Gain-of-function mutations in the human SCN11A-encoded voltage-gated Na+ channel NaV1.9 cause severe pain disorders ranging from neuropathic pain to congenital pain insensitivity. However, the entire spectrum of the NaV1.9 diseases has yet to be defined. Applying whole-exome sequencing we here identify a missense change (p.V1184A) in NaV1.9, which leads to cold-aggravated peripheral pain in humans. Electrophysiological analysis reveals that p.V1184A shifts the voltage dependence of channel opening to hyperpolarized potentials thereby conferring gain-of-function characteristics to NaV1.9. Mutated channels diminish the resting membrane potential of mouse primary sensory neurons and cause cold-resistant hyperexcitability of nociceptors, suggesting a mechanistic basis for the temperature dependence of the pain phenotype. On the basis of direct comparison of the mutations linked to either cold-aggravated pain or pain insensitivity, we propose a model in which the physiological consequence of a mutation, that is, augmented versus absent pain, is critically dependent on the type of NaV1.9 hyperactivity.
Voltage-gated Na+ (NaV) channels of peripheral afferents are essential for pain perception because they initiate action potentials in nociceptive nerve fibres. The family of mammalian NaV channels consists of nine members (NaV1.1–1.9) of which NaV1.7, NaV1.8 and NaV1.9 are the most abundant isoforms in nociceptive neurons1 of dorsal root ganglia (DRG). While NaV1.7- and NaV1.8-mediated currents are the main contributors to the fast action potential upstroke in nociceptors, NaV1.9 channels modulate the threshold of nociceptor excitability by influencing the resting membrane potential (RMP)2,3,4.
Several monogenic human pain disorders are linked to altered NaV channel function5. For example, biallelic loss-of-function mutations in SCN9A, encoding NaV1.7, result in inability to experience pain by impairing the electrical signalling of nociceptors6,7. In contrast, gain-of-function mutations in SCN9A result in hyperexcitability of nociceptors and cause debilitating pain disorders such as primary erythromelalgia and paroxysmal extreme pain disorder8,9. Notably, environmental warmth aggravates pain in primary erythromelalgia patients while cooling of affected extremities relieves pain, suggesting a marked temperature dependence of the phenotype10,11. More recently, NaV1.7 variants with increased activity have been associated with paroxysmal itch12 and painful degeneration of sensory nerve terminals (small-fiber neuropathy)13. Painful neuropathies have also been linked to gain-of-function variants of NaV1.8, encoded by SCN10A (ref. 14).
The role of NaV1.9 in human pain perception is less clear and has only recently begun to be elucidated. The first pathogenic mutation identified in human SCN11A, the gene encoding NaV1.9, was the heterozygous de novo mutation p.L811P, which confers gain-of-function properties to NaV1.9 and causes congenital insensitivity to pain15,16. Further studies have linked gain-of-function mutations in NaV1.9 to familial episodic pain and painful neuropathy17,18,19. At present it is not clear how the gain-of-function of NaV1.9 channels can result in such opposing pain phenotypes.
We here describe a NaV1.9 mutation (p.V1184A) that causes early onset cold-aggravated familial episodic pain. Electrophysiological evaluation reveals that the mutation enhances the activity of NaV1.9 by left shifting the voltage dependence of channel opening, thereby giving rise to hyperexcitability of nociceptors. In line with the temperature sensitivity of the patients’ phenotype, p.V1184A-dependent nociceptor excitability is less attenuated by cold than the excitability of wild-type neurons, suggesting a temperature-dependent contribution of the novel NaV1.9 variant to nociceptor function.
Clinical description and whole-exome sequencing
We studied a three-generation family of mixed European ancestry with severe episodic pain of unclear aetiology (Fig. 1a and Table 1). Onset of chronic pain in the 6-year-old female proband III.4 was within the first year of life. Pain comes on quickly and lasts for about 20–30 min. Reported triggers of pain are gluten and notably low ambient temperature. Pain usually starts in the joints and radiates to the arms and legs. Occasionally, it is accompanied by flushing of the neck and face. The lower extremities are primarily affected but her upper extremities can also be symptomatic. Pain episodes most commonly occur in the late afternoon or early evening. Her symptoms have responded to ibuprofen, colchicine and naproxen. Her motor milestones and intellectual development are typical. Her father (II.3), paternal aunt (II.1), paternal aunt’s daughter (III.2) and paternal grandmother (I.1) had similar symptoms suggesting an autosomal-dominant disorder underlying the pain phenotype. The patient’s father’s pain episodes were first noticed at ∼18 months of age and were associated with flushing of his neck and chest when he was younger. His pain originates in his joints, radiates distally and primarily affects his lower extremities. Less often the upper extremities may be involved. The sensation is described as feeling ‘on fire’. The duration of episodes is between 20 and 30 min during which fine motor ability may be impaired and ambulation is uncomfortable. The frequency of pain episodes is typically two to three times per month when controlled with ibuprofen and a gluten-free diet. Episodes may occur any hour but most often begin at night and may also be provoked by stressors such as exhaustion and illness. The proband’s father also reports frequent constipation since the age of 18. The proband’s grandmother’s symptoms reportedly began in early infancy and similarly occur in the lower extremities and on occasion the upper extremities. Her pain also begins in the joints and radiates outward. Affected joints are limited to the wrists, elbows, knees and ankles. She reports taking ibuprofen prophylactically and avoiding gluten as a means to reduce the number of episodes to a frequency of two to three times per month. In the absence of medication, the episodes last ∼3 h consisting of alternating cycles of pain and no pain in intervals of 20 min. The pain impairs her fine motor manipulation, makes ambulation uncomfortable and can be partially alleviated by positional changes. She has had gastrointestinal symptoms including episodic constipation and diarrhoea since the age of 18. The proband’s paternal aunt and paternal first cousin also experience similar pain episodes but of lesser severity. Similar to other family members, the pain originates in their joints and radiates distally. Non-steroidal anti-inflammatories have reduced the frequency of pain episodes. The aunt uses ibuprofen and the cousin uses ibuprofen and naproxen. The aunt’s pain is somewhat eased by warmth but this is not the case for other affected family members. Of note, cold ambient temperatures can trigger episodes in the aunt. There have been no appreciable developmental or neurologic deficits.
Quantitative evaluation of skin biopsies stained for PGP9.5 revealed a prominent decrease of the intra-epidermal nerve fiber density in the skin biopsies of the father (II.3; Fig. 1d), of the paternal aunt (II.1) and of the grandmother (I.1), compared with published reference values20, indicating a small-fiber neuropathy (6.0, 7.4 and 8.8 nerve fibres/mm, respectively, compared with the reference value of 17.07±6.51 nerve fibres/mm (ref. 20)). Electron microscopy of dermal nerve fascicles demonstrated stacking of Schwann cell processes indicative for a loss of unmyelinated axons (Fig. 1e) and signs of altered endoplasmic reticulum and lysosomal function as well as autophagy in axons and Schwann cells (Fig. 1f–i). Whole-exome sequencing was performed in the index case and her affected cousin and the data were filtered for shared rare variants that were absent from dbSNP, 1000-Genomes project, the Exome Variant Server, or had a low prevalence in the ExAC browser. No causal mutation was identified in known genes involved in episodic pain syndromes (SCN9A, SCN10A and TRPA1). Of the rare heterozygous genetic variants shared by both individuals, a missense change in SCN11A, c.3551T>C, p.V1184A (chr3:38913144A>G, hg19), was the most likely candidate to cause the disorder. The variant was confirmed by Sanger sequencing (Fig. 1b), and segregation with the pain phenotype was verified by genotyping of available family members (Fig. 1a). The variant affects a highly conserved amino-acid residue in the S5 segment in domain III of NaV1.9 (Fig. 1c).
Assessment of p.V1184A in voltage-clamp experiments
To analyse the consequences of mutation p.V1184A for the function of NaV1.9, we performed whole-cell voltage-clamp experiments in ND7/23 cells heterologously expressing either human wild-type NaV1.9 or NaV1.9-V1184A mutant channels. All recordings were carried out at 30 °C, which is close to peripheral skin temperature21,22. To assess the temperature sensitivity of channel function, data were furthermore collected at 20 °C, a temperature selected to simulate cooling that triggers painful episodes in the proband and her aunt.
Both, wild-type and mutant channels gave rise to currents with slow activation and inactivation kinetics typical for NaV1.9 (Fig. 2a). Compared with the wild type, NaV1.9-V1184A channels yielded larger current densities particularly at low voltages, being significant between −97 and −57 mV (P<0.05, two-tailed t-test) at both temperatures tested (Fig. 2b,c). Mean current densities of wild-type and mutant channels showed no significant temperature dependence in the entire voltage range analysed (P>0.05 in all cases, two-tailed t-test). However, at both temperatures the larger current densities of cells expressing mutant p.V1184A were accompanied by three major effects: mutated channels displayed (i) a strongly left-shifted voltage dependence of channel activation, effectively increasing Na+ influx at resting membrane voltages (Fig. 2b,c), (ii) accelerated channel opening kinetics (Fig. 2e,f) and (iii) slowed channel closing kinetics (Fig. 2d). Analysis of the voltage dependence of peak current amplitudes (Fig. 2b,c) and the voltage dependence of channel opening and closure kinetics (Fig. 2e,f) according to a one-step gating scheme (equations (1) and (5)) revealed that the mutation shifted the half-maximal voltage for channel activation (Vm) from −52.0±2.6 to −69.5±2.9 mV at 30 °C (P<0.001, two-tailed t-test) and from −47.5±2.5 to −67.0±2.7 mV at 20 °C (P<0.001, two-tailed t-test). The associated slope factors (km), which reflect the voltage dependence of channel activation, were not affected by the mutation (9.1±0.7 and 10.1±0.8 mV for NaV1.9 at 30 and 20 °C; 9.8±1.0 and 9.8±0.7 mV for p.V1184A at 30 and 20 °C, respectively; both P>0.05, two-tailed t-test). The voltage dependence of opening and closing kinetics were compatible with a gating charge transfer of 2.8±0.5 e0 and 2.6±0.3 e0 and associated symmetry factors specifying the charge fraction assigned to channel opening of 0.53±0.08 and 0.47±0.02 at 30 and 20 °C, respectively. The Q10 temperature coefficients of the channel’s opening kinetics, τa (1.50±0.11 for NaV1.9 between −57 and −17 mV; 1.45±0.06 for p.V1184A between −67 and −27 mV), and the closing kinetics, τd (1.49±0.07 for NaV1.9 between −117 and −77 mV; 1.31±0.04 for p.V1184A between −117 and −87 mV), were not markedly affected by the mutation (P>0.05, two-tailed t-test), suggesting that temperature changes affect opening and closing of wild-type and mutant channels in a similar manner.
At either temperature, mutation p.V1184A did not affect the kinetics of fast channel inactivation (Figs 2a,b and 3a,b). Likewise, the Q10 values of the fast inactivation time constant, τfast, were also not significantly different between wild-type and mutant channels (1.62±0.06 for NaV1.9 between −57 and −17 mV; 1.81±0.25 for p.V1184A between −67 and −27 mV). The half-maximal voltage of channel inactivation, Vh, measured after 500 ms conditioning episodes at various voltages, was only marginally shifted in the mutant from −69.1±3.9 to −64.8±3.3 mV at 30 °C and from −71.5±3.5 to −65.6±1.2 mV at 20 °C, without reaching the level of significance (both P>0.05, two-tailed t-test). The associated slope factors (kh) of wild-type (−10.0±1.1 mV) and mutant channels (−11.2±0.8 mV) characterizing the voltage dependence of channel inactivation were not significantly different at 20 °C; however, at 30 °C the mutation decreased kh from −9.3±1.2 to −12.8±1.0 mV (P<0.05, two-tailed t-test), thus effectively increasing the availability of mutated channels (Fig. 3c,d).
In summary, the mutation p.V1184A confers gain-of-function properties to NaV1.9 by enhancing channel opening at RMPs and increasing channel availability at both temperatures analysed.
Influence of p.V1184A on DRG neuron excitability
NaV1.9 channels are expressed at high levels in nociceptors and are proposed to influence excitability of these neurons by modulating their RMP3. To analyse the impact of mutation p.V1184A on the excitability of primary nociceptive neurons, we performed current-clamp recordings on small (<25 μm in diameter) isolated DRG neurons from wild-type mice transfected with constructs encoding either human wild-type or NaV1.9-V1184A mutant channels. To assess the temperature sensitivity of DRG neuron excitability, data were collected at 30 °C (Fig. 4a) and 20 °C (Fig. 4b).
When overexpressed in DRG neurons, p.V1184A mutant channels depolarized the cell membrane at rest (RMP) by 5.8 mV (P<0.05, two-tailed t-test) and 5.2 mV (P<0.05, two-tailed t-test) at 30 and 20 °C, respectively, when compared with cells overexpressing NaV1.9 wild type (Fig. 4c). In addition, mutant channels increased the action potential after-hyperpolarization voltage (Vmin) at 30 °C by 4.4 mV (P<0.05, two-tailed t-test) while they did not influence the after-hyperpolarization voltage at 20 °C. Other parameters characterizing the shapes of single evoked action potentials, that is, the voltage threshold for action potential firing (Vth), the action potential peak voltage (Vmax), the action potential duration (Width), as well as the time constant describing the relaxation of the action potential after-hyperpolarization back to the resting level (τAHP) were—at both temperatures—not significantly different between cells expressing NaV1.9 or NaV1.9-V1184A (Fig. 4c; P>0.05, two-tailed t-test). However, lowering the temperature from 30 to 20 °C increased the duration of action potentials by factors of 1.92±0.32 (P<0.001, two-tailed t-test) and 1.52±0.36 (P<0.001, two-tailed t-test) when cells were transfected with NaV1.9 and NaV1.9-V1184A, respectively. Temperature-dependent changes were furthermore observed for the relaxation time constant τAHP, although statistically significant only for neurons expressing NaV1.9-V1184A (P<0.05, two-tailed t-test).
Firing rates of neurons were determined by evoking repetitive action potentials with escalating current injections for periods of two seconds. Representative trains of action potentials recorded from neurons transfected with either human NaV1.9 or NaV1.9-V1184A at 30 and 20 °C are shown in Fig. 5a,c, respectively. Systematic assessment of action potential firing as a function of injected current revealed that neurons transfected with NaV1.9-V1184A fired—at either temperature—more action potentials than neurons transfected with wild-type NaV1.9, demonstrating pro-excitatory properties of NaV1.9-V1184A channels (Fig. 5b,d). Interestingly, cooling from 30 to 20 °C reduced the firing frequency of neurons expressing wild-type NaV1.9 by a factor of 3.2±0.1 in contrast to a factor of 1.6±0.1 (P<0.001, two-tailed t-test) for mutant p.V1184A (Fig. 5b,d). Thus, attenuation of DRG neuron excitability by low temperature is diminished in the presence of NaV1.9-V1184A, which is in line with the temperature dependence of the clinical symptoms.
Comparison of mutation p.V1184A with p.L811P
The phenotypes associated with mutation p.V1184A in NaV1.9 as well as those with mutations in NaV1.9 causing neuropathic pain conditions17,18,19 are in marked contrast to that of the NaV1.9 gain-of-function mutation p.L811P, which results in pain insensitivity15,16. The basis of this fundamental difference in the clinical outcome remained elusive. Therefore, we analysed the impact of p.L811P on excitability of DRG neurons under identical experimental conditions as used for p.V1184A. As illustrated in Supplementary Fig. 1, the RMP of neurons expressing p.L811P was increased by 5.9±1.4 mV (P<0.01, two-tailed t-test) at 30 °C and by 5.3±1.0 mV (P<0.01, two-tailed t-test) at 20 °C compared with neurons expressing wild-type NaV1.9. Parameters characterizing the shape of single evoked action potentials were only marginally affected by p.L811P (Supplementary Fig. 1c). Analysis of repetitive firing, evoked with current injections for 2 s, revealed that p.L811P rendered neurons hyperexcitable at both temperatures tested. Thus, this experimental protocol did not reveal overt differences between excitability of neurons transfected with p.L811P or p.V1184A. However, longer trains of action potentials revealed clearly distinguishable firing patterns between neurons expressing p.L811P or p.V1184A (Fig. 6). As illustrated in Fig. 6a,b, 76% of repetitively firing neurons transfected with wild-type NaV1.9 and 81% of repetitively firing neurons expressing p.V1184A maintained stable action potential amplitudes; that is, Vmax diminished by <10 mV throughout the 30-s stimulus of 40 pA current injection, while the same criterion was fulfilled for only 35% of neurons expressing p.L811P (P<0.01, Z-test). Thus, p.L811P channels increase the probability of cumulative loss of action potential integrity in DRG neurons during extended firing periods.
Our study identified a heterozygous missense mutation (p.V1184A) in NaV1.9 as a cause for early onset cold-aggravated episodic peripheral pain. The mutation segregated with the disease phenotype in the affected family and showed slightly variable expressivity. Anti-inflammatory medication reduced the frequency of painful events, which was highest in childhood and gradually decreased with age. Similar age-dependent reduction of painful events as well as beneficial effects of anti-inflammatory drugs were reported for patients from two pedigrees suffering from NaV1.9-associated episodic peripheral pain19. The pain-alleviating effects of the anti-inflammatory therapy correlate with an observed upregulation of NaV1.9 under inflammatory conditions2,23,24 and emphasize a role of NaV1.9 in mediating inflammatory pain.
We demonstrated that mutation p.V1184A confers gain-of-function attributes to NaV1.9 channels primarily by a hyperpolarizing shift in the voltage dependence of channel activation and a smaller voltage dependence of steady-state fast inactivation. The resulting increase in overlap of activation and inactivation of mutated channels predicts a larger steady-state window current25, which is expected to depolarize nociceptors resulting in hyperexcitability2,3,24 (Fig. 7b). On the basis of the models of KV and NaV channel structures26,27,28,29, mutation p.V1184A is located within a conserved sequence at the intracellular end of transmembrane segment 5 in domain III of NaV1.9 (Fig. 1c), a region highly relevant for transferring voltage-sensor movements to the channel pore30. Mutations in this region are expected to interfere with voltage-dependent channel gating.
Furthermore, NaV1.9-V1184A channels diminished the RMP in isolated small-diameter DRG neurons by >5 mV and increased the firing rate of nociceptive neurons in response to standardized current injections. This observation is consistent with previous studies showing similar pro-excitatory properties of gain-of-function variants of NaV1.9 linked to familial episodic pain19 and painful neuropathy17,18. Because low ambient temperature can trigger painful episodes in carriers of the p.V1184A mutation, we analysed the effect of temperature changes on the electrical properties of DRG neurons. Interestingly, cooling from 30 to 20 °C attenuated the excitability of neurons expressing NaV1.9-V1184A much less compared with neurons expressing wild-type NaV1.9, demonstrating that the relative impact of NaV1.9-V1184A on nociceptor excitability is larger at low temperature. We further showed that the mutation p.V1184A did not affect the Q10 values of the gating processes of NaV1.9, indicating that a cool environment does not per se augment the activity of NaV1.9-V1184A relative to the wild type.
The cold-aggravated pain symptoms in humans as well as the reduced attenuation of excitability of nociceptors expressing NaV1.9-V1184A are in line with a previous report showing that NaV1.9 is a key determinant of rodent cold-pain sensation31. Using NaV1.9-deficient animals, Lolignier et al.31 demonstrated that NaV1.9 channels are functionally upregulated specifically in cold-sensitive nociceptors and are required for normal cold-pain sensation. The authors proposed a model in which NaV1.9 in nociceptors serves as amplifier of signals generated by an as yet unknown cold transducer. This hypothesis is appealing because NaV1.9 is expressed not only in the cell bodies of nociceptors32,33 but also in the corresponding nerve terminals in the skin34, which express temperature-sensitive transducer proteins and are exposed to large variations in environmental temperatures. Accordingly, NaV1.9-V1184A channels may confer hypersensitivity to cold-responsive nociceptors because of overamplification of cold transducers. Such a scenario would be in line with our data showing that p.V1184A does not affect the intrinsic temperature dependence of NaV1.9.
The clinical symptoms caused by mutation p.V1184A in NaV1.9 are reminiscent of primary erythromelalgia, which is attributed to gain-of-function mutations of NaV1.7 channels35. Both conditions are characterized by episodic pain attacks in the lower and upper body extremities but seem to differ with respect to the temperature sensitivity of pain sensation. Specifically, p.V1184A-related pain is mostly aggravated by cooling and partly relieved by warming while primary erythromelalgia-associated pain is augmented by warming and relieved by cooling5. This is best illustrated by comparing the NaV1.9-V1184A-related disease with a primary erythromelalgia phenotype caused by the homologous mutation p.V1316A in NaV1.7 (ref. 10): p.V1316A in NaV1.7 causes warmth-aggravated severe burning pain in the body extremities, erythema in the affected body regions, and pain relief on cooling. A hallmark of NaV1.7 mutations linked to primary erythromelalgia—including p.V1316A—is a hyperpolarizing shift in the voltage dependence of channel activation with only minor impairment of channel inactivation5. As demonstrated here, the homologous mutation p.V1184A alters the properties of NaV1.9 channels in a very similar manner but instead results in a cooling-aggravated and thus a clinically distinguishable phenotype. Compatible with our report on the NaV1.9-V1184A-induced clinical symptoms, Huang et al.18 have reported low ambient temperature as a trigger of pain episodes in a patient suffering from a similar episodic peripheral pain phenotype caused by mutation p.I381T in NaV1.9. Likewise, Zhang et al.19 reported pain amelioration on warming of affected body areas in patients carrying NaV1.9 mutation p.R225C or p.A808G. Notably, Han et al.36 described mutation p.G699R, located in the S4/S5 linker in domain II of NaV1.9, which causes painful peripheral neuropathy with a temperature dependence reminiscent of erythromelalgia; that is, in this case, pain episodes are aggravated by warmth and relieved by cooling.
The gain-of-function mutations in NaV1.9 reported previously17,18,19, as well as this report on mutation p.V1184A are in marked contrast to the NaV1.9 gain-of-function mutation p.L811P that results in pain insensitivity15,16. The basis of this fundamental difference in the clinical outcome remained elusive. To infer potential differences between p.V1184A and p.L811P we assessed the functions of both mutations under identical experimental conditions (Figs 6 and 7). Both mutations affect amino acids on the intracellular face of the channel pore in domains II and III (Fig. 1c)—regions well-known to be involved in the gating of NaV channels37. A comparison of current responses revealed substantial differences with respect to fast channel inactivation (Fig. 7a,c), a process largely mediated by the interaction of a hydrophobic IFM (Isoleucine–Phenylalanine–Methionine) motif in the loop connecting channel domains III and IV with the intracellular face of the pore (Fig. 1c). Interestingly, fast inactivation kinetics of NaV1.9-V1184A channels are almost indistinguishable from inactivation of the wild type, whereas mutation p.L811P causes profound slowing of channel inactivation, thus augmenting Na+ influx through NaV1.9 (ref. 15). In addition, both mutations marginally affect the voltage dependence of channel inactivation. However, p.L811P shifts the voltage dependence of opening of NaV1.9 by −29 mV, whereas mutation p.V1184A shifts the same parameter by only −20 mV, clearly demonstrating that mutation p.L811P facilitates opening of NaV1.9 more strongly than mutation p.V1184A (Fig. 7b). As a result, the window current generated by the overlap of activation and inactivation—here used as an operational indicator of channel activity—is largest for mutation p.L811P followed by p.V1184A and wild-type NaV1.9 (Fig. 7b). These data demonstrate that both mutations confer quantitatively and qualitatively different gain-of-function properties to NaV1.9.
Consistent with the gain-of-function on the channel level, both NaV1.9-V1184A and NaV1.9-L811P increased the action potential firing frequency of DRG neurons on stimulation with short current injections for 2 s (Fig. 5 and Supplementary Fig. 1d–g). Thus, neurons expressing either p.V1184A or p.L811P must be considered hyperexcitable under these experimental conditions. Intriguingly, analysis of extended periods of repetitive firing revealed that, in contrast to p.V1184A, mutation p.L811P leads to a substantial instability of DRG neuron excitability; that is, the probability of progressive loss of action potential amplitude is increased in a substantial portion of neurons expressing p.L811P mutant channels (Fig. 6). This instability may be caused by increased influx of Na+ through p.L811P as it is predicted by the larger window current (Fig. 7b) and the slower inactivation kinetics of p.L811P compared with p.V1184A or wild-type NaV1.9 (Fig. 7a). Excessive Na+ influx during longer periods of action potential firing may therefore lead to a conduction block in the transfected neurons. However, chronic NaV1.9 dysfunction in patients will additionally result in secondary effects, including altered gene expression and changes in the synaptic plasticity. In summary, the missense change p.V1184A, which causes cold-aggravated peripheral pain in humans, leads to higher open probability of mutated NaV1.9 channels and to hyperexcitability of DRG neurons; this hyperexcitability is less attenuated at low ambient temperature compared with wild-type neurons. The degree and quality of functional change on the level of the ion channel, however, differs from the gain-of-function mutation p.L811P; the latter only transiently results in DRG neuron hyperexcitability and ultimately leads to loss-of-function and pain insensitivity. Correlations between a clinical pain phenotype and NaV1.9 channel function thus require a very detailed analysis of the channel’s gating parameters where the exact relationship of voltage-dependent channel activation and inactivation appears to be decisive for the overall outcome.
The study was approved by the local research ethics committee or institutional review board of the participating institutions. Informed consent was obtained from all participating family members.
For whole-exome sequencing, 1 μg of DNA from two family members with episodic pain was fragmented using sonication technology (Covaris, Woburn, MA, USA). The fragments were end-repaired and adaptor-ligated including incorporation of sample index barcodes. After size selection, the libraries were subjected to an enrichment process (NimbleGen SeqCap EZ Human Exome Library v2.0, Roche NimbleGen). Samples were sequenced on an Illumina HiSeq 2000 sequencing instrument. This resulted in 6.6 (individual 1) and 6.4 (individual 2) Gb of mapped sequences with a mean coverage of 77/78 and a 30 × coverage of 78/84% and a 10 × coverage of 95.8/96.4% of target sequences. For data analysis, the Varbank pipeline v.2.3 and interface was used (https://anubis.ccg.uni-koeln.de/varbank/). Primary data were filtered according to signal purity with the illumina real-time analysis software v1.8. Subsequently, the reads were mapped to the human genome reference build hg19 using the Burrows-Wheeler alignment algorithm. GATK v.1.6 was used to mark duplicated reads, to perform a local realignment around short insertion and deletions, to recalibrate the base quality scores, and to call single nucleotide polymorphisms and short indels. Subsequent Sanger sequencing of SCN11A exons was performed using standard procedures. Primer sequences are available on request.
Punch biopsies (3 mm) were taken from the volar forearm. The biopsies were fixed with Zamboni solution for immunohistochemistry and with 3.9% buffered glutaraldehyde for electron microscopy. For immunohistochemistry 40 μm cryostat sections were prepared and stained with anti-PGP9.5 primary antibody at 1:100 dilution (DCS-Diagnostics, catalogue number PI647C01), and Alexa Fluor 488-labelled goat anti-rabbit secondary antibody at 1:2,000 dilution (Thermo-Fischer, catalogue number A-11008)38. Intra-epidermal nerve fiber density was quantified following the second set of counting rules39, counting both fibres crossing the epidermal basement membrane and isolated nerve fragments in the epidermis that did not cross the basement membrane38. These counting rules were followed because they had been used by the group that had established the reference values for distal forearm skin innervation20. The glutaraldehyde-fixed tissues were post-fixed with 1% OsO4 in 0.1 M cacodylate buffer and embedded in epoxy resin. Ultrathin sections, after contrast enhancement with uranyl acetate and lead citrate, were examined under a Philips EM 400 T electron microscope. Images were taken with an Olympus Veleta camera system.
cDNA constructs for human NaV1.9 and mutants
Human NaV1.9 cDNA (NM_014139.2) in pcDNA3.1 was used as template15. The c.3551T>C (p.Val1184Ala) mutation was introduced by PCR-based mutagenesis and replaced a cDNA fragment flanked by BlpI on both sites. Correct orientation of the BlpI-fragment was confirmed, and the coding sequence of SCN11A was verified by Sanger sequencing.
Isolation and transfection of mouse DRGs
Animal care and experimental procedures followed the guidelines established by the animal welfare committee of the University of Jena. For action potential recordings, DRG from all levels of the spinal cord of 6–11-weeks-old wild-type C57BL6 mice were extracted and processed as described40. Isolated DRG neurons were transfected by electroporation using a 4D-Nucleofector (Lonza, Basel, Switzerland) with the P3 Primary Cell 4D-Nucleofector X Kit S (V4XP-3032). Briefly, DRG neurons from each animal were split in two equal lots to enable experiments with wild-type and mutant NaV1.9 channels using the same batch of cells. After centrifugation (100 g for 3 min) both cell pellets were resuspended individually in 20 μl of P3 primary cell solution containing supplement 1 and 0.3 μg of a plasmid encoding the enhanced green fluorescent protein. Subsequently, one lot was supplemented with 1.2 μg of a NaV1.9-encoding plasmid, while the second lot was supplemented with 1.2 μg of a vector encoding mutant NaV1.9 variants. Transfection was performed using the electroporation protocol CA137 of the 4D-Neucleofector. After electroporation, 150 μl of low calcium Roswell Park Memorial Institute (Invitrogen) 1640 medium was added to each cell suspension and cells were allowed to recover for 10 min in a 10% CO2 incubator at 37 °C. The cell suspensions were then diluted in 300 μl DRG medium and immediately seeded on poly-D-lysin/laminin-coated glass coverslips, which were placed in the slots of a 24-well plate containing 1 ml of DRG medium per well. DRG medium contained 89.5% DMEM/F12 (Dulbecco’s Modified Eagles Medium with Ham’s F12; Invitrogen) supplemented with 9.5% fetal calf serum and 1% penicillin/streptomycin (Invitrogen). Transfected cells were incubated in a 10% CO2 incubator at 37 °C and used for electrophysiological experiments 15–24 h after transfection. Current-clamp recordings were restricted to successfully transfected small-diameter (<25 μm) DRG neurons, which were identified visually by their green florescence using a 50 W HBO lamp as light source and a green fluorescent protein filter set.
Cell culture and transfection
ND7/23 cells—a hybrid of mouse neuroblastoma and rat DRG neurons—, were maintained in 90% DMEM supplemented with 10% fetal calf serum in a 10% CO2 incubator at 37 °C. Cells were trypsinized, diluted with culture medium, and grown in 35 mm dishes. When grown to 30–50% confluence, cells were transfected with a 5:1 ratio of a DNA plasmid encoding either NaV1.9 or NaV1.9 mutants and a vector encoding the CD8 antigen using the Rotifect transfection kit (Carl Roth, Karlsruhe, Germany) as described earlier15. Transfected cells were maintained in a 10% CO2 incubator at 28 °C for up to 12 h. Voltage-clamp recordings were performed after an additional 1 h recovery period at 37 °C. Anti-CD8-coated Dynabeads (Deutsche Dynal GmbH, Hamburg, Germany) were used for visual identification of individual transfected cells.
Current and voltage recordings were obtained in the whole-cell configuration of the patch-clamp method using an EPC-10 patch-clamp amplifier operated by PatchMaster software (HEKA Elektronik, Lambrecht, Germany). Patch pipettes were fabricated from Kimax borosilicate glass of about 1.0–2.5 MΩ resistance and coated with room temperature vulcanization silicone adhesive (Dow Corning GmbH, Wiesbaden Germany) to reduce tip capacitance. Series resistance was corrected electronically up to 85% and all voltages were corrected for the liquid junction potential. Bath solution for current-clamp recordings contained (in mM) 120 NaCl, 3 KCl, 2.5 CaCl2, 1 MgCl2, 30 HEPES, 15 glucose (pH 7.4 with NaOH), and the pipette 125 KCl, 8 NaCl, 1 CaCl2, 1 MgCl2, 0.4 Na2-GTP, 4 Mg-ATP, 10 EGTA, 10 HEPES (pH 7.3 with KOH). Bath solution for voltage-clamp recordings contained (in mM) 150 NaCl, 2 KCl, 1.5 CaCl2, 1 MgCl2, 10 HEPES (pH 7.4 with NaOH) and was supplemented with 0.0003 tetrodotoxin to block endogenous Na+ currents in ND7/23 cells; the pipette contained (in mM) 35 NaCl, 105 CsF, 10 EGTA, 10 HEPES (pH 7.3 with CsOH). Temperature was controlled by continuous perfusion of cells with tempered bath solution using a SHM-8 in-line solution heater feedback-controlled by a TC-324B temperature controller (both Warner Instruments, Hamden, USA).
Current-clamp recordings. The resting membrane voltage was measured by zero current injection directly after establishing the whole-cell configuration. Single action potentials were evoked at 30 or 20 °C by injecting a current of 100–200 pA for a period of 5 or 10 ms, respectively, followed by a 200-ms pulse without current injection. Sampling interval for voltage measurements was 50 μs. The voltage threshold of action potential firing, Vth, was defined as voltage at which dV/dt reached the level of 0.03 × (dV/dtmax−dV/dtmin)+dV/dtmin. Trains of action potentials were evoked repetitively by 2 s current injections increasing in steps of 20 pA.
Voltage-clamp recordings. In voltage-clamp experiments with ND7/23 cells the holding potential was set to –137 mV. Data were low-pass filtered at 5 kHz and digitized with a sampling interval of 40 μs. Leak and capacitive currents were measured at –117 and –127 mV and subtracted manually.
Channel activation. To measure channel activation, test depolarizations between –127 and 23 mV were applied in steps of 10 mV every 3 s. The voltage dependence of channel activation was estimated from mean current densities using the following formalism:
with the cell capacitance Cm, conductance density (Γ), and the reversal potential (Erev). Vm is the half-maximal activation voltage and km the corresponding slope factor.
Gating kinetics. The kinetics of activation and fast inactivation of NaV1.9 and NaV1.9-V1184A channels were analysed between –67 and –7 mV with a model assuming one activation gate and one inactivation gate:
with the current amplitude I0. m(t) and h(t) describe the kinetics of channel activation and inactivation, respectively; τm and τh are the associated time constants, and h∞ characterizes the fraction of non-inactivating current after infinite time.
Steady-state inactivation. NaV1.9 channels were activated with a first 50 ms test pulse to –47 mV followed by a conditioning interval of 500 ms at voltages ranging from –127 to –17 mV in steps of 10 mV. Peak currents of not inactivated channels were measured in a subsequent 50 ms test pulse. The repetition interval was 20 s. The current amplitude after conditioning (I500 ms) normalized to the control current amplitude before conditioning (I0) was described with the following Boltzmann formalism:
with the maximal and minimal channel availability hmax and hmin, the half-maximal inactivation voltage Vh and the corresponding slope factor kh.
Channel deactivation. Channels were first activated with a 25-ms depolarization to −47 mV. Subsequently, deactivation was triggered with a 150-ms repolarization period at voltages ranging from –117 to –77 mV in steps of 5 mV with a repetition interval of 10 s. The current decay during the repolarization period was fitted according to:
where I0 is the maximal current amplitude and I∞ the current remaining after infinite time. τd is the deactivation time constant. The voltage dependence of activation and deactivation time constants was described with a formalism assuming a one-step process for channel opening and closing:
τ0 is the voltage-independent, limiting speed of deactivation, and α0 is the rate at the equilibrium voltage Vm, and kT is the thermal energy. q is the total gating charge transfer and δ is the symmetry factor specifying the gating charge fraction associated to channel activation.
Temperature dependence. Q10 temperature coefficients, specifying the change of reaction rates in response to a temperature change of 10 °C were calculated according to:
where k1 and k2 are the reaction rates obtained at temperatures T1 and T2, respectively.
Data were analysed with FitMaster (HEKA Elektronik) and IgorPro (WaveMetrics, Lake Oswego, OR, USA) software. Data are presented as mean±s.e.m., (n) with n being the number of independent experiments. Statistical comparisons of two groups of data were made using the two-tailed Student’s t-test or the Z-Test; P values are given explicitly when appropriate.
How to cite this article: Leipold, E. et al. Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant. Nat. Commun. 6:10049 doi: 10.1038/ncomms10049 (2015).
Dib-Hajj, S. D., Cummins, T. R., Black, J. A. & Waxman, S. G. Sodium channels in normal and pathological pain. Annu. Rev. Neurosci. 33, 325–347 (2010).
Baker, M. D., Chandra, S. Y., Ding, Y., Waxman, S. G. & Wood, J. N. GTP-induced tetrodotoxin-resistant Na+ current regulates excitability in mouse and rat small diameter sensory neurones. J. Physiol. 548, 373–382 (2003).
Herzog, R. I., Cummins, T. R. & Waxman, S. G. Persistent TTX-resistant Na+ current affects resting potential and response to depolarization in simulated spinal sensory neurons. J. Neurophysiol. 86, 1351–1364 (2001).
Waxman, S. G. & Zamponi, G. W. Regulating excitability of peripheral afferents: emerging ion channel targets. Nat. Neurosci. 17, 153–163 (2014).
Bennett, D. L. & Woods, C. G. Painful and painless channelopathies. Lancet Neurol. 13, 587–599 (2014).
Cox, J. J. et al. An SCN9A channelopathy causes congenital inability to experience pain. Nature 444, 894–898 (2006).
Goldberg, Y. P. et al. Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. Clin. Genet. 71, 311–319 (2007).
Fertleman, C. R. et al. SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes. Neuron 52, 767–774 (2006).
Yang, Y. et al. Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia. J. Med. Genet. 41, 171–174 (2004).
Wu, M. T., Huang, P. Y., Yen, C. T., Chen, C. C. & Lee, M. J. A novel SCN9A mutation responsible for primary erythromelalgia and is resistant to the treatment of sodium channel blockers. PLoS ONE 8, e55212 (2013).
Han, C. et al. Temperature dependence of erythromelalgia mutation L858F in sodium channel Nav1.7. Mol. Pain 3, 3 (2007).
Devigili, G. et al. Paroxysmal itch caused by gain-of-function Nav1.7 mutation. Pain 155, 1702–1707 (2014).
Faber, C. G. et al. Gain of function NaV1.7 mutations in idiopathic small fiber neuropathy. Ann. Neurol. 71, 26–39 (2012).
Faber, C. G. et al. Gain-of-function Nav1.8 mutations in painful neuropathy. Proc. Natl Acad. Sci. USA 109, 19444–19449 (2012).
Leipold, E. et al. A de novo gain-of-function mutation in SCN11A causes loss of pain perception. Nat. Genet. 45, 1399–1404 (2013).
Woods, C. G., Babiker, M. O., Horrocks, I., Tolmie, J. & Kurth, I. The phenotype of congenital insensitivity to pain due to the Na1.9 variant p.L811P. Eur. J. Hum. Genet. 23, 561–563 (2015).
Han, C. et al. The domain II S4-S5 linker in Nav1.9: a missense mutation enhances activation, impairs fast inactivation, and produces human painful neuropathy. Neuromolecular Med. 17, 158–169 (2015).
Huang, J. et al. Gain-of-function mutations in sodium channel Na(v)1.9 in painful neuropathy. Brain 137, 1627–1642 (2014).
Zhang, X. Y. et al. Gain-of-function mutations in SCN11A cause familial episodic pain. Am. J. Hum. Genet. 93, 957–966 (2013).
Chien, H. F. et al. Quantitative pathology of cutaneous nerve terminal degeneration in the human skin. Acta Neuropathol. 102, 455–461 (2001).
Redisch, W., Sheckman, E. & Stelle, J. M. Skin temperature response of normal human subjects to various conditions. Circulation 6, 862–867 (1952).
Shusterman, V., Anderson, K. P. & Barnea, O. Spontaneous skin temperature oscillations in normal human subjects. Am. J. Physiol. 273, R1173–R1181 (1997).
Rush, A. M. & Waxman, S. G. PGE2 increases the tetrodotoxin-resistant Nav1.9 sodium current in mouse DRG neurons via G-proteins. Brain Res. 1023, 264–271 (2004).
Ostman, J. A., Nassar, M. A., Wood, J. N. & Baker, M. D. GTP up-regulated persistent Na+ current and enhanced nociceptor excitability require NaV1.9. J. Physiol. 586, 1077–1087 (2008).
Cummins, T. R. et al. A novel persistent tetrodotoxin-resistant sodium current in SNS-null and wild-type small primary sensory neurons. J. Neurosci. 19, RC43 (1999).
Sato, C. et al. The voltage-sensitive sodium channel is a bell-shaped molecule with several cavities. Nature 409, 1047–1051 (2001).
Jiang, Y. et al. X-ray structure of a voltage-dependent K+ channel. Nature 423, 33–41 (2003).
Bezanilla, F. The voltage-sensor structure in a voltage-gated channel. Trends Biochem. Sci. 30, 166–168 (2005).
Long, S. B., Campbell, E. B. & Mackinnon, R. Crystal structure of a mammalian voltage-dependent Shaker family K+ channel. Science 309, 897–903 (2005).
Ferrer, T., Rupp, J., Piper, D. R. & Tristani-Firouzi, M. The S4-S5 linker directly couples voltage sensor movement to the activation gate in the human ether-a'-go-go-related gene (hERG) K+ channel. J. Biol. Chem. 281, 12858–12864 (2006).
Lolignier, S. et al. The Nav1.9 channel is a key determinant of cold pain sensation and cold allodynia. Cell Rep. 11, 1067–1078 (2015).
Dib-Hajj, S. D., Tyrrell, L., Black, J. A. & Waxman, S. G. NaN a novel voltage-gated Na channel, is expressed preferentially in peripheral sensory neurons and down-regulated after axotomy. Proc. Natl Acad. Sci. USA 95, 8963–8968 (1998).
Dib-Hajj, S., Black, J. A., Cummins, T. R. & Waxman, S. G. NaN/Nav1.9: a sodium channel with unique properties. Trends Neurosci. 25, 253–259 (2002).
Persson, A. K. et al. Sodium-calcium exchanger and multiple sodium channel isoforms in intra-epidermal nerve terminals. Mol. Pain 6, 84 (2010).
Dib-Hajj, S. D., Yang, Y., Black, J. A. & Waxman, S. G. The Na(V)1.7 sodium channel: from molecule to man. Nat. Rev. Neurosci. 14, 49–62 (2013).
Han, C. et al. The domain II S4-S5 linker in Nav1.9: a missense mutation enhances activation, impairs fast inactivation, and produces human painful neuropathy. Neuromolecular Med. 2, 158–169 (2015).
Catterall, W. A. From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels. Neuron 26, 13–25 (2000).
Weis, J. et al. Small-fiber neuropathy in patients with ALS. Neurology 76, 2024–2029 (2011).
Ebenezer, G. J., Hauer, P., Gibbons, C., McArthur, J. C. & Polydefkis, M. Assessment of epidermal nerve fibers: a new diagnostic and predictive tool for peripheral neuropathies. J. Neuropathol. Exp. Neurol. 66, 1059–1073 (2007).
Dib-Hajj, S. D. et al. Transfection of rat or mouse neurons by biolistics or electroporation. Nat. Protoc. 4, 1118–1126 (2009).
We are grateful to the family who participated in the research study. ND7/23 cells were generously provided by Dr C. Nau (Lübeck, Germany). The work was supported by the Deutsche Forschungsgemeinschaft (DFG) to I.K. (KU 1587/3-1), to E.L. (LE 2338/3-1), and a ‘DFG Heisenberg Professorship’ to I.K. (KU 1587/4-1).
The authors declare no competing financial interests.
About this article
Cite this article
Leipold, E., Hanson-Kahn, A., Frick, M. et al. Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant. Nat Commun 6, 10049 (2015). https://doi.org/10.1038/ncomms10049
Neurobiology of Pain (2020)
Scientific Reports (2020)
Pflügers Archiv - European Journal of Physiology (2020)
A 49-residue sequence motif in the C terminus of Nav1.9 regulates trafficking of the channel to the plasma membrane
Journal of Biological Chemistry (2020)