Cell Calcium 2009-01-01

Calcineurin activation by slow calcium release from intracellular stores suppresses protein kinase C regulation of L-type calcium channels in L6 cells

Jay D. Turner, Andrew P. Thomas, John P. Reeves, Basil M. Hantash

Index: Cell Calcium 46(4) , 242-7, (2009)

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Abstract

L-type Ca 2+ channel activity was assayed in L6 cells as the rate of nifedipine-sensitive Ba 2+ influx in a depolarizing medium. In the absence of extracellular Ca 2+, activation of protein kinase C (PKC) with phorbol-12-myristate-13-acetate (PMA) or thymeleatoxin (TMX) inhibited Ba 2+ influx by 38%. Thapsigargin (Tg), a selective inhibitor of the Ca 2+-ATPase in the sarcoplasmic reticulum, evoked a rise in the cytosolic Ca 2+ concentration ([Ca 2+] i) in a Ca 2+-free medium from 30 to ∼80 nM. This [Ca 2+] i increase declined slowly, giving rise to a modest elevation of [Ca 2+] i that persisted for >5 min. The inhibitory effects of PMA and TMX on channel activity were abolished when tested in Tg-treated cells in a Ca 2+-free medium. However, when the Ca 2+ ionophore, ionomycin, was applied with Tg, PMA and TMX retained their inhibitory effect on L-type Ca 2+ channel activity, suggesting that a lower amplitude and prolonged release of Ca 2+ stores is necessary for abrogating PKC-mediated inhibition of LCC. Cyclosporin A (5 μM) and ascomycin (5 μM), inhibitors of the Ca 2+/calmodulin-dependent protein phosphatase, calcineurin, fully restored the inhibitory effect of PMA and TMX on channel activity. Addition of 1 mM CaCl 2 to the Tg-treated cells increased [Ca 2+] i to ∼165 nM and also restored the inhibitory effects of PMA and TMX. These results indicate that a small, relatively prolonged [Ca 2+] i increase elicited by passive depletion of internal Ca 2+ stores led to activation of calcineurin, giving rise to an increase in protein phosphatase activity that counteracted the inhibitory effects of PKC on channel activity. A larger increase in [Ca 2+] i via store-dependent Ca 2+ entry enhanced the activity of PKC sufficiently to overcome the protein phosphatase activity of calcineurin. This study is the first to demonstrate that the regulation of L-type Ca 2+ channels in a myocyte model involves a balance between the differential Ca 2+ sensitivities and opposing actions of PKC and calcineurin.