Abstract
Light activation of Drosophila photoreceptors leads to the generation of a depolarizing receptor potential via opening of transient receptor potential and transient receptor potential-like cationic channels. Counteracting the light-activated depolarizing current are two voltage-gated K+ conductances, IA andIK, that are expressed in these sensory neurons. Here we show that Drosophilaphotoreceptors IA andIK are regulated by calcium–calmodulin (Ca2+/calmodulin) via a Ca2+/calmodulin-dependent protein kinase (CaM kinase), with IK being far more sensitive than IA. Inhibition of Ca2+/calmodulin by N-(6 aminohexyl)-5-chloro-1-naphthalenesulfonamide or trifluoperazine markedly reduced the K+ current amplitudes. Likewise, inhibition of CaM kinases by KN-93 potently depressedIK and accelerated its C-type inactivation kinetics. The effect of KN-93 was specific because its structurally related but functionally inactive analog KN-92 was totally ineffective. In Drosophila photoreceptor mutantShKS133 , which allows isolation ofIK, we demonstrate by current-clamp recording that inhibition of IK by quinidine or tetraethylammonium increased the amplitude of the photoreceptor potential, depressed light adaptation, and slowed down the termination of the light response. Similar results were obtained when CaM kinases were blocked by KN-93. These findings place photoreceptor K+ channels as an additional target for Ca2+/calmodulin and suggest thatIK is well suited to act in concert with other components of the signaling machinery to sharpen light response termination and fine tune photoreceptor sensitivity during light adaptation.
Phototransduction in vertebrates and invertebrates is a complex signal transduction cascade, based on rhodopsin–G-protein coupling interactions (Hardie and Minke, 1995;Ranganathan et al., 1995; Baylor, 1996; Minke and Selinger, 1996;Zuker, 1996). The phototransduction process has the capacity to amplify single photon events into large electrical signals and to regulate the photoresponse output in a broad dynamic range. Major advances have been made in characterizing the molecular components of phototransduction and the mechanisms of light adaptation and response termination (Baylor, 1996; Minke and Selinger, 1996; Zuker, 1996). However, the modulation of these latter processes is not yet fully understood. The powerful combination of molecular genetics and electrophysiology makesDrosophila photoreceptors an exquisite preparation for studying these processes. In Drosophila, light activation of rhodopsin activates phospholipase C via G-proteins, which hydrolyzes phosphatidylinositol-4,5-bisphosphate into inositol trisphosphate (IP3) and diacylglycerol (DAG). This process leads within a few tens of milliseconds to the opening of cation-selective channels encoded by the trp and trp-like genes (Hardie and Minke, 1995; Ranganathan et al., 1995; Minke and Selinger, 1996). The feedback control of the activation process was recently shown to involve calcium–calmodulin (Ca2+/calmodulin), which tightly regulates the adaptation and termination of the light response (Arnon et al., 1997a,b; Scott and Zuker, 1997; Scott et al., 1997).
The photoreceptor potential has a complex waveform that arises from the opening of light-activated channels as well as from voltage-dependent conductances. Interestingly, Drosophila photoreceptors are endowed with high densities of voltage-gated K+channels (Hardie, 1991; Hardie et al., 1991). In neurons, K+ channels were recognized to regulate action potential duration, firing patterns, and resting membrane potential (Rudy, 1988; Hille, 1992). A great diversity of K+channel subtypes appear to underlie these pleiotropic functions (Pongs, 1992; Doupnik et al., 1995; Salkoff and Jegla, 1995; Wickman and Clapham, 1995; Jan and Jan, 1997). Analysis of Drosophilamutants enabled the initial molecular characterization of several classes of K+ channels (Kamb et al., 1987; Tempel et al., 1987; Pongs et al., 1988). Four different voltage-sensitive K+ channel genes were initially identified inDrosophila: Shaker and Shal, encoding A-type K+ currents (IA), and Shab andShaw, encoding delayed-rectifier K+currents (IK) (Salkoff and Wymann, 1981; Wu and Haugland, 1985; Broadie and Bate, 1993; Tsunoda and Salkoff, 1995a,b). Subsequently, other classes of K+channels were characterized molecularly in Drosophila(Warmke et al., 1991; Goldstein et al., 1996; Titus et al., 1997; Wang et al., 1997).
Drosophila photoreceptors express bothIA and IK currents, with the former mediated by subunits encoded by the Shaker locus (Hardie, 1991; Hardie et al., 1991). However, the genes encoding the delayed-rectifier channel subunits have not yet been identified, and very little is known about IK modulation. Although the functional significance of IA andIK remains to be clarified inDrosophila phototransduction, in Limulus and in the blowfly Calliphora vicina they may regulate the gain and frequency response during light and dark adaptation (Fain and Lisman, 1981; Weckstrom et al., 1991). In Drosophila photoreceptors, the sustained depolarization generated by light activation of transient receptor potential (TRP) and transient receptor potential-like (TRPL) cationic channels is expected to open voltage-gated K+ channels. One can predict that the subsequent hyperpolarizing K+ currents will oppose the light-induced depolarizing currents to shape the photoreceptor potential.
In the present study, we show that Drosophila photoreceptorIK and IA channels are positively regulated by Ca2+/calmodulin via a Ca2+/calmodulin-dependent protein kinase (CaM kinase), with IK being more sensitive thanIA. Using the current-clamp technique, we demonstrate that inhibition of IK with K+ channel blockers or with a CaM kinase inhibitor increases the amplitude and broadens the transient component of the photoreceptor potential, weakens adaptation, and slows the termination of the light response. We suggest that IKrepresents an additional calmodulin-sensitive component ofDrosophila phototransduction.
MATERIALS AND METHODS
Preparation. Wild-type (WT) Drosophila of the Canton S strain and of ShKS133 mutant (both red-eyed) were used for the experiments (Wu and Ganetzky, 1992). The ShKS133 allele, which eliminates theIA, is a missense point mutation in the pore-forming H5 region of the Shaker channel protein (Lichtinghagen et al., 1990). Ommatidia dissociated from stage p15 pupae (Bainbridge and Bownes, 1981) were prepared as described previously (Hardie, 1991; Peretz et al., 1994). Retinae were rapidly dissected in Ca2+/Mg2+-free Ringer’s solution, transferred to normal Ringer’s solution supplemented with 10% fetal calf serum and 25 mm sucrose, and gently triturated with a fire-polished glass pipette of ∼200–400 μm tip diameter. During the dissociation procedure, which requires no enzyme treatment, the surrounding pigment cells disintegrate, exposing the photoreceptor membrane. The dissection procedure was performed under dim red light illumination (Schott OG630 filter). Dark-adapted ommatidia were used immediately after dissection, for whole-cell patch-clamp recording.
Electrophysiology. Aliquots (∼10 μl) of ommatidia were allowed to settle in a small chamber onto a clean coverslip mounted on the stage of an Axiovert 35 inverted microscope (Carl Zeiss). Recordings were made at 22 ± 1°C, using patch pipettes pulled from borosilicate glass capillaries (fiber filled) with resistance of 4–8 MΩ. Whole-cell recordings were performed using standard techniques (Hamill et al., 1981; Hardie, 1991; Peretz et al., 1994). In experiments investigating the light response, we applied the current-clamp mode of the whole-cell patch-clamp technique in isolatedDrosophila photoreceptors. The resting potential of the photoreceptors was adjusted to −60 mV by applying a constant current. Series resistances were compensated by 85–90%. A tungsten halogen lamp (20 V, 150 W; Olympus Highlight 3000), attenuated by neutral density filters (1.5–2.0) via a Uniblitz shutter (Vincent Associates, Rochester, NY), provided illumination of photoreceptors. The peak transmission of the excitation and viewing filters was 520 and 630 nm, respectively. Signals were amplified using an Axopatch 200A patch-clamp amplifier (Axon Instruments, Foster City, CA), filtered below 2 kHz, via a four-pole Bessel filter. Data were sampled at 4–5 kHz and analyzed using pClamp 6.0.2 software (Axon Instruments) on an IBM-compatible 486 computer interfaced with DigiData 1200 (Axon Instruments). Further data analysis was performed using Axograph 3.0 software (Axon Instruments) and Excel 5.0 (MicroSoft) on an Apple Macintosh computer. All data were leakage-subtracted off line by the Clampfit program of the pClamp software. Activation and steady-state inactivation data were fitted with the Boltzmann distribution (assuming a reversal potential VK of −85 mV):
Equation 1where V50 is the voltage of half-maximal activation (at which I = 1/2Imax), or the voltage at which half of the steady-state inactivation was removed, and s is the slope of the curve. In WT photoreceptors, IA was measured at the peak, whereas IK was measured at the end of the trace (∼90 msec). All data were expressed as mean ± SEM. Statistically significant differences were assessed by Student’s t test.
Solutions. Bath Ringer’s solution contained 120 mm NaCl, 5 mm KCl, 1.5 mm CaCl, 8 mm MgSO4, and 10 mmN-tris[hydroxymethyl]methyl-2-aminoethanesulfonic acid (TES), pH 7.15. Stock solutions of KN-62, KN-92, and KN-93 (Calbiochem, La Jolla, CA) were made in DMSO. N-(6 aminohexyl)-5-chloro-1-naphthalenesulfonamide (W7), trifluoperazine (TFP) TEA-Tetraethyfammonium, and quinidine (Sigma, St. Louis, MO) were added to the bath solution at the final concentrations indicated in text and figure legends. The pipette solution contained 135 mm potassium gluconate, 2 mm MgCl, 4 mm Mg-ATP, 0.5 mm Na-GTP, and 10 mmTES, pH 7.15.
RESULTS
Activation and inactivation characteristics ofIK and IA inDrosophila photoreceptors
The whole-cell configuration of the patch-clamp technique (Hamill et al., 1981) was used to study the modulation of K+currents in dissociated Drosophila ommatidia. As shown in Figure 1, wild-type Drosophilaphotoreceptors are endowed with two main voltage-gated K+ conductances, the rapidly activating/inactivatingIA and the slowly inactivatingIK currents (Hardie, 1991). The delayed-rectifier IK current has previously been shown to be composed of two kinetically different components,IKf and IKs (Hardie, 1991). Using our activation protocol (Fig. 1), we were unable to discriminate accurately between these two IKcomponents, mainly because of the kinetic overlap of the various voltage-dependent rise times of activation. We could distinguish two different kinetic components of IK in the mutant allele Shaker KS133 (ShKS133 ) subjected to steady-state inactivation, when photoreceptor cells were treated with CaM kinase inhibitors (in five of eight cells; see below and Fig. 5). However, for the sake of clarity we have considered the delayed-rectifier K+ current as oneIK component, distinguishable from theIA current. Representative traces are shown in Figure 1A (left). IsolatedIK measurement was achieved by using theShKS133 mutation, which eliminatesIA (Fig. 1B, left).ShKS133 is a missense point mutation in the H5 pore-forming region of the Shaker channel protein (Lichtinghagen et al., 1990). IK was also measured in WT photoreceptors at the end of depolarizing pulses (∼90 msec) after IA has inactivated. The normalized current–voltage (I–V) relation ofIK as measured in WT or inShKS133 photoreceptors showed thatIK activated above −40 mV and saturated at potentials greater than +50 mV (Fig. 1C, left). In ShKS133 , the normalized conductance during IK activation was described by a single Boltzmann function with V50 = +12.5 ± 4.7 mV, slope = −12.3 ± 0.9 mV (n = 5) (Fig.2; see Table 2). A slight negative shift in the IK current–voltage relation and normalized conductance curves measured in WT was seen when compared with those measured in ShKS133 (Figs.1C, 2C,D). This could result from incomplete inactivation of IA in WT at the end of the depolarizing pulse, although a major part of IAinactivated in our protocol. Alternatively, there could be a modulation of IK activity attributable to developmental hyperexcitability of the ShKS133 photoreceptors. Along this line, we found thatIK amplitude inShKS133 tends to be slightly higher than that measured in WT (Tables 1, 3). Such compensatory mechanisms are observed sometimes in transgenic knock-out mice.
Activation and inactivation characteristics ofIA and IK inDrosophila photoreceptors. A, Representative wild-type (WT) whole-cell recordings of photoreceptor potassium currents using the activation (left) and inactivation (right) protocols. Usually, we can clearly differentiate the inactivatingIA component (arrowheads) separated from the slowly inactivating IK.B, Representative whole-cell recordings of activation (left) and inactivation (right) protocols of the Shaker mutant alleleShKS133 . C(left), The current density (pA/pF) is plotted against the voltage steps for WT (■) andShKS133 (▪). TheIK component is characterized (Boltzmann fitting, assuming a reversal potentialVK = −85 mV) byImax = 85.5 ± 4.1 pA/pF and 87.8 ± 5.6 pA/pF for WT (n = 11) andShKS133 (n = 8), respectively. Right, Steady-state inactivation ofIK in WT (■) andShKS133 (▪). For Boltzmann fitting parameters, see Table 2. D (left), The current density/voltage curve of IA is presented (Table 1). IA is characterized (Boltzmann fitting, measured at peak outward current, assuming a reversal potential VK = −85 mV) byImax = 92.3 ± 7.8 pA/pF (n = 11). Right, The Boltzmann fitting of IA steady-state inactivation gave the values V50 = −42.1 ± 1.0 mV and slope = 10.0 ± 0.8 (n = 4). In all voltage-clamp experiments throughout this study, the holding potential was −100 mV. For the activation protocol, cells were stepped from −100 mV to +60 mV in 10 mV increments, during a 100 msec test pulse (left column). In the steady-state inactivation protocol, the cell membrane was subjected to inactivating prepulses of 1 sec duration from −90 mV to +10 mV in 10 mV increments, before 80 msec test pulse to +30 mV (right column).
Inhibition of the delayed-rectifier current (IK) by the calmodulin antagonist W7. The activation protocol as in Figure 1 is used to detect the steady-state effect of the calmodulin antagonist W7 onIK currents. Traces were recorded 3–4 min after drug treatment. A, Whole-cell potassium currents, recorded in WT photoreceptors, were inhibited by W7 in a concentration-dependent manner. In response to 2.5 μm W7,IK was reduced by >50% (middle), whereas 25 μm W7 almost completely abolished the current (right), as compared with control (left). B, Similar results were obtained in the ShKS133 mutant, which lacks the IA. C, D, The current density/voltage curve for WT (C, left) andShKS133 (D, left) and their corresponding normalized conductance (C, D, middle) are shown for control (■), 2.5 μm W7 (▪), and 25 μm W7 (•) data. The steady-state inactivation protocol was the same as in Figure 1(right; traces not shown). Because of almost complete inhibition of IK, no steady-state inactivation curves could be determined after treatment with 25 μm W7. The curves were fitted by the Boltzmann distribution function. For fitting values see Tables 1 and 2.
W7 effect on the Imax in WT andShKS133
As shown in the normalized I–V curve,IA activated at potentials more negative than those required for IK, above a threshold of approximately −60 mV (Fig. 1D, left). The normalized conductance of IA activation was fitted with a single Boltzmann distribution ofV50 = −7.9 ± 2.9 mV and slope = −13.8 ± 0.3 mV (n = 5) (Fig.3; Table2). Both currents inactivated in response to a depolarizing prepulse, with the IA being inactivated at more hyperpolarized potentials. The steady-state inactivation of IA and IKcould be described by a V50 = −42.1 ± 1.0 mV, slope = 10.0 ± 0.8 (n = 4), andV50 = −18.9 ± 2.1 mV, slope = 11.0 ± 0.2 (n = 6), respectively (Figs.1C,D, right, 3, right; Table 2). TheV50 values for IAactivation and steady-state inactivation of the present work are significantly shifted to more depolarized potentials (more than +10 mV) when compared with a recent study on a semi-intact retina preparation (Hevers and Hardie, 1995). Differences in recording conditions and solutions may account for these variations.
The effect of W7 on IA. The current density/voltage curve (left), their normalized conductance (middle), and the corresponding steady-state inactivation curves (right) are shown for control (■), 2.5 μm W7 (▪), and 25 μmW7 (•) data. Because little effect on IAwas observed in the presence of 2.5 μm W7, only the data obtained with 25 μm W7 were included in the normalized conductance and steady-state inactivation curves. All of the curves were fitted by Boltzmann distributions. For details of the fitting values, see Tables 1 and 2.
Effect of W7 on the steady-state activation and inactivation parameters in WT and ShKS133
Ca2+/calmodulin-dependent modulation ofIK
In view of the pivotal role played by Ca2+/calmodulin in adaptation and termination of the light response (Arnon et al., 1997a,b; Scott et al., 1997), we tested whether photoreceptor IA andIK would be subjected to modulation by Ca2+/calmodulin-dependent processes, and if so, to what extent it would affect the light response. To examine the possible Ca2+/calmodulin-dependent modulation ofIK, we perfused the photoreceptor cells extracellularly with the calmodulin antagonist W7 at two different concentrations. Similar results were obtained using TFP, another calmodulin antagonist (data not shown). For all experiments, the currents were recorded on the same cell before and after application of the drug. Application of 2.5 μm W7 to WT photoreceptor cells led to a reduction of ∼62% of the maximalIK current density (Imax), whereas exposure of 25 μm W7 produced an almost complete inhibition ofIK (Fig. 2A,C; Table 1). The onset of W7 action was at ∼1–2 min, and the effect reached steady state within ∼5–7 min. Similar results were obtained whenIK was reordered in isolation in theShKS133 mutant, with 55% inhibition ofIK current density at 2.5 μm W7 and an almost complete IK suppression on exposure to 25 μm W7 (Fig. 2B,D; Table1). The normalized conductance of activation indicated that there was a small negative shift of V50 in the presence of 2.5 μm W7 (5.6 and 7 mV as measured in WT andShKS133 , respectively) (Fig.2C,D; Table 2). Generally, the steady-state inactivation properties of IK did not change significantly in response to 2.5 μm W7, as measured either in WT or inShKS133 mutant (Fig. 2C,D; Table 2).
Ca2+/calmodulin regulation ofIA
Qualitatively, similar results were obtained for W7 action onIA, except that the effects onImax were much weaker. Furthermore, the effect of W7 on IA might be slightly overestimated because of a minor contribution of the IK rise. At 2.5 μm W7, current density at the peak ofIA was not significantly altered, with a decrease of <10% (Fig. 3; Table 1). At 25 μm W7, maximal IA was substantially reduced (by 67%). The voltage dependence of activation and steady-state inactivation were significantly affected by W7. The V50 ofIA activation was negatively shifted from −7.9 ± 2.9 mV to −19.8 ± +1.7 mV (n = 5) in response to 25 μm W7. In addition, there was a negative shift of the steady-state inactivation fromV50 = −42.1 ± 1.0 mV toV50 = −48.8 ± 2.5 mV in response to 25 μm W7 (n = 4) (Fig. 3; Table 2).
A CaM kinase, identified as a calmodulin-dependent modulator of photoreceptor K+ channels
The next question we asked was what type of calmodulin-dependent process was involved in the regulation of the photoreceptor K+ currents. To examine this issue, we used the specific CaM Kinase inhibitors KN-93 (Sumi et al., 1991) and KN-62 (Tokumitsu et al., 1990). Only the data of KN-93 are presented here, because essentially the same results were obtained with KN-62 (data not shown). We focused on the IK current because it proved to be more sensitive to W7. For this purpose, we used theShKS133 mutant to exclude anyIA contamination. AlthoughIK inactivated very little in the range of 100 msec (Fig. 1B, left), it underwent C-type inactivation (Hoshi et al., 1990) in a longer stimulation range (1 sec), and its inactivation could reach >50% (Figs.4D, 5). We measuredIK amplitudes both at the peak and at the end of the pulse (plateau). After exposure to 5 μm KN-93, the amplitudes of the peak and plateau components ofIK were reduced by 62% (from 107.1 ± 6.8 pA/pF to 40.7 ± 6.1 pA/pF) and 85% (from 65.7 ± 6.3 pA/pF to 10.1 ± 1.2 pA/pF), respectively (n = 6) (Fig.4A,D, top traces; Table3). The effect of KN-93 was very specific because the application of its structurally related but functionally inactive analog KN-92 (5 μm) did not produce any effect on IK even after longer exposure (>15 min) (Fig. 4D). Furthermore, to exclude the possibility that KN-93 could act as an open-channel blocker, we used a train protocol. KN-93 inhibition was obtained at the first pulse (+60 mV) after a 5 min exposure to the drug, and the effect did not significantly increase further after subsequent stimulations. The onset of KN-93 inhibitory action was at ∼2 min after application, and it peaked at ∼5–6 min. Because KN-93 was delivered along with the carrier DMSO at a final concentration of 0.1%, we checked for possible effects of the solvent carrier. We found that DMSO alone affected neither IK nor the light response (data not shown). KN-93 caused a significant change in the voltage dependence of activation. The normalized conductance curves indicated a negative shift of the V50 by 11.5 and 8.7 mV for the peak and plateau components, respectively (Fig. 4B; Table3). KN-93 also caused the IK to inactivate at more negative potentials. The V50 of steady-state inactivation was shifted from −12.7 ± 0.6 mV to −22.3 ± 2.4 mV (n = 6) (Fig. 4C; Table 3), an effect not seen in response to W7 treatment (see Discussion).
Modulation of IK by the CaM kinase inhibitor KN-93 in theShKS133 mutant. The specific CaM kinase inhibitor KN-93 modulates the peak and plateau components ofIK in theShKS133 mutant. In the experiments, the currents were recorded on the same cell before and after 6 min application of the drug. Except for C, the cells were stepped from −100 to +60 mV in 10 mV increments, and the peak and plateau currents were measured during the 1 sec pulse. The curves were fitted by a single Boltzmann distribution. Results were obtained from six pupae. A, The current density/voltage curve is shown for control (■) and in response to 5 μm KN-93 (▪) at the peak (left) and plateau (right) ofIK. B, The normalized conductance curves are shown for the peak (left) and plateau component (right) ofIK. The same symbols were used as inA. For the fitting values, see Table 3.C, The steady-state inactivation curve ofIK is shown. Here the inactivation protocol was the same as in Figure 1. For detailed Boltzmann fitting values see Table 3. D (top traces), Representative example of the KN-93 (5 μm) effect onIK. From a holding potential of −100 mV, a step to +60 mV (1 sec) was given before and after (9 min) drug application. Bottom traces, Cell stepped from a holding potential of −100 to +60 mV (100 msec) before and 10 min after KN-92 treatment (5 μm).
Effect of KN-93 on Imax, normalized conductance and steady-state inactivation of IKin ShKS133
CaM kinase inhibition accelerated IKinactivation kinetics
It is known that K+ channels exhibit two different mechanisms of inactivation, referred to as N- and C-type inactivations (Hoshi et al., 1990; Choi et al., 1991; Yellen et al., 1994). Although N-type inactivation is a fast process involving the occlusion of the inner mouth of the channel pore by the amino terminus (ball and chain model), C-type inactivation is a slower process occurring after prolonged depolarization and involving conformational changes at the external mouth of the pore and the S6 transmembrane domain. As shown in Figure 5, after step depolarization of 1 sec duration from −100 mV to +60 mV,IK underwent a slow C-type inactivation process by >50%. In Figure 5A,B, the traces have been normalized to compare the kinetics. After 6 min of 5 μm KN-93 application on ShKS133 photoreceptor cells, IK decreased in amplitude and inactivated with faster kinetics when compared with control (Fig. 5A). Similar results were obtained with 10 μm W7 application (Fig. 5B). After a 5 min W7 washout, there was a partial recovery in terms of both amplitude and kinetics. Note that neither the deactivation kinetics [as reflected by the tail current decay (Fig.5A, inset)] nor the rising phase of current activation was changed in the presence of W7 or KN-93 (Fig. 5A, right).IK inactivation kinetics was best fitted with two exponentials. In response to 5 μm KN-93, the decay time constants were significantly reduced from τ1 = 86 ± 10 msec and τ2 = 767 ± 29 msec to τ1 = 30 ± 3 msec and τ2 = 514 ± 34 msec (n = 6, p < 0.005). Regarding the activation kinetics, we have considered the photoreceptorIK to be one component. As mentioned earlier, it was suggested by Hardie (1991) that the Drosophiladelayed-rectifier currents are composed of two conductances,IKf and IKs, with fast and slow activation kinetic components. Results consistent with this suggestion were obtained in KN-93-treatedShKS133 photoreceptors by using a steady-state inactivation protocol (Fig. 5C). In the control traces, it was difficult to discriminate between the two kinetic components (Fig. 5C, left). However, when photoreceptor cells (in four of seven cells) were exposed to 5 μm KN-93 for 6 min (Fig. 5C, right), it became obvious that a fast component was more sensitive to inactivating prepulse potentials, as compared with a slower activating component that inactivated more weakly at the same prepulses. Similar results were obtained with W7 in seven of eight cells recorded. Nevertheless, it was difficult to distinguish between these two components when fitting the steady-state inactivation curve (Fig. 4C). Thus, it is possible that inhibition of CaM kinase affects differently the two kinetic components of C-type inactivation, thereby reflecting the existence of two different IK conductances. However, we cannot exclude the possibility that these kinetic components represent different conformational kinetic transitions of the same channel complex.
Changes in IK kinetics in response to W7 and KN-93. Using theShKS133 mutant, photoreceptor cells were stepped from −100 to +60 mV for 1 sec to allow the C-type inactivation of IK to occur.A (left), The currents were recorded before (control) and after 6 min application of 5 μm KN-93. Traces have been normalized for kinetic comparison. Right, The same normalized traces are shown at a smaller time scale. Inset, The normalized tail currents are shown. The C-type inactivation kinetics are well described by two exponential fits. In response to 5 μm KN-93, the fast and slow time constants (τ1 and τ2) decreased from 86 ± 10 to 30 ± 03 msec and from 767 ± 29 to 514 ± 34 msec, respectively (n = 6, p < 0.01). B (left), Similar results were obtained in response to 2 min exposure of 10 μm W7, with a partial recovery 5 min after washout of the drug.Right, Another experiment demonstrates the same phenomena at a smaller time scale and higher sampling rate.C, Steady-state inactivation traces, before and 5 min after application of 5 μm KN-93. The same steady-state inactivation protocol was used as in Figure 1.
Inhibition of IK reduced the light adaptation and delayed the response termination
To test whether photoreceptor K+ currents oppose the light-induced depolarizing currents and shape the light response, we investigated their role in phototransduction by pharmacological means using the current-clamp technique in isolated photoreceptors of the WT and the Drosophila mutantShKS133 , which eliminatesIA. To quantitatively estimate the drug effects on photoreceptor potential waveform, we used the quotientQ50 defined as a ratio value (Q50 =TD/TC) of the measurements made in the presence (TD) and absence (TC) of the drug.TD and TC are temporal parameters (in milliseconds) measuring the width of the light response at 50% of the maximal receptor potential amplitude evoked by illumination. First, we studied in WT photoreceptors the voltage light response before and after CaM kinase inhibition by application of 5 μm KN-93 (Fig.6A). After a 10 msec flash stimulus, KN-93 (6 min preincubation) significantly increased the light response amplitude and markedly delayed its termination, as compared with control with a Q50 = 1.84 ± 0.15 (p < 0.05, n = 4) (Fig.6A, left). To evaluate the effects of KN-93 on the light adaptation process, a 500 msec light stimulus was given before and after application of the drug. As shown in Figure6A (right), KN-93 not only increased the amplitude of the receptor potential but also broadened the transient component of the light response and weakened the dip between the peak and the plateau (Q50 = 1.99 ± 0.17,n = 4, p < 0.05). To focus on the K+ channel contribution, we investigated the effects of two different K+ channel blockers, TEA and quinidine (Fig. 6B). After a 10 msec flash stimulus, there was an enhancement of the receptor potential amplitude and a marked slowing of light response termination in the presence of the general K+ channel blocker TEA (20 mm) (Q50 = 1.76 ± 0.36, n = 6,p < 0.05). Similar results were obtained with 0.2 mm quinidine, previously shown to block delayed-rectifier K+ channels in Drosophila (Singh and Wu, 1989), with a Q50 = 2.12 ± 0.17 (n = 4, p < 0.05). After a 500 msec light stimulus, quinidine (0.2 mm) strongly inhibited the light adaptation process with a much broader transient and an almost complete elimination of the plateau (Q50 = 2.21 ± 0.33, n = 5, p < 0.01) (Fig. 6B, right). Figure 6C illustrates to what extent quinidine (0.2 mm) preferentially blockedIK currents in WT photoreceptors (compare withShKS133 in Fig.7C). However, we noticed that at this concentration (0.2 mm), quinidine also reduced by ∼20% the IA currents in WT cells (Fig.6C).
Effect of K+ channel blockers and a CaM kinase antagonist on the light response of WT photoreceptors.A, B, Whole-cell current-clamp recordings of the light response were performed in WT photoreceptors. In the current-clamp mode the resting potential was adjusted to −60 mV. The resting potential before adjustment ranged between −35 and −45 mV. Left, A light flash (10 msec, arrow) was given to dark-adapted photoreceptors (>2 min), and the light response was recorded before and 4 min after exposure of 5 μm KN-93 or 3 min after application of 20 mm TEA. Traces shown are representative of four similar experiments. Right, The same procedure was used except the light stimulus duration was 500 msec. Effects of the IK channel blocker quinidine (0.2 mm, five experiments) and of the CaM kinase inhibitor KN-93 (5 μm, five experiments) are shown in representative traces. C, Whole-cell voltage-clamp recordings of cells before (control, left) and 2 min after application of 0.2 mm quinidine (right). The activation protocol was the same as in Figure 1.
Effect of K+ channel blockers on the light response of ShKS133 photoreceptors. A, B, Whole-cell current-clamp recordings of the light response were performed inShKS133 photoreceptors.A, Voltage responses to light stimuli (500 msec) recorded in WT (right; representative of seven cells) and ShKS133 (left; representative of six cells) photoreceptors. B, Voltage responses of ShKS133 photoreceptors to a 10 msec flash in the absence and presence of 0.2 mmquinidine (left; representative of five cells) and 20 mm TEA (right; representative of four cells). C, Whole-cell voltage-clamp recordings ofShKS133 photoreceptors before (control, left) and 2 min after application of 0.2 mm quinidine (right). The activation protocol was the same as in Figure 1.
To evaluate the contribution of IA in light response adaptation and termination, we performed the same experiments in ShKS133 photoreceptor cells (Fig. 7). The photoreceptor potential waveform was very similar inShKS133 mutants as compared with WT photoreceptors after either a 10 msec flash or a 500 msec light stimulus (Figs. 6, 7A,B). TheShKS133 mutation affected neither the light adaptation nor the voltage waveform, including the transient, the dip, and the plateau phases (Fig. 7A). As compared with WT cells, essentially the same effects of TEA and quinidine were obtained in ShKS133 photoreceptors, with an increased amplitude and a broadening of the photoreceptor potential as well as a slowing down of the turn-off responses to flash stimuli (Fig.7B). After a 10 msec flash, the Q50of TEA (20 mm) and quinidine (0.2 mm) was 1.41 ± 0.04 (n = 5, p < 0.001) and 2.00 ± 0.26 (n = 4, p < 0.05), respectively. Similar results were obtained with KN-93 (data not shown). Figure 7C shows that quinidine (0.2 mm) blocked virtually all IK currents inShKS133 photoreceptors.
Finally, we investigated the possible modulation ofIK by light. We comparedIK in dark-adapted cells and during a 10–100 msec flash stimulus that generates an approximately +10 mV depolarization. IK was measured under voltage-clamp by stepping cells for 100 msec from −80 mV to −10 mV. After subtracting the light-induced current, we found no significant effects on IK kinetics or amplitude (<10%) (data not shown).
DISCUSSION
For what functional purpose are Drosophilaphotoreceptors endowed with high densities of voltage-gated K+ channels (Hardie, 1991; Hevers and Hardie, 1995)? Given their magnitude, voltage operating range, and kinetics, it was crucial to elucidate whether these K+ conductances are subject to modulation and to evaluate their functional significance in phototransduction. The present work shows that Drosophilaphotoreceptor K+ channels are modulated by a CaM kinase, and as such may act in concert with other calmodulin-sensitive components to play a role in the feedback control of the light response.
Drosophila photoreceptor neurons have evolved an exquisitely sophisticated signaling machinery to turn on the light response. This leads to the opening of TRP and TRPL cationic channels and generates a depolarizing receptor potential (Ranganathan et al., 1995; Minke and Selinger, 1996; Zuker, 1996) that is expected to activate the voltage-gated K+ channels. On light stimulation, photoreceptor cells are likely to operate within potentials ranging from approximately −60 mV to +10 mV. Considering the voltage operating range values we found for IA andIK (Figs. 1, 3; Table 2), it is reasonable to assume that these K+ conductances will be operative within the voltage limits of photoreceptor activity.
Our data show that photoreceptors IK andIA are specifically inhibited by different Ca2+/calmodulin antagonists such as W7 or TFP, withIK being far more sensitive thanIA. Interestingly, this modulation was mimicked by two selective CaM kinase antagonists, KN-62 and KN-93. The inability of KN-92 (inactive structural analog of KN-93) to affectIK demonstrates the specificity of KN-93 action. The mechanisms whereby IK andIA are depressed after exposure to CaM kinase inhibitors are not elucidated yet, but may involve either a direct channel phosphorylation or an indirect modulation. With respect to indirect regulation, it is possible that the CaM kinase mediates its effect via the eag channel subunit, as suggested previously (Zhong and Wu, 1993). A striking consequence of CaM kinase inhibition was the accelerated C-type inactivation kinetics ofIK as revealed by exposure ofShKS133 photoreceptors to KN-93 or W7. Blockade of CaM kinase-mediated phosphorylation may alter the local charge distribution in a specific channel domain, thereby affecting directly or allosterically the kinetics of C-type inactivation, through long-range electrostatic interactions. A very similar modulation by CaM kinase has been reported recently for Kv1.4 K+channels (Roeper et al., 1997). Blockade of CaM Kinase II by KN-93 was found to accelerate the Kv1.4 inactivation rate constants by 5- to 10-fold, suggesting that CaM kinase phosphorylation is likely to affect the interplay between N- and C-type inactivation (Roeper et al., 1997). The origin of the shift toward negative potentials (∼10 mV) in steady-state activation of IK andIA evoked by KN-93 and W7, respectively, is unclear. However, blockade of CaM kinase-mediated phosphorylation may alter the net charge in the vicinity of the channel voltage sensor and thus affect the voltage-dependent gating (Perozo and Bezanilla, 1990). It is worth noting that W7 did not produce a substantial leftward shift in the steady-state activation and inactivation curves ofIK (Fig. 2), suggesting that the Ca2+/calmodulin effects may not be mediated solely by a CaM kinase.
Our results indicate that IK is more sensitive than IA to modulation by a CaM kinase in photoreceptor cells. A similar higher sensitivity ofIK as compared with IAwith regard to CaM kinase modulation was recently found in culturedDrosophila neurons (W.-D. Yao and C.-F. Wu, personal communication). The channel subunit gating theIA current in Drosophilaphotoreceptors was found to be encoded by the Shaker locus (Hardie et al., 1991). Although the native oligomeric structure ofIA is not known, Hardie et al. (1991) suggested previously that it is encoded by some of the Shakerisoforms, possibly ShA1, ShA2, ShG1, or ShG2. The situation is even more complex for the identity of IK. We found by PCR thatShab 1 and Shab 2 isoforms as well asShaw transcripts are expressed in Drosophilaretina (our unpublished data), indicating that Shaband Shaw gene products could possibly be direct or indirect substrates of CaM kinase regulation. In this regard, it is worth noting that the Shab channel subunit contains four consensus sites for phosphorylation by CaM kinase [XRXXS (Pearson and Kemp, 1991)] at its intracellular amino and C termini.
Ca2+/calmodulin is known to regulate various downstream targets, including CaM kinase as well as additional components involved in phototransduction (Arnon et al., 1997a,b; Scott et al., 1997). Modulation of IK mediated by CaM kinase thus represents one of the effects of Ca2+/calmodulin on receptor potential. Considering that photoreceptor cells were recorded in the dark, our data imply that in resting dark-adapted conditions there is a marked basal phosphorylation of K+ channels by CaM kinase. Resting cytoplasmic free Ca2+ levels in the dark (in the presence of 1.5 mm external Ca2+) range within 130 and 180 nm (Hardie, 1996). These values are apparently sufficient to elicit substantial CaM kinase activity in the dark (Friedman et al., 1986; Braun and Schulman, 1995; Soderling, 1996). Within the operating window of the photoreceptor potential (−60 mV to +10 mV), the activation of IK andIA is still far from saturation, leaving many K+ channels to be recruited by increased CaM kinase activity after light stimulation. However, we could not detect a significant upregulation of IK by light. This result does not exclude a role for CaM kinases in regulatingIK activity during light stimulation. Indeed, under our experimental conditions light stimulation could also activate Ca2+/calmodulin-dependent phosphatases (e.g., calcineurin), which may tightly interact with the channel complex leaving a steady-state phosphorylation almost unchanged. Thus,IK channel activity may be accounted for by a fine tuning of Ca2+/calmodulin-dependent kinases and phosphatases. Interestingly, a recent report described the existence of a signaling complex consisting of the stable association of the protein phosphatase PP2A with CaM kinase IV (Westphal et al., 1998). PP2A dephosphorylates CaM kinase IV and functions as a negative regulator of CaM kinase IV signaling (Westphal et al., 1998).
From a functional point of view, our current-clamp data show for the first time in Drosophila that voltage-gated K+ channels play a significant role in adaptation and termination of the light response. Similar observations were reported in photoreceptors of the blowfly C. vicina(Weckstrom et al., 1991), in which K+ channels were suggested to reduce the membrane time constant, thus enabling the photoreceptors to code high frequencies in light-adapted cells. Previous work performed in Limulus suggested that the dip between the transient and the plateau phase of the photoreceptor potential could be accounted for by the IAchannel activity (O’Day et al., 1982). This dip was consistently observed in the voltage light response recorded fromShKS133 photoreceptors (Fig.7A), excluding a significant contribution ofIA to this phase of the receptor potential waveform. Furthermore, inhibition of CaM kinase by KN-93 or blockade ofIK channels by quinidine and TEA reproduced the same effects on either ShKS133 mutant or WT photoreceptors. Although we did not notice major differences in the potential waveforms between WT andShKS133 mutants, we cannot totally exclude a possible role of IA in the light response. Clearly, the decreased light adaptation and the slowing down of the turn-off kinetics produced by TEA and quinidine point toIK as the main K+ conductance involved in the regulation of the light response. It is worth noting that KN-93 broadened the transient component of the light response but did not reduce the plateau phase as elicited by K+channel blockers. A likely explanation is that 5 μm KN-93 did not completely abolish IK (Fig. 4; Table 3), whereas 0.2 mm quinidine almost totally suppressedIK in ShKS133 photoreceptors (Fig. 7).
The gating mechanisms of light-activated channels remain a matter of controversy. It has been proposed that calcium release from internal stores is required for activation of phototransduction and that the TRP channel functions as a store-operated channel. In this view, TRP is gated by the depletion of internal stores (Minke and Selinger, 1996;Arnon et al., 1997a,b). However, recent studies challenged this hypothesis and suggest that IP3 receptors and internal stores are not required for the activation of the light response (Scott et al., 1997). However, Ca2+/calmodulin was recently found to tightly control the light response by modulating the various components previously established in the Drosophilaphototransduction process. Ca2+/calmodulin was shown to mediate light adaptation through its negative feedback on IP3- and ryanodine-sensitive stores, thereby dampening the Ca2+-induced Ca2+ release amplification process (Arnon et al., 1997a,b). Likewise, Ca2+/calmodulin was found to control termination of the light response via its inhibitory action on TRPL channels and its positive regulation of arrestin activity (Scott et al., 1997). For example, arrestin I (also called phosrestin I in photoreceptors) undergoes light-induced phosphorylation on a subsecond time scale, via CaM kinase II activity (Matsumoto et al., 1994; Kahn and Matsumoto, 1997). A recent study in Limulus photoreceptors showed that Ca2+/calmodulin could even exert its control via inhibition of phospholipase C, and this may also apply to theDrosophila phototransduction process (Richard et al., 1997). The modulation of IK by CaM kinase supports the notion that K+ channels represent an additional calmodulin-sensitive component of the negative feedback control of the light response. We suggest that IK acts in concert with other Ca2+/calmodulin-sensitive elements of the transduction cascade to regulate the gain, to control the waveform of the light-activated receptor potential, and to extend the operating range of photoreceptors.
Footnotes
This research was supported by grants from the Israel Academy of Science, the Minerva Foundation, and the Dominic Einhorn Foundation (B.A). Dr. A. Peretz was supported by a Weizmann Institute postdoctoral fellowship (Koret fund) and by the Human Frontier Science Program. B.A. is an incumbent of the Philip Harris and Gerald Ronson Career Development chair. We thank Drs. Vivian Teichberg, Baruch Minke, and Eitan Reuveni for critical reading of this manuscript and helpful discussions. We are grateful to Emily Levine for careful reading of this manuscript. We also thank Wei-Dong Yao for communication of unpublished work.
Correspondence should be addressed to Dr. Bernard Attali, Department of Neurobiology, The Weizmann Institute of Science, Rehovot 76100, Israel.
