Abstract
The potassium chloride cotransporter KCC2 is crucial for Cl- extrusion from mature neurons and thus key to hyperpolarizing inhibition. Auditory brainstem circuits contain well-understood inhibitory projections and provide a potent model to study the regulation of synaptic inhibition. Two peculiarities of the auditory brainstem are (i) posttranslational activation of KCC2 during development and (ii) extremely negative reversal potentials in specific circuits. To investigate the role of the potent phospho-site serine 937 therein, we generated a KCC2 Thr934Ala/Ser937Asp double mutation, in which Ser937 is replaced by aspartate mimicking the phosphorylated state, and the neighbouring Thr934 arrested in the dephosphorylated state. This double mutant showed a twofold increased transport activity in HEK293 cells, raising the hypothesis that auditory brainstem neurons show lower [Cl−]i. and increased glycinergic inhibition. This was tested in a mouse model carrying the same KCC2 Thr934Ala/Ser937Asp mutation by the use of the CRISPR/Cas9 technology. Homozygous KCC2 Thr934Ala/Ser937Asp mice showed an earlier developmental onset of hyperpolarisation in the auditory brainstem. Mature neurons displayed stronger glycinergic inhibition due to hyperpolarized ECl−. These data demonstrate that phospho-regulation of KCC2 Ser937 is a potent way to interfere with the excitation-inhibition balance in neural circuits.
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Introduction
Proper brain function relies on a fine tuned balance between excitation and inhibition1,2. Excitatory synaptic transmission is mainly mediated through glutamatergic synapses and inhibitory synaptic transmission through GABAergic and glycinergic signalling2. Binding of GABA (gamma aminobutyric acid) and glycine to ionotropic GABAA and glycine receptors, respectively3, results in Cl- influx into mature neurons leading to hyperpolarizing inhibitory postsynaptic potentials (IPSPs). In contrast, in immature neurons GABA and glycine cause a depolarisation of the membrane due to Cl- efflux driven by high [Cl-]i4,5,6,7,8,9. Depolarisation in immature neurons facilitates opening of voltage-gated Ca2+ channels thereby evoking local Ca2+ transients10,11,12,13,14,15,16. Ca2+ in turn activates intracellular signalling cascades, which are important to establish and stabilize synaptic connections12,15,17. The developmental shift from depolarisation to hyperpolarisation (D/H shift) is conserved throughout the nervous system (e.g. brainstem, cortex, hippocampus, hypothalamus, and spinal cord)4,6,8,12,13,18,19,20 and occurs during early postnatal life in most rodents21,22.
The key players regulating the D/H shift are NKCC1 (sodium potassium chloride cotransporter 1) and KCC2 (potassium chloride cotransporter 2)23,24,25,26. Both membrane transporters are secondary active mediating the Cl- coupled transport of K+ and/or Na+27,28. In immature neurons, NKCC1 is the predominant transporter mediating Cl- uptake and intracellular accumulation29,30,31,32. In mature neurons, KCC2 is the central Cl- extruder that lowers [Cl−]i and thus enables fast hyperpolarizing postsynaptic inhibition33,34. The physiological relevance of NKCC1 and KCC2 is underlined by the severe phenotypes of knock-out mice models. Mice with disruption of the gene Slc12a5 encoding both splice variants of KCC2 (KCC2a and KCC2b) die shortly after birth due to severe motor deficits that compromise respiration35,36. Mice with disruption of the gene Slc12a2 encoding NKCC1 are viable, but suffer from deafness, increased pain perception, and male infertility31,37,38,39.
In most brain areas including cortex, hippocampus and the cerebellum, the D/H shift is caused by a decrease in NKCC1 and an increase in KCC2 expression during development31,33,40,41,42,43,44,45,46. Interestingly, auditory brainstem neurons perinatally express KCC2 at high levels in the plasma membrane, but in a transport-inactive form47,48,49. Here, the developmental increase in KCC2 transport activity correlates with an increase in the oligomer/monomer ratio49 and a switch from membrane rafts to non-membrane rafts50. In addition, phospho-regulation may play an essential role in the developmental activation of KCC251,52, but detailed knowledge of the multiple phosphorylation sites is lacking.
In the mature auditory brainstem, synaptic inhibition is key in various computational tasks during neural signal processing. This is reflected by well-defined inhibitory projections and circuit-specific hyperpolarizing glycine reversal potentials (EGly). The superior paraolivary nucleus (SPN) is involved in encoding sound offsets53 and displays an exceptionally negative EGly = − 90.6 mV, compared to other auditory nuclei, such as the auditory lateral superior olive (LSO) (EGly = − 68.6 mV) and the medial superior olive (MSO) (EGly = − 75.8 mV) in mice54.
Differential phosphorylation of KCC2 could be one mechanism underlying different EGly in neuronal subtypes. KCC2 harbours several phosphorylation sites that are present at the N-terminus and C-terminus and have been shown to impact its transport activity28,55,56,57. Interestingly, both dephosphorylation of Thr6 in KCC2a, Thr906, Thr1007, Thr1009, and Tyr1087 and phosphorylation of Ser932, Thr934, Ser937, and Ser940 enhances KCC2 activity52,57,58,59,60,61,62,63,64,65,66,67,68,69. The latter phospho-sites are all encoded by exon 22, which is only present in KCC2 and non-therian KCC4 (Fig. 1)65,66,69,70,71. These complex phosphorylation and dephosphorylation combinations provide KCC2 with a rich-regulatory tool-box to achieve graded activity and the integration of different signalling pathways60,66.
Here, we used CRISPR/Cas9 gene editing to generate transgenic mice with a Thr934Ala/Ser937Asp double mutation in KCC2 to probe for a functional link between KCC2 phosphorylation and its transport activity.
Results
Phosphorylation of Ser937 in the KCC2a Thr934Ala/Ser937Asp double mutant enhances KCC2 transport activity
Serine 937 represents an experimentally proven phosphorylation site58,65. It might sometimes be flanked by phosphorylation of threonine 93458. A previous analysis demonstrated that single mutation of threonine 934 or serine 937 into aspartate (mimicking the phosphorylated state) increases KCC2 activity twofold, whereas mutation of either of the two residues into alanine (mimicking the dephosphorylated state) does not impair KCC2 activity65. Here, we generated a KCC2 Thr934Ala/Ser937Asp double mutant that traps Ser937 in the phosphorylated state (Thr934Ala) and the nearby Thr934 in the dephosphorylated state (Ser937Asp). Importantly, the latter mutation Thr934Ala alone does not alter KCC2 activity65. This Thr934Ala/Ser937Asp mutant enabled us to specifically investigate the effect of Ser937 phosphorylation on the activity. The double mutation also prevents a possible confounding action of phosphatases and kinases on threonine 934, which might render interpretation of the results difficult. Immunocytochemical analyses of the transiently transfected KCC2 constructs in HEK293 cells revealed similar transfection rates between KCC2a wild-type (KCC2aWT) and KCC2a Thr934Ala/Ser937Asp (Fig. 2B). To analyse the transport activity, we used the well-established Tl+ flux measurement method65,66,72,73. HEK293 cells transfected with KCC2aWT showed higher transport activity than in mock transfected cells (100 ± 9.05% vs. 28.92 ± 14.23%; p = 1.93 × 10−10) (Fig. 2A, Table 1). In comparison, the KCC2a Thr934Ala/Ser937Asp double mutant showed twofold higher transport activity compared to KCC2aWT (199 ± 44.96%; p = 0.001) (Fig. 2A, Table 1). These data reveal that phosphorylation of Ser937 in Thr934Ala/Ser937Asp double mutant enhances the activity.
Homozygous KCC2 Thr934Ala/Ser937Asp mice show no obvious phenotypic changes
To analyse the in vivo impact of Ser937 phosphorylation, we generated a KCC2 Thr934Ala/Ser937Asp mice via CRISPR/Cas9 located in exon 22 (Fig. 3A). The two mutations were verified by genotyping and DNA sequencing. Heterozygous and homozygous KCC2 Thr934Ala/Ser937Asp mice, which we here name KCC2+/AD (heterozygous) and KCC2AD/AD (homozygous) are viable, fertile, showing no abnormalities in the nutritional state, posture, motor skills and coat. The genotypes of the littermates show the expected Mendelian inheritance of the two alleles (χ2-test 1:2:1; Table 2). Compared to KCC2+/+ littermates, heterozygous KCC2+/AD and homozygous KCC2AD/AD mice show no differences in weight gain from P0 to P16 (Fig. 3B, Table 3, p-value = 0.76, see ANOVA output in Table 4). As usual, male mice become slightly heavier than females (p-value = 0.025, see Table 4), without a genotype-specific effect (p-value = 0.65). Thus, heterozygous KCC2+/AD and homozygous KCC2AD/AD mice show no obvious phenotypic changes.
Next, we performed morphometric measurements in the auditory brainstem. Quantitative analysis of Nissl-stained sections of the brainstem revealed no significant changes in volume of major auditory nuclei. Both the dorsal (DCN) and ventral (VCN) parts of the cochlear nucleus complex (DCN: KCC2+/+: 0.192 ± 0.022 mm3, KCC2AD/AD: 0.171 ± 0.025 mm3, p = 0.334; VCN: KCC2+/+: 0.249 ± 0.037 mm3, KCC2AD/AD: 0.223 ± 0.014 mm3, p = 0.315; Fig. 4A,B) were not affected. Nuclei of the superior olivary complex showed also no morphological differences. All three examined nuclei, the lateral superior olive (LSO), the superior paraolivary nucleus (SPN), and the medial nucleus of the trapezoid body (MNTB) showed no change in volume (LSO: KCC2+/+: 0.054 ± 0.003 mm3, KCC2AD/AD: 0.050 ± 0.003 mm3, p = 0.208; SPN: KCC2+/+: 0.027 ± 0.005 mm3, KCC2AD/AD: 0.023 ± 0.001 mm3, p = 0.239; MNTB: KCC2+/+: 0.034 ± 0.005 mm3 KCC2AD/AD: 0.034 ± 0.001 mm3, p = 0.315; Fig. 4A,C). Thus, the phosphorylation mimic of Ser937 does not affect gross morphology of the auditory brainstem, probably ruling out effects on cell migration or cell viability.
Earlier D/H shift in LSO neurons of homozygous KCC2 Thr934Ala/Ser937Asp mice
The action of glycine, the main inhibitory neurotransmitter in the brainstem, shows a D/H shift between P4 and P8 in LSO neurons8,20,47,74,75. To access whether phosphorylation of KCC2 affects its transport activity, we performed gramicidin perforated patch clamp recordings in LSO neurons at the ages P3 and P5, as previously described76,77,78. To this end, the reversal potential of glycine-evoked currents was determined while leaving the [Cl−]i undisturbed through gramicidin-pores that are exclusively permeable to monovalent cations and small, uncharged molecules79,80. Glycine was applied via puff-application (100 ms) at saturating concentration of 1 mM, while neurons were held at different membrane potentials. Synaptic stimulation can not be used to reliably estimate ECl− at this immature stage, due to ongoing development of inhibitory inputs20,81,82,83. In control mice, we measured a depolarized ECl− at P3 compared to P5 (Fig. 5) and hypothesized in homozygous KCC2AD/AD mice a more hyperpolarized ECl− with respect to controls. In the control data set containing cells from wild type (KCC2+/+) littermates and C57Bl/6N animals, we recorded the average ECl− at P3 = − 36.6 mV (n = 7) and at P5 = − 63.8 mV (n = 5), in agreement with a developmental shift toward hyperpolarizing values (**, p = 0.002). In contrast, recordings in KCC2AD/AD LSO neurons showed the average ECl− = − 79.4 mV (n = 5) already at P3, with no further change at P5 (ECl− = − 71 mV, n = 5, p = 0.155). These data demonstrate that the phospho-mimetic mutation of KCC2 at Ser937 causes an early D/H shift of ECl− compared to the control (− 79.4 mV vs. − 36.6 mV at P3, ***p < 0.001), suggesting an important role of this phospho-site in developmental regulation of KCC2.
Adult homozygous KCC2 Thr934Ala/Ser937Asp mice show more hyperpolarized IPSC-reversal potentials
Based on the increased Cl− extrusion activity of KCC2 observed in HEK293 cells and immature neurons, we predicted more hyperpolarized reversal potentials for synaptically evoked inhibition (EIPSCs) in mature LSO and SPN neurons. We tested this hypothesis by taking advantage of whole cell patch-clamp recordings that allowed to set high intracellular Cl- concentrations of 34.5 mM in order to further challenge KCC2’s Cl- extrusion activity. Based on the Nernst equation, the compositions of pipette solution, the ACSF, the junction potential correction and the assumption that glycinergic synaptic currents are mainly carried by Cl−, the predicted EIPSC was − 36 mV. However, electrical stimulation of the inhibitory fibre tracts leaving the MNTB, the major source of glycinergic inhibition in the superior olivary complex (Fig. 6A,B), reliably elicited pharmacologically isolated glycinergic IPSCs with EIPSCs of at least − 70 mV in wild type KCC2+/+ and homozygous KCC2AD/AD mice. The driving force of the IPSCs, or else the strength of inhibition, is governed by the difference between the resting (in our case holding) potential and the reversal potential of the IPSC. IPSCs of homozygous KCC2AD/AD neurons reversed at more hyperpolarized membrane potentials compared to wild type neurons, suggesting a larger driving force for inhibition in homozygous KCC2AD/AD mice and thus increased KCC2 activity (Fig. 6C,D). These more hyperpolarizing IPSCs resulted in a leftward shift of the current–voltage relationship in both LSO and SPN neurons (Fig. 6E,F), which changed from − 72.0 ± 2.6 mV (n = 11) in LSO wild type neurons to − 80.6 ± 2.7 mV (n = 12) KCC2AD/AD neurons (two-tailed t-test: p = 0.034; Fig. 6G). A hyperpolarizing shift was also observed from − 82.0 ± 2.1 mV (n = 19) in wild type SPN neurons to − 92.8 ± 1.4 mV (n = 13) KCC2AD/AD neurons (two-tailed t-test: p ≤ 0.001; Fig. 6G). Thus, the phospho-mimetic mutation at Ser937 affects not only the developmental shift in immature auditory neurons, but also increases the driving force for inhibition in mature neurons.
Discussion
We generated a transgenic KCC2 Thr934Ala/Ser937Asp mouse, in which serine 937 is replaced by aspartate mimicking the phosphorylated state and analysed its role in the auditory brainstem. This approach was motivated by the observation that the phospho-mimetic mutation of serine 937 is among the most effective ways to increase KCC2 activity in a heterologous expression system65, and since the auditory brainstem shows peculiarities concerning synaptic inhibition, such as posttranslational activation of KCC2 to induce D/H shift47,49 and the most negative ECl− observed so far in neurons54.
A fundamental process during development of the nervous system is the shift from depolarizing to hyperpolarizing action of inhibitory neurotransmitters. This is often accompanied by an increase in the expression or increase in the activity of KCC233,40,41,42,43,44,46. In the auditory brainstem, especially in rat LSO neurons, the D/H shift occurs during the first postnatal week8,20,74,75,84. Here, KCC2 is perinatally expressed, but transport-inactive47,49. This raises the question how KCC2 activation is achieved during development47,49. Based on previous studies, three possible scenarios can be envisaged, which might be causally related: increase in the oligomer/monomer ratio49, a shift from membrane rafts to non-membrane rafts50, and phospho-regulation51,85.
Here, we hypothesized that the potent phospho-site serine 937 plays an important role and, therefore, generated KCC2 Thr934Ala/Ser937Asp mice. These mice are viable and bred normally. They thus provide an excellent tool to explore in vivo the effect of phosphorylation on KCC2 activation and activity. By performing electrophysiological analyses in LSO neurons of acute brainstem slices, we showed that the developmental maturation of Cl- dependent inhibition is shifted to earlier stages in homozygous KCC2 Thr934Ala/Ser937Asp mice. These results are consistent with in vitro analyses, as the KCC2 Thr934Ala/Ser937Asp double mutant leads to activation of KCC2 in HEK293 cells. Such enhanced KCC2 activity lowers the [Cl−]i and increases the strength of glycinergic inhibition. Thus, phosphorylation of Ser937 is sufficient to induce KCC2 activity causing an earlier D/H shift in LSO neurons.
Similarly, (de)phosphorylation of Thr906/Thr1007 or Ser940 induce the onset of hyperpolarisation during development86,87. The decrease in phosphorylation of Thr906 and Thr100752,67 increased KCC2 activity60. In transgenic KCC2 Thr906Ala/Thr1007Ala mice, mimicking the dephosphorylated state of these two phospho-sites, an accelerated onset of hyperpolarisation in hippocampal neurons was observed, pointing to its importance for the D/H shift in this brain area86. In contrast, heterozygous KCC2 Thr906Glu/Thr1007Glu mice, mimicking a phosphorylated state, showed a delayed D/H shift in CA3 pyramidal neurons and hippocampal slices87. These mice showed increased ultra-sonic vocalization, seizure susceptibility and long-term abnormalities in social behaviour87 in comparison to transgenic KCC2 Thr906Ala/Thr1007Ala mice. In the latter, the dephosphorylation-mimicking status limits the onset and severity of seizure64. Ser940 is another phosphorylation site highly phosphorylated in cultured hippocampal neurons in the first postnatal week86. This enhances the KCC2 activity in cultured hippocampal neurons69,86,88. The importance of Ser940 phosphorylation is further corroborated by a delayed D/H shift in Ser940Ala knock-in mice86. These mice suffer from profound social interaction abnormalities like in autism spectrum disorders24,86. Thus, phospho-regulation is a common mechanism to regulate KCC2 activity and to initiate the onset of hyperpolarisation. In view of its rich phospho-site tool box, it will be interesting to study in the future, whether individual phospho-sites have brain area-specific functions. The increasing number of site-specific KCC2 transgenic mice pave the way for such an analysis.
So far, it is unclear whether the stronger Cl- extrusion in the transgenic KCC2AD/AD mice has an implication for the auditory function. Presently, our gramicidin-perforated patch-clamp recordings revealed a conspicuous early D/H shift in KCC2AD/AD mice (hyperpolarizing Cl- gradient present at P3), suggesting early onset of KCC2-mediated Cl- extrusion. This result implies a shorter depolarizing phase of inhibitory inputs onto LSO neurons during postmitotic differentiation. In this phase of neuronal maturation, GABA/glycine triggered depolarisation increase [Ca2+]i, thus contributing to synaptic maturation during development of neuronal circuits9. In the early postnatal LSO, GABA/glycine synaptic inputs evoke depolarizing EPSPs which induce Ca2+ transients spreading to dendritic processes and even trigger action potentials8,15,20,89. During the first postnatal week, such excitation likely facilitates NMDA-dependent developmental plasticity, thereby contributing to synaptic refinement of the MNTB-LSO projections90. It remains to be investigated whether a shorter depolarizing phase, caused by early KCC2 activity onset, affects the development of excitatory and inhibitory synapses on LSO or SPN neurons.
The D/H shift in the auditory brainstem is staggered in time, occurring before postnatal day 1 (P1) in the SPN to about P12 (i.e. at hearing onset) in the MNTB (cochlear nucleus:48,76; superior olivary complex:8,47,74,91). While the mechanisms underlying cell-type-specific regulation remain to be elucidated, these differences point to the importance of precise Cl- homeostasis regulation for maturation of the brainstem circuit.
Another peculiarity of the auditory brainstem is an extremely negative EGly specifically in mature SPN neurons54. This is important for the precise offset firing after sound termination53. The neuron-type-specific regulation of ECl− in auditory brainstem neurons might be due to a different phosphorylation pattern of KCC2 that specifically attunes the strength of inhibition. Consistent with this notion, the phosphorylation status correlates with hyperpolarizing Cl− gradient, as shown for EGABA in adult hippocampal neurons of Thr906Ala/Thr1007Ala transgenic mice64. Our analyses of KCC2AD/AD mice demonstrate a more negative EIPSC both in SPN and LSO neurons compared to KCC2WT. However, the present data do not explain the ECl− difference between SPN and LSO neurons, as the mutation caused a similar hyperpolarizing shift of about − 10 mV in both nuclei. Therefore, it is tempting to presume additional regulatory mechanisms rendering EGly more negative in the SPN. In the future, phospho-proteomic studies or phospho-site specific immunohistochemistry will be helpful to investigate the different phosphorylation pattern of KCC2 in SPN and LSO neurons. What effect will the more negative reversal potential have in SPN neurons? Remarkably, SPN neurons show very stable, strongly hyperpolarized IPSC reversal potentials after the D/H shift has taken place, without further changes after hearing onset around P1292. This suggests that the crucial window for adjusting the strength of inhibition is indeed around the D/H shift. Behavioural effects are to be expected in difficult sound localization tasks as well as gap-detection or sound duration discrimination tasks. Indeed, a reduction of KCC2 activity results in reduced gap detection in a cellular paradigm54. This loss of temporal resolution is present in ageing, hearing loss, and neurodegeneration54. Our results suggest that phosphorylation of Ser937 enhances KCC2 activity resulting in more negative reversal potential in SPN neurons, which in turn might enhance gap detection. Therefore, pharmaceuticals that mediate a neuronal-targeted increase in phosphorylation of Ser937 may represent a novel therapeutic strategy to prevent for example age-related hearing loss. In a high-throughput screening the compound CLP257 and its carbamate prodrug derivate CLP290 were found as promising KCC2 agonist compounds that enhance the activity of KCC293,94 and increase the phosphorylation of Ser94095. However, a follow-up study did not confirm the effect of CLP257 on KCC2 activity96. Future studies should test whether this compound also has an influence on the phosphorylation of Ser937.
In conclusion, we showed that a phospho-mimetic mutation of serine 937 enhances KCC2 activity in the mammalian auditory brainstem. This shifted the onset of hyperpolarisation, i.e. ECl−, to an earlier timepoint in development and rendered EIPSC in mature LSO and SPN neurons more negative. Thus, phospho-regulation of KCC2 is a potent way to increase its transport activity. As such, pharmaceuticals that directly interfere with phosphorylation of KCC2 may be a novel therapeutic strategy.
Material and methods
Construction of the expression clones
Site-directed mutagenesis of mouse KCC2a (NM_001355480.1) was performed according to the QuikChange mutagenesis system (Stratagene, Heidelberg, Germany)65,66,97. The sequence for the forward oligonucleotide for the generation of the KCC2 Thr934Ala/Ser937Asp mutant is CGGGAGATCCAGAGCATCGCAGACGAGGACCGGGGCTCCATTCGGAG. The generated clone was verified by sequencing (LGC genomics, Berlin).
Cell culturing
For immunocytochemistry and measurement of K+-Cl− cotransporter activity, HEK293 cells were transiently transfected with the respective constructs, using Turbofect (Fermentas, Schwerte, Germany). Cells were seeded in a 6-well plate 24 h prior transfection. The DMEM medium was replaced four hours before transfection. 150 µl Opti-MEM (Invitrogen, Karlsruhe, Germany), 6 µl Turbofect and the corresponding DNA amount were thoroughly mixed and incubated for 20 min at room temperature. The mixture was applied to the cells which were then shaken at 300 rpm for 10 min at room temperature.
For K+-Cl− cotransporter activity measurements, transfected HEK293 cells were plated at a concentration of 1 × 105 cells/well in a 0.1 mg/ml poly-L-lysine coated black-well 96 well culture dish (Greiner Bio-One, Frickenhausen, Germany) 24 h after transfection. Each transfected construct was plated out three times, and represents three technical replicates. For the generation of independent biological replicates, the constructs were transfected separately. At least five biological replicates were done. The remaining cells were plated on 0.1 mg/ml poly-L-lysine-coated glass coverslips. After ~ 18 h, coverslips were proceeded for immunocytochemical analysis to determine transfection rates, which were routinely between 20 and 30%.
Immunocytochemistry
For immunocytochemistry, all steps were performed at room temperature. HEK293 cells grown on poly-L-lysine-coated coverslips were fixated for 10 min with 4% paraformaldehyde in 0.2 M phosphate buffer. Afterward, the cells were washed three times with PBS before the blocking solution (2% bovine serum albumin and 10% goat serum in PBS) was applied for 30 min. Primary antibody solution (anti-KCC2 N1-12; 1:1000; Neuromab, California, USA) was added in carrier solution (0.3% Triton X-100, 1% bovine serum albumin, 1% goat serum in PBS) and incubated for 1 h. After washing three times with PBS the secondary antibody, which was conjugated to a fluorescent probe (Alexa Flour 488 goat anti-mouse; 1:1000; Thermo Fisher Scientific, Bremen, Germany) was added to the carrier solution and incubated for 1 h. Again, the cells were washed three times with PBS and completely dried. The dried coverslips were mounted onto glass slides with Mowiol (Roth) and 4′,6-diamidine-2-phenylindole (DAPI, 1:1000; Roth). Photomicrographs were taken using an Olympus fluorescence microscope (Olympus BX63).
Determination of the K+-Cl-cotransport activity
Transport activity of KCC2 was determined by Cl−-dependent uptake of Tl+ in HEK293 cells as described previously72,73,98. To initiate the flux measurement, the medium in the 96-well culture dish was replaced by 80 µl hypotonic preincubation buffer (100 mM N-methyl-D-glucamine-chloride, 5 mM (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid) (Hepes), 5 mM KCl, 2 mM CaCl2, 0.8 mM MgSO4, 5 mM glucose, pH 7.4; osmolarity: 175 mmol/kg ± 2) with 2 µM FluoZin-2 AM dye (Invitrogen) plus 0.2% (wt/vol) Pluronic F-127 (Invitrogen) and incubated for 48 min at RT. Afterward, cells were washed three times with 80 µl preincubation buffer and incubated for 15 min with 80 ml preincubation buffer including 0.1 mM ouabain to block the activity of the Na+/ K+ ATPase. Then, the 96-well plate was placed into a fluorometer (Fluoroskan FL, Thermo Scientific), and each well was injected with 40 µl 5 × Thallium stimulation buffer (12 mM Tl2SO4, 100 mM N-methyl-D-glucamine 5 mM Hepes, 2 mM KCl, 2 mM CaCl2, 0.8 mM MgSo4, 5 mM glucose, pH 7.4). The fluorescence was measured in a kinetic-dependent manner (excitation 485 nm, emission 538 nm, one frame in 6 s in a 200-speriod) across the entire cell population in a single well. By using linear regression of the initial values of the slope of Tl+- stimulated fluorescence increase, the transport activity was calculated.
Statistical Analysis: Transport activities of the respective mutant were tested against control samples (mmKCC2aWT and mock), using a two-sample t-test after Student’s t-test for similar variances between samples. In exceptional cases, where the standard deviation differs by more than a factor of 2, Welch's t-test was used99. To avoid pseudo-replication, the number of degrees of freedom was deflated according to the size of independent preparations each with three technical replicates. The false-discovery rate was controlled and p-values were corrected using the Benjamini–Hochberg method100. The chance of false positive results (type 1 errors) was reduced by choosing p-values < 0.01.
The distribution of genotypes in the F1 generation was tested with the χ2 test under the null hypothesis of a Mendelian ratio of 1:2:1. The age-dependent weight (P0–P16) was tested with repeated measurement two-way ANOVA against the null hypothesis of no difference in mean weight, using sex, genotype, and the interaction of sex and genotype as fixed factors and the mouse id as random factor, i.e., aov(weight ~ sex*genotype + Error(id)).
Animals
All protocols were in accordance with the German Animal Protection Law and approved by the local animal care and use committee (LAVES (Niedersächsisches Landesamt für Verbraucherschutz und Lebensmittelsicherheit), Oldenburg) and followed the NIH guide for the care and use of laboratory animals. Mice of both sexes were used. The KCC2AD/AD mouse line was generated with CRISPR/Cas (clustered, regulatory interspaced, palindromic repeats (CRISPR)-associated (Cas) system) at the transgenic core facility at the Max Planck Institute of Molecular Cell Biology and Genetics (Dresden, Germany). For this purpose the guide RNA 5′cucguagugucugcucagag 3′ and the repair template: CATCCACTGTAGTAATGGCTCTTGGCAGGGCGTGGGTGGTGACCCCCCAGCAGAGCTGGCACCAACCTGTGTCACTCCCCAGATCCAATCGATTGCCGATGAAGACCGAGGCTCCATTCGGAGGAA was used. These mice were kept on a C57Bl/6N genetic background. Primers for genotyping KCC2 wild-type are as follows : for : ATGGGCCCTTGAAGGACAGG and rev : CCGAGACTCGTCTGTGATGCT. For the genotyping of the T934A/S937D mutation in KCC2 the following primers were used: for: ATGGGCCCTTGAAGGACAGG, and rev: TCGGTCTTCATCGGCAATCGA.
Morphometric volume analysis
Adult KCC2AD/AD and KCC2+/+ mice (aged between postnatal day (P) 30–P60) were transcardially perfused with phosphate buffered saline (PBS; 136.9 mM NaCl, 2.7 mM KCl, 10.1 mM Na2HPO4, 1.8 mM KH2PO4, pH 7.4) followed by 4% paraformaldehyde solution. Brains were dissected and postfixed for 2–4 h in 4% PFA and stored in 30% sucrose in PBS for cryoprotection. The brainstem was cut in coronal sections with a thickness of 30 µm using a cryostat (Leica Biosystems, Wetzlar, Germany). Nissl staining was performed on consecutive sections of the auditory brainstem. Sections were imaged with an automated slide scanning microscope (AxioScan Z1, Carl Zeiss, Oberkochen, Germany). The volume of individual nuclei was obtained as described previously101,102,103. Shortly, images were analysed by outlining the auditory nuclei using Fiji104 and multiplying this area with the thickness of each section. Three animals per genotype were analysed. The experimentalist was blind to the respective genotype. Statistical analysis was performed using Student’s t-test after testing for Gaussian distribution using Prism version 9 (GraphPad, San Diego, California). Reported values are mean ± SD.
Patch-clamp recordings
Slice preparation: Coronal slices (200 µm) containing the superior olivary complex including LSO and SPN were cut from P3 to P29 mice of either sex. The brainstem was sliced with a vibratome (Leica VT1200 S), in ice-cold, low-calcium artificial cerebrospinal fluid (ACSF) solution containing (in mM): 125 NaCl, 2.5 KCl, 0.1 CaCl2, 3 MgCl2, 1.25 NaH2PO4, 25 NaHCO3, 25 glucose, 2 sodium pyruvate, 3 myo-inositol, 0.5 ascorbic acid, continuously bubbled with 5% CO2 and 95% O2, pH 7.4. Slicing solution contained lower Ca2+ and higher Mg2+ concentration than the standard ACSF in order to avoid Ca2+-dependent signalling and activation of NMDAR. Slices were incubated in the standard recording solution (ACSF same as for slicing, except CaCl2 and MgCl2 were changed to 2 mM and 1 mM, respectively) for 30–45 min at 37 °C before being stored at room temperature until recordings.
Gramicidin perforated patch recordings were conducted at room temperature (22 ± 1 °C) in LSO neurons of P3 and P5 day old mice of both genotypes and either sex. Gramicidin perforated patch recordings were acquired as previously described77,78. In brief, patch pipettes were pulled with DMZ-Universal-Electrode horizontal puller from filamented borosilicate glass capillaries (Science Products) to have resistances of 5–6 MΩ when filled with a K+-gluconate-based internal solution. Pipettes were tip-filled as follows (mM): 97.5 potassium-gluconate, 32.5 KCl, 1 MgCl2, 10 HEPES, 5 EGTA, 10 HEPES, pH 7.34 with KOH (290 mOsm). The remainder of the pipette was back-filled with the same solution including gramicidin (50 µg/ml gramicidin A, Sigma) and 25 µM ATTO 488. The latter was used to confirm that the perforated patch was not ruptured. At the end of the experiment, the rupture of the perforated patch yielded EGly around the Nernst potential for Cl− of − 34 mV, thus confirming that the gramicidin ionophores were impermeable for Cl− and that our recordings were not affected by the [Cl−]pip. The progress of perforation was evaluated by monitoring the steady-state current responses to a − 5 mV voltage command (with access resistance dropping from 1 GΩ to around 20 MΩ). Recordings were done when series resistance reached a steady level (mean Rs = 20.8 ± 5 MΩ, n = 22), typically within 30–40 min after the giga-seal formation. Glycine (1 mM) was prepared in standard recording ACSF and pressure applied (100 ms) over the soma of recorded neuron using a Picospritzer (General Valve Corp.). Current responses to glycine puff were recorded while cells were held at different holding potentials (from − 82 to − 12 mV with increment of 10 mV, offline corrected for liquid junction potential). The constant stimulation conditions were assured by controlling the pipette diameter, application pressure and duration, and distance from the cell (3 µm, 5 psi, 5 ms, 10 µm, respectively). The perfusion was turned off just prior to each puff application to avoid unequal dilution of the agonist. Significance of the responses was determined by employing the z-test, i.e., level of acceptance was set at z < − 3.3 (Im), which corresponds to p < 0.001 [z = (A-BL)/SDBL, with A being the maximal amplitude of the response, BL the mean of the baseline (2 s prior to stimulation), SDBL the standard deviation of the baseline]. Pressure-ejection of ACSF under the same condition evoked no response (mean ACSF response = − 0.34 ± 0.2 pA, z = − 0.21 ± 0.13, p > 0.73, n = 4), while glycine evoked significant membrane currents in the same neurons.
Synaptic stimulation experiments were performed on LSO and SPN neurons of P14–P29 mice of both genotypes and either sex. Recordings were conducted at 37 ± 1 °C, maintained by an inline feedback temperature controller and heated stage (Warner Instruments) with the recording chamber being continuously perfused with ACSF at a rate of 1–2 ml min−1. Whole-cell patch-clamp recordings were made from visually identified LSO and SPN neurons. Patch pipettes were pulled from borosilicate glass capillaries (Warner Instruments) using a DMZ Universal electrode puller (Zeitz-Instuments Vertriebs GmbH), filled with an internal solution containing (in mM): K-gluconate 97.5, KCl 32.5, HEPES 40, EGTA 5, MgCl2 1, Na2phosphocreatine 5, pH was adjusted to 7.2 with KOH. Synaptic responses were evoked by afferent fibre stimulation with concentric bipolar electrodes (FHC inc., #CBARC75). Voltage pulses were generated by the HEKA amplifier and post-amplified by an isolated pulse stimulator (AM Systems). Inhibitory currents were recorded in ACSF containing 6,7-dinitroquinoxaline-2,3-dione (DNQX; 10 µM) and D-2-amino-5-phosphonopentanoic acid (D-AP5; 50 µM) to block AMPA and NMDA glutamate receptors, respectively. Stated voltages are corrected for a liquid junction potential of − 11 mV.
The patch clamp recordings were acquired using a HEKA EPC 10 amplifier (HEKA Elektronik). Recorded signals were digitized at 50–100 kHz and filtered with a 6–10 kHz Bessel low-pass filter. Data were examined with FitMaster (HEKA) software followed by the analysis on the same software. Amplitude of the current responses from individual cells were plotted against holding potential under which they were recorded (IV diagram) and reversal potential was derived from linear fit of those values.
Statistics: Data sets were tested for Gaussian distribution prior to comparison with the Shapiro–Wilk test. Statistical analyses were carried out in Sigma Plot (Sigma Plot 14, Systat Software). Values are reported as mean ± SEM and compared using t-test (*p < 0.05, **p < 0.01, ***p < 0.001). The studies reported are in accordance with ARRIVE guidelines.
Data availability
All data generated or analysed during this study are included in this published article and its supplementary information files.
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Acknowledgements
We thank the transgenic core facility at the Max Planck Institute of Molecular Cell Biology and Genetics (Dresden, Germany) for the generation of the transgenic mice. Authors are also grateful to Dr. Antje Cordshagen, Lauredana Alessandra Dos Santos Ferreira Grani, Natalie Ubben, and the animal facility at the University of Oldenburg. This work was supported by the Deutsche Forschungsgemeinschaft (Grants NO428/14-1 to H.G.N; KO2207/3-1 to C.K-S. and HA 6338/2-1 to A.-M.H).
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T.R., C.K.S., L.E., I.M., H.G.N. and A.M.H. designed the experiments, performed the experiments and analyzed the results. T.R., C.K.S. and M.W. performed statistical analyzes. A.M.H. wrote the paper with T.R., C.K.S., L.E., H.G., I.M., and M.W.
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Radulovic, T., Rajaram, E., Ebbers, L. et al. Serine 937 phosphorylation enhances KCC2 activity and strengthens synaptic inhibition. Sci Rep 13, 21660 (2023). https://doi.org/10.1038/s41598-023-48884-x
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DOI: https://doi.org/10.1038/s41598-023-48884-x
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