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      Depolarisation-evoked Ca2+ waves in the non-excitable rat megakaryocyte.

      The Journal of Physiology
      Adenosine Diphosphate, pharmacology, Animals, Calcium, metabolism, Calcium Signaling, Cell Nucleus, physiology, Cell Polarity, Electrophysiology, Endoplasmic Reticulum, Immunohistochemistry, Intracellular Membranes, Male, Megakaryocytes, Microscopy, Confocal, Patch-Clamp Techniques, Rats, Rats, Wistar

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          Abstract

          1. A combination of patch clamp, confocal microscopy and immunohistochemistry was used to examine the spatial properties of Ca2+ signalling in the rat megakaryocyte, a non-excitable cell type in which membrane potential can markedly modulate agonist-evoked Ca2+ release. 2. Intracellular calcium ion concentration ([Ca2+]i) increases, stimulated by both ADP and depolarisation, frequently originated from a peripheral locus and spread as a wave throughout the cell. Spatially restricted [Ca2+]i increases, consistent with elementary Ca2+ release events, were occasionally observed prior to ADP-evoked waves. 3. ADP- and depolarisation-evoked Ca2+ waves travelled approximately twice as fast around the periphery of the cell compared to across its radius, leading to a curvilinear wavefront. There was no significant difference between wave velocities generated by the two stimuli. 4. Immunohistochemical staining of type III IP3 receptors, the endoplasmic reticulum-specific protein GRP78/BiP and calreticulin indicated a major peripheral location of the cellular Ca2+ stores which probably accounts for the accelerated wave velocity at the cell periphery. 5. These data demonstrate that [Ca2+]i increases, stimulated by depolarisation or the agonist ADP, have indistinguishable spatial properties, providing evidence that similar underlying mechanisms are responsible for their generation.

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