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. 2015 Oct 8;10(10):e0139865. doi: 10.1371/journal.pone.0139865

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© 2015 Guo et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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Fig 4 — Several inorganic calcium channel blockers, including La³⁺ (200 μM), Gd²⁺ (100 μM), and Ni²⁺ (300 μM), and store-operated calcium channel (SOC) blockers, including 2-APB (100 μM) and SKF96365 (10 μM), inhibit cathode-directed cell migration, but Sr²⁺ (1 mM), a substitute for calcium, nifedipine (20 μM), a voltage-dependent channel inhibitor, and BAPTA-AM (25 μM), an intracellular calcium chelator, failed to inhibit cellular responses to EF. * (p < 0.05) and ** (p < 0.01) vs EF 5 V/cm control. Error bars indicate standard error.