FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W1947607762> ?p ?o ?g. }

• W1947607762 endingPage "6038" @default.
• W1947607762 startingPage "6029" @default.
• W1947607762 abstract "Non-technical summary Ion channels are pores that allow the exchange of molecules across cell membranes. In nerve cells (neurons) of the hippocampus (a brain region involved in learning and memory), the potassium KV7 channel is present predominantly in the cell body (the soma) and in its axon, a projection from the cell body that produces brief electrical signals known as action potentials. We have previously shown that axonal KV7 channels control action potential initiation and so regulate cell excitability. However, cells also receive inputs from other cells connected to them, resulting in longer lasting electrical signals known as synaptic potentials. In this study, we show that only somatic KV7 channels influence synaptic potential shapes and summation, whereas axonal channels increase the ability of synaptic potentials to generate action potentials. Hence, axonal and somatic KV7 channels differentially contribute to information processing within hippocampal neurons, which may be important for processes such as cognition Abstract The KV7/M-current is an important determinant of neuronal excitability and plays a critical role in modulating action potential firing. In this study, using a combination of electrophysiology and computational modelling, we show that these channels selectively influence peri-somatic but not dendritic post-synaptic excitatory synaptic potential (EPSP) integration in CA1 pyramidal cells. KV7/M-channels are highly concentrated in axons. However, the competing peptide, ankyrin G binding peptide (ABP) that disrupts axonal KV7/M-channel function, had little effect on somatic EPSP integration, suggesting that this effect was due to local somatic channels only. This interpretation was confirmed using computer simulations. Further, in accordance with the biophysical properties of the KV7/M-current, the effect of somatic KV7/M-channels on synaptic potential summation was dependent upon the neuronal membrane potential. Somatic KV7/M-channels thus affect EPSP–spike coupling by altering EPSP integration. Interestingly, disruption of axonal channels enhanced EPSP–spike coupling by lowering the action potential threshold. Hence, somatic and axonal KV7/M-channels influence EPSP–spike coupling via different mechanisms. This may be important for their relative contributions to physiological processes such as synaptic plasticity as well as patho-physiological conditions such as epilepsy. KV7 channels underlie the so-called ‘M’-current, a subthreshold active neuronal K+ current (Brown & Passmore, 2009). All five known subtypes (KV7.1–7.5) are likely to be expressed in central neurons (Brown & Passmore, 2009; Goldman et al. 2009). Although early reports indicated that these neurons may have a somato-dendritic expression pattern (Roche et al. 2002; Shah et al. 2002), recent reports suggest that these channels are expressed at a higher density in axons (Devaux et al. 2004; Chung et al. 2006; Pan et al. 2006). Here, they play a role in regulating the resting membrane potential and action potential threshold (Shah et al. 2008), and thereby influence post-synaptic spike firing. This may be one of the potential mechanisms that enhance neuronal excitability during benign familial neonatal convulsions (BFNC) as mutations in KV7/M-channels associated with this condition can result in disrupted axonal KV7 channel function (Chung et al. 2006). In vivo, though, excitatory synaptic potential (EPSP) integration is an important factor in determining action potential generation (Debanne, 2004; Clark & Hausser, 2006). Since KV7 channels are active at rest (Shah et al. 2008), it is possible that they may contribute to synaptic potential integration. Indeed, the summation of a train of EPSPs generated by extracellular stimulation in hippocampal CA1 pyramids is affected by KV7/M-channel modulation (Hu et al. 2007). However, since KV7/M-channels may also be present pre-synaptically in the hippocampus (Martire et al. 2004; Peretz et al. 2007), it is not clear whether this effect is pre- or post-synaptic in origin. In this study, we injected EPSP waveforms (αEPSPs) in the soma and dendrites of CA1 pyramids to investigate how EPSP integration is affected in these neuronal subcellular compartments. We also used a competing peptide, ankyrin G binding peptide (ABP; Shah et al. 2008) to determine if axonal KV7 channels contribute to somatic EPSP summation. Computer simulations were performed to corroborate our findings. We show that somatic, but not axonal, KV7/M-channels affect synaptic integration in a voltage-dependent manner in peri-somatic locations only. Axonal KV7 channels, on the other hand, alter EPSP–spike coupling by lowering the action potential threshold. Modulation of EPSP–spike coupling may be another mechanism by which modification in KV7/M-channel function may have a substantial impact on neuronal excitability and therefore, physiological processes such as learning and memory as well as patho-physiological conditions such as epilepsy (Jentsch, 2000; Peters et al. 2005; Wu et al. 2008). All experimental procedures were approved by the UK Home Office (Project licence PPL No. 70/06372) as well as the School of Pharmacy and UCL research ethics committees. All measurements were made using Clampfit (v8.0). The summation ratio was calculated as the amplitude of the fifth EPSP divided by the amplitude of the first. Group data are expressed as mean ± SEM. Statistical significance was determined using either paired or unpaired Student's t tests as appropriate. Statistical significance of P < 0.05 is indicated as * in all figures. All chemicals were obtained from Sigma (St Louis, MO, USA) apart from XE991, CNQX, CGP 55845, bicuculline and APV, which were purchased from Tocris (USA). Retigabine was provided by NeuroSearch (Ballerup, Denmark) through EU grant LSHM-CT-2004-503038. ABP and sABP was custom made by Genscript (USA). Stock solutions of bicuculline and CGP 55845 were made in DMSO and stored at −20°C until use. These were then dissolved in the external solution such that the final DMSO concentration was less than 0.1%. Aqueous stock solutions of XE991, linopirdine, CNQX and APV were also kept at −20°C until use. All simulations were implemented and run with the NEURON program (v7.1) (Hines & Carnevale, 1997) using the variable time step feature. The 3D reconstruction of the CA1 pyramidal neuron was one of those used in a previous work (neuron 9068802, Migliore et al. 2005). The same standard, uniform, passive properties were used for control conditions (τm = 28 ms, Rm = 28 kΩ cm2, Ra = 150 Ω cm). Resting potential was set at −65 mV and at 35°C. All channel kinetic and distribution were from a previously published model (Shah et al. 2008), and based on the available experimental data for CA1 pyramidal neurons (reviewed in Migliore & Shepherd, 2002). Sodium and delayed rectifier potassium conductances were uniformly distributed throughout the dendrites, whereas an A-type potassium and a non-specific Ih conductance were linearly increasing with distance from the soma. The KV7-type potassium conductance was inserted into the soma and at a 3-fold higher density in the axon (Shah et al. 2008). To take into account for Ca2+ channels open around resting potential (reviewed in Marder & Goaillard, 2006), a low-threshold Ca2+ and Ca2+-dependent K+ conductances together with a simple Ca2+ extrusion mechanism were included at uniform density and distribution in all compartments. The simulation files are available for public download under the ModelDB section (Migliore et al. 2003) of the Senselab database (http://senselab.med.yale.edu). The effects of XE991 application were modelled by deleting the KV7/M-conductance. To determine if Kv7 (M-) channels affect post-synaptic EPSP kinetics and summation at the soma and dendrites, individual EPSPs as well as 20 and 40 Hz trains of EPSPs were induced post-synaptically by injecting an alpha waveform current (Poolos et al. 2002; Shah et al. 2004) (see Methods) into either the soma or dendrite. These somatic and dendritic αEPSPs had similar kinetics to those evoked by stimulating the Schaffer collaterals in the stratum radiatum. We chose this method to avoid complications due to possible pre-synaptic effects of KV7 channels (Martire et al. 2004; Peretz et al. 2007; Luisi et al. 2009; Huang & Trussell, 2011). Experiments were done in the presence of 1 μm TTX to prevent spontaneous action potential firing in the presence of the KV7/M-channel inhibitor, XE991 (Shah et al. 2008). At −60 mV, 3 μm XE991 enhanced the amplitude of somatic αEPSPs by 34.7 ± 11% (n= 6, P < 0.05, Fig. 1A) and lengthened the decay time constant (τ) by 92.3 ± 28% (n= 6, P < 0.05, Fig. 1A). Consistent with the M-current biophysical properties in these neurons (Shah et al. 2008), the actions of XE991 were voltage dependent with significantly smaller effects at −70 mV (% change in amplitude and τ were 23.2 ± 3.1% (n= 6) and 28.7 ± 7.4% (n= 6, P < 0.05), respectively, Fig. 1A). The KV7/M-channel enhancer, retigabine (10 μm), on the other hand, had little effect on somatic αEPSP amplitudes at either −70 mV or −60 mV (Fig. 1B). It significantly reduced τ at −60 mV by 41.8 ± 3.8% (n= 9, P < 0.05) but not at −70 mV (Fig. 1B). Neither retigabine nor XE991 had any effect on dendritic αEPSPs (Fig. 1A and B), as would be expected for a significantly lower dendritic KV7 channel density (Yue & Yaari, 2006; Hu et al. 2007; Shah et al. 2008). Example traces showing the effects of (A) the KV7/M-channel blocker XE991 (3 μm) and (B) the KV7/M-channel enhancer retigabine (10 μm) on simulated EPSP (αEPSP) shapes at the soma and dendrites when evoked at a potential of −60 mV Black traces represent controls whereas the grey traces are those obtained following bath application of the KV7/M-channel modulator. Shown below the traces are the average (mean and SEM) somatic and dendritic αEPSP amplitudes in the absence and presence of (A) XE991 and (B) retigabine at potentials of −60 mV and −70 mV. The observations for each point are indicated in brackets next to the potential. Within each panel, the percentage change in the decay time constant (τ) of αEPSPs at the soma and dendrites at either −60 mV or −70 mV is illustrated in the graph on the far right. In these particular graphs, the numbers of observations are indicated above each bar. *Significance at P < 0.05. Since the KV7 modulators affected somatic αEPSP decay time constants at −60 mV, it is likely that they may also modulate αEPSP integration at that voltage. Indeed, at −60 mV XE991 and retigabine significantly enhanced and reduced, respectively, the summation of 20 Hz and 40 Hz trains of somatic 5 αEPSPs (Fig. 2A and B). Removal of TTX, in the presence of XE991, resulted in spikes during the somatic αEPSP train irrespective of the frequency, indicating that EPSP–spike coupling had increased (data not shown). Representative illustrations showing trains of 20 Hz or 40 Hz somatic and dendritic αEPSPs in the absence (black) and presence (grey) of either (A) 3 μm XE991 or (B) 10 μm retigabine at a potential of −60 mV The summation ratio was calculated as the amplitude of the fifth αEPSP divided by the amplitude of the first αEPSP (see Methods). Below each of the examples are graphs showing the mean and SEM of the summation ratio for the particular frequency at potentials of either −60 mV or −70 mV. The numbers of observations for each frequency at a particular potential are indicated in parentheses within each graph. *Significance at P < 0.05. Interestingly, retigabine, unlike XE991 (Fig. 2A), affected somatic αEPSP summation at −70 mV (Fig. 2B). The effects were less than that at −60 mV (Fig. 2B), consistent with the much reduced effect of the compound on the decay time constants of single αEPSPs (Fig. 1B). Retigabine shifts the activation curve of KV7/M-current to the left in neurons (Tatulian et al. 2001; Shah et al. 2008). Hence, in the presence of retigabine, channel opening occurs at lower voltages and so summation is likely to be more affected by retigabine at −70 mV than by XE991. Neither XE911 nor retigabine altered dendritic αEPSP summation (Fig. 2A and B), in agreement with the lack of effects of the compounds on single dendritic αEPSPs and the notion that fewer KV7 channels are located in dendrites (Yue & Yaari, 2006; Hu et al. 2007; Shah et al. 2008). To verify the interpretation of the above results, we performed computer simulations using a model that we had previously found best mimicked the changes in firing patterns of CA1 neurons following KV7 channel inhibition (see Shah et al. 2008). Na+ channels were not included in these simulations as in our experimental conditions Na+ channels had been inhibited by TTX. Compatible with the experimental results, KV7 channel deletion throughout the neuron enhanced 20 Hz (Fig. 3A) and 40 Hz EPSP summation at the soma at −60 mV. The increase in summation was less than at −70 mV (Fig. 3A), consistent with the biophysical properties of KV7 channels in hippocampal pyramidal cells (Shah et al. 2008). Dendritic EPSP summation, though, was not affected at either frequency at −60 mV or −70 mV (Fig. 3B for example traces at 20 Hz). These findings support the idea that KV7 channels are principally located at the soma/axon and affect peri-somatic post-synaptic EPSP integration. Twenty hertz trains of EPSPs obtained using computer simulations with (black) and without (red) KV7/M-channels at the soma (A) and dendrites (B) The simulations were obtained at −70 mV and −60 mV. C, computer simulations showing 20 Hz αEPSP traces under control (black) conditions and following the selective removal of either somatic or axonal KV7/M-channel density (grey). The simulations were performed at −60 mV. The scale bar shown applies to both traces. We next asked whether axonal or somatic KV7 channels differentially affect EPSP integration. In computer simulations, removal of axonal KV7 channels but leaving somatic channels intact, had little impact on EPSP summation at the soma (Fig. 3C). In contrast, elimination of somatic KV7 channels with axonal KV7 channels still present significantly enhanced summation (Fig. 3C). These results indicate that only somatic KV7 channels affect peri-somatic EPSP summation. To test if this is so experimentally, we used a competing peptide, ABP (YIAEGESDTD), that is designed to selectively disrupt the coupling of KV7 channels to ankyrin G, and thereby alter KV7 channel function in the axon (see Shah et al. 2008). Hence, unlike XE991 or retigabine, bath application of which would affect all channels within the neuron, this peptide only affects axonal KV7 channels. Indeed, we have previously shown that the peptide had little effect on somatic M-current measured with voltage clamp (Shah et al. 2008). Inclusion of this peptide (10 mm) in the intracellular pipette solution caused RMP depolarization from −68 ± 0.7 mV to −60.9 ± 1.4 mV (n= 8, P < 0.05) within 25 min (Fig. 4A). The action potential threshold was also lowered by 4.9 ± 1.3 mV (n= 7, P < 0.05, Fig. 4A) as described previously (Shah et al. 2008). As a consequence, the action potential firing rate increased substantially, with 5 out of 8 neurons firing spontaneously as reported previously (Shah et al. 2008). However, unlike XE991 (Hu et al. 2007; Shah et al. 2008), the somatic input resistance as measured using a 400 ms, 50 pA depolarizing step from a fixed potential of −70 mV was unaffected by ABP (% change =−2.9 ± 22.6%, n= 7). Inclusion of a scrambled ABP (TSEYDAEDIG, 10 mm) had little effect on resting membrane potential (Fig. 4B), action potential firing (Fig. 4B), action potential threshold (Fig. 4B) or input resistance (% change = 13.9 ± 21.8%, n= 3) over a period of 45–60 min. Effects of ABP and sABP on action potential firing and resting membrane potential Aa, Ba, Ab and Bb, examples of traces 5 min and 25 min after obtaining whole-cell patch clamp when ABP (A) or sABP (B) is included in the patch pipette solution. Ac and Bc, representative traces showing the influence of ABP and sABP on action potential threshold 5 min (black) and 25 min (grey) after breakthrough. The alterations in resting membrane potential, the number of action potentials and the action potential threshold when either ABP or sABP are present in the patch pipette are shown in Ad, Bd, Ae, Be, Af and Bf. In panels Af and Bf, the filled squares represent the mean and standard error whereas the open squares show the individual responses. We then tested the effects of ABP on single and trains of αEPSPs generated at the soma. In contrast to XE991 (Fig. 1A), in the presence of TTX, single αEPSPs were unaffected by ABP at −60 mV (% increase in amplitude and τ= 4.3 ± 12.0% (n= 4) and −6.5 ± 10.7% (n= 4), respectively). Thus, not surprisingly, trains of 20 Hz and 40 Hz αEPSPs were unaffected by 30 min ABP treatment at −60 mV (Fig. 5A). Removal of TTX resulted in action potentials being elicited in 60% (3/5) of neurons with 40 Hz αEPSP trains and in 50% (2/4) of neurons with 20 Hz αEPSP trains (Fig. 5A), presumably because ABP lowers the action potential threshold (Fig. 4A). Inclusion of scrambled ABP (sABP) in the pipette solution for 45 min had no effect on single (% increase in amplitude and τ= 9.2 ± 12.3% (n= 6, P= 0.7) and 9.0 ± 14.7% (n= 6, P= 0.4), respectively) or trains of αEPSPs (n= 6, Fig. 5). Further, washing out TTX did not result in spikes with αEPSP trains if sABP was included in the patch pipette. Hence, disruption of axonal or somatic KV7 channel function is likely to alter EPSP–spike coupling. However, only somatic KV7 channels affect EPSP integration at the soma. Axonal KV7 channels have little effect on somatic αEPSP summation A, example traces showing the effects of including the ankyrin G binding peptide (ABP, 10 mm) in the intracellular pipette solution on 20 Hz and 40 Hz trains of αEPSPs. The traces within 5 min of going whole cell are deemed control (see (Shah et al. 2008) and are in black. The maximal effect of ABP occurs within 25 min (Shah et al. 2008) and is shown in red. TTX was present throughout. Washout of TTX resulted in spikes (AP; green trace). Generation of spikes will cause an afterdepolarization and/or afterhyperpolarization, which will affect αEPSP summation. Indeed, in the particular example shown, the action potential resulted in an afterdepolarization followed by an afterhyperpolarization, thereby distorting the αEPSP summation. For this reason, αEPSP summation ratios were calculated from traces in the which TTX was present in the external solution. The average (mean and SEM; filled squares) and individual (open squares) calculated summation ratios following 5 min and 25 min of patching with pipettes containing ABP in the presence of external TTX are shown below the traces. B, representative traces showing the effects of scrambled ABP (sABP, 10 mm) on 20 Hz and 40 Hz trains of αEPSPs within 5 min of going whole cell (control, black) or after 25 min (red). All experiments were performed in the presence of TTX. The individual (open squares) and mean (filled squares) calculated summation ratios for all cells in which sABP was included in the pipette are shown below. Post-synaptic KV7/M-channels have been shown to modulate action potential firing in a number of different cell types (pyramidal neurons as well as interneurons; Brown & Passmore, 2009). Here, we show that post-synaptic KV7 channels also affect synaptic integration in a location-dependent manner in CA1 pyramids. Bath application of KV7 channel modulators affected somatic but not dendritic synaptic potential shapes (Fig. 1) and summation (Fig. 2) in a voltage-dependent manner, in agreement with the reported biophysical properties of the M-current in hippocampal CA1 pyramids (Shah et al. 2008). These results were reproducible by computer modelling (Fig. 3). Hence, KV7/M-channels are likely to be primarily located in the peri-somatic region (Yue & Yaari, 2006; Hu et al. 2007; Shah et al. 2008). In our experiments, most synaptic transmission was blocked. KV7/M-channels may be present on pre-synaptic terminals in the hippocampus (Martire et al. 2004; Peretz et al. 2007). Therefore, though post-synaptic KV7/M-channels do not affect dendritic synaptic potentials directly, modulation of synaptic release by pre-synaptic KV7/M-channels may additionally affect dendritic excitability and synaptic integration. KV7/M-channels are likely to be present predominantly in the axon initial segment (Devaux et al. 2004; Chung et al. 2006; Pan et al. 2006; Shah et al. 2008). However, our data suggested that only somatic channels altered somatic synaptic potential shapes and summation as bath application of XE991 and retigabine (which would affect all KV7 channels in a neuron) modified somatic EPSP summation (Fig. 2) whereas use of the competing peptide, ABP, had little effect (Fig. 5). In these neurons, ABP modulates only axonal KV7 channels as it lowered the action potential threshold without changing the input resistance (Fig. 4 and Results). In contrast, treatment with XE991, which would inhibit all KV7 channels, reduced the action potential threshold and increased the input resistance (see Shah et al. 2008). Further, we have previously shown that bath application of XE991 after ABP has had its full effect causes little further decrease in action potential threshold (Shah et al. 2008). These data thus suggest that ABP affects axonal KV7 channels only. In addition, the notion that somatic but not axonal KV7 channels affected summation was supported by data obtained using computer simulations (Fig. 3C). Since somatic KV7 channels influence somatic input resistance (Shah et al. 2008), and variations in input resistance lead to changes in synaptic potential shapes (Magee, 2000), this may explain why only KV7 channels located at the cell body modified synaptic integration. These results therefore suggest that the effects of KV7 channels on synaptic integration are locally mediated. Since recent evidence suggests synaptic potentials can propagate along axons (Clark & Hausser, 2006), we cannot exclude the possibility that axonal KV7 channels may influence shapes and summation of synaptic potentials within these structures. Indeed, recent evidence shows that KV7 channels located in immature synaptic terminals alter inhibitory depolarizing synaptic potential shapes and integration in the bouton, suggesting that KV7 channels exert a local effect on synaptic integration within a particular neuronal subcellular compartment (Huang & Trussell, 2011). By modulating spike threshold and the resting membrane potential of neurons (Fig. 4; Shah et al. 2008), axonal KV7 channels can affect global cell excitability too. Thus, though ABP did not affect somatic synaptic integration per se, EPSP–spike coupling was enhanced as the action potential threshold was reduced (Fig. 5). This also raises the possibility that the manner in which KV7 channels affect cell excitability may depend on the cellular compartment in which they are expressed. Since these channels are modulated by a variety of neurotransmitters and intracellular signalling molecules (Delmas & Brown, 2005), this may provide an exquisite mechanism by which KV7 channels can fine-tune a cell's intrinsic activity in response to changing neural network excitability and thereby influence physiological processes such as plasticity and learning as well as prevent neurological disorders such as epilepsy (Jentsch, 2000; Peters et al. 2005; Wu et al. 2008). M.M.S. and D.A.B. designed experiments. M.M.S. performed and analysed all experiments. M.M. performed computer simulations. M.M.S. and D.A.B. wrote the manuscript. All authors approved the final version. The work was supported by a Wellcome International Prize Travel Research Fellowship (M.M.S.) and a Wellcome Trust Project Grant (WT087363MA; M.M.S., D.A.B.)." @default.
• W1947607762 created "2016-06-24" @default.
• W1947607762 creator A5027714194 @default.
• W1947607762 creator A5084672179 @default.
• W1947607762 creator A5085113626 @default.
• W1947607762 date "2011-12-14" @default.
• W1947607762 modified "2023-10-16" @default.
• W1947607762 title "Differential effects of Kv7 (M‐) channels on synaptic integration in distinct subcellular compartments of rat hippocampal pyramidal neurons" @default.
• W1947607762 cites W1559348600 @default.
• W1947607762 cites W1736719008 @default.
• W1947607762 cites W1963878275 @default.
• W1947607762 cites W1964272828 @default.
• W1947607762 cites W1970747055 @default.
• W1947607762 cites W1973826704 @default.
• W1947607762 cites W1992455733 @default.
• W1947607762 cites W2009560301 @default.
• W1947607762 cites W2010185947 @default.
• W1947607762 cites W2031915049 @default.
• W1947607762 cites W2039804216 @default.
• W1947607762 cites W2043204092 @default.
• W1947607762 cites W2046728093 @default.
• W1947607762 cites W2055127006 @default.
• W1947607762 cites W2059668389 @default.
• W1947607762 cites W2064354742 @default.
• W1947607762 cites W2068805802 @default.
• W1947607762 cites W2071032731 @default.
• W1947607762 cites W2079373480 @default.
• W1947607762 cites W2083402348 @default.
• W1947607762 cites W2111710361 @default.
• W1947607762 cites W2112272723 @default.
• W1947607762 cites W2117120818 @default.
• W1947607762 cites W2127457810 @default.
• W1947607762 cites W2128325566 @default.
• W1947607762 cites W2140894987 @default.
• W1947607762 cites W2157152005 @default.
• W1947607762 cites W2165094762 @default.
• W1947607762 cites W2168858520 @default.
• W1947607762 doi "https://doi.org/10.1113/jphysiol.2011.220913" @default.
• W1947607762 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3245855" @default.
• W1947607762 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22041186" @default.
• W1947607762 hasPublicationYear "2011" @default.
• W1947607762 type Work @default.
• W1947607762 sameAs 1947607762 @default.
• W1947607762 citedByCount "49" @default.
• W1947607762 countsByYear W19476077622012 @default.
• W1947607762 countsByYear W19476077622013 @default.
• W1947607762 countsByYear W19476077622014 @default.
• W1947607762 countsByYear W19476077622015 @default.
• W1947607762 countsByYear W19476077622016 @default.
• W1947607762 countsByYear W19476077622017 @default.
• W1947607762 countsByYear W19476077622018 @default.
• W1947607762 countsByYear W19476077622019 @default.
• W1947607762 countsByYear W19476077622020 @default.
• W1947607762 countsByYear W19476077622021 @default.
• W1947607762 countsByYear W19476077622022 @default.
• W1947607762 countsByYear W19476077622023 @default.
• W1947607762 crossrefType "journal-article" @default.
• W1947607762 hasAuthorship W1947607762A5027714194 @default.
• W1947607762 hasAuthorship W1947607762A5084672179 @default.
• W1947607762 hasAuthorship W1947607762A5085113626 @default.
• W1947607762 hasBestOaLocation W19476077622 @default.
• W1947607762 hasConcept C121332964 @default.
• W1947607762 hasConcept C148762608 @default.
• W1947607762 hasConcept C169760540 @default.
• W1947607762 hasConcept C185592680 @default.
• W1947607762 hasConcept C2778437258 @default.
• W1947607762 hasConcept C2781161787 @default.
• W1947607762 hasConcept C86803240 @default.
• W1947607762 hasConcept C93226319 @default.
• W1947607762 hasConcept C97355855 @default.
• W1947607762 hasConceptScore W1947607762C121332964 @default.
• W1947607762 hasConceptScore W1947607762C148762608 @default.
• W1947607762 hasConceptScore W1947607762C169760540 @default.
• W1947607762 hasConceptScore W1947607762C185592680 @default.
• W1947607762 hasConceptScore W1947607762C2778437258 @default.
• W1947607762 hasConceptScore W1947607762C2781161787 @default.
• W1947607762 hasConceptScore W1947607762C86803240 @default.
• W1947607762 hasConceptScore W1947607762C93226319 @default.
• W1947607762 hasConceptScore W1947607762C97355855 @default.
• W1947607762 hasIssue "24" @default.
• W1947607762 hasLocation W19476077621 @default.
• W1947607762 hasLocation W19476077622 @default.
• W1947607762 hasLocation W19476077623 @default.
• W1947607762 hasLocation W19476077624 @default.
• W1947607762 hasOpenAccess W1947607762 @default.
• W1947607762 hasPrimaryLocation W19476077621 @default.
• W1947607762 hasRelatedWork W1501306774 @default.
• W1947607762 hasRelatedWork W2010108080 @default.
• W1947607762 hasRelatedWork W2101607104 @default.
• W1947607762 hasRelatedWork W2138730144 @default.
• W1947607762 hasRelatedWork W2147243983 @default.
• W1947607762 hasRelatedWork W2783633930 @default.
• W1947607762 hasRelatedWork W2796344372 @default.
• W1947607762 hasRelatedWork W2980640576 @default.
• W1947607762 hasRelatedWork W3033872672 @default.
• W1947607762 hasRelatedWork W4317939744 @default.
• W1947607762 hasVolume "589" @default.
• W1947607762 isParatext "false" @default.

• next