast, blockade of L-type Ca 2+ channels with nifedipine prevented ET-1 from inducing near-synchronous Ca 2+ transients and resultant action potentials, leaving only asynchronous Ca 2+ transients and local Ca 2+ waves. These data were well simulated by a model of lymphatic smooth muscle with: 1), oscillatory Ca 2+ release from IP 3R-operated Ca 2+ stores, which causes depolarization; 2), L-type Ca 2+ channels; and 3), gap junctions between cells. Stimulation of the stores caused global pacemaker activity through coupled oscillator-based entrainment of the stores. Membrane potential changes and positive feedback by L-type Ca 2+ channels to produce more store activity were fundamental to this process providing long-range electrochemical coupling between the Ca 2+ store oscillators. We conclude that lymphatic pacemaking is mediated by coupled oscillator-based interactions between active Ca 2+ stores. These are weakly coupled by inter- and intracellular diffusion of store activators and strongly coupled by membrane potential. Ca 2+ store-based pacemaking is predicted for cellular systems where: 1), oscillatory Ca 2+ release induces depolarization; 2), membrane depolarization provides positive feedback to induce further store Ca 2+ release; and 3), cells are interconnected. These conditions are met in a surprisingly large number of cellular systems including gastrointestinal, lymphatic, urethral, and vascular tissues, and in heart pacemaker cells.

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