Open access peer-reviewed chapter

Altered Potassium Ion Homeostasis in Hearing Loss

By Viktoria Szuts, Janos Andras Jarabin, Nikoletta Nagy, Ferenc Otvos, Roland Nagy, Attila Nagy, Katalin Halasy, Laszlo Rovo, Marta Szell and Jozsef Geza Kiss

Submitted: November 9th 2017Reviewed: April 24th 2018Published: October 10th 2018

DOI: 10.5772/intechopen.77732

Downloaded: 691


Connexins, Kv-type ion channels, and pannexins have a dominant role in maintaining the potassium ion homeostasis in the cochlea. The cellular background currents are sustained by Kir2.1 ion channels; however, their involvement in the hearing system is less clear. In this study, the mutations of gap junction proteins beta 2 (GJB2), beta 3 (GJB3) and beta 6 (GJB6) were screened in the white Caucasian population in Hungary using gene mapping and immunofluorescence methods from translated proteins of these genes—connexins on blood cells. Expression of connexins and Kir2.1 ion channels was investigated in the blood cells of deaf patients prior to cochlear implantation, and the results show significantly decreased amounts of connexin26 and connexin43. In addition, the coexpression of Kir2.1 ion channels with synapse-associated 97 proteins was partially impaired. Our investigation revealed a reduced level of Kir2.1 channels in deaf patients indicating a crucial role for the functional Shaker superfamily of K+ channels in the non-diseased hearing system.


  • hearing loss
  • cochlea
  • GJB gene mutation
  • connexin26
  • connexin43
  • Kir2.1 ion channels
  • lymphocytes

1. Introduction

Mutations in connexin26 (Cx26) and connexin30 (Cx30) have frequently been associated with hearing loss and deafness, and some Cx26 mutations have also been found to contribute to over 50% of hearing loss or nonsyndromic deafness cases in different human populations investigated in the last decades [1, 2, 3, 4, 5, 6].

Recently, a fast and new non-invasive method has been developed in our laboratory to identify mutated genes for GJB2 leading to hearing loss or deafness [7]. This method has allowed us to collect and store the dried blood spots (DBS) in Guthrie cards for mutation analysis or expressed proteins of genes. The early detection of genetic mutations for inner ear impairment is crucial to provide hearing rehabilitation with an outstanding functional outcome, i.e. to maintain the development of the peripheral and central auditory pathway for unhindered future benefits. There are a number of modern technologies in the field of cochlear implantation and to fulfill this aim it is crucial to address the audiological and logopedical progress in a timely manner.

Cx26 and connexin43 (Cx43) have a major role in cell-to-cell interactions and in the permeability of the channels for diverse ions and small molecules, which maintain the physiological condition of the cochlea [1, 8]. Connexins form hemichannels in the cochlea where the Cx26 channels are the most abundant and are involved in the potassium-recycling pathway of the cochlea. Translated proteins from GJ genes make up channels by head-to-head docking of two connexin hexamers referred to as hemichannels (HCs) or connexons; one from each neighboring cell [9, 10]. Cx26 proteins were localized in the outer membrane of the cochlea.

The position of mutations in the GJB2gene (Cx26 protein) is different across certain populations. The known mutation in the populations of northern European descent is a base pair deletion at position 35 in the GJB2 gene (known as 35delG; Cx26 protein) while the 235delC mutation, which occurs more frequently in Asian populations, misses a base pair at position 235 (Cx26 protein) [11, 12, 13]. Furthermore, patients with a single base pair deletion at position 167 (167delT) (Cx26 protein) are commonly found in communities of eastern European (Ashkenazi) Jewish ancestry [14, 15].

Different connexins may be important factors in the flawless cell-to-cell interactions that maintain the fast electrogenic mechanisms between the cochlea and neuronal system [16]. Other ion currents are also involved in this process. The voltage-dependent inward rectifier potassium current (IK1) has a role in maintaining the resting membrane potential, contributing to the beginning and the final repolarization in all cells. The IK1 current in different tissues is sustained mostly by Kir2.x (Kir2.1, Kir2.2, and Kir2.3) ion channels [17, 18, 19, 20, 21, 22, 23]. Auxiliary subunits and the synapse-associated protein 97 (SAP97) modulate the function of these channels [24, 25]. IK1 currents have a fundamental role in muscle cells, but their molecular background in the hearing system is still uncertain. We have limited information on the impact of the altered gap-junctions [26] and Kir2.1 in the inner membrane of the cochlea [20, 21, 27], the neural connection and the expressed potassium ion channels on blood cells. The exploration of the type and mechanism of these channels is one of the aims of the present work.

Hereditary hearing diseases are known to be associated with mutations, such as the autosomal recessive non-syndromic hearing loss (ARNSHL), seizures, sensorineural deafness [5, 28, 29, 30], Pendred syndrome (PDS) [5, 29, 30, 31], deafness [7, 27, 28, 29, 30, 31, 32, 33, 34, 35], and rarely the hearing loss overlaps with Andersen-Tawil syndrome [2, 36, 37]. The Andersen-Tawil syndrome is characterized by mutated KCNJ2 genes expressing malfunctioned Kir2.1 proteins, which leads to functional abnormalities and causing deafness with cardiomyopathy [36, 37, 38].

The IK1 current is sustained -by ion channels that consist of heteromeric assemblies of Kir2.1, Kir2.2, and Kir2.3 α-subunits [22, 39]. This current significantly contributes to the maintenance and regulation of the resting membrane potential [17, 40] and strongly affects the final repolarization of the action potential (AP) [8, 9, 17, 18, 41]. The Kir2.x channels are under the control of the intracellular scaffolding, trafficking and regulatory proteins, which strongly adjust their physiological functions. Kir2.x isoforms colocalize with membrane associated guanylate kinase (MAGUK) proteins [24, 42]. One of these is the SAP97 anchoring protein, which has an important interaction with Kir2.x channel complexes in neuronal cells and myocytes [25, 42, 43]. Various Kir2.x isoforms may cooperate differently with the MAGUK proteins in the complexes that traffic Kir2.x ion channels to the plasma membrane (PM), and anchor and stabilize these channels into the sarcolemma of cardiac muscle [22, 25, 43]. The Kir2.1 channels may be exported from the Golgi in a signal-dependent manner and this process may be disrupted by certain diseases [44]. The age-dependent SAP97 expression in the human heart was evaluated for the first time in our laboratory [45], and it seems that the regulation and modulation of these ion channel complexes have a strong effect in the development of different tissue types in diverse hereditary diseases associated with cardiomyopathy and deafness too [36, 37, 38, 39, 46]. These genes have demonstrated a gender differences and have been remodeled in cardiomyopathy [40, 41]. IK1 currents are active during the time course of AP [20, 21, 47, 48], but their molecular background basis is poorly characterized on blood cells.

Our hypothesis states that connexins and Kir2.x ion channels, which are impaired at the transcription and translated protein level in deafness, have an essential function in the hearing system. The aim of this study was to monitor the mutations of expressed GJsand KCNJ2 genes in the Hungarian population and to screen the expression of hearing-related genes and proteins involved in the maintenance of the ionic homeostasis in the cochlea. An additional goal was to find an opportunity to obtain cells from the body that present the disrupted ionic status control characteristic of the pathophysiological condition of deafness. For this purpose, we used non-invasive methods to find the representative and irrevocable changes in peripheral blood cells of patients. Our group has previously demonstrated that connexin ion channels, especially the Cx26 mutations, are characteristic indicators in patients with hearing loss [7, 48]. In this study we investigated ion channels related to connexins in patients with altered hearing and detected the expression level of Cx26, Cx43 and Kir2.1 channels in the blood cells. Patients have hearing defects and these results highlight to the role of gap junctions and hemichannels in K+ removal and recycling in the inner ear, as well as possible roles for nutrient passage in the cochlea [9, 26, 48].


2. Material and methods

2.1. Human patients

Eighty consecutive, non-randomized profoundly hearing-impaired cochlear implant candidates were recruited in this study cohort; 45 females and 35 males aged between 0.5 and 72 years (average: 25.8 ± 24.4 years). The control group was made up of 13 subjects with objectively measured binaural normal hearing sensitivity; 7 females and 6 males aged between 3 and 59 years (average: 27.4 ± 17.2 years) (Tables 1 and 2). Details of patient demographics, clinical diagnoses, and genetic investigations are presented in Table 1. All patients in the diseased group had nonsyndromic sensorineural hearing loss, without any organic abnormalities (neither anatomical nor developmental alterations) including overlapping diseases. Prior to cochlear implantation, patients did not receive medication. The investigations conformed to the Declaration of Helsinki. Experimental protocols were authorized by the University of Szeged and National Scientific Research Ethical Review Boards (No. 38/2014). The blood cells were taken and kept in cold (4–6°C) for 2–4 h prior to investigations.


Table 1.

Data of non-diseased patients without mutations in GJB2 (Cx26) genes in Hungarian population: non-diseased patients.

ND: Non-Diseased; F: female; M: male.

1M1.7Hearing loss
2M46.3Hearing loss
3M2.5Hearing lossGJB2 (heterozygote c.35delG)
4F4.4Hearing loss
5F1.1Hearing loss
6M2.8Hearing loss
7M16.1Hearing loss
8M23.5Hearing loss
9M1.4Hearing lossGJB2 (homozygote c.35delG)
10F14.5Hearing loss
11F26.9Hearing loss
12F27.6Hearing lossGJB2 (homozygote c.35delG)
13M14.5Hearing loss
14F1.8Hearing loss
15F65.7Hearing loss
16F64.6Hearing lossGJB2 (homozygote c.35delG)
17M2.1Hearing lossGJB2 (heterozygote c.35delG)
18M70.4Hearing loss
19F70.0Hearing loss
20F41.9Hearing loss
21F1.8Hearing loss
22F71.0Hearing loss
23F2.2Hearing lossGJB2 (heterozygote missense c.101 T/C p.Met34Thr (rs35887622, CM077555, CM970679))
24F9.9Hearing lossGJB2 (homozygote c.35delG)
25M6.9Hearing lossGJB2 (heterozygote c.35delG)
26F1.9Hearing lossGJB2 (homozygote c.35delG)
27M2.7Hearing lossGJB2 (homozygote c.35delG)
28M1.3Hearing loss
29F2.9Hearing lossGJB2 (homozygote c.35delG)
30M5.4Hearing lossGJB2 (heterozygote c.35delG)
31M69.6Hearing loss
32F11.3Hearing loss
33F54.0Hearing loss
34F69.5Hearing loss
35F23.7Hearing loss
36M3.1Hearing loss
37M61.6Hearing loss
38F15.4Hearing loss
39F27.7Hearing loss
40F76.9Hearing loss
41F41.7Hearing loss
42M2.0Hearing loss
43M1.2Hearing loss
44M2.6Hearing lossGJB2 (heterozygote missense c.119c/a p.Ala40Glu (rs111033296, CM051511)
45F48.0Hearing loss
46F59.1Hearing lossGJB2: c.101 T/C p.Met34Thr rs35887622 homozygote,
GJB2: c.139G/T p.Glu47Ter rs104894398 homozygote
47M52.7Hearing lossGJB2: c.35delG homozygote
48M19.7Hearing loss
49M2.6Hearing lossGJB2 (homozygote c.35delG)
50M6.6Hearing loss
51M58.5Hearing loss
52M13.2Hearing loss
53F27.3Hearing loss
54F34.9Hearing loss
55F58.9Hearing loss
56F29.8Hearing loss
57F49.2Hearing loss
58F77.3Hearing loss
59M51.2Hearing loss
60M3.1Hearing lossGJB2 (homozygote c.35delG)
61M52.6Hearing loss
62F40.9Hearing lossGJB2 (heterozygote c.35delG)
63F5.7Hearing loss
64M1.5Hearing lossGJB2 (homozygote c.35delG)
65F2.5Hearing loss
66F2.0Hearing loss
67F64.6Hearing loss*GJB3 (c.316C/T p.Arg106Cys (rs147106166) heterozygote)
68F2.8Hearing loss
69F7.1Hearing loss
70M23.7Hearing loss
71F66.5Hearing loss
72M68.7Hearing loss
73F5.9Hearing lossGJB2 (heterozygote c.35delG)
74M6.2Hearing loss
75F20.9Hearing loss
76M9.4Hearing lossGJB2 (heterozygote c.35delG)
77F45.2Hearing loss
78M1.4Hearing loss
79F3.4Hearing loss
80F55.8Hearing loss

Table 2.

Data of hearing loss patients carrying mutations in GJB2 (Cx26) genes in Hungarian population: patients with hearing loss.

Mutation of GJB3 gene.

F: female; M: male.

2.2. Objective tests used for the evaluation of hearing sensitivity

2.2.1. Impedance audiometry Tympanometry

A measurement of compliance change in the middle ear apparatus to transmit sounds to the inner ear as air pressure is varied in the external auditory canal [49, 50]. Equipment used: r36m Clinical Middle Ear Analyzer (Resonance, Gazzaniga, Italy). Acoustic reflex test

Following high intensity acoustic stimulation, a sudden decrease in compliance occurs with an approximate 10 ms delay as a consequence of the contraction of the stapedius muscle. Equipment used: r36m Clinical Middle Ear Analyzer (Resonance, Gazzaniga, Italy).

2.2.2. Otoacoustic emission (OAE)

Spontaneous and evoked sound waves that originate from the inner ear are transmitted through the ossicles and the eardrum into the external auditory meatus can be measured. Equipment used: Eclipse EP15 (Interacoustics A/S, Middelfart, Denmark [51].

2.2.3. Auditory brain stem responses (ABR)

Auditory brain stem responses are far-field potentials that measure all ranges of the early auditory evoked potentials (AEP) using signal averaging [52, 53]. It consists of a series of seven waves (I-VII.) occurring within about 10 ms from stimulus onset [54]. Applied stimuli: Click and CE-Chirp LS. Equipment used: Eclipse EP15 (Interacoustics A/S, Middelfart, Denmark). Click stimulus: used to test the critical high frequency region (approximately 2–4 kHz). Chirp stimulus: applied to activate the entire cochlea instantaneously.

2.2.4. Auditory steady state responses (ASSR)

Auditory steady state responses are AEPs that are used to objectively estimate the hearing sensitivity in individuals with normal hearing sensitivity and with various degrees and configurations of sensorineural hearing loss (SNHL) [55]. Equipment used: Eclipse EP15 (Interacoustics A/S, Middelfart, Denmark) [50, 55].

2.3. Genetic investigations

Peripheral blood samples were drawn from the affected patients (n = 80). Genomic DNA was isolated following the instructions of QIAamp DNA Blood Mini Kit (Qiagen, USA). The coding regions and the flanking introns of the GJB2, GJB3 and GJB6 genes were amplified by polymerase chain reaction (PCR) using DreamTaq Green PCR Master Mix (Thermo Scientific, USA). Primer sequences used for the genetic analyses were designed with Primer 3 ( online software. The quality and quantity of PCR products were measured by electrophoresis on 2% agarose gel (SeaKem LE agarose, Lonza), which were used as templates for sequencing. Direct sequencing of PCR products was performed on a traditional capillary sequencer (ABI Prism 7000) and compared with the wild-type gene sequences using the Ensemble Genome Browser.

2.4. Immunofluorescence

Blood samples were collected in parallel for protein analyses in tubes containing EDTA as anticoagulant. Blood cells of non-diseased and hearing loss patients were washed with phosphate buffer saline (PBS, pH 7.3) and centrifuged gently. Cells, mostly lymphocytes, were attached to slides, blocked with 2% bovine serum albumin and incubated overnight at 4°C with mouse anti-Cx26 (1:100 dilution, Millipore, USA), or rabbit anti-Cx43 (1:100 dilution, Cell Signaling Technology, USA), or rabbit anti-Kir2.1 antibodies (1:100 dilution, Alomone Ltd., Jerusalem) with mouse anti-SAP97 (1:300 dilution, LifeSpan, USA) [48]. After washing with PBS, the cells were incubated with Alexa 488-labeled anti-rabbit IgG (1:400 dilution; Molecular Probes, USA) plus Cy3-conjugated anti-mouse IgG (1:400 dilution; Jackson Immuno Research Laboratories, Inc., USA) secondary antibodies and counterstained with 2,4 diamino-2-phenylindol (DAPI) (Hoechst 33258) for 10 minutes. Detection was performed using an Olympus FV1000 confocal laser scanning microscope (Olympus Life Science Europa GmbH, Hamburg, Germany). The scale bar was labeled in every figure (n = 2–3 specimens for each antibody staining) from 12 patients and the analysis was performed using Fluoview ver. 4.0 programme.

3. Results

3.1. Examination of patients expecting cochlear implantation

The outer ear was inspected by physical examination and found to be anatomically and functionally intact in all subjects prior to any hearing assessment (Figure 1AH). Hearing sensitivity was subsequently evaluated with objective procedures, applying the crosscheck principle to achieve reliable results, confirmed by multiple analyses [49]. The middle ear is essentially an impedance matching system. Impedance is simply a measure of acceptance or rejection of the energy per unit time. While transmitted through the tympanic membrane and other structures of the middle ear, acoustic signals can be modified, depending on the mass, the elasticity and the resistance of the system that would determine the amount of energy accepted or reflected. The overall configuration of tympanometry and acoustic reflex tests provide greater authority and assurance in the evaluation of middle ear pathologies and conductive hearing loss. Middle ear analysis was performed prior to any other tests to unquestionably exclude any pathology that might alter subsequent results [49, 50]. Otoacoustic emissions (OAEs) indicate the functional integrity of the outer hair cells in the inner ear [49, 51]. The source that generates retrograde sound transmission is the frequency following cell-vibration of the outer hair cells, representing their active, non-linear characteristics. There is a distinction between spontaneous emissions (SOAE) and evoked emissions (EOAE). Several modes of stimulation and registration (i.e. post or pre-stimulatory) are known to provide information about outer hair cell function [49, 50]. Distortion product otoacoustic emission (DPOAE) [49, 51] is one of them. Representative results of a non-diseased subject (Table 1), (Figure 1A, C, E, G) and a hearing-impaired patient (Table 2), (Figure 1B, D, F, H) are presented. All curves are color-coded: red lines represent the right ear while blue lines represent the left ear. Figure 1A and B clearly shows that the active, non-linear vibrations of the outer hair cells to an external sound stimulus are sensitively recordable with DPOAE exhibiting the normal function of the endocochlear cellular amplification mechanisms (Figure 1A). In hearing-impaired patients, DPOAE can be registered up to a moderate degree of sensorineural hearing loss; however, the signal tapers off beyond a certain extent (Figure 1B). Neural responses during an auditory brainstem response test (ABR) are generated subcortically by the auditory nerve and subsequent brain stem fiber tracts and nuclei. Using either click or chirp stimuli is still the gold standard for electro-physiologically assessing the integrity of the auditory nerve and the brain stem pathways as they lead the electrical stimuli towards the cortex [52, 53, 54, 55] (Figure 1C and D). Neuronal junction points in the brainstem as generator relay structures are identified in the form of waves on the electrophysiological recordings in normal subjects (Figure 1C); while these points are not registered in patients with a profound hearing loss (Figure 1D). Using CE Chirp-LS stimuli (Figure 1E and F) while registering ABRs, the synchronous activation is achieved in the cochlea, thus a more prominent wave IV-V is observed in a non-diseased patient (Figure 1E). In patients with profound hearing loss, ABRs are missing (Figure 1F). Auditory steady state responses on amplitude-modulated stimuli are highly relevant, since it takes many years to objectively estimate hearing sensitivity in individuals with normal hearing and with various degrees and configurations of SNHL. The objective estimation of hearing sensitivity is performed by auditory steady-state response (ASSR) tests (Figure 1G and H). In a non-diseased subject, normal thresholds were registered on all the measured frequencies (Figure 1G); while a profound hearing loss is demonstrated in a patient with hereditary sensorineural deafness (Figure 1H).

Figure 1.

Objective clinical measures of the auditory function in patients with hearing loss. Representative results of a non-diseased patient (A, C, E, G) and a patient with impaired hearing (B, D, F, H) are presented. All curves are color-coded. Red represents the right ear, and blue represents the left ear. A-B: The active, non-linear vibrations of the outer hair cells to external sound stimuli are sensitively recordable with the distortion product otoacoustic emission test (DPOAE) exhibiting the normal function of the endocochlear cellular amplification mechanisms (A). In hearing impaired patients, DPOAE can be registered up to a moderate degree of sensorineural hearing loss. However, the signal tapers off beyond a certain extent (B). C-D: Auditory brainstem response tests (ABR) precisely reveals the functional integrity of the vestibulocochlear nerve leading the electrical stimuli towards the cortex. Neuronal junction points in the brainstem as generator relay structures are identified in the form of waves in the electrophysiological recordings in normal subjects (C); however, they are not present in patients with a profound hearing loss (D). E-F: The objective estimation of hearing sensitivity was performed by auditory steady-state response (ASSR) tests. In a non-diseased subject, normal thresholds were registered on all the measured frequencies (E), while a profound hearing loss is shown in a patient with hereditary sensorineural deafness (F). G-H: Used while registering ABRs, synchronous activation is achieved in the cochlea, thus a more prominent CE chirp-LS stimuli wave IV-V is observed in a non-diseased subject (G). In patients with profound hearing loss, ABRs are missing (H).

3.2. Mutation of connexin genes in blood cells in patients with hearing loss

In all patients the most frequently occurring GJ genes in the cochlea were tested for mutations of GJB genes from DNA of blood cells as described above. Figure 2 shows the distribution in patients from Hungary involving 13 non-diseased patients and 80 patients selected for cochlear implantation. The results of the mutation analysis of GJB2, GJB3 and GJB6 genes are shown in Figure 2A. 25.0% of hearing loss patients carried a mutation in the GJB2 gene, and only 1 out of 80 patients (1.2%) had a mutation in the GJB3 gene (Figure 2A). Mutations in GJB6 genes were not detected in this study (Table 1). In the ancestors of the Hungarian Caucasian population, the 35delG mutation in the GJB2 gene appeared most frequently in homozygous state (50%) (Figure 2B) and c.35delG (p.Gly12ValfsTer2 (rs80338939)) in heterozygotes (50%). Among the heterozygotes, the tests showed 35% mutations of heterozygote c.35delG p.Gly12ValfsTer2 (rs80338939), 5% heterozygote missense c.101T>C p.Met34Thr (rs35887622), 5% heterozygote missense c.119C>A p.Ala40Glu (rs111033296) and 5% of compound heterozygous c.101T>C p.Met34Thr (rs35887622), GJB2: c.139G>T p.Glu47Ter (rs104894398). The distribution of these ratios for homozygotes and heterozygotes may change with time, but the rate of this change cannot be estimated at this moment.

Figure 2.

Genetic mutations for GJB genes were tested in hearing loss patients prior to implantation (n = 80). (A) Prevalence of GJB2 and GJB3 gene mutations in subjects with non-syndromic hearing impairment (n = 21/80). (B) Prevalence of different GJB2 mutations in subjects with non-syndromic hearing impairment (n = 20/80).

3.3. Distribution of connexins and Kir2.1 ion channels with modulators on blood cells

The expression of Cx26 and Cx43 channel proteins was abundant in non-diseased patients (control 1 and 2) but much poorer in blood cells of deaf patients as seen in Figure 3 and variable in hearing loss patients (see 1–3 on Figure 4). In all cells, the nuclei were counterstained with DAPI (blue) and scale bars are shown on each image. Thirteen patients with hearing loss were tested for ion channels and compared to controls (with same age and sex) in each experiment. The protein pattern of both Cx26 and Cx43 changed on the surface of blood cells (Figures 3 and 4), appearing as large patches in the control cells and reorganized in smaller groups of connexins in diseased cells. Furthermore, the shape of the area around the nucleus was round in diseased cells and the cytosol was disintegrated. The protein level of Cx26 was variable on the surface of blood cells from patients with hearing loss. We could not identify the GJB2 gene mutation in Patient 1, but Patient 2 and 3 showed mutations with decreased protein level of Cx26. We suppose that Patient 1 has a mutation in another type of gene.

Figure 3.

Pattern of connexin26 ion channels on blood cells of patients expecting cochlear implantation. Cx26: Connexin26, DAPI: 2,4-diamino-2-phenylindole.

Figure 4.

Alteration of protein levels of connexin43 ion channels in blood cells in patients with deafness. Representative figures from non-diseased and hearing loss patients. Cx43: Connexin43; DAPI: 2,4-diamino-2-phenylindole.

The Kir2.1 ion channels colocalized with SAP97 protein in non-diseased patients, but we determined only partial or no overlayed channel complexes (Figure 5) in cells from cochlear implant candidates. The protein pattern was altered and the levels were decreased in hearing loss patients compared to controls. The SAP97 anchoring protein is redistributed in the blood cells and do not colocalize often with Kir2.1 channels in diseased cells. The levels of Kir2.1 protein were varied in each cochlear implant candidates, just as in Patient 1 compared to Patient 2 or 3. The amount of SAP97 declined in the lymphocytes of Patient 2 and 3 with GJB2gene mutations. The Kir2.1 channels did not perfectly colocalize with SAP97 in the lymphocytes of Patients 1– 3 with hearing loss (Figure 5).

Figure 5.

The disrupted protein pattern and coexpression of Kir2.1 ion channel with declined SAP97 on blood cells of hearing loss patients. SAP97: Synapse-associated protein 97; DAPI: 2,4-diamino-2-phenylindole.

4. Discussion

The main purpose of this study was to detect the mutations of genes GJB2, GJB3 and GJB6 as well as the translated proteins Cx26, Cx43 and Kir2.1 ion channels from blood cells in cochlear implant candidates. The cochlear implantation was required in hearing impaired patients for based on indication criteria. Hearing sensitivity was evaluated with objective methodologies [56], applying the crosscheck principle. The outer and middle ear anatomy and function proved to be normal in all the recruited subjects of this cohort.

The study provided the following key results: (1) the different GJB mutations were detected in hearing loss in 50% homozygote and 50% heterozygote form for GJB genes in a Hungarian population. (2) Cx43 levels decreased moderately in blood cells. (3) Our investigation revealed a reduced level for Kir2.1 channels as well as for the SAP97 protein. (4) The extent of colocalization of Kir2.1 ion channels with SAP97 anchoring proteins was less marked or partially redistributed in blood cells from patients with hearing loss. (5) Cx26 mutation impacts hearing loss.

4.1. Significance of connexins in hearing system and alteration in deafness

These data are consistent with earlier reports on the decrease of GJB2 gene expression in deafness [7, 57], and this study is the first to demonstrate the declined Cx26 protein level in patients carrying these mutations. Recently, more than 100 mutations have been reported, among which the GJB2 gene mutations are the most common cause of nonsyndromic deafness [1]. In this study we demonstrated a similar ratio of GJB2 gene mutations in a Hungarian population in accordance with the earlier findings of Nagy et al. [7]. Additionally, more heterozygote forms were identified in this investigation. The position of joint mutations differs across many populations. This very likely holds true for other genes as well, but GJB2 gene is probably the most examined gene among the genes involved in hearing-related problems. The allelic frequency of three GJB2 gene mutations have been shown to exhibit differences based on ethnicity, which in some cases also translated to geographic regions [11]. The 35delG mutation of the coding exon of GJB2 gene has a frequency of 2–4% in the Caucasian population [58]. Geographically this holds true for Europe, the Middle East and some populations in North America.

The GJB2 gene encodes the Cx26 protein, which assembles to form channels between the cells in the cochlea. These gap junction proteins allow the rapid removal of K+ from the base of hair cells, resulting in the recycling of this ion back to the endolymph to maintain the cochlear homeostasis in humans [59]. Kamiya et al. investigated the expression of Cx26 and Cx30 in the gap junction macromolecular complex [60], where Cx26 is the most abundant channel in the cochlea of mice. They concluded that the disruption of Cx26 was the earliest alteration of the Cx26-dependent gap junction plaque during the embryonic development of mice with connexin-associated deafness. The degradation of the gap junction macromolecular complex leads to loss of hearing function [60] caused by diets [61].

The abnormal or missing gap junctions likely alter the level of potassium ions, which may affect the function and survival of cells that are essential for hearing in the inner ear. The spatial and temporal heteromeric associations of Cx26 and Cx30 proteins in the inner ear have been confirmed earlier [26, 62]. This finding has not been reconfirmed until now. Forge’s results had an essential role to understand the pathophysiologic processes of nonsyndromic deafness caused by mutations in GJB2 genes.

Previously, we have demonstrated that the Cx26 mutation frequently occurs in the Hungarian population [7]. In this study we demonstrated that the ratio of homozygotes and heterozygotes is 1.0:1.0 in the mutated GJB2 genes, which suggests that the frequency of heterozygotes is rather high in hearing impaired patients. Further investigations are required to identify additional mutated genes. The combination of heterozygote forms of additional channels may also be involved in the causes leading to deafness in the Caucasian population, because about 73.8% of hearing impaired subjects is not carriers for mutations of the GJB2 gene.

Connexins are 25% more abundant in the sensory epithelial cells of the inner ear than in mammalian supporting cell types and these cells infrequently contain more than 100,000 channels. Forge and co-workers have demonstrated [62] that four connexin isotypes, Cx26, Cx30, Cx31 and Cx43, can be found in different mammalian species, in the cochlea and three of them, Cx26, Cx30 and Cx43, in the vestibular organs. The spatial distribution of connexins in the inner ear has been extensively investigated and it was suggested that these connexin channels are isolated both spatially and functionally. The Cx26 and Cx30 are found in supporting cells of the organ of Corti, in the basal cell region of the stria vascularis, and in type 1 fibrocytes of the spiral ligament, but no other connexin type was detected in this area. Cx31 localizes around the type 2 fibrocytes and below the spiral prominence. Cx30 was not expressed here and the amount of Cx26 expression was low in the above areas [62]. Cx43 was only detected in one region where “tension fibrocytes” line the inner aspect of the otic capsule. It is an important result that Cx26 colocalizes with Cx30 as detected by electron microscopic and immunoprecipitation methods for protein expression.

The majority of gap junction forming proteins in the inner ear potassium-recycling pathway includes Cx26, Cx30 and Cx43. The heteromeric association of Cx26 and Cx30 proteins indicates a fine regulation in the connexin composition of the gap junction channels in the inner membrane of the cochlea, and the altered potassium homeostasis might also be related to the redistributed ion channels on blood cells. The heteromeric coexpression of Cx40-Cx43-Cx45 was evaluated by Desplantez et al. [63, 64] in liver cells, and low levels of Cx40/Cx43 coexpression was detected in heart tissues demonstrating that the Cx40:Cx43 ratio regulates the composition and electrical properties of gap junctions [65, 66, 67, 68], which may also be the case in the cochlea.

The age of the 35delG mutation was estimated by Van Lear and co-workers [12]. This mutation was tested in ancestors for about 500 generations, indicating an approximate age of 10,000 years in various populations. The mutations in the Hungarian Caucasian population demonstrate a European average.

We saw a high expression of Cx26 and Cx43 proteins in the blood cells of non-diseased patients where the high intensity staining on the surface of cells indicated a high abundance of Cx26. In the presence of the GJB2 gene mutation, the Cx26 protein level decreased and the pattern of the distribution was disrupted. These results suggest that the expression of GJB2 gene is regulated at the level of transcription and translation in non-diseased patients. Furthermore, it supported the results that the GJB2 gene deficiency is presumably associated with cochlear developmental disorders [66].

Our results indicate that the absence or a reduced presence of Cx26 channels contributes to the development of deafness in humans, which is in support of earlier results [1, 7, 57]. The widely distributed Cx26 and Cx30 and Cx43 proteins have an essential role in the regulation of early ear development [9, 26, 35] and also in the regulation of potassium pathways in the inner ear of adults [26, 62, 67].

4.2. The possible role of Kir2.1 ion channels in the cochlea

Kir2.x ion channels have an important physiological function in transporting potassium ions back into the cells, but the mutations of these ion channels are rarely detected. The role of Kir2.1 ion channels, well-known in Andersen-Tawil syndrome, has only recently been confirmed for deafness [36, 37, 69], and this suggests the importance of in the auditory system. The spatial and temporal localization of Kir2.x channels has been mapped in the inner ear by Forge et al. [62], Jagger et al. [26] and its significance has been described by Meredith et al. [70]. Kir2.1 was characterized as a strong inwardly rectifying ion channel in the vestibular type II hair cells by Zampini et al. [18], Correia et al. [71] in avian and mammalian settings too [47, 69]. An inwardly rectifying potassium channel itself, Kir5.1 plays a vital role in regulating cochlear K+ circulation which is necessary for normal hearing, and it has age-related reduction in expression [71] just like SAP97, but contrary to the Kir2.1 ion channels [45]. The developmental study by Ruan et al. [20, 21] carried out in mouse has shown the temporal pattern of Kir2.1 channels in different parts of the hearing system. Kir2.1 has a temporal expression in the hair cells of mouse cochleae that correlates with the functional maturation of the hair cells and the neurons. The stronger signals were generally detected in the apical parts of the cochlea and on row 3 outer hair cells after birth. However, the Kir2.1 ion channels in human adults have been detected mostly in the vestibular system. In all types of cells the mutations of these channels still indicated that the homomer and heteromer Kir2.x channel compositions are necessary in the mammalian inner ear. Lewin and Holt [47], and also Meredith and Rennie [70] identified the functional contribution of Kir2.1 in the IK1 current in utricle hair cells. They demonstrated that Kir2.1 is required for IK1 currents in type II utricle hair cells and that Kir2.1 contributes to the hyperpolarized resting potentials [46] and also to the fast, small amplitude receptor potentials.

The effective functioning of the Kir2.x protein tripartite complex, requires an association of proteins involving SAP97 and calcium calmodulin kinase II (CaMKII) with Kir2.1 ion channels, and Kir2.6 ion channel also has an essential role to deliver the matured Kir2.x protein to the membrane surface [42, 43]. In this study, we showed that the amount of Kir2.1 channel was close to the control in hearing loss patients where we could not detect GJB2 gene mutations. The low level of SAP97 anchoring protein decreased drastically in hearing loss patients. Our results confirmed the colocalization of Kir2.1 ion channel with SAP97 anchoring protein in non-diseased patients but only partial colocalization with disrupted clustering occurred on the surface of blood cells in patients with deafness. This redistribution of the Kir2.1 channel complex, and also the clearly visible reorganization of Cx26 and Cx43 channels, suggests the instability of Kir2.1 and connexin macromolecule complexes in blood cells. This redistribution of Kir2.1 ion channels and Cx26 on the surface of blood cells may lead to a weakened physiological function of Kir2.1 channels and gap junctions, which, in turn, may influence the potassium homeostasis in the sensorineural system [73, 74]. These direct or indirect interactions are essential for the normal physiological function of the Kir2.1 complex and inward rectifier currents contributing to normal potassium ion homeostasis [71, 72].

The development of new diagnostic techniques for molecular biology analysis together with deep insights into molecular physiology requires subcellular nanotechnology tools in biomedical research and clinical diagnostics. In this study, we report on hearing impaired patients with a series of hearing screenings using modern equipment, and we have developed a new molecular method to study the critical potassium ion channels contributing to normal cochlear function.

5. Conclusion

Altered expression of Cx26 with Kir2.1 ion channel complex in hearing loss patients profoundly determines the potassium-recycling pathway and the alteration of these channels in blood cells in deafness detectable using molecular tools.

The Kir2.x ion channels and connexin channels may have an essential role in the IK1 currents of the cochlea and vestibule during the development process and may serve as diagnostic markers in the early stage of the pathophysiology of hearing loss.



This study was supported by grant EFOP-3.6.2-16-2017-00009, which supported MSz, NN, JGK, JAJ, and RN. VSz was supported through the NKFIH-112688 and OTKA K112688 grants. The authors thank Professor Dr. Gyozo Garab and his group for complementary protein studies, Dr. Ferhan Ayaydin, Zsuzsanna Koszo, Ildiko Kelemen Valkonyne, and Peter Deak for their assistance in confocal microscopy.

Conflict of interest

The authors have nothing to disclose.

Author contributions

MS was the mentor who guided the genetic research study; JAJ and LR tested patients and wrote the manuscript; NN designed and performed the genetic analyses; JGK, AN, RN KH, VSZ carried out protein experiments, analyzed data, and VSZ, FO, JAJ and KH wrote the first draft of the manuscript.


ABRauditory brain stem responses
AEPauditory evoked potentials
APaction potential
ARNSHLautosomal recessive non-syndromic hearing loss
ASSRauditory steady-state responses
CaMKIIcalcium calmodulin kinase II
DBSdried blood spots
DNAdeoxyribonucleic acid
DPOAEdistortion product otoacoustic emission
EDTAethylenediaminetetraacetic acid
EOAEevoked otoacoustic emissions
GJB2gap junction protein beta 2
GJB3gap junction protein beta 3
GJB6gap junction protein beta 6
Kv-typevoltage-gated potassium channel
Kir2.xpotassium inward-rectifier ion channel 2.x
MAGUKmembrane associated guanylate kinase
OAEotoacoustic emission
PCRpolymerase chain reaction
PDSPendred syndrome
PMplasma membrane
SAP97synapse-associated protein 97
SNHLsensorineural hearing loss
SOAEspontaneous otoacoustic emission

© 2018 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Viktoria Szuts, Janos Andras Jarabin, Nikoletta Nagy, Ferenc Otvos, Roland Nagy, Attila Nagy, Katalin Halasy, Laszlo Rovo, Marta Szell and Jozsef Geza Kiss (October 10th 2018). Altered Potassium Ion Homeostasis in Hearing Loss, Ion Channels in Health and Sickness, Kaneez Fatima Shad, IntechOpen, DOI: 10.5772/intechopen.77732. Available from:

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