Purkinje cells (PC) control deep cerebellar nuclei (DCN), which in turn inhibit inferior olive nucleus, closing a positive feedback loop via climbing fibers. PC highly express potassium BK channels but their contribution to the olivo-cerebellar loop is not clear. Using multiple-unit recordings in alert mice we found in that selective deletion of BK channels in PC induces a decrease in their simple spike firing with a beta-range bursting pattern and fast intraburst frequency (~200 Hz). To determine the impact of this abnormal rhythm on the olivo-cerebellar loop we analyzed simultaneous rhythmicity in different cerebellar structures. We found that this abnormal PC rhythmicity is transmitted to DCN neurons with no effect on their mean firing frequency. Long term depression at the parallel-PC synapses was altered and the intra-burst complex spike spikelets frequency was increased without modification of the mean complex spike frequency in BK-PC−/− mice. We argue that the ataxia present in these conditional knockout mice could be explained by rhythmic disruptions transmitted from mutant PC to DCN but not by rate code modification only. This suggests a neuronal mechanism for ataxia with possible implications for human disease.
BK channels are large-conductance voltage and Ca2+-activated K+ channels acting as important signals modulators in many types of neurons1,2,3. They are activated by the conjunction of membrane depolarization and intracellular Ca2+ concentration ([Ca2+]i), and yield strong K+ currents. These currents play different roles ranging from regulation of transmitter release4 to shaping of dendritic Ca2+ spikes5 and modulation of action potential repolarization6,7. The functional link between BK channels activation and elevation in [Ca2+]i is reinforced by a macromolecular complex formed by the association of BK and voltage-gated Ca2+ channels (Cav). This requires a rise in [Ca2+]i3, which can be provided by activated N-methyl-D aspartate (NMDA) receptors8.
In cerebellar Purkinje cells (PC), BK channels are highly expressed in the soma and dendrites9,10. They are activated by Ca2+ provided by P/Q-type Cav11. In turn, BK channels activation counteracts the inward Ca2+ current effect5. This mechanism plays an important role with respect to climbing fiber (CF) response characterized by a burst of three to five Na+ spikes and a dendritic Ca2+ spike in the target PC12,13,14,15. The CF triggers one of the most important Ca2+ entrance in a brain cell16. In accordance with Ca2+ influx control exerted by the BK channels, Chen et al.17 demonstrated that the CF–evoked dendritic Ca2+ transients had larger amplitude in PC-BK−/− mice. Consequently, the BK channel could play a key role in PC by limiting Ca2+ entrance during CF input18. This tight regulation underlies crucial Ca2+ functions in neuronal excitability and plasticity. This calls for the investigation of long term depression (LTD) at the parallel fiber-PC-BK−/− synapse for which the calcium signaling is central19. In humans, the recent description20 of cerebellar ataxia associated with KCNMA1 gene mutation, presumably causing BK channel loss of function, reinforces the importance of the study of PC-BK−/− mice.
In alert animals BK channels deletion in the cerebellum led to the emergence of beta oscillation phase-locked with ultra-rhythmic PC and Golgi cells21. As the sole output of the cerebellar cortex, the PC exhibits a double rhythmicity which is associated with ataxia21. The functional link between ataxia and the deletion of BK channels in the cerebellum is strengthened by the fact that we could reproduce the PC firing pattern (including abnormal rhythmicity) and the ataxic behavior by micro-injection of BK channels blocker (paxillin) in the cerebellum of alert WT mice21. Nevertheless, the precise role played by the PC-BK channels has not been elucidated in the alert state. In this perspective, the generation of a mouse line with a PC-specific deletion of BK channels (PC-BK−/−) offers an ideal model for studying the PC-BK channels’ role in cerebellar physiology. Interestingly, Chen et al. (2010)17 demonstrated the presence of an ataxic behavior in those mutant mice (PC-BK−/−). Thus, there is a physiological link between PC-BK channels deletion and ataxia. However, cerebellar rhythmicity has not been studied to date in this model. If there is a functional link between increased rhythmicity and ataxia21, (1) selective suppression of PC-BK channels should produce abnormal rhythmicity in the cerebellar cortex and (2) this abnormal rhythm should be transmitted to the deep cerebellar nuclei (DCN).
The role of the DCN is crucial as they are not only the final stage of the cerebellar circuit receiving PC inhibitory modulation but also an integrating network combining this inhibition with direct mossy fiber and CF excitatory inputs, and intrinsic properties22,23,24,25,26,27,28,29,30. Therefore, studying DCN modulation is essential to understand the pathophysiology of cerebellar ataxia31. Based on rate code modulation only, a decrease in PC discharge frequency should logically increase DCN output frequency toward the premotor target and also increase inhibition of the IO, reducing CF output frequency, which would in turn destabilize the PC networking, as demonstrated in anesthetized animal17. However, the mean firing rate of the different components of the olivo-cerebellar system does not describe the dynamics of the systems accurately. As demonstrated by Person and Raman30 the mode of firing of PC and their synchronicity strongly influence DCN firing in a way that the firing rate code only cannot predict. An increase of PC synchronization (without any firing rate modification) may ‘paradoxically’ lead to an increase of the DCN firing rate. Moreover, the temporal pattern of PC firing is highly dependent on alertness32,33,34.
To address these issues we used multiple-unit extracellular electrodes in awake mice and analyzed the rhythmicity of the PC simultaneously with the DCN neurons. We showed in alert mice that selective deletion of the PC-BK channels –as convincingly demonstrated in supplementary Figure S117– induces increased simple spikes (SS) rhythmicity of the PC, increased frequency of the complex spike (CS) spikelets, and alters LTD at the parallel-PC synapse. We also demonstrate that an abnormal PC rhythmicity is transmitted to the DCN neurons. Rather than rate code modification, rhythm disruptions transmitted from PC to DCN is probably underlying the ataxic phenotype. Therefore, despite strong recurrence in the cerebellum, suppression of a single membrane ion channel type in PC population markedly disrupts cerebellar function. Our findings suggest a possible neuronal mechanism for cerebellar ataxia.
Using multi-electrode extracellular recording techniques in the alert animal, we recorded the firing behavior of the PC of Crus IIa and the DCN neurons identified from antidromic activation from the red nucleus and their electrical activation from the inferior olive (IO) (see Methods) (Fig. 1).
Firing behavior of PC-BK−/− PC in alert state
A total of 194 PC (127 in PC-BK−/− and 67 in WT) were recorded and analyzed in 33 mice (18 PC-BK−/− and 15 WT mice). SS firing may be considered as an important criterion reflecting the functional interaction between intrinsic PC pacemaker properties and the influence of afferent- and network-related input. As previously observed in alert total BK channels–deficient mice21 and in anesthetized PC-BK−/− 17, SS firing frequency was lower in PC-BK−/− (61.7 ± 33.0 Hz; n = 127 cells and 18 mice) than in WT mice (80.5 ± 37.7 Hz; n = 67 and 15 mice; P < 0.0004) (Fig. 2e). There was no difference in the coefficient of variation (CV) (0.32 ± 0.27 in PC-BK−/−, versus 0.35 ± 0.25 in WT, P = 0.44) (Fig. 2f).
In order to verify that the selective suppression of the BK channels in the PC is able to produce increased PC rhythmicity, the rhythm index (RI) was measured during spontaneous PC activity. This analysis demonstrated that the RI considerably increased in the PC-BK−/− mice reaching a mean value of 0.22 ± 0.36 (n = 127 cells) contrasting with 0.06 ± 0.08 (n = 67 cells) in WT; P < 0.0005 (Fig. 2g). Figure 2 illustrates the rhythmic alteration of the SS firing behavior in PC-BK−/− compared to WT mice. A clear oscillation in the beta band (19.3 Hz in the present case) emerges with numerous side peaks in the PC-BK−/− PC (Fig. 2c,d) in contrast to WT (Fig. 2a,b).
Among the 127 PC recorded in PC-BK−/− mice, 61 (48%) showed a double rhythmicity with a periodic bursting pattern in the beta range (17.6 ± 5.9 Hz) and fast intraburst frequency (190 ± 57.2 Hz) (Fig. 3a–d). 55 PC (43.3%) showed tonic firing with fast rhythmicity (140.5 ± 48.5 Hz). The remaining 11 cells (8.7%) showed a similar pattern to the majority (61%) of PC recorded in WT animals, i.e. SS firing without any consistent rhythmicity (RI ≤ 0.05), as illustrated by flat autocorrelogram (Fig. 2b). Paired recordings showed that the SS firing of the PC-BK−/− was synchronous along the parallel fiber beam (Fig. 3). Figure 3 illustrates this highly rhythmic SS firing pattern in two PC distant from each other by 250 µm. Both autocorrelograms show the double rhythmicity, the slow one peaking at about 14 Hz and the fast one showing two fast side peaks in the second PC (Fig. 3c,d). In addition, the crosscorrelogram of these two cells shows the same beta rhythmicity (~14 Hz) indicating in-phase synchrony of these abnormal synchronized firing patterns. This in-phase synchronicity was quantified by means of the synchrony index (SI), showing a highly significant difference (P < 0.00002) between PC-BK−/− (0.13 of ±0.04, n = 18) and PC-WT pairs (0.03 ± 0.02, n = 7).
Figure 4a–g illustrates the alteration of the CS behavior: CS frequency was similar in PC-BK−/− and WT mice (1.02 ± 0.67 Hz, n = 127 cells in PC-BK−/−, 18 mice versus 0.93 ± 0.36 in WT, n = 67 cells, 15 mice; P = 0.30) (Fig. 4d). In contrast, intraburst of spikelets frequency was significantly higher in PC-BK−/− (1517.7 ± 406.5 Hz (n = 34 cells) than in WT mice (722.1 ± 343.3 Hz, n = 41 cells; P < 0.0000) (Fig. 4b,e). FFT analysis performed on isolated CS confirmed this increase in spikelets frequency in the mutant mice (Fig. 4c). Accordingly, the number of spikelets was higher in PC-BK−/− mice (3.7 ± 1.3 n = 98 cells) (Fig. 4b,f) than in WT mice (2.3 ± 0.9, n = 67 cells; P < 0.000001) (Fig. 4a,f) while CS duration was similar (6.8 ± 3.3 ms, n = 64 cells in PC-BK−/− versus 7.1 ± 1.7 ms, n = 62 cells in WT; P = 0.49). The silencing of SS firing evoked by the CS was longer in PC-BK−/− mice (17.6 ± 11.0, n = 79 cells) (Fig. 4b,g) than in WT (12.4 ± 4.5 n = 67 cells; P < 0.0003) (Fig. 4a,g).
Firing behavior of the DCN neurons in alert state
A total of 154 DCN neurons (90 in PC-BK−/− and 64 in WT) were recorded and analyzed in 33 mice (18 PC-BK−/− and 15 WT mice). In order to facilitate online recognition of the DCN among these neurons, 41 (27 in PC-BK−/−, 14 in WT) were antidromically activated from the red nucleus (Fig. 5a) at a mean latency of 1.11 ± 0.40 ms, which was not different for the two groups of mice (P = 0.18) (Fig. 5b). Figure 5a illustrates the antidromic activation of one DCN neuron from the red nucleus and a spontaneous collision with an orthodromic spike occurring just before the stimulation.
Although the logical consequence of the SS firing decrease in the mutant would be to induce disinhibition of the DCN neurons, the mean frequency (48.4 ± 28.5 Hz in the PC-BK−/− (n = 90) versus 49.7 ± 25.6 Hz in WT, n = 64) (Fig. 5c) was not different (P = 0.76) but the CV was increased in the PC-BK−/− (0.27 ± 0.14) with respect to the WT (0.21 ± 0.09)(P < 0.003)(Fig. 5d). As for the PC, the DCN neurons showed a significant RI increase reaching a mean value of 0.08 ± 0.14 (n = 90) in the PC-BK−/− mice in place of 0.02 ± 0.06 (n = 64) in the WT; P < 0.005 (Fig. 6a). Figure 6 illustrates the marked change in the rhythmic behavior of one representative DCN neuron in a PC-BK−/− mouse showing beta bursting (Fig. 6d) that gives rise to a constant oscillatory profile as shown in an autocorrelogram (Fig. 6e) instead of the tonic firing (Fig. 6b) and flat profile (Fig. 6c) seen in the WT DCN neuron. The beta oscillatory profile has been identified in 41% of the DCN neurons of the PC-BK−/− mice, reaching a mean value of 16.9 ± 5.7 Hz, n = 37. Interestingly, the mean oscillatory profile of these DCN neurons was not statistically different (P = 0.58) from the one recorded in the PC of the same mutant mice.
When the DCN neurons antidromically activated by a stimulation of the red nucleus were separately analyzed from the DCN neurons that were not identified as providing input to the red nucleus, the same differences in firing parameters (frequency rate, CV and RI) between the mutant and WT mice were found. The mean total duration of the DCN neuron spikes (n = 139) was 6.2 ± 2.8 ms and the depolarization phase was 0.36 ± 0.19 ms. These spike parameters were not different in mutant and WT mice (P = 0.41 and P = 0.66, respectively).
Effects of IO stimulation on DCN neurons
In order to verify the functional integrity of the IO action on the DCN, the effect of IO stimulation was analyzed in 48 DCN neurons (28 in PC-BK−/− and 20 in WT). This stimulation evoked a negative field potential (Fig. 7a) at the latency of 3.2 ± 0.5 ms in the majority of these neurons (n = 35) and no difference was found between the mutant and WT mice (P = 0.12) (Fig. 7b). Although the placement accuracy of the stimulating electrode (online) in the IO was confirmed by the fact that they induced a specific negative field in the PC layer (as demonstrated in the ferret)35 and followed by evoked CS at a latency ranging from 10 to 20 ms and resembling to the spontaneous one (Fig. S1), we never succeeded in recording antidromic activation of DCN neurons from the IO stimulation.
IO stimulation also induced an increase in DCN neurons firing rate expressed in different peaks in the stimulus histogram (Fig. 7c–e). All these sequences (excitatory and inhibitory) were not different in the mutant with respect to the WT mice. The first peak occurred at the latency of 5.9 ± 1.3 ms in PC-BK−/−, (n = 24) versus 6.2 ± 1.8 ms in WT, (n = 20), (P = 0.45); the second one at 12.7 ± 2.6 ms, in PC-BK−/−, (n = 17) versus 11.2 ± 2.5 ms in WT (n = 16), (P = 0.10); the third at 20.7 ± 1.2 ms in PC-BK−/−, (n = 8) versus 25.5 ± 2.5 ms in WT (n = 12), (P = 0.079); and the fourth at 50.0 ± 16.1 ms in PC-BK−/−, (n = 10) versus 46.3 ± 4.4 ms in WT (n = 6), (P = 0.79). This excitatory sequence was ended by a period of inhibition of variable duration centered on 110.7 ± 31.9 ms at the onset latency of 82.5 ± 42.3 ms in PC-BK−/−, (n = 10) versus 76.0 ± 24.1 ms in WT (n = 6), (P = 0. 79). All these sequences (excitatory and inhibitory) were not different between the knockout and the WT mice.
Rhythmic communication between PC and DCN in PC-BK−/−
In some exceptional recordings performed in PC-BK−/− mice, we were able to simultaneously record pairs of PC and DCN neurons. Figure 8 illustrates one PC showing the double rhythmic pattern (Fig. 8a) and one DCN neuron presenting the same beta rhythmicity at about 15.3 Hz (Fig. 8b) in an exact out-of-phase relationship (Fig. 8d). It is technically difficult to keep one PC and one identified DCN neuron in alert animal for quality recording, but the existence of such functional pairs (n = 6) may contribute to a better understanding of the olivo-cerebellar network. The magnification part of Fig. 8 illustrates a series of 5 to 6 SS spikes followed by one or 2 DCN spikes (while the PC were silent). The autocorrelograms of the PC (Fig. 8c) and DCN neuron firing (Fig. 8d) confirm the presence of the same beta rhythm. The crosscorrelogram between these two units demonstrated their functional out-of-phase correlation (Fig. 8e). This suggests a transmission of the abnormal beta rhythm by PC inhibition to the DCN neuron. In addition, the analysis of the relationship inside the PC-DCN pairs between the firing activity of the DCN neuron and the CS activity of the related PC demonstrated a phase-locked of the DCN firing to the generation of the CS of the original PC (Fig. 9). This corroborates the existence of the closed loop between the DCN to the PC via the IO. When the DCN firing is aligned with the CS occurrence a clear beta oscillation was recorded in the DCN firing. The major peak of DCN discharge preceded the CS by 29.2 ± 3.9 ms (n = 6) (26 ms in Fig. 9).
8Hz LTD-inducing paradigm
In order to highlight the potential role of PC-BK channels in the sensory-stimulation plasticity observed in the cerebellar cortex of WT alert mice36, we investigated the local field potentials (LFP) plasticity recorded in the Crus I or Crus II area, evoked by electrical stimulation of the whisker pad. Ten recordings were performed for each group and were obtained in 6 mutant and 5 WT mice. This stimulation evoked three early negative waves, designated as N1, N2 and N3, peaking at 1.8 ± 0.4 ms, 3.3 ± 0.3 ms, and 4.5 ± 0.2 ms (n = 15), respectively, after stimulus onset. The mean peak-to-peak amplitude of these components corresponded to 0.19 ± 0.15 mV, 0.43 ± 0.18 mV, and 0.48 ± 0.19 mV, respectively (mean ± SD; n = 15). The short latency and small amplitude of N1 correspond to the classical P1–N1 presynaptic input component37 originating in the mossy fiber in the granule cell layer. N2 and N3 are related to PC activation mainly supported by the ascending axon–PC synapse and the parallel fiber-PC synapses, respectively36. In WT mice, we observed long-term modifications (lasting at least 30 min) after 8-Hz stimulation, characterized by a specific decrease of the N3 amplitude accompanied by an increase of the N2 and N3 latency peaks (Fig. 10) expressing an LTD effect (P < 0.05). In contrast, neither effects on N3 amplitude nor on N2, nor on N3 latency peaks occurred in the PC-BK−/− (Fig. 10). These results strongly suggested that PC-BK channels play a major role in the LTD timing-plasticity.
Our results showed that specific ablation of BK channels in PC induced a stereotyped SS firing rhythmic alteration that was transmitted to DCN neurons, and enhanced intra-burst CS frequency. Moreover, LTD at the parallel-fiber-PC synapse was abolished. This emphasizes the importance of the olivo-cerebellar loop in the transmission between the cerebellar cortex and the DCN, and the PC-BK channels role in this network and cortical plasticity. These new findings contribute to a better understanding of the physiological link between specific deletion of a single type of K+ channels in a single cell population in the cerebellar cortex and cerebellar ataxia.
SS firing reduction similar to what we found in alert mice was previously observed in anesthetized preparation17. A causal role for decreased SS firing in the emergence of ataxia was originally hypothesized when decreased SS rate induced DCN neurons disinhibition, which in turn enhanced IO inhibition17. Following this IO inhibition, reduced CS frequency is expected, and was actually observed in anesthetized preparation17. However, our results in alert PC-BK−/− mice did not reproduce these findings, suggesting that reduced CS frequency per se is not a pathophysiological mechanism and that they may reflect an effect from anesthesia. Another major difference with the anesthetized preparation is the absence of increase in mean discharge frequency of DCN neurons in alert PC-BK−/− mice. More generally, DCN neurons discharge frequency has been reported to be much lower compared to our findings in alert mice (e.g. 10.5 ± 2.3 Hz in WT mice and 14.7 ± 1.9 Hz in PC-BK−/− mice17, or 18.0 ± 13.1 Hz in L7-ChR2-eYFP mice38, versus 49.7 ± 25.6 Hz in WT and 48.4 ± 28.5 Hz in the PC-BK−/− mice in the present alert condition). The absence of effect of the PC-BK deletion on DCN mean firing rate does not mean that alteration of PC output has no effect on DCN neurons. Another important parameter is the regularity of the PC, represented by the CV. In agreement with experimental evidences that irregularity of PC39 firing is strongly associated with cerebellar ataxia, we have also reported such irregularity in the PC of alert mice with BK channel deletion in the cerebellum21. However, this PC irregularity was not reproduced in the present PC-BK−/− mice, but it was well expressed in the DCN neurons letting open the possibility that such irregularity in the firing output of the cerebellum could be an element sustaining ataxia.
We showed here that another parameter than the rate code is a major element in the PC-DCN transmission in alert mice. Rhythmicity of both PC and DCN neurons is dramatically increased, expressing beta oscillation. This abnormal rhythm is similar to the oscillation recorded in whole-BK mutant, as well as the one induced by BK-blocker (paxillin) in WT mice21. In both situations, beta oscillation was also accompanied by ataxia. Though we argued that rate code modification is insufficient to underlie ataxia but rhythmicity of different cerebellar nuclei should be taken into account, we do not exclude that other factors could also contribute to the ataxic phenotype. Indeed, enhanced excitability31,41,40 and firing irregularity39 have been shown to be important parameters in relation to ataxia.
The functional link between the rhythmic DCN output alteration and ataxia is supported by a number of electrophysiological evidences. Experiments using optogenetic stimulation in mice42 demonstrated that movements evoked by stimulation of the cerebellum are initially produced via a direct pathway through the red nucleus and/or the reticular formation and not by the motor cortex. This reinforces findings with electrical stimulation of the cerebellum demonstrating the powerful influence exerted by the inhibitory PC signal on descending motor pathways resulting in actual movement43,44,45. However, this feedforward control perspective is challenged by the presence of different feedback loops inside the cerebellar cortex, e.g. from the PC collaterals to the molecular interneurons, Golgi cells and other PC44 and from the olivo-cerebellar loop46,47.
We also found that this beta rhythm was functionally transmitted in an out-of-phase way. Indeed, the DCN neurons fired one or two spikes only in the absence of SS firing (at beta frequency). We showed that this rhythmic coupling is extended to the olivo-cerebellar loop as we documented the correlation between the rhythmic behavior of the DCN neurons and the CS occurrence of the related PC. This is in accordance with the recent studies of Tang et al.48 performed in anesthetized rat. They demonstrated that synchronized CS were able to induce DCN neuron inhibition which was preceded as in the present case by a short firing increase of the DCN neurons. In the same way, it was also demonstrated38,42 that optogenetic stimulations of a set of PC triggering restricted DCN inhibition were able to induce transient disinhibition of IO cells that project onto this specific set of PC. This optogenetic experimental strategy elegantly demonstrated in anesthetized preparation that the time between PC excitation and CS occurrence is about 64 ms (Fig. S4 in Chaumont et al.)38. In the present case, CS occurred about 29 ms after the beta firing peak of the DCN neurons. This delay is compatible with the total loop time of ~64 ms. Indeed, it takes about 20 ms for the PC to inhibit DCN neurons38, about 29 ms for the DCN neurons to inhibit (or disinhibit) IO neurons, the rest of the time corresponding to PC activation by the IO (~15–20 ms, Fig. S1). This looping time is also suitable for the generation of beta oscillation as we found in PC-BK−/− mice.
Spontaneous recruitment of this closed cortico-nucleo-olivary loop by BK-channels deletion of PC could explain both the ataxic behavior probably sustained by the abnormal beta oscillation of the DCN output and the alteration of the LTD at the level of parallel-PC synapses. This LTD plasticity controlling the sensitivity of the excitatory input of the PC49 may participate in the formation and storage of internal models reproducing the sensorimotor system dynamic properties50,51. In this model, the cerebellar cortex integrates the current state of the sensorimotor system and internally generates motor commands to predict future action and related sensation. These predictions are transmitted via the DCN to the IO acting as comparator of the expected and ongoing action or sensation and generating the CF ‘error’ signals acting as a supervisor of cerebellar learning. This CF signal is also considered as one of the key elements of the parasagittal organization of the cerebellar module, which is subdivided in different microzones considered as the operational units of the cerebellum52. Acting as a supervisor on these operational units, the nucleo-olivary output requires a precise tuning47. Although, the preservation of the CS frequency rate in the alert PC-BK−/− mice, the presence of ongoing beta rhythm coming from the DCN output probably impacts the precise tuning and accurate coupling between parallel fibers and CF input necessary for inducing LTD. As theoretically advanced by Medina and Mauk53, conjunction of mossy and climbing fiber input in the DCN is unable to retain memories in presence of background activities and only a plasticity rule concerning PC activity can keep a memory trace resistant to ongoing activities in the network preclude the possibility for the DCN to compensate for the PC alteration in the PC-BK−/− mice. Other important elements which may explain the absence of LTD are the modification of the CS configuration and the increase of the SS silent period following the CS. It was demonstrated that in spite of the fact that the CF elicits prominent dendritic calcium spikes14,15 these dendritic spikes are not directly linked to the CS spikelets but well to the duration of the SS silent period triggered by the CS54. It was demonstrated that the silent period was correlated with the amplitude of the dendritic afterhyperpolarization54. The Ca2+ influx triggered by the CF at the dendritic level activates Ca2+-dependent potassium conductance7 inducing hyperpolarization and the modulation of the silent period in SS firing. Although, small (SK) and large (BK) conductance Ca2+-activated potassium channels contribute to the action potential shape and spike afterhyperpolarization, respectively7, the fact that the silent period was increased and not decreased in the absence of BK channels in the PC-BK−/− mice (present results) and also in the whole BK−/− mice and after paxilline microinjection in WT21 indicates that the BK channels are not implicated in this process or that their absence are compensated by another hyperpolarizing channels. It cannot be ruled out, however, that PC may compensate for the absence of BK channels by over- or under-expressing other proteins following genetic knock out.
Our finding of increased number of spikelets and SS silent period in alert PC-BK−/− mice could be explained by larger amplitude CF-evoked dendritic Ca2+ transients as demonstrated on slice in PC-BK−/− mice17. In addition, the increase of the number of spikelets for a same CS duration indicates that the BK channels may also regulate the production of axonal spikelets. Recent view55 and experimental evidences56,57,58 point out that CS configuration, namely the number of spikelets, which are directly related to the number of spikes in the CF59, plays a major role in PC learning. During ‘trials over trials’ learning of pursuit eye movement, Yang and Lisberger (2014, 2017)57,58 demonstrated that longer-duration CS related to a greater number of spikelets induced stronger learning responses than medium or short CS duration. In contrast, the SS silent period triggered by the CS did not affect learning. In the present work, increased CS spikelets number in PC-BK−/− mice should favor PC learning. However, this spikelet increase was not accompanied by an increase of the CS duration but rather by an increase in spikelets intraburst frequency. Two mechanisms can be proposed to explain this: (1) as already demonstrated in slice17 the absence of BK disturbed PC membrane properties in such a way that a ‘conserved’ CF signal was not normally transmitted or treated by the membrane properties of the PC or (2) as it was clearly demonstrated that the phase of the subthreshold oscillation present in the IO could regulate the number of spikes in the CF burst corresponding to the CS spikelet59, the rhythmic alteration of the DCN inhibitory input on the IO may potentially increase the intraburst frequency of the CS. Whatever the pathophysiological pathway the alteration of the CS waveform may play a role in both the absence of LTD and the ataxia in the PC-BK−/− mice.
Another important finding was the specific alteration in DCN neurons firing behavior. DCN neurons exhibit pacemaker firing properties with a mean frequency of about 25 Hz in slices24 and reaching higher frequencies around 90 Hz in vivo22,30. Over this ongoing activity, excitatory input from the mossy and CF collaterals and the PC inhibition are integrated to produce a tonic firing discharge that has been documented in alert animals from different species22,23,25,29. The specific contribution of PC has been described as convergent transduction of PC inhibitory inputs to DCN neurons, with about 11 PC projecting on to 1 DCN neuron60,61. It must be recognized, however, that the DCN neuron population is heterogeneous61. It is therefore important to identify at least one subpopulation. This can be achieved electrophysiologically by using antidromic stimulation of the red nucleus. In the alert cat DCN neurons projecting onto the red nucleus (antidromic activation at a latency of 0.76 ± 0.12 ms) have thus been characterized (firing rate from 10 to 45 Hz)25. Here in the alert mice we found DCN neurons antidromically activated from the red nucleus at a latency of 1.11 ± 0.40 ms. There were no differences in the firing rate of the DCN neurons projecting to the red nucleus (n = 27) compared with those which were not antidromically activated from the red nucleus (n = 81), for both groups the mean firing was about 45 Hz. The lack of statistical difference between WT and PC-BK−/− mice in terms of frequency rate argued against a determining role of the DCN rate code in ataxia.
Another physiological property of the DCN operation mainly based on a timing code transmission of synchronized PC output to the DCN has recently been defended by Pearson and Raman62. They clearly demonstrated on slice and in anesthetized mice that the existence of a high intrinsic firing rate of the DCN neuron (91.5 ± 7.4 Hz) is differently modulated by the type of the rhythmic input of PC30. Asynchronous GABAergic IPSC of the PC exerts a potent inhibitory effect on the DCN neurons, but in contrast the same inhibitory input produced by synchronous PC entrains the spiking of DCN neurons in a perfect phase-locking with the rhythmic PC. This is in accordance with the present data where abnormal PC beta rhythm of the PC-BK−/− mice is transmitted to the DCN neurons. The PC synchronicity observed in the present mutant may facilitate this phase-locked transmission as demonstrated by Pearson and Raman30 in WT mice. The present sculpting of the DCN neurons firing by the abnormal PC rhythmic pattern is accordance with the disinhibition hypothesis50 and with recent finding that specific inhibition of the PC by optogenetic stimulation of the basket cells in mice is able to control the timing and the kinematic properties of the cerebellar motor output via graded disinhibition of the DCN neurons63.
The fact that DCN response to IO stimulation was not modified in PC-BK−/− mice indicates that the excitatory action of the CF collaterals on the DCN neurons is not responsible for the observed impairments, which further reinforces the importance of PC upstream signals on the DCN final output64,65,66.
Multiple conditions induce ataxia, including cerebellar ablation26, PC degeneration67 and PC firing rate reduction9,10. All these situations result in a decrease of GABA synaptic input on the neurons in the DCN that are targeted by PC. This has been proposed as one pathophysiological mechanism of ataxia31. However, in calcium-binding knockout mice32,33,68, and in mouse model of fetal alcohol syndrome69, Angelman syndrome70 and myotonic dystrophy40 ataxia has been reported in presence of SS firing increase, which is not expected to reduce the GABA synaptic input of the DCN but dramatically change the rhythmicity and the synchrony of the PC population. In addition, such SS firing increase was accompanied by abnormal fast oscillation of the local field potential disturbing the control exerted by the cerebello-olivary loop. Other, more subtle modifications of PC physiology, such as irregular PC firing, have been reported to induce ataxia71.
If the functional link between the absence of the classical LTD (mainly in vitro studies) and the behavioral learning remains controversial72,73, the alteration of the cerebellar LTD is often accompanied by ataxia74,75,76,77,78. Although the present LTD paradigm using 8 Hz electrical stimulation of the whiskers in alert mice is not largely used, we are confident that the N3 component is generated by the parallel fiber-PC synapse as demonstrated by collision between the activation of the granular cell axons by the peripheral stimulation and the antidromic stimulation of the parallel fiber on the cerebellar surface36. In addition, we have also demonstrated that both the classical LTD on slice and the 8 Hz LTD in alert mice were altered in PTPRR knockout mice79. This protein tyrosine phosphatase receptor type R is involved in maintaining low basal MAPK activity in PC. The same approach was also initiated in order to test the idea that cerebellar LTD may be determinant for inducing normal plasticity in the somatosensory cortex. We demonstrated that after a 8 Hz LTD inducing protocol, the cerebellar LTD accompanied by a delayed response in the WT mice was missing in Angelman syndrome mouse model and that the LTD induced in the barrel cortex following the same peripheral stimulation in WT is reversed into a LTP in the Angelman syndrome mice80. A mouse model for the human disease spinocerebellar ataxia type 1 (SCA1) offers another example where the presymptomatic mice showed reduced PC firing rate both in slices and in alert preparation, even before morphological alteration could be identified81. Interestingly, the gross motor behavior was not impaired at this stage of the disease, indicating that an important decrease in the firing rate (71 Hz in WT to 28 Hz in the SCA1 mice), which would logically reduce the PC GABAergic action on the DCN neurons, was not the prime inductor of ataxia. In addition, in spite of this PC frequency decrease, CS frequency was not significantly reduced in the SCA1 mice. This is consistent with the idea that the rate code alteration initiated by the PC output along the olivo-cerebellar loop is not able to explain ataxia.
In conclusion, the cell-specific genetic deletion of the BK channels in the PC, which is the sole output from the cerebellar cortex, appears to be the initial and determining element inducing an abnormal beta rhythm in both PC and DCN, LTD impairment and related ataxia. This study underlies the crucial need to understand oscillation as a way of neuronal communication and is certainly all the more important as a novel mutation in the KCNMA1 gene has been associated with a cerebellar ataxic phenotype in a human patient20, presumably caused by a BK channel loss of function mutation.
Materials and Methods
PC-BK−/− and WT littermate control mice with the same SV129xC57Bl6 background, used as experimental animals, were generated as follows17: Constitutive heterozygous BK L1/+ mice (SV129 background) were intercrossed with transgenic mice (C57BL/6 background) expressing the Cre recombinase under the control of the Purkinje protein 2 (PNP2) gene. The generation of this PNP2-Cre mouse line was described in detail by Barski et al.82. Progenies both carrying one BK L1 allele and being transgenic for PNP2-Cre were then crossed with mice carrying two loxP-flanked L2 alleles (BK L2/L2; SV129 background) of the BK gene KCNMA1 to obtain PNP2-Cre transgenic BK L2/L1 (PN-BK−/−) and PNP2-Cre transgenic BK L2/+ (PN-BK-Control) mice. The correct genotype was analyzed by PCR amplification as described previously9,17. Mice were bred and maintained at the animal facility of the Institute of Pharmacy, Department of Pharmacology, University of Tübingen, Germany. Either litter- or age-matched mice (at an age of 3 to 4 months) were randomly assigned to the experimental procedures with respect to the German legislation on animal protection. All animal procedures were approved by the University of Mons Ethics Committee and conducted in conformity with the European Union directive 609/86/EU. Every effort was made to minimize the number of animals and their discomfort. All animal procedures were approved by the University of Mons Ethics Committee and conducted in conformity with the European Union directive 609/86/EU. Every effort was made to minimize the number of animals and their discomfort.
Animals were prepared for chronic recordings of local field potential (LFP) and PC single-unit activity33 (Fig. 1). Mice were anesthetized with xylido-dihydrothiazin (Rompun©, Bayer, 10 mg/kg) and ketamine (Ketalar©, Pfizer, 100 mg/kg). Animals were administered an additional dose of xylido-dihydrothiazin (3 mg/kg) and ketamine (30 mg/kg) when they demonstrated agitation or marked increases in respiration or heart rate during the procedure. In addition, local anesthesia (0.5 mL of 20 mg/mL lidocaine and adrenaline [1:80000, Xylocaine©, Astra Zeneca]) was administered subcutaneously during the soft tissue removal. During surgery, two small bolts were cemented perpendicular to the skull to immobilize the head during the recording sessions, and a silver reference electrode was placed on the surface of the parietal cortex. To allow access to the vermis and the Crus I and II areas in the cerebellum, an acrylic recording chamber was constructed around a posterior craniotomy (2 × 2 mm) and covered with a thin layer of bone wax (Ethicon©, Johnson & Johnson).
In addition, bipolar silver stimulating electrodes were vertically implanted in the magnocellular division of the red nucleus (RN) (stereotaxic coordinate: 3.6 mm posterior, 0.5 mm lateral and 3.5 mm deep) and in the IO: 7.2 mm posterior, 0.25 mm lateral and 4.5 mm deep with respect to Bregma) following the method developed in the cat by Gruart and Delgado-Garcia24. Electrodes were aimed to the center of the mentioned structures and inserted contralaterally from the site of DCN recording following stereotaxic coordinates from the atlas of Franklin and Paximos83.
Histological identification of the recording and stimulating sites
At the end of the experiment, electrolytic marks were placed in selected recording sites with quartz–platinum/tungsten microelectrodes (1 mA for 10 s). Then animals were deeply anesthetized with sodium pentobarbital (50 mg/kg, i.p.) transcardially perfused with saline and phosphate-buffered formalin. The location of the stimulating electrodes was made on serial 50-µm-thick sections of the brainstem and cerebellum mounted on glass slides and stained with Neutral Red.
Electrical stimulation of the whisker region
Facial dermatomes of the whisker regions were electrically stimulated with a pair of small cutaneous needles inserted under the skin (inter-electrode distance 3–4 mm). Electrical stimulation consisted of a single square pulse, 0.2 ms in duration and <2 mA current intensity, delivered by an isolation unit (Isoflex, AMPI, Israel) connected to an analog pulse generator (Master 8, AMPI, Israel). The amplitude of the current delivered at intervals of 10 ± 3 s in the whisker region was adjusted in order to avoid overt movements and animal discomfort. The movement of the whisker was recorded by means of a home-made system using the A3515/16 BiCMOS linear Hall-effect sensors measuring the displacement of a micro-magnet of 0.003 g (1.0 mm diameter and 0.5 mm height), glued onto one whisker.
Paradigm for inducing LTD
Paradigm used for inducing plasticity was the same as those developed by Marquez-Ruiz and Cheron36. It consisted of 15-min control situation in which single electrical stimuli were given at intervals of 10 ± 3 s in the whisker region. This period was immediately followed by 10 min of 8-Hz stimulation and then by 30 min of control during which the same single stimuli were applied at the same frequency as in the control situation. Electrophysiological responses to electrical stimulation in the whisker region were assessed by both the configuration of the LFP (which must show P1-N1-N2-P2-N3 components and by the identification of appropriate PC firing (modulated by spontaneous whisker movements and electrical stimulation). The P1/N1 component was taken to reflect the evoked activity in the mossy fibers of the granule cell (GC) layer while N2 and N3 are related to the activity of the synaptic link between the ascending axon of the granular and PC dendrite and between the parallel fiber and the PC dendrite, respectively. Data were analyzed off-line for amplitude and latency quantifications of N1, N2, and N3. For this analysis, 30 successive evoked field potentials were averaged to obtain one average data point every 5 min. The amplitude was computed by peak-to-peak measurements. For this calculation, negative peaks were compared to the trough of the preceding positive wave. When the P1 positive peak was not evident, we used the inflection point observed in the averaged trace for the N1 measurement. For N3 measurements, the amplitude was set as the difference between the positive peak between N2 and N3 and the negative peak of N3. Latency was determined as the time difference between stimulus onset and N1, N2, or N3 averaged peaks. For comparisons between animals, amplitude values for each one of the components of the LFP were normalized for statistical analysis.
Single-unit and multiple-unit recordings in alert mice
Twenty-four hours after anesthesia, alert mice were restrained for the recording session. The dura was removed over the cerebellum to expose the tissue in the recording chamber. Recordings were performed in the Crus II area, and the depths of the electrodes were noted. To avoid unnecessary stress for the animals and movement artifacts, recording sessions were performed in a quiet room, when the animals were awake and calm. The alertness level was controlled by looking for the maintenance of whisking activity during the recording session. We used quartz–platinum/tungsten microelectrodes (1.2–3 MΩ) in a seven-channel Eckhorn microdrive (Thomas Recordings©, Giessen, Germany). All measures of impedance were made with a 1 kHz sinusoidal current and checked throughout the recording session. In the present study, the exploration were made with one or two microelectrodes separated from 250 µm (outer and shaft diameters of 80 µm and 25 µm, respectively). The microelectrode was mounted into a stretched elastic rubber tube to enable proper positioning via DC-micromotors (resolution of 0.27 μm).
Neural activity signal recordings were filtered at 100 Hz high-pass and 10 kHz low-pass. LFP and unitary electrical activities were stored digitally on a computer after conversion with an analog-digital converter (Power 1401, CED©, Cambridge, UK). The recorded data were digitized continuously at 20 kHz. Off-line analysis and illustrations were performed with Spike 2 CED software (CED©, Cambridge, UK).
The rhythmic frequency was defined as the reciprocal of the latency of the first peak in the autocorrelogram of SS firing (width = 1 s, bin size = 1.0 ms). Consequently, rhythmic frequency could not be determined on flat autocorrelograms. The strength of the rhythmicity was quantified with a rhythm index (RI) introduced by Sugihara et al.84. Briefly, peaks and valleys were recognized if their heights and depths exceeded the mean baseline level ± SD (measured at time lags of 250–300 msec). The RI was defined by the following formula: RI = a1/z + b1/z + a2/z + b2/z + …, in which ai (i = 1, 2, …) is the absolute value of the difference between the height of the ith peak and baseline level, bi (i = 1, 2, …) is the absolute value of the difference between the height of the ith valley and baseline level, and z was the difference between the height of the zero time bin and the baseline level. The strength of synchronicity between pair of PC was quantified by a synchronicity index (SI), measured on the cross-correlogram (width = 1 s, bin size = 1 ms). This was calculated by dividing the difference between the central peak of the cross-correlogram and the baseline level by the total number of spikes during the same period of time (the higher the synchronicity, the higher the synchronicity index). The central peak was defined as the highest peak in a 20 ms interval centered on the 0 ms time-bin35.
The regularity of the neuron was measured by the coefficient of variation (CV), defined as the quotient between the standard deviation and the mean of the interspike intervals. The recording and analysis of the different neurons were made the by an investigator blind to the genotype. Results are expressed and illustrated as mean ± S.D. and are considered significant if p < 0.05. All statistical analyses were performed using Statistica 7.0.
Purkinje cells recordings
A neural signal was considered to originate from a PC when it presented two types of spiking activities: SS, characterized by a single depolarization (300–800 μs) that occurred between 20 and 200 Hz; and CS, characterized by an initial fast depolarization (300–600 μs), followed by smaller, and relatively constant wavelets. SS and CS were considered to originate from the same PC when a transient pause (>5.0 ms) in SS firing followed each CS. Recordings were analyzed when a stable signal was present for longer than 60 s. The configuration of the CS was studied by the measure of its duration, the number of spikelets, the intra CS frequency and the transient pause induced on the SS firing.
Identification and recording of the DCN neurons
The deep cerebellar nuclei were located with the help of stereotaxic coordinates and the antidromic field potentials induced in interpositus and dentate nuclei by electrical stimulation of the red nucleus. Then, the region of interest was explored during this bipolar stimulation. The cathodic square pulses used for stimulation had a duration of 0.05 ms and an intensity ranging from 30 to 60 µA (below the threshold for eliciting overt movement). To be qualified as antidromically activated, a neuron had to meet three conditions: 1) it had to follow stimulation up to at least 200 Hz; 2) during a near-threshold stimulation the latency had to remain constant (±50 µs); 3) it had to show a collision of the antidromic spike with naturally occurring action potentials, demonstrable for spike-stimulus intervals as long as the antidromic latency period43. The differentiation between a somatic versus an axonic recording were made following the criteria adopted by Gruart and Delgado-Garcia25 which are based on the slope of the extracellular recording, the possibility of recording it over 100 µ; and the occurrence of an initial segment/somatodendritic break. In order to take into account the diversity of the neuronal type present in the DCN our analysis was not restricted to the neurons antidromically identified from the red nuclei. The neurons recorded in the close vicinity of an antidromically identified neurons were also studied and considered as a DCN neuron. The effects of the electrical stimulation of the IO on these DCN neurons were systematically analyzed by means of peri-stimulus time histogram (bin size of 2 ms) representing the neural discharge from 100 ms before to 400 ms after the repeated stimulation (n = 30). A firing rate response to a given stimulus was taken into account when their amplitude in the per-stimulus histogram represented more than the double or less than half of the mean resting value.
Data were analyzed using a one–way ANOVA test and Bonferroni’s post-hoc test after assessing their normality by Kolmogorov-Smirnov test. For the analysis of the N1, N2 and N3 components during the 8 Hz LTD paradigm we used ANOVA for repeated measurements and Dunnett’s methods (post-hoc) when data were normally distributed and Friedman Repeated measurements analysis and Student-Newman-Keuls method (SNK) (post-hoc) when data were not normally distributed. Differences were considered significant at P < 0.05. Results are expressed as mean ± 1 SD.
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
The authors thank T.D’Angelo, M. Dufief, E. Hortmanns, M. Petieau, E. Toussaint, and R. Sánchez-Campusano for expert technical assistance. This work was funded by the Belgian Federal Science Policy Office, the European Space Agency (AO-2004, 118), the Belgian National Fund for Scientific Research (FNRS), the Research Funds and the Leibu Fund of the Université Libre de Bruxelles and the Université de Mons (Belgium). This work was also supported by the Ministerio de Educación y Ciencia Programa Nacional de Movilidad de Recursos Humanos del Plan Nacional de I-D+I 2008–2011 of the Spanish Government.
Electronic supplementary material
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.