A novel mutation in GPD1‑L associated with early repolarization syndrome via modulation of cardiomyocyte fast sodium currents
- Authors:
- Published online on: January 8, 2020 https://doi.org/10.3892/ijmm.2020.4454
- Pages: 947-955
Abstract
Introduction
Unexplained cardiac death is mainly caused by malignant ventricular tachycardia, ventricular fibrillation, or both (1). On electrocardiography, an early repolarization pattern (ERP) appears to be common among cardiac death cases (2). ERP is characterized by J point (QRS-ST junction) elevation of >0.1 mV in at least two leads on the electrocardiogram, accompanied by J-wave slurring and notching changes (3). Patients with an ERP and unexplained cardiac arrest, but without structural heart disease, have early repolarization syndrome (ERS) (4).
ERPs are common among the relatives of patients with ERS. Therefore, heredity of a genetic mutation may play a key role in the occurrence of ERPs (5). The main mechanism of ERP is disordered ion currents during the depolarization stage and during the early stages of repolarization of cardiomyocyte action potentials (6). These abnormal ion currents mainly include transient outward potassium currents (7), fast sodium currents (8), inward-rectifier ATP-dependent K+ channel currents (9), and L-type calcium currents (10). Study results suggest that the 'loss of function' caused by mutations of CACNA1C (11), CACNB2b (12), CACNA2D1 (12), SCN5A (8) and SCN10A (13), and 'gain of function' caused by mutations of KCNJ8 (14) and ABCC9 (15), are associated with ERS.
The glycerol-3-phosphate dehydrogenase 1-like (GPD1-L) gene is located on chromosome 3. GPD1-L is mainly expressed near, but not on the cell membrane (16), and it may affect the action potentials of cardiomyocytes via regulation of sodium channel function (16). The objective of the present study was to examine the effects of changes in GPD1-L using co-expression of GPD1-L with Nav1.5 in 293 cells in order to determine whether there is an association between ERS and of a loss of function in INa secondary to mutations in GPD1-L.
Materials and methods
Ethics approval
The present study was performed in accordance with the principles for ethical human genetic disease research formulated by the World Medical Association and the Helsinki Declaration. The investigation was approved by the Ethics Committee of the First Affiliated hospital of Sun Yat-Sen University. All family members agreed to participate in the study and signed the informed consent forms.
Clinical study
Patients with ERS admitted to the First Affiliated Hospital of Sun Yat-Sen University in 2015 were selected for the study. All clinical data, including those obtained from records of routine and specialized cardiovascular disease examinations (electrocardiogram, Holter electrocardiogram, X-ray, echocardiography, coronary angiography, and electro-physiological examination) were collected. ERP was defined as J point (QRS-ST junction) elevation of >0.1 mV on the electrocardiogram, in at least two leads, accompanied by J-wave slurring or notching changes. Detailed family histories of the probands were investigated, and the family pedigrees were drawn. Full and reliable clinical phenotype data were collected as well as possible. Peripheral venous blood was extracted from each proband for genetic testing.
Genetic sequencing and analysis
QIAamp DNAKits (Qiagen GmbH) were used to extract blood DNA according to the standard operating manual method recommended by the manufacturer. The samples used to build the libraries met the requirements for new-generation high-throughput gene sequencing. Whole-genome sequencing was performed using Next Generation Sequencing and the HiSeq X Ten (Illumina, Inc.).
The reference sequences were compared with the sequencing results. Bioinformatics methods were used to detect and annotate single-nucleotide variants (SNVs) and InDel results. The gene frequency of each SNV was determined using comparison with standard databases (e.g., the 1000 Genomes Project and dbSNP). Candidate genes for malignant arrhythmias have been described previously (17). SNVs with allele frequencies <1% were selected during screening to facilitate further investigation and identification of sudden death-related genes. Protein function prediction software [PROVEAN Protein, version 1.1 (http://provean.jcvi.org/seq_submit.php) and SIFT, version 6.2.1 (http://sift.bii.a-star.edu.sg/)] and conservation of gene sequences analysis software [PhyloP (https://ccg.epfl.ch//mga/hg19/phylop/phylop.html) and Grantham (https://gist.github.com/danielecook/501f03650bca6a3db31ff3af2d413d2a)] were used to predict the protein functions encoded by the mutant genes. The candidate genetic mutation present in each proband was verified using Sanger sequencing.
Mutagenesis, cell culture and transfection
Nav1.5 cDNA (SCN5A, NM_198056) was subcloned into the mammalian expression vector, pENTER. For western blotting and electrophysiological study, GPD1-L cDNA (NM_015141.3) was amplified using PCR and subcloned into pIRES2-EGFP. When the plasmid was transfected into 293 cells, the 293 cells expressed enhanced green fluorescent protein (eGFP) and GPD1-L protein. For the confocal microscopy examination, GPD1-L cDNA (NM_015141.3) was amplified using PCR and subcloned into pEGFP-N1. When the plasmid was transfected into 293 cells, the 293 cells expressed eGFT-GPD1-L fusion protein to trace the trafficking of GPD1-L. The p. P112L mutation of GPD1-L was introduced by site-directed mutagenesis using the QuikChange II kit (Stratagene; Agilent Technologies, Inc.). 293 cells were cultured in DMEM containing 10% fetal bovine serum, and under the conditions of 5% CO2 and 37̊C. 293 cells were transfected with SCN5A plasmid and WT/MT GPD1-L plasmid (1:1 molar ratio) using Lipofectamine 3000 transfection reagent (Invitrogen; Thermo Fisher Scientific, Inc.). The electrophysiological recordings, western blotting, and confocal microscopy observations were performed according to the manufacturers' instructions.
Western blotting
After transfection for 24 h, the medium was discarded and the cells were washed twice using pre-cooled PBS; 120 µl ice-cold RIPA buffer (Beyotime Institute of Biotechnology) was added to each well of 6-well plates, and the plates were shaken on ice for 15 min. Intermittent ultrasound (200 W, 25% power) was used to lyse the cells (working for 3 sec and stopping for 5 sec), until the lysates were clear and bright. After centrifugation at 12,580 × g for 15 min at 4°C, the supernatant was collected as the protein sample.
The protein samples were quantified using the BCA Protein Quantitation kit (Thermo Fisher Scientific, Inc.) according to the manufacturer's instructions. Each protein sample was diluted using 5X loading buffer and was denatured in 95̊C water for 10 min. Protein samples (10 µg/lane) were separated by 10% SDS-PAGE gel and transferred to PDVF membranes. The PVDF membranes were blocked using 5% BSA solution (Thermo Fisher Scientific, Inc.) and incubated with anti-GPD1L antibody (1:500, cat. no. NPB1-32279, Novus Biologicals, Ltd.) and anti-tubulin antibody (1:5,000, cat. no. 66031-1-Ig, Proteintech Group, Inc.) overnight on a shaker at 4̊C. The PVDF membranes were washed four times (10 min each time) using TBS/0.1% Tween-20 (TBST) solution and were incubated with HRP-conjugated goat-anti-mouse secondary antibody (1:10,000, cat. no. 15134-1-AP, Proteintech Group, Inc.) for 1 h at room temperature. After the secondary antibody incubation, the PBST solution was used to wash the membranes four times (10 min each time). The proteins were visualized using enhanced chemiluminescence on an X-ray film in a dark room. The results were quantified using Image J software, version 1.52a (National Institutes of Health). For the analysis, the GPD1-L blots were standardized to the corresponding tubulin blots in each sample.
Electrophysiological recordings
Electrophysiological recordings were performed using a microelectrode manipulator (MP285, Sutter Instruments) under an inverted microscope (IX71, Olympus Corporation). The recording electrodes were prepared from capillary glass tubes (BF150-86-10, Sutter Instruments), which were modified using three steps and a microelectrode puller (P97, Sutter Instruments). The patch pipette resistance was 2-3 MΩ when filled with pipette solution. The bath solution contained 140 mM NaCl, 4 mM KCl, 1 mM MgCl2, 2 mM CaCl2, 5 mM D-glucose monohydrate, and 10 mM HEPES (pH 7.4, adjusted using NaOH). The pipette solution contained 145 mM CsCl, 0.1 mM CaCl2, 2 mM MgCl2, 10 mM NaCl, 0.5 mM Na2-GTP, 2 mM Mg-ATP, 1.1 mM EGTA, and 10 mM HEPES (pH 7.2, adjusted using CsOH). After the patch pipette contacted the cell membrane, negative pressure was used to form a GΩ seal and break the cell membrane to create the whole-cell recording mode. All electrophysiological experiments were performed at room temperature. Currents were filtered and digitized using default settings. Series resistance (80%) was compensated by computer. The data were collected using an EPC-10 amplifier (HEKA Elektronik) and stored in PatchMaster software, version 2×90.5 (HEKA Elektronik). The results were analyzed using PatchMaster and IGOR Pro 6.0 software.
The activation INa values were measured by providing cell pulsing voltages ranging from −120 to 30 mV (10-mV step pulse), with a holding potential at −120 mV; the peak INa value was also recorded. The peak current was fitted using the Boltzmann function: GNa/Gmax =[1+exp −1 (V1/2−Vc)/k] , where k is the slope factor and V1/2 is the half-maximal voltage of activation. GNa=INa/(V−Vrev), where V is the membrane potential and Vrev is the reversal potential. The inactivation INa values were measured using a two-step protocol, with a holding potential at −120 mV. The first step was a 30-msec conditional pulse; the voltage range was from −120 to −20 mV (10-mV step pulse). The second step was the test pulse (−20 mV), and the peak sodium current was recorded. The current was fitted using the Boltzmann function: I/I =[1+exp −1 max (Vc-V1/2)/k] , where Vc is the membrane potential. The recovery INa values were measured using a three-step protocol, with a holding potential at −120 mV. The duration (30 msec) and voltage (−20 mV) of the condition pulse and test pulse amplitudes were consistent, and the two pulses were spaced from 1 to 60 msec, in 1-msec steps. The values for the peak currents induced by the test pulses were recorded. The current was fitted using an exponential function: I/Imax=A+A1*exp(−t/t), where t stands for time and t is the recovery time constant. All data were plotted using Origin 8 software (OriginLab CorporationA).
Immunofluorescence and confocal microscopy
All treated 293 cells expressing eGFP-GPD1-L fusion protein were imaged at room temperature using a Zeiss LSM 780 confocal system with ZEN software (black edition, version 11.0.0190). The images were acquired using a ×63 oil immersion objective and ×10 ocular lens.
After the 293 cells were transfected with the plasmid for 48 h, they were digested using 0.25% trypsin (2520056, Gibco; Thermo Fisher Scientific, Inc.), resuspended, and attached to tissue culture-treated confocal dishes (BDD012035, Jet Biofil). Cell membranes were stained using 1,1′-diocta-decyl-3,3,3′,3′-tetramethylindocarbocyanine perchlorate (Dil; 3 µM, D4010, US Everbright, Inc.) for 5 min at 37̊C. The cells were then fixed using 4% paraformaldehyde for 15 min at room temperature. DAPI (1 µg/ml, D4054, US Everbright, Inc.) was then added. The cells were then exposed to a Dil excitation wavelength of 549 nm, and emission sections were collected between 560 and 580 nm. The EGFP-GPD1-L fusion protein excitation wavelength was 488 nm, and emission sections were collected between 505 and 530 nm. The DAPI excitation wavelength was 360 nm, and emission sections were collected at 460 nm.
Statistical analysis
The data were analyzed using an SPSS 20.0 software package (IBM Corp.) and the results were expressed as mean ± standard deviation values. Student's t-tests were used for between-group comparisons. One-way ANOVA and Student-Newman-Keuls tests were used for comparisons of multiple groups. P<0.01 was considered to indicate a statistically significant difference.
Results
Clinical data
A family whose electrocardiograms showed ERP from January 2013 to June 2015 was investigated. The mean age of the patients was 50 years (standard deviation, 22.62 years). The details of the family members are presented in Table I. Blood samples were collected from the proband (black arrow) for whole-genome sequencing analysis. The whole-genome sequencing and bioinformatics analysis of the proband genomic DNA revealed a total of 22,205 missense SNV sites in the exon regions. After screening for candidate genes for malignant arrhythmias, allele frequencies <1% and protein function prediction, GPD1-L was identified as the suspected pathogenic mutation (NCBI Reference Sequence: rs1201810677, https://www.ncbi.nlm.nih.gov/snp/rs1201810677). The results for the mutation sites of the GPD1-L gene are presented in Fig. 1B. The mutation in the proband was verified using Sanger sequencing (Fig. 1C). This mutation resulted in the conversion of a hydrophilic proline to a hydrophobic leucine at position 112 of the GPD1-L protein.
The proband was a 34-year-old man who suffered from recurrent palpitations with dizziness, fatigue and amaurosis fugax. The patient's electrocardiogram results are presented in Fig. 1D. The electrocardiogram revealed J-point elevations (>0.1 mV) in leads II, III and aVF, and a slurring J wave. The chest X-ray, echocardiography, serum electrolyte levels, coronary angiography, multiple myocardial enzyme tests and treadmill test results were within the reference ranges. The results of the patient's electrocardiogram monitoring indicated the presence of ventricular premature contractions and short polymorphic ventricular tachycardia. Based on these results, ERS was diagnosed in the proband. A clinical investigation of all members of the family (brother, sister and both parents of the proband) revealed that the father's electrocardiography results indicated the presence of ERPs, but the siblings' electrocardiograms did not.
GPD1-L was successfully transfected in 293 cells and P112L mutant decreased the expression of GPD1-L
Western blotting of whole-cell lysates was performed to verify the successful transfection of GPD1-L and study the effects of gene mutation on protein expression. Tubulin, with a molecular weight of 55 kDa, was used as an internal reference protein. The results indicated that both the WT and MT groups expressed the GPD1-L protein, but the mock group did not (Fig. 2A), which suggested that GPD1-L was successfully transfected in 293 cells. The expression level of MT-GPD-1L was significantly reduced in the MT group compared with the WT group (P<0.01; Fig. 2B).
P112L mutation decreased INa activation
293 cells were transfected with both SCN5A plasmid and WT/MT GPD1-L plasmid. The results for representative activation of INa in the 293 cells of the WT and MT groups are presented in Fig. 3A. The voltage stimulation protocol for activation of INa is presented in Fig. 3B. The whole-cell patch-clamp recording experiment revealed that the maximum current densities for the WT and MT groups were −599.50±103.80 pA/pF (n=9) and −197.25±78.53 pA/pF (n=9), respectively (Fig. 3C). The P112L mutation reduced the current by ~60% compared with the WT group (P<0.01). The IV curve morphology was basically the same between the two groups. The Boltzmann function was used to obtain the V1/2 and slope factor k (Fig. 3D). The results indicated that the steady-activation curves for both groups began to activate at ~ −60 mV. There were no significant between-group differences for V1/2 (P=0.43) or slope factor k values (P=0.17). These results indicated that the mutation exerted little effect on activation of INa (Table II). Representative results for inactivation and recovery of INa and stimulation protocols are presented in Fig. 4A-D. The Boltzmann inactivation curve function was used to obtain the V1/2 and slope factor k (Fig. 4E). Compared with the WT group, a negative voltage change was detected in the MT group. There were no significant between-group differences in V1/2 (P=0.54) or slope factor k values (P=0.38). These results indicated that the mutation exerted little effect on the inactivation of INa (Table II). An exponential reactivation curve function was fitted to obtain the τ (Fig. 3F). The results indicated that the mutation exerted little effect on recovery of INa (P=0.77; Table II).
The P112L mutant reduces localization of GPD1-L adjacent to the cell surface
To investigate the effect of the P112L mutation on GPD1-L localization in cells, 293 cells were transfected with SCN5A plasmid and eGFP-WT/MT GPD1-L fusion plasmid (1:1 ratio). After a 48-h transfection period, the cells were treated for confocal microscopy observation. Dil was used to stain the cell membranes. The eGFP-GPD1-L fusion protein was used to track the localization of GPD1-L in the 293 cells. The results indicated that the expression levels of GPD1-L near the membrane were higher in the WT group compared with those in the MT group (Fig. 5). Both the WT and MT GPD1-L were mainly distributed in the cytoplasm, whereas the distribution in the nuclei was lower in both groups (Fig. 5).
Discussion
In the present study, the whole-cell patch-clamp recording experiment results indicated that, compared with the WT group, the activation of INa was 60% lower in the MT group. The western blotting results indicated that GPD1-L was successfully transfected in 293 cells and the expression of the mutant GPD1-L protein was lower in the MT group. The evaluation using confocal microscopy revealed that the MT GPD1-L was less expressed near the cell membrane and more expressed in the cytoplasm.
Research on the mechanism of ERS and severe ventricular arrhythmia has reached the ion level (18). The change in the action potential notch of the epicardial membrane is related to the J wave, and the increase in repolarization current (secondary to the decrease in inward current or the increase in outward current) leads to an increase in the J waves or elevation of ST segments (19). The gene mutation leading to the morphological change in the action potential notch may result in the formation of ERPs. Currently, the genetic variations associated with both ERP and ERS include seven types: KCNJ8 (9) and ABCC9 (15), which regulate pore formation of the IK-ATP channel and the ATP-sensitive subunit; CACNA1C (11), CACNB2b (12), CACNA2D1 (12), and related subunits of the L-type calcium channel; and SCN5A (20) and SCN10A (13) of the INa channel. The enhanced repolarization dispersion is prone to form 2-phase reentry, which may result in premature ventricular contractions and ventricular tachycardia (19).
GPD1-L, a glycerol-3-phosphate dehydrogenase 1-like gene, plays an important role in the function regulation of myocardial sodium channels; it is an important susceptibility gene for sudden unexpected death syndrome (21), sudden infant death syndrome (21), and Brugada syndrome (22). The human GPD1-L gene is located on chromosome 3 and encodes a protein composed of 351 amino acids. GPD1-L may interact with proteins associated with ion channels, such as ankyrin-G, syntrophin, caveolin-3 and Nedd4-2 (23). GPD1-L regulates endoplasmic reticulum signaling by affecting the protein kinase A-dependent phosphorylation (24). GPD1-L also affects the oxidative state to regulate the function of cardiac sodium channels (16).
The first reported association for GPD1-L was in type II Brugada syndrome (25), where it is co-expressed with Nav1.5 in the cardiomyocytes. Van Norstrand (21) detected three mutation sites for GPD1-L (E83K, I124V and R273C) in 83 cases of sudden unexpected death syndrome and in 221 cases of subsequent sudden infant death syndrome. All sites were highly conserved, and none were detected in the 300 control group patients. Experiments with 293 cells and neonatal rat myocardial cells transfected with the aforementioned mutants demonstrated that the mutants may cause an instantaneous decrease in sodium current density (21).
We found that the activation current density of the MT group decreased by 60% compared with the WT group. A recent study found that GPD1-L is expressed near the cell membrane (26) and can regulate the redox state of sodium channels via PKC-dependent phosphorylation, thus affecting the function of sodium channels (16). It was inferred that the decrease in the activation of INa can increase the relative inward current of the action potential during repolarization through the mechanisms mentioned above and, thus, alter the notch morphology of action potentials in myocardial cells and form J waves and J-point elevations in the electrocardiogram. Further study is required to confirm the effects of GPD1-L P112L on action potentials and elucidate the exact mechanisms underlying the association between GPD1-L and sodium channels. The western blotting results indicated that the mutation decreased the total expression of GPD1-L. Although confocal microscopic observation found that GPD1-L somewhat co-located with cell membrane markers, a previous study demonstrated that GPD1-L is localized near rather than on the cell membrane (26). Therefore, the results may be interpreted as follows: MT GPD1-L was less expressed near the cell membrane and more expressed in the cytoplasm compared with WT GPD1-L. Our results indicate that the difference in total expression level and distribution of GPD1-L caused by mutations may also be implicated in the occurrence of ERS. Further research is required to investigate the mechanisms of expression and abnormal intracellular transport of GPD1-L affected by mutations.
In summary, it was herein demonstrated that GPD1-L P112L decreased the activation of INa. The decreased total cell GPD1-L expression and the decreased expression of GPD1-L near the cell membrane may also contribute to the development of abnormal sodium currents. Our study results suggested that GPD1-L P112L may be a novel pathogenic genetic mutation of ERS.
Funding
This study was supported by the National Natural Science Foundation of China (grant nos. 81370285 and 81970206), and the Guangzhou City Science and Technology Program (grant no. 201508020057).
Availability of data and materials
The datasets generated and/or analyzed during the present study are available from the corresponding author on reasonable request.
Authors' contributions
WSH and JF made substantial contributions to the design of the present study. JF, JCC, YH, CYJ, CXM and ZZH performed the experiments; JF, JCC, YH, CYJ, CXM and ZZH analyzed the data; JF, WSH, JCC, CYJ wrote the manuscript. All authors have read and approved the final version of the manuscript.
Ethics approval and consent to participate
The investigation was approved by the Ethics Committee of the First Affiliated Hospital of Sun Yat-Sen University. All family members agreed to participate in the study and signed the informed consent forms.
Patient consent for publication
All patients provided written informed consent regarding the publication of their data, including clinical and genetic information.
Competing interests
All the authors declare that they have no competing interests.
Acknowledgments
Not applicable.
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