Modulation of type A K+ current inDrosophila larval muscle by internal Ca2+; effects of the overexpression of frequenin |
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Authors: | C Poulain A Ferrús A Mallart |
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Institution: | (1) Unité de Physiologie Neuromusculaire, Laboratoire de Neurobiologie Cellulaire et Moléculaire, CNRS, Gif-sur-Yvette, France;(2) Present address: Instituto Cajal, CSIC, E-28002 Madrid, Spain |
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Abstract: | The calcium-dependent modulation of type A K+ current (I
A) has been investigated using a two-electrode voltage clamp on larval muscle cells ofDrosophila. It was found that the amplitude ofI
A increases when Ca2+]0 is changed from 0.2 mM to 2 mM. The increase inI
A amplitude is not due to overlap with the Ca2+-dependent fast K+ current,I
CF, since it is observed also inslo
1 mutants, which are deficient for this current. This effect is not due to Ca2+-dependent shifts in the steady-state activation/inactivation kinetics. The phenomenon is probably due to elevations in internal calcium since it is abolished by Ca2+ channel blockers and promoted by caffeine (5 mM) if added in the absence of external calcium. This calcium effect was dose-dependent since it was not observed in the presence caffeine plus 2 mM calcium in the bath nor for values of Ca2+]0 above 4 mM. The Ca2+-dependent modulation ofI
A is absent inV7, a mutation that causes overexpression of frequenin, a recoverin-like Ca2+-binding protein which stimulates guanylyl cyclase 31]. One possible explanation for the loss ofI
A modulation in theV7 mutation is that the excess of frequenin alters intracellular cGMP-dependent metabolic pathways responsible for the internal calcium homeostasis. |
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Keywords: | Drosophila melanogaster Muscle A current Calcium Frequenin |
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