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B. L. Prosser and E. O. Hernández-Ochoa contributed equally to this work.
Corresponding author M. F. Schneider: 108 N. Greene Street, Baltimore, MD 21201, USA. Email: email@example.com
S100A1 is a Ca2+ binding protein that modulates excitation–contraction (EC) coupling in skeletal and cardiac muscle. S100A1 competes with calmodulin for binding to the skeletal muscle SR Ca2+ release channel (the ryanodine receptor type 1, RyR1) at a site that also interacts with the C-terminal tail of the voltage sensor of EC coupling, the dihydropyridine receptor. Ablation of S100A1 leads to delayed and decreased action potential evoked Ca2+ transients, possibly linked to altered voltage sensor activation. Here we investigate the effects of S100A1 on voltage sensor activation in skeletal muscle utilizing whole-cell patch clamp electrophysiology to record intra-membrane charge movement currents in isolated flexor digitorum brevis (FDB) muscle fibres from wild-type and S100A1 knock-out (KO) mice. In contrast to recent reports, we found that FDB fibres exhibit two distinct components of intra-membrane charge movement, an initial rapid component (Qβ), and a delayed, steeply voltage dependent ‘hump’ component (Qγ) previously recorded primarily in amphibian but not mammalian fibres. Surprisingly, we found that Qγ was selectively suppressed in S100A1 KO fibres, while the Qβ component of charge movement was unaffected. This result was specific to S100A1 and not a compensatory result of genetic manipulation, as transient intracellular application of S100A1 restored Qγ. Furthermore, we found that exposure to the RyR1 inhibitor dantrolene suppressed a similar component of charge movement in FDB fibres. These results shed light on voltage sensor activation in mammalian muscle, and support S100A1 as a positive regulator of the voltage sensor and Ca2+ release channel in skeletal muscle EC coupling.
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Skeletal muscle excitation–contraction (EC) coupling is the process by which membrane depolarization triggers sarcoplasmic reticulum (SR) Ca2+ release and subsequent contractile activation. Depolarization of the transverse (T) tubule system is detected by the voltage sensor of EC coupling, the dihydropyridine receptor (DHPR), an L-type Ca2+ channel (CaV1.1). Upon depolarization there is a reorientation of positively charged residues in the transmembrane domain of DHPR that triggers Ca2+ release from the coupled ryanodine receptor (RyR1) in the SR membrane (Schneider & Chandler, 1973; Horowicz & Schneider, 1981b; Huang, 1988; Ríos & Pizarro, 1991).
RyR-mediated Ca2+ release is modulated by Ca2+ and Mg2+, as well as by endogenous proteins such as FKBP12, calmodulin, calsequestrin and, more recently, S100A1 (Tripathy et al. 1995; Ikemoto et al. 1989; Jayaraman et al. 1992; Meissner, 1994; Treves et al. 1997). S100A1 is a small Ca2+ binding protein highly expressed in striated muscle and localized to the Ca2+ release units of skeletal and cardiac muscle cells (Haimoto & Kato, 1987; Zimmer et al. 1991; Most et al. 2003; Prosser et al. 2007). S100A1 interacts with both skeletal and cardiac RyR isoforms and enhances SR Ca2+ release. In the heart, S100A1 improves Ca2+ cycling and contractile performance (for a detailed review see Most et al. 2007), and is being rapidly pursued as a gene therapeutic agent for the treatment of cardiomyopathy (Pleger et al. 2007; Vinge et al. 2008). The ablation of S100A1 results in ventricular conduction defects and increased mortality following myocardial infarction (Ackermann et al. 2008; Desjardins et al. 2009). While skeletal muscle research has been less extensive, several groups have demonstrated direct effects of S100A1 on skeletal muscle EC coupling. Specifically, S100A1 binds to RyR1 with nanomolar affinity and increases the open probability of the channel (Treves et al. 1997), and exogenous S100A1 enhances Ca2+ release and force in skinned slow and fast twitch muscle fibres (Most et al. 2003). We recently have shown that S100A1 competes with calmodulin (CaM) for the CaM binding site on RyR1, and have mapped this interaction using NMR spectroscopy (Prosser et al. 2007; Wright et al. 2008). Furthermore, we showed that compared to muscle fibres from wild-type (WT) animals, muscle fibres from an S100A1 knock-out (KO) animal demonstrate smaller and more slowly developing Ca2+ transients when stimulated with an action potential, which can be reversed with adenoviral delivery of S100A1 (Prosser et al. 2007).
Enhancement of SR Ca2+ release could be the result of a direct interaction between S100A1 and RyR1, as supported by studies with the purified channel (Treves et al. 1997). A second, not mutually exclusive possibility is that modulation of the voltage sensor mediates S100A1's effect on Ca2+ release. This hypothesis is supported by the following. (1) S100A1 modulates the DHPR L-type Ca2+ channel in cardiomyocytes (Reppel et al. 2005). (2) S100A1 binds to the CaM binding site on RyR1 (Prosser et al. 2007; Wright et al. 2008), a site proposed to bind and stabilize the C-terminal tail of the DHPR (Sencer et al. 2001). (3) S100A1 binds RyR1 and enhances Ca2+ signalling, which may contribute to bi-directional crosstalk between RyR1 and DHPR, a previously documented pathway (Nakai et al. 1996; Avila & Dirksen, 2000). For these reasons we sought to explore the effect of S100A1 on the activation of the voltage sensor of EC coupling.
A classical approach to studying DHPR activation in skeletal muscle is to record gating currents elicited by sarcolemmal and transverse tubule depolarization. This is performed by eliminating ionic and linear capacitive currents, thereby allowing the isolation of non-linear capacitive currents arising primarily from the movement of intra-membrane charged residues in the DHPR (Schneider & Chandler, 1973; Chandler et al. 1976). Initial studies in frog muscle showed that a certain amount of charge must be moved to trigger Ca2+ release and fibre contraction (Kovacs et al. 1979; Horowicz & Schneider, 1981a). Since then, recording of charge movement has been used extensively to study DHPR mediated activation of Ca2+ release in skeletal muscle, at first largely in amphibian muscle (Hui, 1983; Pizarro et al. 1989; Csernoch et al. 1991; García et al. 1991), and more recently in mammalian muscle (Wang et al. 1999; Avila & Dirksen, 2000; Royer et al. 2008). Here we utilize whole-cell patch clamp electrophysiology to record charge movement currents in mammalian skeletal muscle fibres from WT and S100A1 KO animals. We show that WT mammalian fibres exhibit two components of charge movement, including a temporally delayed, steeply voltage-dependent component reminiscent of ‘Qγ’ previously identified in amphibian muscle fibres (Adrian & Almers, 1976; Adrian & Peres, 1977). We also demonstrate for the first time that the absence of an endogenous protein can markedly affect voltage sensor charge movement, as Qγ is suppressed in fibres lacking S100A1. Furthermore, we show that Qγ can be restored in KO fibres by transient application of S100A1, and is at least partially suppressed by the RyR1 inhibitor dantrolene. These results shed light on the nature of voltage sensor charge movement in mammalian muscle, as well as furthering our understanding of S100A1's modulation of EC coupling. A detailed examination of the relationship between voltage sensor charge movement and RyR Ca2+ release in both wild-type and S100A1 deficient muscle fibres is provided in a companion paper.
All animals were housed in a pathogen-free area at the University of Maryland, Baltimore. The animals were killed according to authorized procedures of the Institutional Animal Care and Use Committee, University of Maryland, Baltimore (Baltimore, MD), by regulated delivery of compressed CO2 overdose followed by decapitation.
FDB fibre preparation
Fibres were prepared using enzymatic dissociation of FDB muscles of 6- to 7-week-old C57 × 129 WT and S100A1 KO mice, and were cultured as previously described (Liu et al. 1997). S100A1−/− animals and WT littermate control animals were obtained from Dr Danna Zimmer, Texas A&M University. The generation and genotyping of these animals has been previously reported (Prosser et al. 2007).
For whole-cell Ca2+ current measurements bath (external) solution contained (in mm): 150 TEA-CH3SO3, 2 CaCl2, 10 Hepes, 1 MgCl2, 0.001 TTX, 1 4-aminopiridine, 0.025 N-benzyl-p-toluene sulphonamide (BTS), pH adjusted to 7.4 with CsOH. For non-linear capacitive current recording we use a similar external solution, except we added 0.5 CdCl2 and 0.5 CoCl2, and CaCl2 was reduced to 1 to keep the total divalent concentration constant.
The standard pipette solution (internal solution) contained (in mm): 140 Cs-CH3SO3, 10 Hepes, 20 EGTA, 4 MgCl2, 4 Na2ATP, 14 creatine PO4, 0.3 Na2GTP and 0.1 leupeptin, pH adjusted to 7.4 with CsOH. The choice of such solution was the result of a large series of trial and error tests in preliminary experiments. Compared with large non-permeable inorganic (NMG+ and TEA+) or organic (aspartate and glutamate) cations, we obtained with a Cs+-based solution a large improvement in sealing, durability, blocking of ionic currents, and comparability with experiments at the level of ionic current.
Alexa-Fluor-488 labelled S100A1 protein was a generous gift from Drs Nathan Wright and David Weber, University of Maryland, Baltimore.
Electrophysiology and data analysis
Membrane current measurements were performed using the whole-cell configuration of the patch-clamp technique (Hamill et al. 1981) as previously detailed by Wang et al. (1999) for mammalian FDB fibres but with some modifications. We use an EPC-10 (HEKA Instruments Inc., Bellmore, NY, USA) amplifier and Parafilm coated pipettes of borosilicate glass (WPI-TW150F3) with resistance of 1.2–1.6 MΩ when filled with the internal solution. Once the whole-cell configuration was established, cells were held at −60 mV and the capacitance compensation partially adjusted. Series resistance was compensated to 50–65%. Fibres with signs of qualitative clamp error, such as unstable series resistance, unstable holding current, or a stable holding current above 8 nA, were rejected from the analysis. Measurements were started 20 min after whole-cell configuration was established.
Voltage protocols were generated and current responses were digitized and stored using Patchmaster and Fitmaster (HEKA Instruments). Command pulses were delivered at 10 s intervals to the levels and duration indicated in each figure from a holding potential of −80 mV, unless otherwise indicated. Currents were typically low-pass-filtered at 3–10 kHz (3-pole Bessel filter). Currents were sampled at 10 kHz. Linear capacitive and ionic currents were routinely subtracted by a P/4 protocol from a subholding potential of −20 mV. Gating charge moved during each test depolarization (QON) was quantified by calculating the area under the curve of each trace of non-linear current using the post-transient level of each trace as a steady-state value of non-linear ionic current. Total charge moved during repolarization (QOFF) was calculated similarly. Total charge movement was normalized to the linear fibre capacitance, which was estimated using the following equation: C=Q/V. C was determined by measuring linear capacitive current elicited by a ±5 mV test pulse from the holding potential and integrating the area under the capacitive current trace to estimate Q.
Temporal differences in charge development at different voltage steps and between WT and KO groups were considered in setting the time to integrate during a typical 80 ms pulse. To minimize ionic contamination of the ON current, the time of integration for QON was set to the nearest approximation of the end of Q development. As such, for steps to −70 through −40 mV, and for steps above 0 mV, the time of integration for the ON current was set between 15 and 25 ms. For steps to −30 through 0 mV, the time of integration was increased to between 25 and 35 ms due to the presence of a temporally delayed component in WT fibres. In KO fibres lacking a temporally delayed component, an increase in integration time was not required. As a visual depiction of these different integration time points, hash marks have been included on the ON current traces in Fig. 1C to mark the end of the integration time. The time of integration for the OFF current was always set to 50 ms after the pulse. Quantification of charge movement will be considered further in the results.
Western blots were performed as in Liu et al. (2009) with modifications. Tibialis anterior muscles were isolated from WT and S100A1−/− animals, frozen in liquid nitrogen, and stored at −80°C. Muscles were ground to a fine powder at −20°C with mortar and pestle, then lysed and centrifuged, and the soluble fraction collected as previously described (Liu et al. 2009). Protein content was determined using the Bradford assay (Bio-Rad, Hercules, CA, USA). Approximately 50 μg of protein from each sample was separated by SDS-PAGE using a 4–12% gradient gel and transferred to PVDF membrane. Blots were then processed and probed with the appropriate antibodies. The antibody for DHPR α1s was purchased as tissue culture supernatant from Developmental Studies Hybridoma Bank (Iowa City, IA, USA) and used at a 1: 100 dilution. The antibody for glyceraldehyde phosphate dehydrogenase (GAPDH) was from Sigma (St Louis, MO, USA). Immunoreactive bands were visualized by ECL Western Blotting Detection Reagents (GE Healthcare (Amersham), Piscataway, NJ, USA).
Fluo-4AM Ca2+ transient recordings
Action potential evoked Ca2+ transients were monitored using the fluorescent indicator Fluo-4AM and ultra high-speed confocal microscopy (Zeiss LSM 5 LIVE system) as previously described (Prosser et al. 2007).
All statistical analysis was performed using OriginPro8.0 (OriginLab Corp., Northampton, MA, USA). All data are presented as mean values ± standard error of the mean (s.e.m.) unless otherwise noted. Normality of data sets was ensured for each statistical calculation. Significance was determined using Student's t-test and set at P < 0.05.
Non-linear charge movement currents are different in WT and S100A1 KO fibres
Figure 1 presents non-linear capacitive current records obtained from a FDB fibre from an S100A1 KO mouse (Fig. 1B) and from a WT littermate (Fig. 1A). The current components were elicited with 80 ms depolarizing test pulses to voltages ranging from −70 to +20 mV in 10 mV increments. The displayed records are typical of those obtained from 11 fibres from KO mice and 12 fibres from WT littermates. The transient positive (outward) non-linear current at the start of each depolarization was primarily due to outward movement of intramembrane charged voltage sensors. The more slowly developing or maintained inward or outward current following the transient charge movement current during the larger pulses represents slowly developing or constant voltage-dependent ionic current. The transient negative (inward) current at the end of the pulse was primarily due to the return of these mobile intramembrane charges when the membrane potential was restored to the holding voltage, with a possible additional contribution from non-linear tail currents flowing through ion channels activated during the depolarization. Ionic current interference with the charge movement currents was typically minimal for depolarizations to voltages ranging from −70 to −10 mV, but became increasingly important for larger depolarizations. Procedures for minimizing the influence of such ionic current components on charge movement characterization and quantification will be presented in the following section.
Simple visual comparison of the representative non-linear current records in Fig. 1 reveals several similarities and differences between charge movement currents recorded from the KO and WT fibres. (1) For depolarizations to −70 to −40 mV, the amplitude of the transient currents and their relatively simple time course were similar for KO and WT fibres. (2) During pulses to −30 to 0 mV the charge movement records from the WT fibres exhibited a temporally delayed ‘hump’ component after the initial peak, whereas KO fibres continued to display a time course consisting of a relatively rapid rise followed by a simple decay (see superimposed records in Fig. 1C). A temporally delayed component of charge movement that arises at intermediate depolarizations and produces a ‘hump’ in non-linear current records has been previously described in amphibian fibres and termed Qγ (Adrian & Almers, 1976; Adrian & Peres, 1977). We will adapt this terminology for the temporally delayed component seen in mammalian fibres here. Due to the similar initial phase in WT and KO fibres, but the presence of a delayed extra component only in the WT fibre, the charge moved by the charge movement current became larger for the WT than for the KO fibre over this intermediate voltage range. (3) For even larger depolarizations (to +10 and +20 mV), a kinetically delayed component was no longer obviously distinguishable. However, the amplitude of the transient charge movement current (and its area) continued to be larger for the WT than for the KO fibre, indicating greater charge moved in the WT fibre. These observations were generally characteristic of WT and KO fibres studied.
Isolation, verification and quantification of charge movement currents
Before quantifying the observations in the preceding paragraph, it is important to establish measures of charge movement that are not appreciably contaminated by non-linear ionic current contributions. The successful elimination of ionic current results in a charge movement current that saturates at extreme voltages, and demonstrates an equal amount of charge moved during depolarization (QON) and repolarization (QOFF). As seen in Fig. 2B, QON and QOFF demonstrated ON/OFF equality with minimal ionic contamination during and after 80 ms steps to −70 mV to −10 mV (Fig. 2A, top and 2B). However, QOFF became significantly larger than QON after 80 ms steps to 0 mV and more positive voltages, suggesting ionic contamination of the OFF recordings, as can be visualized with the longer depolarizing step in Fig. 2A, bottom. To minimize possible non-linear ionic current contamination of the OFF current, we used shorter, 25 ms steps to 0, +10 and +20 mV. This step was of adequate duration to achieve complete charge movement at these voltages, and minimizes the ionic contamination of the OFF, as seen in the ON/OFF equality of the open and filled circles in Fig. 2B and with the shorter depolarizing step in Fig. 2A, bottom. For approximately half the fibres tested we also used 25 ms steps to +30 mV and +40 mV, and found that despite increasing ionic contamination, ON and OFF charge movement were completely saturated at these voltages. These short steps could not be used for the less depolarized voltages, as fibres that exhibited a temporally delayed component elicited charge movement currents lasting longer than 25 ms (demonstrated in Fig. 1C). Ionic contamination of the ON current also appears to have led to a slight underestimation of charge moved at the most positive steps. For this and the other reasons detailed above, to achieve our measure of charge movement (Q) we integrated the ON current traces for 80 ms steps from −70 to −10 mV, and averaged the ON and OFF integrations from short 25 ms pulses for steps from 0 to +20 mV. Following these parameters fibres demonstrated ON/OFF equality, as demonstrated by the linear relationship between the ON and OFF charge seen in Fig. 2C.
As the P/4 protocol was used to subtract linear capacitive currents and isolate non-linear charge movement currents during depolarizing pulses, we sought to ensure linearity of membrane properties over the voltage range used to obtain these subtraction templates. Figure 2D demonstrates a sum response (black trace) to opposite polarity 20 mV voltage steps from a holding potential of −120 mV. The red and grey traces represent the total current from the depolarizing and hyperpolarizing steps, respectively. As can be seen the sum of these two currents is essentially zero, suggesting linearity of membrane currents at these very negative potentials. Figure 2E shows the remaining non-linear current elicited by an 80 mV step to 0 mV in a representative WT fibre (blue trace), after subtraction with the P/4 protocol. Below is the amplitude of the subtraction template (middle current trace) and the template scaled up by a factor of 4 (bottom current trace), as would be used in the subtraction from an 80 mV step. Remaining non-linear currents in the control pulses appear negligible compared to the relatively large charge movement currents, validating the use of this technique to isolate non-linear capacitive currents in FDB fibres.
Figure 3 further demonstrates charge movement conservation in WT FDB fibres. Charge movement currents were recorded in response to depolarizing pulses of different duration (starting at 2 ms and increasing in 2 ms increments) to −10 mV (Fig. 3A top), where we typically saw a pronounced temporally delayed component in WT fibres, and to +20 mV (Fig. 3A bottom), where a temporally delayed component was not apparent. Figure 3B shows the relationship between QON or QOFF and pulse duration for the set of pulses in Fig. 3A. The normalized charge-pulse duration relationship was fitted to a single exponential function (continuous lines) of the form:
The calculated QON time constants were 12.7 ms for pulses to −10 mV, and 2.3 ms for pulses to +20 mV. Similar values were obtained for QOFF.
Charge movement in S100A1 KO fibres lacks the temporally delayed, steeply voltage-dependent Qγ component
Figure 4A shows the average charge vs. voltage (Q–V) relationship of 12 WT and 11 KO fibres. Consistent with simple visual comparison of charge movement currents between WT and KO fibres, the Q–V relationship was very similar between groups for steps to −70 to −30 mV. However, at −20 mV the data began to diverge and the charge moved in WT fibres (QWT) was considerably larger than their KO counterparts (QKO), consistent with the development of a second component. As a first approximation, the Q–V relationship of each individual fibre tested was fitted to a single Boltzmann function, as described by the equation:
where Qmax gives the maximum charge movement, Vhalf defines the potential where Q= 0.5 of Qmax and 1/k is a measure of the steepness of the Q–V relationship. The KO data were typically well fitted by a single Boltzmann, with average Boltzmann parameters of Qmax= 37.3 ± 3.2 nC μF−1, Vhalf=−25.8 ± 1.04 mV and k= 13.0 ± 0.9 mV. A single Boltzmann fit to each WT data set gave average parameters of Qmax= 53.0 ± 4.9 nC μF−1, Vhalf=−21.5 ± 2.5 mV and k= 9.5 ± 0.5 mV. Using these parameters both Qmax and k values were found to be significantly different between WT and KO fibres (P= 0.016 and P= 0.003, respectively).
Upon inspection of the fits to the average data in Fig. 4A, it is clear that while a single Boltzmann function accurately fits the KO data (R2= 0.998), several points are missed along the WT curve (R2= 0.955). Based on the similar Q–V relationship of WT and KO fibres at lesser depolarizations and the presence of a second, Qγ component of charge movement seen in WT, but not KO fibres, a double Boltzmann fit was applied to the WT data:
where Qmax is the limiting charge movement, Q1 and Q2 are the amplitudes of the charge components, and Vhalf and k are half-activation voltage and slope factor for each component, respectively. For this fit we used all fixed Q1, Vhalf,1, and k1 parameters from the KO fibres for the first Boltzmann component and allowed free values for the second component. As can be seen in Fig. 4B, this double Boltzmann function very accurately fitted the WT data (R2= 0.998). As all parameters were fixed to KO values for the first component, the improved fit cannot be attributed to an increased number of free parameters; instead it appears the WT and KO data contained a very similar first component, with a second component only present in the WT fibres. The second component of the double Boltzmann fit displayed a steep voltage dependence, with parameters of Qmax= 15.2 nC μF−1, Vhalf=−13.0 mV and k= 4.8 mV. A curve of this theoretically derived difference component (QWT-KO) is simulated in green, and represents Qγ suppressed in the KO fibres.
To evaluate the properties of the current elicited by the difference component of charge movement we subtracted the average KO current records from the average WT current records for each depolarizing voltage step. This average difference current, IWT-KO, is plotted vs. the average WT and KO charge movement currents (IWT and IKO, respectively) in Fig. 5. IWT-KO was negligible with steps to −70 through −40 mV. At −30, and more prominently −20 mV, IWT-KO began to develop a temporally delayed ‘hump’ which further increases in amplitude and area with steps to −10 and 0 mV while shifting back to earlier in time during the pulse. This current saturates in area around 0 mV.
To quantify QWT-KO we subtracted the average IKO record from individual IWT records for steps to −50 through +20 mV. We then integrated the resulting difference records to get a Q–V relationship for each individual difference component. These Q–V relationships were averaged and fitted to a single Boltzmann function, as plotted in Fig. 6A (AVG Q–V fit). The curve displays parameters Qmax= 12.1 nC μF−1, Vhalf=−17.7 mV and k= 5.0, which agree nicely with the steeply voltage-dependent component theoretically derived in Fig. 4B. The individual QWT-KOQ–V relationships were also fitted to single Boltzmann functions, and their subsequent Boltzmann parameters averaged. These revealed average parameters of Qmax= 12.9 ± 2.4 nC μF−1, Vhalf=−17.4 ± 2.9 mV and k= 3.7 ± 0.6 mV. A simulated curve from these average parameters (AVG of Fits) is superimposed over the fit of the average Q–V relationship. The most noticeable difference in the curves was the increased steepness of the fit to the average parameters, quantified by the lower k value. The fit to the average Q–V relationship was slightly less steep due to the variable appearance of Qγ along the voltage axis, which manifested itself as a larger range for Vhalf (range =−27 mV to −10 mV) and blurring of the steepness of the curve. This slight variability in the voltage dependence of Qγ also accounted for the larger variation in WT Vhalf parameters compared to KO Vhalf parameters. Furthermore, it blurred the kinetic properties of the two distinct components in WT fibres when viewed as an average current record (Fig. 5). A more accurate visual depiction of the two temporal components is seen in traces from individual fibres, as in Fig. 1A, Fig. 7B and Fig. 9B. Figure 6B plots QWT-KOvs. QWT and QKO for comparison. Figure 6C plots the Q–V curves normalized to Qmax, allowing a better visualization of the steeply voltage dependent difference component.
It is important to note that there was some variability in the presence or absence of the Qγ component within the groups of KO and WT fibres. Two out of a total of 11 KO fibres did show clear indications of a delayed Qγ component at one or more intermediate depolarization, and 1 out of 12 WT fibres did not exhibit a clear delayed Qγ component over the same voltage range.
Thus, the presence or absence of the delayed Qγ component is not absolutely determined by the presence of absence of S100A1. In the companion paper we show that the presence of the delayed Qγ component in a few atypical KO fibres and its absence in a few atypical WT fibres is correlated with a relatively larger Ca2+ release in these atypical KO fibres, and a relatively smaller Ca2+ release in the atypical WT fibres. If these atypical fibres were excluded from the Boltzmann fits to the Q vs. V data sets for each individual fibre, the mean parameter values for the KO fibres (without noticeable delayed Qγ component) were Qmax= 34.2 ± 2.6 nC μF−1, Vhalf=−25.8 ± 1.1 mV and k= 13.8 ± 0.8 mV. Excluding the atypical WT fibres lacking clear Qγ and using mean Q1 parameter values obtained only from KO fibres without any obvious delayed Qγ component, the mean parameter values for the second charge component from the double Boltzmann fit are Qmax= 16.1 ± 2.6 nC μF−1, Vhalf=−16.1 ± 3.1 mV and k= 2.8 ± 0.4 mV.
These refined values are likely to reflect a better estimate of Qβ and Qγ than obtained by using all KO fibres to define Qβ and all WT fibres (together with all KO fibres for Qβ) to define Qγ.
Intracellular application of S100A1 protein restores Qγ in S100A1 KO fibres
Next we sought to evaluate whether the Qγ component of charge movement suppressed in the KO fibres could be rescued by transient intracellular application of S100A1. To this end, we dialysed KO fibres with purified S100A1 protein and recorded charge movement currents. After our standard 20 min dialysis time, but now with 10 μm Alexa-488-S100A1 added to the pipette solution, non-linear capacitive currents were recorded using the same pulse protocol as detailed in the description of Fig. 1. Additionally, a confocal fluorescence image was taken of the dialysed fibre and a second image was taken of the tip of the pipette. Comparing the fluorescence in the pipette (with a known 10 μm Alexa-488-S100A1) to that of the fibre we could estimate the protein concentration achieved in the cell at the time of the recordings. The mean concentration of purified Alexa-488-S100A1 in the fibre at the time of charge movement recordings was 2.8 ± 0.2 μm, approximating the concentration of endogenous S100A1 in fast twitch skeletal muscle (Haimoto & Kato, 1987; Zimmer et al. 1991). As can be seen in Fig. 7A, dialysis of S100A1 into KO fibres almost completely restored the Q–V relationship of charge movement to the WT level, with restoration of both the total charge moved and the steepness of the curve. These data were well fitted by a double Boltzmann function (R2= 0.998), again using fixed KO parameters for the first Boltzmann and free parameters for the second. The restored (second) component obtained from this fit demonstrated Boltzmann parameters of Qmax= 14.8 nC μF−1, Vhalf=−12.7 and k= 6.1, similar to the difference component between WT and KO fibres. Figure 7B compares the ON current record of a KO fibre dialysed with Alexa-488-S100A1 compared to the average KO fibre recording. It is clear that transient application of S100A1 can restore the kinetic properties of the charge movement current in KO fibres, as the characteristic temporally delayed hump component of charge movement becomes evident after application of S100A1.
S100A1−/− fibres do not have significant alteration in L-type channel expression or Ca2+ current activation
Suppressed maximal charge movement could be the result of decreased DHPR expression in KO muscle. To test this hypothesis, we performed Western blot analysis for the α1s subunit of the DHPR in WT and KO muscle lysates. Figure 8A shows that protein expression of the DHPR was not altered in KO muscle, suggesting that decreased channel expression did not account for the differences in charge movement seen in KO fibres. Moreover, although S100A1 KO fibres lack Qγ, they did not exhibit any noticeable difference in both the amplitude and the activation of L-type Ca2+ currents compared to WT fibres. Figure 8B presents representative time courses of Ca2+ currents from WT and KO fibres in response to 1 s depolarizing steps to −60 mV to +20 mV as illustrated above the graph. Current onset was slow and maximum inward current peaked at approximately 80 ms with a pulse to 0 mV. The voltage dependence of activation and peak current density appear similar between WT and KO fibres. The current vs. voltage (I–V) relationship for pooled data from 11 WT and eight KO fibres is shown in Fig. 8C. There were no significant differences in current density at any of the voltages tested, including the maximum inward current elicited by a step to 0 mV (WT ICa=−5.8 ± 0.5 pA pF−1, KO ICa=−5.1 ± 0.5 pA pF−1, P= 0.27). I–V plots from WT and KO fibres were fitted to a Boltzmann Ohmic function, described by the following equation (Nakai et al. 1996):
where Gmax is the maximum conductance, V is the membrane potential, Vrev is the reversal potential, Vhalf is the half-activation potential, and k is a measure of the steepness. Average parameter values for Gmax, Vhalf and k for WT fibres were 108.7 pS pF−1, −14.7 mV and 5.4 mV, respectively. For KO fibres Gmax, Vhalf and k were 106.0 pS pF−1, −9.6 mV and 7.6 mV, respectively. These parameters were used to derive the activation curves for WT and KO fibres, as plotted in Fig. 8C (bottom). Other than a slight rightward shift in the Vhalf of KO fibres, there were no noticeable differences in L-type current activation. This suggests that despite suppression of Qγ in KO fibres, the activation of L-type Ca2+ currents was not significantly affected.
Application of dantrolene suppresses the Qγ component in WT fibres
It has been suggested that the Qγ component of charge movement identified in amphibian fibres is a consequence of Ca2+ released from the SR (Csernoch et al. 1991). If the decreased charge movement in KO fibres is a consequence of their decreased Ca2+ release (Most et al. 2003; Prosser et al. 2007), then a pharmacological intervention that reduces Ca2+ release should suppress the second component of charge movement. Therefore, we sought to reduce Ca2+ release with dantrolene, an inhibitor of RyR1, and measure the effect on charge movement. To this end we first identified a suitable concentration of dantrolene that mimicked the reduction of the Ca2+ transient inherent to fibres lacking S100A1. As shown in Fig. 9A, we found that after 3 min exposure to 40 μm dantrolene the peak amplitude of the action potential evoked Ca2+ transient was reduced by about 35%. The effect was consistent, relatively stable over time, and in general mimicked the reduction of the Ca2+ transient previously reported for fibres lacking S100A1 (Prosser et al. 2007). We then recorded the effect of this concentration of dantrolene on charge movement in control fibres. Figure 9B (left) shows representative ON charge movement currents of a control fibre before and after 3 min exposure to dantrolene, and the resulting difference record. Exposure to dantrolene did not affect the first component of charge movement but at least partially suppressed the temporally delayed component seen at intermediate depolarizations. Figure 9B (right) shows the average ON charge movement currents of four KO fibres before and after dantrolene, and the resulting difference current. There was no temporally delayed component in these KO fibres prior to exposure to dantrolene, and, notably, exposure to dantrolene caused no further suppression in charge movement in any of these fibres. The only detectable difference was a slight increase of the Qβ component of charge movement, as indicated by the minor negative deflection in the difference current. Figure 9C shows the pooled Q versus V relationship from six control fibres before and after treatment with dantrolene. The Q–V relationship of the integrated difference records is also displayed for comparison. The difference component over the voltage range of −50 mV to −10 mV was fitted by a single Boltzmann function with parameters Qmax= 6.3 nC μF−1, Vhalf=−21.5 mV and k= 3.0 mV. It should be noted that this fit only accurately described the Q vs. V relationship of the dantrolene isolated difference component for steps to −50 mV to −10 mV. Upon further depolarizations the difference component appears to decrease monotonically with voltage, and therefore has been fitted with a straight linear function over this voltage range. These findings suggest that 40 μm dantrolene partially suppresses and/or shifts the voltage dependence of Qγ in control fibres to higher potentials, but has minimal or no affect on KO fibres which initially lack Qγ.
La3+ profoundly modifies charge movement currents in FDB fibres, but Cd2+ and Co2+ do not
As the temporally delayed Qγ component of charge movement has not been consistently demonstrated in mammalian fibres, we next evaluated possible explanations for this discrepancy. Since Cd2+ has been suggested previously to alter the kinetic properties of charge movement (Francini et al. 2001), we first evaluated charge movement in the absence of Cd2+ and Co2+ by using our standard internal and external solutions, except with the elimination of Cd2+ and Co2+ from the external solution. To block inward Ca2+ currents and allow the evaluation of charge movement currents, we added 10 mm Mg2+ to the external solution. This set of control experiments, both for Cd2+/Co2+ and for La3+ (see below), were carried out on FDB fibres from mice of the C57Black strain. Figure 10A shows representative recordings from one such control fibre bathed in the high Mg2+, Cd2+ and Co2+ free external solution. The presence of a temporally delayed ‘hump’ component is clearly evident in the current records at similar voltages to where it is typically seen in control fibres bathed in our standard Cd2+/Co2+ based external solution. Figure 10B shows the pooled Q vs. V relationship of three control fibres exposed to high Mg2+, Cd2+ and Co2+ free external solution and three control fibres exposed to Cd2+/Co2+solution. The Q vs. V relationship of fibres treated with high Mg2+, Cd2+ and Co2+ free solution was very similar in both slope and amplitude to that of fibres exposed to Cd2+/Co2+, with only a slight, 2–3 mV shift in the half-maximal voltage. The data were fitted by a double Boltzmann function with the following parameters: Qmax,1= 33.8 nC μF−1, Qmax,2= 14.2 nC μF−1, Vhalf,1=−19.0 mV, Vhalf,2=−13.0 mV, k1= 12.8 mV and k2= 4.0 mV.
La3+ is another common and widely used Ca2+ channel blocker. In preliminary experiments using a recording solution containing La3+ we did not detect the presence of two kinetically distinct components of charge movement in FDB fibres. We therefore sought to further evaluate the effects of La3+ on charge movement. Figure 10C shows representative charge movement currents from fibres exposed to 0.3 mm La3+ in our standard external solution containing Cd2+/Co2+. These fibres exhibited dramatically increased current kinetics and did not display any clear temporally delayed ‘hump’ component in the current records. Figure 10D plots the Q vs. V relationship of pooled data from five control fibres exposed to La3+ compared with the control fibres exposed to Cd2+/Co2+ from Fig. 10B. As a first approximation the La3+Q vs. V data were fitted to a single Boltzmann function, with parameters Qmax= 27.0 nC μF−1, Vhalf=−10.4 mV and k= 16.6 mV, R2= 0.987. Therefore, the addition of La3+ led to a reduction in both Qmax and the steepness of the Q vs. V relationship, as well as a rightward shift in the voltage dependence of charge movement.
Figure 10E compares charge development with increasing pulse duration from a step to −10 mV in a fibre treated with our standard external solution (top) vs. one supplemented with 0.3 mm La3+ (bottom). A temporally delayed hump component is clearly distinguishable in the fibre exposed to Cd2+/Co2+, and noticeably absent in the La3+ exposed fibre, which exhibits markedly increased current kinetics. Figure 10F plots the charge vs. pulse duration relationship for these two fibres. The calculated time constant for charge development in the Cd2+/Co2+ exposed fibre was 13 ms, compared to 2.4 ms for the fibre exposed to La3+. Thus the addition of La3+ to our standard external solution dramatically increased the kinetics of charge movement and decreased the amount of charge moved in control fibres.
Gating charge movement in muscle
Gating charge movement was first predicted by Hodgkin & Huxley (1952) to explain the voltage-dependent origin of Na+ and K+ conductance in the nerve. The first recordings of these gating currents were applied to the activation of muscle contraction by Schneider & Chandler (1973), who proposed that voltage-dependent intra-membrane charge movement was a key step in skeletal muscle EC coupling. Evidence has accumulated demonstrating that the α1 subunit (α1S) of the DHPR is the primary source of this charge movement (Tanabe et al. 1988; Nakai et al. 1996) that triggers Ca2+ release from the mechanically linked RyR1 (Block et al. 1988; Protasi et al. 2002) and promotes skeletal-specific muscle contraction (Horowicz & Schneider, 1981a).
Recent groups using the whole cell patch-clamp technique on FDB fibres have demonstrated charge movement currents with a single rise and simple decay (Wang et al. 1999, 2002; Royer et al. 2008). Here using this same technique we demonstrate a clear, consistent, temporally delayed component in the ON charge movement currents of WT murine FDB fibres. As an explanation for this discrepancy, we propose that the use of the trivalent cation lanthanum as a Ca2+ channel blocker (Wang et al. 1999, 2002; Royer et al. 2008) may alter charge movement currents and mask Qγ in mammalian fibres. We use a channel blocking cocktail of Cd2+ and Co2+, with no added La3+, to minimize ionic currents; in our hands the addition of La3+ dramatically increased the kinetics of charge movement currents and abolished any temporally distinct components (Fig. 10C, E and F), leaving recordings that kinetically resemble those of these recent reports. We also noted a reduction in the maximum charge moved (Qmax) and rightward shift in the voltage dependence of charge movement (Vhalf) in the presence of La3+, when compared to our control solution. The La3+Qmax value reported here is about 30% less than that reported by Wang et al. (1999) and Royer et al. (2008). Potential explanations for this discrepancy include different strains and age (5–7 weeks here vs. 5–7 months in the study of Wang et al.) of mice studied. Additionally, the studies by both Wang et al. and Royer et al. used a higher concentration of Mg2+ in their external solution (2 and 3.5 mm, respectively) than our 1 mm Mg2+. Increased Mg2+ could potentially blunt some of the effects of La3+ on the voltage sensor. A final possibility to consider is that part of the decrease in charge movement seen here in the La3+ containing solution could be due to a partial detubulation of the fibres in La3+. There was a slight, but not significant, decrease in the total fibre linear capacitance from 1.33 ± 0.05 nF and 1.32 ± 0.05 nF for WT and KO fibres (n= 38 and 29, respectively) measured in our standard external solution to 1.20 ± 0.11 nF for the 13 fibres measured in La3+ containing solution (P= 0.24), indicating that detubulation was likely not to be a major factor. To our knowledge the effects of La3+ on skeletal EC coupling have not been thoroughly explored; however La3+ has been shown to alter both sodium and potassium voltage-dependent channel gating in a manner that cannot be explained by surface charge considerations alone (Armstrong & Cota, 1990; Tytgat & Daenens, 1997). We additionally observed both time- and use-dependent effects of La3+ on charge movement currents and therefore suggest that the use of this trivalent cation as an L-type Ca2+ channel blocker should be approached with caution.
Effects of S100A1 on voltage sensor charge movement
A striking finding of this work is the modulation of intra-membrane charge movement by an endogenous Ca2+ binding protein, S100A1. Qγ was selectively suppressed in fibres lacking S100A1, resulting in reduced sensitivity to activation (decreased steepness of the Q–V relationship), and reduced maximal activation (decreased Qmax) of the voltage sensor. Notably, the first component of charge movement (Qβ) appeared unaffected by ablation of S100A1, as can be seen by the identical current traces at voltages hyperpolarized to the development of Qγ (Fig. 4), as well as by the accurate double Boltzmann fit to the WT Q–V relationship with fixed KO parameters describing the first component. These data suggest a selective suppression of a distinct component of charge movement in fibres lacking S100A1.
Moreover, several lines of evidence presented here support that effects on charge movement appear to be specific to S100A1, and not a result of compensatory changes in KO animals. First, a 20 min intracellular application of S100A1 restored both the total charge moved and the kinetics of Qγ in KO fibres, arguing against a developmental role of S100A1 in the modulation of charge movement. Second, Western blot analysis suggests that protein expression of the DHPR is not changed in KO fibres. Third, the L-type Ca2+ current density and voltage-dependent activation do not appear to be significantly altered in KO fibres. The last two pieces of evidence suggest that the total expression of DHPR Ca2+ channels, as well as the functional fraction of these Ca2+ channels, is preserved in fibres lacking S100A1, implying that the suppressed charge in KO fibres is independent of channel expression and/or developmental or compensatory changes due to genetic manipulation. This is a unique finding, as multiple groups have demonstrated a reduction in charge movement with the alteration of endogenous proteins, but as a by-product of reduced functional L-type channels. For example, mutations to the β1 subunit of the DHPR lead to reduced α1S expression at the membrane and a concomitant decrease in charge movement (Gregg et al. 1996; Schredelseker et al. 2009), and expression of the RGK family member Rem reduces the functional number of DHPRs and charge movement in myotubes (Bannister et al. 2008). To our knowledge, this specific modulation of gating charge by S100A1 is the first example of an endogenous protein regulating skeletal muscle charge movement independent of channel expression.
This reduction in charge movement is consistent with our previous findings that fibres lacking S100A1 have depressed SR Ca2+ release (Prosser et al. 2007). In that work we showed that action potential evoked Ca2+ transients are smaller in KO fibres compared to WT counterparts, a finding predicted if there is decreased activation of the voltage sensor. Additionally, as DHPR expression levels and L-type Ca2+ currents in KO fibres do not differ from their WT counterparts (Fig. 8B and C), the suppressed Qγ component does not appear to be linked to gating of the DHPR Ca2+ channel, but instead is likely to be linked to the excitation–contraction coupling machinery. One interpretation of these findings is that S100A1 modulates intra-membrane voltage sensors that regulate Ca2+ release, but not the gating of the DHPR Ca2+ channel. However, we have also previously proposed that S100A1's modulation of Ca2+ release is a direct effect of S100A1 binding to RyR1 and enhancing RyR1 release. This was supported by previous reports of S100A1 increasing the open probability of the purified RyR1 in single channel recordings (Treves et al. 1997), and our demonstration, in conjunction with our collaborators, that S100A1 competes with calmodulin for binding the CaM binding domain (CaMBD) of RyR1 (Prosser et al. 2007; Wright et al. 2008), a site previously demonstrated to modulate the channel's activation (Tripathy et al. 1995; Moore et al. 1999; Rodney & Schneider, 2003).
While these two proposed mechanisms for S100A1's modulation of EC coupling may appear contradictory, they are not mutually exclusive. The DHPR and RyR interact in both an ‘orthograde’ manner, where the DHPR signals RyR1 to open, and a ‘retrograde’ fashion, where RyR1 prevents DHPR inactivation (Nakai et al. 1996). Interestingly, the CaMBD where S100A1 binds RyR1 is involved with mechanical coupling and bi-directional signalling with the DHPR. Specifically, the CaMBD of RyR1 interacts with the carboxyl-terminal tail of the DHPR (Sencer et al. 2001), and the region of RyR1 containing the CaMBD elicits a retrograde signal to the DHPR (Nakai et al. 1998). It is tempting to speculate that S100A1 interacting with this same region of RyR1 may affect retrograde coupling between the two proteins, enhancing voltage sensor activation and/or Ca2+ release. However, studies on retrograde signalling in myotubes suggest that while L-type Ca2+ currents are dramatically affected by interaction with RyR1, voltage sensor charge movement is minimally influenced, undermining this hypothesis (Nakai et al. 1996). Nonetheless, myotubes lack Qγ and demonstrate less than 20% of the total charge moved in adult fibres (Nakai et al. 1998; Avila & Dirksen, 2000), validating the exploration of the interaction between the CaMBD of RyR1 and the DHPR and its effects on charge movement in adult fibres.
Origin of Qγ
An alternative explanation for the enhanced charge movement in the presence of S100A1 is that Qγ appears as a consequence of RyR-mediated Ca2+ release. This is not a novel concept; the nature of the delayed component has been widely debated. Several groups proposed Qγ to be the primary charge moved by the voltage sensor that causes Ca2+ release (reviewed in Huang, 1988). Yet Qγ has also been well argued to be a consequence of release, in a model put forth primarily by Pizarro et al. (1991). Our findings with the RyR1 inhibitor dantrolene support this hypothesis. Dantrolene rapidly suppressed the temporally delayed hump in charge movement currents of control fibres, isolating a component with similar initial voltage dependence to the component suppressed in KO fibres. These results suggest that Qγ may be a function of optimal RyR-mediated Ca2+ release. In KO fibres, where Qγ is already suppressed (in conjunction with suppressed release, as is documented in the companion paper), dantrolene treatment caused no further suppression of charge, as would be expected if Qγ is a consequence of optimal release.
However, our data with dantrolene treatment of control fibres do not completely mimic the difference in charge movement between WT and KO fibres. The difference component isolated by dantrolene peaks around −10 mV and then begins to decrease monotonically with voltage, suggesting a rightward shift in the voltage dependence of Qγ. We cannot determine whether this difference component would diminish to zero upon further depolarization beyond +20 mV, mostly due to the presence of ionic contamination at these large depolarizations which precluded an accurate isolation of charge movement currents. In contrast to the dantrolene isolated component, we did not see rescue of Qγ at larger depolarizations in KO fibres, where differences in maximal saturating charge in WT compared to KO fibres were maintained even at steps to +30 or +40 mV. These findings suggest a more complex mechanism than simply the amount of Ca2+ release dictating the presence or absence of Qγ (with Qγ defined here as the difference component between WT and KO fibres). A detailed examination of the relationship between charge movement and Ca2+ release in WT and KO fibres is needed to address these questions, and is provided in the companion paper (Prosser et al. 2009).
Regardless of this discrepancy, it is clear from our studies and previous work that Qγ is selectively affected when the RyR1 Ca2+ release channel is altered (Lamb, 1986b; Hollingworth et al. 1990; Csernoch et al. 1991; García et al. 1991; Gonzalez & Rios, 1993). This does not appear to be a function of global myoplasmic [Ca2+], as all of our recordings were performed in high intracellular EGTA. Instead our data suggest a process, dependent on optimal RyR1 activation and/or local Ca2+ release, that can be modulated by S100A1, and that positively feeds back on voltage sensor charge movement. The mechanistic underpinnings of the relationship between S100A1, Ca2+ release and Qγ are further explored in the companion paper.
In conclusion, here we demonstrate that mammalian muscle fibres exhibit two distinct components of intra-membrane charge movement (Fig. 11A), a relatively rapid initial rise to peak (Qβ), and a temporally delayed hump component (Qγ). The use of La3+ as a Ca2+ channel blocker altered the kinetics and voltage dependence of intra-membrane charge movement. We showed that Qγ is selectively suppressed in muscle fibres lacking S100A1 (Fig. 11B, red curve), a protein known to bind to RyR1 and enhance Ca2+ release. We also found that the RyR-inhibitor dantrolene selectively suppresses a similar component of voltage sensor charge movement (Fig. 11B, orange curve), suggesting that Qγ may be a product of cross talk between RyR1 and DHPR. Transient application of S100A1 rescues Qγ in KO fibres (Fig. 11B, black curve), suggesting a specific effect of S100A1 on charge movement. These results further support S100A1 as a positive regulator of the t-tubule voltage sensor and SR Ca2+ release channel in skeletal muscle-type EC coupling.
B.L.P. performed the majority of experimentation, analysis, and writing involved with this work. E.O.H. contributed to all aspects of this work, particularly to experimental design and interpretation of results. D.B.Z. designed and provided the S100A1−/− animal and WT counterparts, and also critically revised and approved the final manuscript. M.F.S contributed to experimental design, analysis, and discussion. All the experiments presented above were performed in the lab of M.F.S., at the University of Maryland, Baltimore.
We would like to thank Drs Nathan Wright and David Weber for providing the Alexa labelled S100A1, as well as for insightful discussion stemming from their expertise with the S100 family of proteins. The project described was supported by grant no. RO1 QR055099 from the National Institute of Arthritis and Musculoskeletal and Skin Diseases. B.L.P. was supported by NIAMS training grant T32 AR007592 to the Interdisciplinary Program in Muscle Biology, University of Maryland School of Medicine.