- Research article
- Open Access
Transient change in GABAA receptor subunit mRNA expression in Lurchercerebellar nuclei during Purkinje cell degeneration
© Linnemann et al; licensee BioMed Central Ltd. 2006
- Received: 10 March 2006
- Accepted: 27 July 2006
- Published: 27 July 2006
Lurcher mice suffer from a complete Purkinje cell (PC) loss in the first four postnatal weeks. Parallel to this degeneration, GABAergic synapses in the deep cerebellar nuclei (DCN), the major recipient of the inhibitory PC projection, increase synaptic conductance. Here, we further investigated this phenomenon, using real-time RT-PCR to assess GABAA receptor subunit gene expression during PC degeneration.
We observed a specific reduction in γ2 subunit gene expression, while α1–5, β1–2, γ1,3 and δ subunits were unaffected. We made two further specific findings. First, the difference in gene expression was shown in tissue from DCN only. Neither the hippocampus nor coronal sections through the forebrain showed such effects. Furthermore, the involvement of different levels of corticosterone, a possible humeral trigger for differences in gene expression, could be excluded. Second, like the known potentiation of GABAergic synapses, the γ2 down-regulation was present only after the onset of degeneration at p14. The difference in γ2 mRNA expression, however, appeared transient, since it was no longer detectable in adult Lurcher mice.
In conclusion, the down-regulation of γ2 subunits may be related to differences in synaptic efficacy and, as such, may reflect the initial phase of adaptive responses of DCN tissue to massive GABAergic deafferentation. Its transient course, however, does not support the idea that modulations in GABAergic transmission are at the basis of the well-known DCN-based functional benefit of Lurcher mice present throughout their life.
- Purkinje Cell
- GABAA Receptor
- Deep Cerebellar Nucleus
- Single Channel Conductance
- Synaptic Conductance
Inhibitory projections are sometimes placed at decisive locations within the motor system and are therefore important for programming and controlling the execution of movement. One of these projections is the GABAergic Purkinje cell (PC) projection onto the deep cerebellar nuclei (DCN) neurons. This projection system undergoes a degeneration in the spontaneous, autosomal semidominant mouse mutation Lurcher, yielding nonviable homozygous mice, while heterozygous individuals (Lc/+) show ataxia expressed by a tendency to fall . The syndrome is based on a complete loss of Purkinje cells during postnatal development followed by a secondary degeneration of intracerebellar and precerebellar cells [2–4]. The phenotype arises from a mutation in the orphan receptor subunit glutamate δ2  which is expressed almost exclusively in PCs and thus determines the specificity of the primary effect . The first signs of PC degeneration are observed at postnatal day 8 (p8; ) and by p26, approximately 90% of PCs have disappeared . The majority of DCN neurons survive, albeit deprived of their inhibitory PC input [8, 9].
Behaviorally, Lc/+ show deficits in standard tests of motor behavior like the rotarod and other tests of equilibrium [10–15]. However, the symptoms are mild, since differences to wild type animals were seen only in test situations that confront the motor system with higher demands such as, for instance, higher rotation frequencies in the rotarod test . Experiments using lesions of the DCN in Lc/+ clearly showed that the mild symptoms reflect a residual functionality of the cerebellar system because lesioned animals showed a grossly deteriorated motor performance in comparison with non-lesioned mutants. Scores measured with the rotarod test dropped virtually to zero without recovery during repeated sessions . Furthermore, spatial orientation, which is mildly impaired in Lc/+ [17, 18], deteriorated drastically after DCN lesions [19, 20]. These behavioral data suggest that the DCN play a beneficial role for the motor performance of Lc/+. Electrophysiological recordings in DCN neurons of Lc/+ strongly support this hypothesis. Lc/+ exhibited a potentiation of GABAA-receptor-mediated average synaptic conductance (gsyn) in close temporal relationship to PC death . This potentiation of gsyn in the DCN might have an adaptive value, compensating for the loss of the extrinsic inhibition. A possible basis for the modulation of GABAergic synaptic transmission are changes in the subunit composition of GABAA receptors . We asked in the present study whether the DCN change their GABAA receptor subunit composition in temporal relationship to the degeneration of the inhibitory afferents. Guided by the occurrence of conductance changes between p11 and p14 , we used real-time RT-PCR to investigate the gene expression of GABAA receptor subunits α1–5, β1–2, γ1–3 and δ in DCN tissue of Lc/+ compared with wild type mice at these critical ages and after the completion of PC degeneration at the age of 8 weeks. Furthermore, we addressed the question as to whether the observed changes are specific to the DCN. In addition, we performed whole cell voltage-clamp recordings of CA1 pyramidal neurons in mutants and controls to determine whether the potentiation in gsyn previously observed in DCN is a generalized and ubiquitous phenomenon or specific to the denervated DCN.
Using real-time RT-PCR, mRNA expression levels of GABAA receptor subunits α1–5, β1–2, γ1–3 and δ were investigated in tissue of DCN obtained from Lurcher mutants aged p11 and p14 and compared to wild type controls of the respective age. Since gene expression of GABAA receptor subunits  and of internal controls such as hypoxanthine-phosphoribosyltransferase (HPRT) [24, 25] are known to be subject to changes during postnatal development, we restricted our comparison of gene expression to age-matched mutants and controls.
The residual motor functionality of Lurcher mice is based on the intactness of the DCN and outlasts the period in which PCs degenerate . To elucidate the role of candidate cellular mechanisms for this compensation, their specificity for the structure (DCN) and time of occurrence (degeneration of PCs) must be investigated. Mechanisms showing no clear specificity and relationship to the DCN (or connected structures) or to the occurrence of the PC degeneration can be excluded as a basis for this functional compensation. In a previous study from our laboratory, Lurcher mice displayed a potentiation of miniature IPSCs in the DCN in close temporal relationship to PC degeneration . Our present data complement these earlier results by showing that the synaptic conductance of GABAergic IPSCs is unaffected in another brain structure, the hippocampus.
The responsiveness of the hypothalamo-pituitary-adrenal system is known to be enhanced in Lurcher mice. Under stress, this mutant shows increased levels of serum corticosterone compared to wild type controls [26, 27]. Corticosterone has a known modulatory role for GABAA-receptor-mediated conductance  as well as GABAA receptor subunit gene expression [29, 30]. The absence of significant differences of serum corticosterone between Lurcher and wild type mice (at the ages and under the experimental conditions investigated here), thus supports the idea that the changes observed in DCN of Lurcher mice are not unspecific phenomena that occur throughout the brain. The results instead suggest that these changes are specific to the DCN. The down-regulation of γ2 mRNA matches the spatiotemporal specificity of the electrophysiological changes in GABAergic transmission. This was detected in the DCN, but not in material taken from the hippocampus or from a section through the forebrain. Furthermore, its de novo occurrence at p14 indicates a temporal relationship to the course of PC degeneration. However, since it was not detectable in adulthood (eight weeks of age), the reduction of subunit gene expression cannot be the direct structural cause of the permanent mild expression of ataxia in Lurcher mice. If future work is to show a functional link between subunit composition and synaptic potentiation, the latter must be subjected to the same reasoning and must be excluded from the candidates of mechanisms directly responsible for functional adaptation in the DCN. The main question to be discussed below is therefore, to what extent can a changed subunit expression relate to changes in synaptic transmission in the Lurcher mouse.
First and foremost, the differences in gene expression were calculated with reference to the ubiquitously expressed HPRT. Therefore, the measurements should be insensitive to known differences of volume and cell densities in Lurcher DCN [8, 9]. This may help to explain apparent conflicting results obtained in adult Lurcher mice using in situ hybridization, where increased γ2 mRNA levels in Lurcher mice aged p108 based on the assessment of autoradiographic grain density were reported . The different results may be partly explained by the different ages of animals and the different methods used, but the shrinkage of the DCN (confere [8, 9]) may well have contributed to an increase in grain density (as discussed in ). The insensitivity of the real-time RT-PCR to shrinkage of the DCN is further supported by the exclusive reduction of the γ2 subunit mRNA expression. If general differences in cell densities, volume and presence of GABAergic synapses in DCNs of Lurcher and wild type mice had accounted for differences in mRNA expression, the consequences should have affected all, or at least many, subunits. Our findings imply that the relative composition of postsynaptic GABAA receptors during the time of PC degeneration was different in Lurcher mice. This conclusion is in line with the probable postsynaptic location of the mechanism, leading to the increment in miniature synaptic conductance . There are two possible explanations as to how the present findings may be related to changes in synaptic conductance. First, it is well established that the compositions of subunits determine single channel conductances [32–35]; see for review . Second, subunit composition specifically affects the dynamic control of GABAA receptor expression at the cell surface and may thus effectively determine its presence at the postsynaptic membrane ([36–39]; see for review also .
If modulation of single channel conductances were at the basis of the synaptic potentiation, then our present data, together with earlier results,  would imply that a reduced γ2 content increases channel conductance and hence synaptic conductance. This prediction, however, would be in conflict with previously published data of several investigators. Verdoorn et al.  analyzed GABA-gated chloride channels expressed in human embryonic kidney cells. When the γ2 subunit was present, the resulting GABAA receptors had a larger conductance. Moreover, Lorez et al.  investigated the channel properties of neuronal GABAA receptors from brains of embryonic and postnatal mice lacking the γ2 subunit and found smaller single channel conductances. To rescue this scenario, one would need to assume that the decrement of the γ2 subunit mRNA expression found here is accompanied by the replacement of γ2 by another subunit that has the potential to increase the gsyn, but that has not been detected so far. Replacements for GABAA receptor subunit composition during postnatal development under physiological conditions are well known. For instance, α2 subunits are partially replaced by α1 subunits in DCN during the first two postnatal weeks . Such switches have indeed the potential to change the synaptic strength of GABAA receptors [41, 42].
The second possibility is that subunit composition is altered to dynamically regulate the receptor availability at the cell surface. DCN neurons in rodents express mainly α1, β2 and γ2 subunits [31, 43]. The presence of the α1 subunit appears to be required for the surface expression of β2 (as investigated in Madin-Darby canine kidney cells  and in COS7 cells ). Our study shows that the content of α1 and β2 mRNA remained unchanged in Lurcher mice compared to the age-matched controls. None of these facts suggest that the amount of generated GABAA receptors and their subsequent transport to the cell membrane is impaired in Lurcher mice. On the other hand, it may also be possible to regulate receptor presence by interfering with the removal of receptors from the membrane. GABAA receptors undergo a constitutive endocytosis after association with the adaptin AP2 complex, a process dependent on the presence of β and γ subunits . Moreover, blockade of endocytosis enhances the amplitude of GABAA-mediated mIPSCs in hippocampal neurons . More specifically, Connolly et al.  ascertained that cell surface stability of GABAA receptors depends on the presence of γ2 subunits. They observed that receptors containing γ2 are selectively removed from the cell surface upon activation of protein kinase C with concomitant reduction of GABA-induced currents. In summary, a tentative hypothesis – to be tested by further experiments – can be formulated from these considerations as follows: The specific γ2 reduction of subunit expression during PC degeneration in Lurcher mice might modulate endocytosis such as to allow the Lurcher DCN neurons to specifically increase the GABAA receptor cell surface levels at the postsynaptic membrane. This speculation receives some experimental support from the results of a non-stationary fluctuation analysis on mIPSCs in wild type and Lurcher mice. This analysis gave no indication of changes of single channel conductances, while the peak number of open receptors underlying Lurcher mIPSCs was estimated to be of a factor two higher than in wild type mice .
Animals and molecular genotyping
Heterozygous B6CBACa-Aw-J/A-Lc (Jackson Laboratories, Bar Harbor, ME, USA) were mated with B6CBA (Harlan-Winkelmann, Borchen, Germany) mice. The animals were kept and used in experiments according to the institutional and national animal care guidelines (also conforming with NIH guidelines on animal care). Animals from the Lurcher progeny not showing the characteristic Lc/+ phenotype (ataxic gait and tendency to fall) were genotyped as described previously .
Primers for GABAA receptor subunits and the internal control
Mice aged p15-18 (without statistically significant age differences between mutants and controls) were deeply anesthetized by application of ketamine (150 mg/kg i.p.). The brains were removed and placed in ice-cold modified artificial cerebrospinal fluid [ACSF, containing (in mM) 126 sucrose, 2.5 KCl, 1.3 NaH2PO4, 3 MgCl2,, 26 NaHCO3, 0.1 CaCl2 and 20 D-glucose] that was bubbled with 95%O2-5%CO2. Horizontal slices of 275 μm thickness that included the hippocampus were obtained using a vibratome (VT1000s, Leica, Nussloch, Germany) and transferred into modified ACSF at room temperature. The modified ACSF was replaced within the next 90 min with ACSF containing (in mM) 125 NaCl, 2.5 KCl, 1.3 NaH2PO4, 2 MgCl2,, 26 NaHCO3, 2 CaCl2 and 20 D-glucose, oxygenated with 95%O2-5%CO2 at room temperature. Experiments were performed with this ACSF to which the selective non-NMDA receptor antagonist 6,7-dinitroquinoxaline-2,3-dione (25 μM; Tocris, Bristol, UK), tetrodotoxine (1 μM, Tocris) and, in some recordings, also the GABAA antagonist bicuculline (10 μM; Sigma, Taufkirchen, Germany) were added.
Whole-cell voltage-clamp recordings of hippocampal CA1 pyramidal neurons were conducted with patch pipettes that had a resistance of 2.5–3.5 MΩ when filled with a solution containing (in mM) 124 CsCl, 10 K+-HEPES, 5 EGTA, 4.6 MgCl2, 4 K+ATP, 0.4 Na+GTP, 0.1 CaCl2, and 5 QX-314 (Tocris), adjusted to pH 7.3 with CsOH, thus obtaining chloride symmetrical experimental conditions. CA1 pyramidal neurons were identified and the patch procedure was visualized using a motorized (Luigs&Neumann, Ratingen, Germany) microscope (Axioscope, Zeiss, Göttingen, Germany) with water immersion objective (×40, Zeiss numerical aperture 0.75), infrared illumination, Normaski optics and infrared sensitive CCD camera (Newvicon C2400-07-C Hamamatsu, Japan). The recordings were performed with an EPC-7 amplifier (Heka, Lambrecht, Germany). The data was sampled at a rate of 25 kHz (Spike2, CED, Cambridge, UK). Neurons were voltage-clamped at -70.6 ± 0.7 mV. Data was not quantitatively analyzed if, under these conditions, the serial resistance (17.9 ± 7.3 MΩ, n = 11) had changed by more than 20% or if the membrane resistance (221.8 ± 66.8 MΩ, n = 11) of the recorded neuron was below 150 MΩ. Neither the membrane nor the serial resistances differed significantly between genotypes.
Analysis of the miniature inhibitory postsynaptic currents (mIPSCs) was performed with the MiniAnalysis program (Synaptosoft, Decatur, GA, USA). For analysis of the synaptic waveforms, only those synaptic events that had not been interrupted by other synaptic events were evaluated. gsyn values were calculated as gsyn = Imean/(Vh - E), where Imean is the mean peak amplitude of the mIPSCs, Vh is the holding potential and E is the measured equilibrium potential for the mPSCs of the respective recording. The decay time mentioned in this paper is the time it takes the current values to decay to 1/e of the peak values of the mIPSC amplitudes.
Following deep anesthesia by application of ketamine (150 mg/kg i.p.), blood was collected by intracardial puncture and immediately transferred into a plasma separator tube filled with lithium heparin (BD Microtainer PST LH, Becton Dickinson, Heidelberg, Germany) on ice. After centrifugation, the sera were stored at -20°C until the 125I radioimmunoassay was performed. The Coat-A-Count Rat Corticosterone (TRKC 1; DPC Biermann, Bad Nauheim, Germany) procedure is a solid-phase 125I radioimmunoassay. 125I-labelled rat corticosterone competed for 2 h at room temperature with corticosterone in the serum specimens for antibody sites immobilized to the wall of the tubes. The counts per minute measured in the tubes with a gamma counter (Multi-Crystal Counter LB 2104, Berthold, Bad Wildbad, Germany), converted by way of a calibration curve yielded to a measure of the corticosterone serum level. The minimal detectable dose is approximately 5.7 ng/ml. The blood collections were always performed in the same time window in the afternoon, to avoid variations due to circadian rhythm.
Statistically significant differences and correlations were tested with the Student's t-test for normally distributed data, and otherwise with the Mann-Whitney-Test (italicized P values throughout the paper). Statistical significance was assumed if P < 0.05.
The sequencing procedures were performed by the sequencing service facility of the Center for Interdisciplinary Clinical Research, Tübingen. We thank Ute Großhennig and Britta Baumann for technical assistance. We are also grateful to Dr. Martin Möck of the Department of Anatomy, University of Tübingen, and Dr. Bernd Wissinger of the Molecular Genetics Laboratory, University Eye Hospital Tübingen for discussions, advice and support.
This work was supported by the German Science Foundation (SFB 430-C6, SCHW 577/5-1), the Center for Interdisciplinary Clinical Research, Tübingen (IZKF IC1) and the Hermann and Lilly Schilling Foundation.
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