kobe university repository : kernel4 52 introduction 53 reactive oxygen species (ros), including...
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Kobe University Repository : Kernel
タイトルTit le
Hearing vulnerability after noise exposure in a mouse model of react iveoxygen species overproduct ion
著者Author(s)
Morioka, Shigefumi / Sakaguchi, Hirofumi / Yamaguchi, Taro / Ninoyu,Yuzuru / Mohri, Hiroaki / Nakamura, Takashi / Hisa, Yasuo / Ogita,Kiyokazu / Saito, Naoaki / Ueyama, Takehiko
掲載誌・巻号・ページCitat ion Journal of Neurochemistry,146(4):459-473
刊行日Issue date 2018-08
資源タイプResource Type Journal Art icle / 学術雑誌論文
版区分Resource Version author
権利Rights
© 2018 Internat ional Society for Neurochemistry. This is the peerreviewed version of the following art icle: [Journal of Neurochemistry,146(4):459-473, 2018], which has been published in final form atht tps://doi.org/10.1111/jnc.14451. This art icle may be used for non-commercial purposes in accordance with Wiley Terms and Condit ionsfor Use of Self-Archived Versions.
DOI 10.1111/jnc.14451
JaLCDOI
URL http://www.lib.kobe-u.ac.jp/handle_kernel/90005448
PDF issue: 2021-05-29
1
Hearing vulnerability after noise exposure in a mouse model of reactive oxygen 1
species overproduction 2
3
Shigefumi Morioka1,2, Hirofumi Sakaguchi2,*, Taro Yamaguchi3, Yuzuru Ninoyu1, Hiroaki Mohri1, 4
Takashi Nakamura1, Yasuo Hisa2,4, Kiyokazu Ogita3, Naoaki Saito1, Takehiko Ueyama1,* 5
6
1Laboratory of Molecular Pharmacology, Biosignal Research Center, Kobe University, Kobe 657-7
8501, Japan; 2Department of Otolaryngology-Head and Neck Surgery, Kyoto Prefectural 8
University of Medicine, Kyoto 602-8566, Japan; 3Laboratory of Pharmacology, Faculty of 9
Pharmaceutical Sciences, Setsunan University, Hirakata 573-0101, Osaka, Japan; 4Faculty of 10
Health and Medical Sciences, Kyoto Gakuen University, Kyoto 615-8577, Japan. 11
12
Running title: Hearing vulnerability after NE in NOX4-TG mice 13
Key words: antioxidant, Hsp47, hearing loss, NOX4, ROS, transgenic mouse model 14
15
*Corresponding authors: 16
Takehiko Ueyama 17
1-1 Rokkodai-cho, Nada-ku, Kobe 657-8501, Japan 18
Tel: +81-78-803-5962, Fax: +81-78-803-5971, E-mails: [email protected] 19
Hirofumi Sakaguchi 20
465 Kajii-cho, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, Japan 21
Tel: +81-75-251-5603, Fax: +81-75-251-5604, E-mail: [email protected] 22
2
Abstract 23
Previous studies have convincingly argued that reactive oxygen species (ROS) contribute to the 24
development of several major types of sensorineural hearing loss, such as noise-induced hearing 25
loss (NIHL), drug-induced hearing loss, and age-related hearing loss. However, the underlying 26
molecular mechanisms induced by ROS in these pathologies remain unclear. To resolve this issue, 27
we established an in vivo model of ROS overproduction by generating a transgenic (TG) mouse 28
line expressing the human NADPH oxidase 4 (NOX4, NOX4-TG mice), which is a constitutively 29
active ROS-producing enzyme that does not require stimulation or an activator. Overproduction 30
of ROS was detected at the cochlea of the inner ear in NOX4-TG mice, but they showed normal 31
hearing function under baseline conditions. However, they demonstrated hearing function 32
vulnerability, especially at high-frequency sounds, upon exposure to intense noise, which was 33
accompanied by loss of cochlear outer hair cells (OHCs). The vulnerability to loss of hearing 34
function and OHCs was rescued by treatment with the antioxidant Tempol. Additionally, we found 35
increased protein levels of the heat shock protein 47 (HSP47) in models using HEK293 cells, 36
including H2O2 treatment and cells with stable and transient expression of NOX4. Furthermore, 37
the upregulated levels of Hsp47 were observed in both the cochlea and heart of NOX4-TG mice. 38
Thus, antioxidant therapy is a promising approach for the treatment of NIHL. Hsp47 may be an 39
endogenous antioxidant factor, compensating for the chronic ROS overexposure in vivo, and 40
counteracting ROS-related hearing loss. 41
3
Abbreviations 42
4-HNE, 4-hydroxynoneal; Ab, antibody; ABR, auditory brainstem response; BCA, bicinchoninic 43
acid; CL, chemiluminescence, HBSS, Hank's balanced salt solution; HC, hair cell; H2O2, hydrogen 44
peroxide; Hsp47, heat shock protein 47; IB, immunoblotting; IHC, inner HC; IP, 45
immunoprecipitation; LB, spiral limbus; mAb, monoclonal antibody; NE, noise exposure; NIHL, 46
noise-induced hearing loss; NOX, NADPH oxidase; Nrf2, nuclear factor erythroid-2 related factor 47
2; OC, organ of Corti; OHC, outer hair cell; PFA, paraformaldehyde; polyA, polyadenylation; ROS, 48
reactive oxygen species; SG, spiral ganglion; SL, spiral ligament; LB, spiral limbus; SNHL, 49
sensorineural hearing loss; SOD, superoxide dismutase; SPL, sound pressure level; SV, stria 50
vascularis; Tempol (4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl); TG mice, transgenic mice 51
4
Introduction 52
Reactive oxygen species (ROS), including superoxide anions, hydroxyl radicals, hydrogen 53
peroxide (H2O2), and singlet oxygen, are known to play key roles in numerous physiological and 54
pathological processes (Leto et al. 2009). Although appropriate levels of ROS are indispensable 55
for cell survival and differentiation (Leto et al. 2009), high levels induce oxidative stress in several 56
organs, including the inner ear, heart, brain, liver, and kidney, thereby triggering pathologies, such 57
as sensorineural hearing loss (SNHL), myocardial infarction, heart failure, neurodegenerative 58
disorders, and liver and renal fibrosis (Altenhofer et al. 2012, Wong & Ryan 2015, Yang et al. 59
2015a, Ma et al. 2017). 60
Hearing loss is one of the most common sensory deficits in humans, and about 90% of the 61
cases are accounted for by SNHL (Li et al. 2017). Most SNHL is caused by loss of hearing 62
sensitivity due to damage and/or cell death in the cochlea, an auditory detection organ (Wong & 63
Ryan 2015). The cochlea contains two types of hair cells (HCs), i.e., inner HCs (IHCs) and outer 64
HCs (OHCs). IHCs are responsible for detecting sounds and transmitting the acoustic information 65
to the brain. In contrast, OHCs are responsible for an active mechanical amplification process that 66
leads to high sensitivity and fine frequency resolution. The cochlea has a tonotopic gradient along 67
the length of the lumen in which the basal turn detects high-frequency sounds, while the apical 68
turn detects low-frequency sounds (Goutman et al. 2015, Wong & Ryan 2015). 69
Previous studies have convincingly argued that ROS contribute to the development of several 70
major types of SNHL, such as noise-induced hearing loss (NIHL), drug-induced hearing loss; 71
including the one caused by cisplatin; and age-related hearing loss (Wong & Ryan 2015, Yang et 72
al. 2015a). Among these pathologies, the ototoxic effect of oxidative stress has been most 73
frequently studied in NIHL. For example, biomarkers of lipid peroxidation, such as 4-74
hydroxynoneal (4-HNE) and malondialdehyde, are reportedly increased in the cochlear sensory 75
5
epithelium after noise exposure (NE) (Choi & Choi 2015, Le Prell et al. 2007, Fetoni et al. 2013). 76
In addition, antioxidants such as N-acetyl-L-cysteine (Le Prell et al. 2007, Coleman et al. 2007, 77
Choi et al. 2008) and 4-hydroxy-2,2,6,6-tetramethylpiperidine-n-oxyl (Tempol) (Murashita et al. 78
2006, Minami et al. 2007) have been reported to have a therapeutic effect on NIHL. Peri-traumatic 79
application of these drugs can decrease the permanent hearing threshold shift induced by NE. 80
Moreover, supplementation of antioxidants in animals and humans has been reported to prevent 81
progression of age-related hearing loss in some studies (Tavanai & Mohammadkhani 2017). 82
NADPH oxidase 3 (Nox3), one of the main NOXs in the inner ear, has been found to be 83
increased in the cochlea after administration of cisplatin in rats, which leads to ROS 84
overproduction and induces apoptosis in the cochlea, including OHC (Mukherjea et al. 2008, Kaur 85
et al. 2016). Subsequently, a small interfering RNA (siRNA) for Nox3 was reportedly effective in 86
reducing OHC damage and hearing function in rats (Mukherjea et al. 2010). On the contrary, Nox3 87
was proposed to be protective against NE based on a genome-wide association study, in which 88
Nox3 knockout (KO) mice were shown to be susceptible to NIHL (Lavinsky et al. 2015). In 89
addition, increased expression of Nox4 and Nox1 as well as Nox3 after administration of cisplatin 90
was reported in the mouse cochlea (Kim et al. 2010). Thus, ROS function and its underlying 91
molecular mechanism inducing SNHL may be different depending on the injury applied and the 92
Nox isoform involved. 93
To advance the understanding of the underlying molecular mechanisms in ROS-induced SNHL, 94
and especially in NIHL, we established an in vivo model for ROS overproduction by generating a 95
transgenic (TG) mouse line expressing human NOX4, which is a constitutively active ROS-96
producing enzyme (Leto et al. 2009). 97
6
Materials and methods 98
Plasmids 99
The human NOX4 in pcDNA3.1 was a kind gift from Dr. Thomas L. Leto (Boudreau et al. 100
2014). NOX4 with HindIII/NotI sites at the 5´ and 3´ ends was amplified by PCR, cloned into the 101
HindIII/NotI site of the p3xFLAG-CMV-10 vector (Sigma-Aldrich, St Louis, MO, USA), and 102
named 3xFLAG-NOX4. NOX4(1-305) in pcDNA3.1 was generated by insertion of a stop codon 103
immediately after Ser305 of NOX4 using the QuikChange Lightning Site-Directed Mutagenesis Kit 104
(Agilent Technologies, Santa Clara, CA, USA). In NOX4(1-305), the C-terminal, FAD-, and 105
NADPH-binding domains have been deleted, leading to loss of the ROS-generating capability 106
(Boudreau et al. 2014). 107
108
Generation of transgenic mice 109
This study was approved by the Institutional Animal Care and Use Committee and carried out 110
according to the Kobe University Animal Experimentation Regulation (24-04-08 and 26-03-05). 111
This study was not pre-registered. 112
Two PCR products, 3xFLAG-NOX4, with an XhoI site at the 5´ end, and the polyadenylation 113
(polyA) signal of the rabbit -globin, with an StuI site at the 3´ end, were amplified by PCR and 114
cloned into the XhoI/StuI sites of the pCAGGS vector, containing the CAG promoter, using the In-115
Fusion HDTM cloning kit (Takara Bio Inc., Tokyo, Japan). The final construct is shown is Fig. 1A. 116
After confirming the identity of the plasmid by sequencing and the protein expression of 117
3xFLAG-NOX4 in HEK293 cells by immunoblotting, its capabilities for ROS production were 118
examined. ROS production was found to be comparable between 3xFLAG-NOX4 and untagged 119
NOX4 (Fig. 1B). Thereafter, a purified fragment digested with SalI and StuI, which contained the 120
CAG promoter, 3xFLAG-NOX4, and polyA, was injected into fertilized eggs obtained at the 121
7
pronuclear stage from C57BL/6 mice (UNITECH, Kashiwa, Japan). Founder (F0) and first 122
generation (F1) mice were screened by PCR using the following primer pair: 5 ′ -123
CCTACAGCTCCTGGGCAACGTGTGCTGGT-3 ′ (located in the CAG promoter) and 5 ′ -124
AGAGGGAAAAAGATCTCAGTGGTAT-3′ (located in the polyA). We obtained four F0 and two 125
F1 mouse lines. The copy number of the transgene (CAG promoter; 3xFLAG-NOX4;polyA), as 126
integrated into the genome, was evaluated by Southern blotting; one line carried 12 and the other 127
carried 17 copies. The second and later generations of heterozygous NOX4-TG mice were used for 128
subsequent analyses. Offspring were genotyped by PCR using the above-mentioned primer pair. 129
All mice were identified by numbered ear tags. Mice were housed in specific pathogen-free 130
conditions using the individually ventilated cage system (Techniplast, Tokyo, Japan), and allowed 131
food and water ad libitum. The animal facility was maintained on a 14 h light and 10 h dark cycle 132
at 23 ± 2 °C and 50 ± 10% humidity. Mice from control group were always treated and assessed 133
first, followed by experimental group. No randomization was performed. Females were used in 134
the analyses unless otherwise indicated (mice younger than 1 week were not differentiated based 135
on sex). Age-matched wild type (WT) siblings were used as control. 136
137
Antibodies and chemicals 138
The following specific antibodies (Abs) were used (monoclonal unless indicated): 4-HNE 139
(HNE-J2; JaICA, Fukuroi, Japan; 1:100), heat shock protein 47 (HSP47) polyclonal (H-300; 140
RRID:AB_2185194, Santa Cruz Biotechnology; Santa Cruz, CA, USA; 1:50 for 141
immunohistochemistry and 1:200 for immunoblotting), and Hsp47 (EPR4217; 142
RRID:AB_10888995, Abcam; 1:200 for immunohistochemistry and 1:1000 for immunoblotting). 143
The anti-p22phox (#449, 1:200) Ab has been described previously (Ueyama et al. 2006). Magnetic 144
bead-conjugated anti-FLAG Ab (RRID:AB_2716804) and horseradish peroxidase (HRP)-145
8
conjugated anti-FLAG (1:2000, RRID:AB_2687989), anti-glyceraldehyde 3-phosphate 146
dehydrogenase (GAPDH; 1:2000, RRID:AB_10699462), anti-tubulin(1:2000, 147
RRID:AB_10695326), and anti-actin-(1:2000, PM053-7) Abs were obtained from MBL 148
International (Nagoya, Japan). Alexa Fluor 488-conjugated phalloidin (1:500, AB_2315147) and 149
HRP-conjugated secondary (1:10,000) Abs were obtained from Invitrogen (Carlsbad, CA, USA) 150
and Jackson Immuno Research Laboratories (West Grove, PA, USA), respectively. Validation data 151
for Abs is available from the companies. Tempol (4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl), 152
an antioxidant metabolizing superoxide and H2O2 (Wilcox & Pearlman 2008), and diphenylene 153
iodonium (DPI) were obtained from Sigma-Aldrich. Chloral hydrate, H2O2, and HistoVT One 154
were obtained from Nacalai Tesque (Kyoto, Japan). 155
156
Cell culture and transfection 157
HEK293 cells (ATCC, Cat# CRL-1573, RRID:CVCL_0045) were maintained in Eagle’s 158
minimal essential medium (Wako Pure Chemical Industries, Osaka, Japan) containing 10% fetal 159
bovine serum (Nichirei Biosciences, Tokyo, Japan), 100 M nonessential amino acids (Wako), 160
100 units/mL penicillin, and 100 g/mL streptomycin at 37 °C in 5% CO2. Stable protein-161
expressing HEKFLAG-NOX4 and HEKcont cells were generated by transfection of the 3xFLAG-NOX4 162
or the control p3xFLAG-CMV-10 plasmids, respectively, by electroporation (NEPA21; NEPA 163
GENE, Ichikawa, Japan), followed by selection with the antibiotic G418 (0.5 mg/mL; Wako). 164
For transfection, HEK293 cells were seeded into 6-well dishes at 2.5 × 105 cells/well, 48 h 165
before. Plasmids were transfected into HEK293 cells using FuGENE6 (Promega, Madison, WI, 166
USA). Six hours after transfection, the cell culture medium was replaced with complete medium. 167
168
Sample preparation and immunoblotting 169
9
The membranous cochleae (two from each mouse) of postnatal day 7 (P7) or P46 pups, and 170
the heart of adult NOX4-TG and control mice were homogenized and lysed in lysis buffer 171
(Nakamura et al. 2017) with 0.1% Triton X and protease inhibitor cocktail (Nacalai Tesque). Forty-172
eight hours after transfection with plasmids or 24 h after treatment with H2O2, HEK293 cells were 173
lysed in the same lysis buffer as above. Each lysate was centrifuged at 13,000 g for 10 min at 4 °C 174
and supernatants were measured with the bicinchoninic acid (BCA) protein assay kit (Thermo 175
Fisher Scientific, Waltham, MA, USA). The supernatants were separated by SDS-PAGE and 176
transferred onto PVDF membranes. The membranes were incubated overnight at 4 °C with the 177
anti-FLAG, anti-HSP47, or anti-p22phox Ab, and then incubated for 30 min at 23 °C with a HRP-178
conjugated secondary Ab. Immunoreactivity was detected using the ECL detection system (Bio-179
Rad Laboratories, Hercules, CA, USA). For quantitative assessment of immunoreactive bands, 180
ImageJ software (National Institutes of Health) was used as previously described (Ueyama et al. 181
2016). Protein expression levels were normalized to those of tubulin, actin-, or GAPDH. 182
183
ROS production assay 184
Twenty-four hours after transfection, 2 × 105 HEK293 cells in Hank's balanced salt solution 185
(HBSS; Wako) were used for assays. For detection of overall ROS, we performed a 186
chemiluminescence (CL) assay. Cells were incubated in the presence of 200 M luminol and 10 187
units/mL HRP (Sigma-Aldrich) for 10 min, and CL signal was detected using a luminometer 188
(Mithras LB940; Berthold Detection Systems, GmbH), as previously described (Ueyama et al. 189
2015). 190
To measure ROS production in the cochleae of NOX4-TG mice, two membranous cochleae 191
were dissected from each NOX4-TG or control mouse at P7. Tissues of the organ of Corti (OC) 192
and the lateral wall of the cochlea, including the spiral ligament (SL) and stria vascularis (SV), 193
10
were collected in HBSS. After homogenization, lysates were centrifuged at 20,000 g for 15 min at 194
4 °C and precipitates containing NOX4 were resuspended in HBSS. After measuring the protein 195
concentration of the membrane pellets using the BCA protein assay kit, equal amounts of protein 196
were used for CL detection of ROS using the luminometer, and incubated for 10 min in the 197
presence of 10 M FAD, 500 M NADPH, 1 mM NaN2, 200 M luminol, and 10 units/mL of 198
HRP, as previously described (Ago et al. 2004, Ueyama et al. 2015). ROS production was inhibited 199
by a 10-min prior incubation with 0.1 M Tempol or 5 M DPI. Because this ROS assay was 200
performed in-vitro (cell-free), Tempol was used at the minimum concentration previously reported 201
(Bhattacharyya et al. 2008). 202
203
Immunohistochemistry 204
To examine surface preparations of the cochleae, dissected tissues were fixed with 4% 205
paraformaldehyde (PFA) in 0.1 M phosphate buffer (PB, pH 7.4) and decalcified in 0.12 M EDTA 206
for 1 week at 4 °C (Ueyama et al. 2014). After permeabilization with phosphate-buffered saline 207
(PBS) containing 0.3% Triton X-100, fixed tissues were incubated with Alexa Fluor 488-208
conjugated phalloidin for 2 h at 23 °C. Stained tissues were mounted in Prolong anti-fade 209
(Invitrogen) with a coverslip and observed under an LSM700 confocal microscope (Carl Zeiss, 210
Jena, Germany). To evaluate OHC loss after NE, the percentages of remaining OHCs were 211
calculated separately at the apical, middle, and basal turns of the cochlea. 212
To analyze cross-sections of cochleae, tissues were isolated from P14 or adult mice and fixed 213
with 4% PFA in 0.1 M PB. Decalcified cochleae were embedded into paraffin blocks and cut into 214
6-m slices on a Leica RM2125 RTS manual rotary microtome (Leica Biosystems, Wetzlar, 215
Germany). Sections were immunostained after deparaffinization through a xylene and ethanol 216
graded series. For antigen unmasking, the slides were bathed in HistoVT One (Nacalai Tesque) for 217
11
20 min at 80 °C. Retrieved tissues were blocked in either 10% normal goat serum and 3% H2O2 218
(Nacalai Tesque) in PBS/0.03% Triton, or in 0.1% phenylhydrazine (Nacalai Tesque) in 219
PBS/0.03% Triton for 20 min at 23 °C. The tissues were incubated with primary Abs for 2 h at 220
23 °C in PBS/0.03% Triton, followed by MACH 2 Universal HRP-Polymer Detection (BIOCARE 221
Medical, Pacheco, CA, USA) for 30 min at 23 °C. 222
To analyze cryosections of hearts, adult mice were transcardially perfused with ice-cold 0.9% 223
saline solution, and subsequently with 4% PFA in 0.1 M PB. Hearts were dissected and post-fixed 224
overnight in the same fresh fixative. Twenty-μm cryosections were immunostained for HSP47, 225
followed by MACH 2 Universal HRP-Polymer Detection, as previously described (Nakamura et 226
al. 2017). Sections were visualized after staining with 3,3-diaminobenzidine tetrahydrochloride 227
(DAB, Sigma-Aldrich) and 0.02% H2O2 in Tris-buffered saline, pH 7.6. Slides were washed in 228
PBS/0.03% Triton and mounted in Entellan New (Merck Millipore, Billerica, MA, USA), 229
coverslipped, and photographed under a light microscope (Axioplan II; Carl Zeiss) equipped with 230
a DP26 camera (Olympus, Tokyo, Japan). 231
For the quantitative assessment of DAB intensity (evaluated using 4-HNE or Hsp47 Ab), we 232
used ImageJ software and the color deconvolution plugin for proper separation of the DAB color 233
spectra, as previously described (Varghese et al. 2014). Briefly, the region of interest (ROI) was 234
manually determined with the polygon or freehand tool, and then the deconvoluted image was 235
analyzed pixel-by-pixel. The color threshold for the positive area was defined in the range of 61–236
125/255, and the ratio of the positive to the total image area was calculated and presented as a 237
percentage of the control sample ratio. 238
239
Auditory brainstem response measurement and NE 240
For ABR measurements (Ueyama et al. 2016), mice were anesthetized with chloral hydrate 241
12
(500 mg/kg, i.p.) and stainless-steel needle electrodes were placed at the vertex and ventro-lateral 242
to the left and right ears. Electroencephalographic recording was performed with BioSigRP 243
Software and the TDT System 3 (Tucker-Davis Technologies, Alachua, FL, USA), in order to 244
generate a click or tone-burst stimulation at 4, 12, or 20 kHz (click, 4, 12, and 20 kHz for mice 245
under baseline conditions; 4, 12, and 20 kHz for mice in the NE experiment). ABR waveforms 246
were recorded for 12.8 ms at a sampling rate of 40,000 Hz with 505,000 Hz bandpass-filter settings. 247
Waveforms from 500 stimuli were averaged. ABR threshold was determined by decreasing the 248
sound intensity by 5-dB steps from 90 dB sound pressure level (SPL) and defined as the lowest 249
stimulus intensity that produced a reliable wave III on the ABR. When there was no response to 250
the stimulation at 90 dB, the threshold was considered as 100 dB. Blinded data analysis was 251
performed by two otologists or two scientists. ABR of control and NOX4-TG mice under baseline 252
conditions was measured at the age of 3, 5 (14.3–15.7 g), 7 and 24 (27.0–30.0 g) weeks. The 253
experiments were terminated if the mice showed signs of unbearable pain. 254
255
For NE experiments, 5-week-old control and NOX4-TG mice were anesthetized with chloral 256
hydrate and exposed to 110 dB SPL of octave-band noise, centered at 8 kHz, for 1 h inside a sound 257
chamber. These conditions of noise exposure were shown to cause a permanent threshold shift in 258
WT mice (Yamaguchi et al. 2017). Each animal was placed in a cage and the cage placed in the 259
sound chamber, which was fitted with a speaker (300 HT; FOSTEX, Akishima, Japan) driven by 260
a noise generator (SF-06; RION, Kokubunji, Japan) and power amplifier (DAD-M100proHT; 261
FLYING MOLE, Hamamatsu, Japan). To ensure the uniformity of the stimulus, we calibrated and 262
measured the sound levels with a sound-level meter (NL-26; RION), positioned at the level of the 263
animal’s head. The ABRs were measured immediately before NE. Then, ABR was sequentially 264
measured immediately after NE (day 0), and on days 1, 2, 5, 7, and 14 after NE. Hearing 265
deterioration due to NE was evaluated by measuring the ABR threshold shift, calculated by the 266
13
differences in ABR threshold before and after the NE test. In the antioxidant rescue experiment, 267
Tempol was injected intraperitoneally twice, immediately before and 24 h after NE, at a 268
concentration of 300 mg/kg, determined based on previous studies (Lahiani et al. 2016). During 269
the experiments, the mice were observed through a small window in the sound chamber, and the 270
experiments were terminated if the mice showed signs of unbearable pain. 271
272
Immunoprecipitation and mass spectrometry 273
HEKcont and HEKFLAG-NOX4 cells were homogenized in ice-cold buffer (20 mM Tris-HCl, pH 274
7.4, 120 mM NaCl, 1 mM EDTA, 5 mM EGTA, and 0.3% CHAPS) containing protease and 275
phosphatase inhibitor cocktails. Lysates were immunoprecipitated with anti-FLAG Ab-conjugated 276
magnetic beads. The immunoprecipitates were washed three times with the homogenization buffer, 277
separated by SDS-PAGE, and then analyzed by silver staining (Silver Stain MS Kit; Wako) or 278
immunoblotting. Subsequently, analysis of protein sequences by mass spectrometry was carried 279
out as described previously (Oshiro et al. 2007). Briefly, the silver-stained gel regions that seemed 280
to be different between the HEKcont and HEKFLAG-NOX4 samples were broadly excised and de-281
stained. The proteins in the gels were reduced and alkylated, followed by in-gel digestion with 282
trypsin in 25 mM ammonium bicarbonate for 15 h at 37 °C. The resulting peptides were then 283
subjected to liquid chromatography electrospray ionization mass spectrometry/mass spectrometry 284
(MS/MS) using the LCQ Advantage ion-trap mass spectrometer (Thermo Finnigan, Somerset, NJ, 285
USA). Protein identification, based on product ion mass lists, was performed by MASCOT 286
“MS/MS ion search.” 287
288
Statistical analysis 289
The exact number of experiments for each condition is provided in the figure legends. All data 290
14
are presented as the mean ± SEM. Two groups were compared using an unpaired, two-tailed 291
Student’s t-test. For comparisons of more than two groups, one-way or two-way ANOVA was 292
performed, followed by Bonferroni’s post-hoc test for pairwise group differences. Statistical 293
analyses were performed using Prism 6.0 software (GraphPad). Sample size calculation was not 294
performed. 295
15
Results 296
Generation of NOX4-TG mice 297
Low levels of Nox4 and Nox1 are detected in the mouse cochlea and these levels are increased 298
after administration of cisplatin in the mouse cochlea (Kim et al. 2010). NOX3 is one of the main 299
NOX isoforms in the inner ear; however, it is a multicomponent enzyme that requires at least four 300
other components (p22phox, Noxo1 or p47phox, Noxa1 or p67phox, Rac) in order to work functionally 301
in mouse cells (Ueyama et al. 2006, Leto et al. 2009). In addition, the effects of NOX3 after injury 302
are still controversial. For example, NOX3 is ototoxic after administration of cisplatin (Mukherjea 303
et al. 2008, Kaur et al. 2016), whereas it is protective after NE (Lavinsky et al. 2015). However, 304
NOX4 heterodimer with p22phox is the only constitutively active enzyme in the seven-membered 305
NOX family, which produces ROS without the need for a co-activator or stimulation (Leto et al. 306
2009). Therefore, to establish a mouse model with overproduction of ROS in the cochlea, we 307
decided to generate NOX4-TG mice. The expression levels of endogenous p22phox protein are 308
upregulated by introduction of exogenous NOX4 (Leto et al. 2009); hence we reconstituted NOX4-309
based ROS production by a single transfection of NOX4 expressing plasmid, without p22phox. By 310
using a luminol-based method and HEK293 cells expressing various NOX4 expression or mock 311
plasmids, we confirmed that untagged and 3xFLAG-tagged NOX4 at the N-terminus (3xFLAG-312
NOX4) showed comparable ROS-production capabilities (Fig. 1B), consistent with a previous 313
report (Martyn et al. 2006). In NOX4-TG mice, the expression of 3xFLAG-NOX4 was systemically 314
controlled by the CAG promoter (Fig. 1A). Hence, we confirmed the capability for ROS production 315
of two F1 NOX4-TG mouse lines obtained, by using primary fibroblasts and astrocytes (data not 316
shown). ROS production was higher in cells from mice carrying 17 copies of the transgene than 317
from mice carrying 12 copies, and thus further studies were performed using the mouse line 318
carrying 17 copies. NOX4-TG mice were fertile and did not show any gross body abnormalities. 319
16
320
Overproduction of ROS in the inner ear of NOX4-TG mice 321
Immunoblotting analysis using a FLAG Ab showed that FLAG-tagged NOX4 protein was 322
expressed in the cochlea and heart of NOX4-TG but not of control mice at P7 (Fig. 1C). We then 323
examined the in vivo function of FLAG-NOX4 in the cochlea of NOX4-TG mice at P7. A ROS 324
production assay using membranous cochleae showed that ROS production was higher in NOX4-325
TG than in control mice. As expected, the generation of ROS in NOX4-TG cochleae was 326
suppressed to control levels after incubation with the antioxidant Tempol (Wilcox & Pearlman 327
2008) or the NOX inhibitor DPI (Fig. 1D). Furthermore, although the morphology of the OC at 328
the basal turn of the cochlea in NOX4-TG mice showed no apparent abnormality, 4-HNE 329
immunoreactivity, a marker for lipid peroxidation (Zarkovic et al. 2017), was higher in the SL, SV, 330
and OHCs of the cochlea in NOX4-TG than in control mice (Fig. 1E). Taken together, these results 331
(ROS overproduction and lipid peroxidation in the cochlea) indicate that NOX4-TG mice can be 332
used as a model for ROS-overproduction in the cochlea. 333
334
Normal hearing function and cochlear morphology in NOX4-TG mice 335
We evaluated the hearing function of 3-, 5-, 7-, and 24-week-old NOX4-TG mice, bred under 336
normal noise conditions, by measuring the ABR to click and tone-burst stimuli, the latter at 337
frequencies of 4, 12, and 20 kHz (Fig. 3D). Unexpectedly, we did not find any significant 338
difference in the ABR between NOX4-TG and control mice regardless of stimulus or age, 339
indicating that there is no direct effect of ROS overproduction on hearing function in mice bred 340
under normal noise conditions. ABR data at 5 and 24 weeks are shown in Fig. 2A. No apparent 341
morphological differences were observed in the basal, middle, and apical turns of the cochleae 342
between 5-week-old NOX4-TG and control mice, with few HC loss detected in the entire area that 343
17
was examined (Fig. 2B). 344
345
Hearing vulnerability of NOX4-TG mice after NE 346
Next, we examined whether ROS overproduction in NOX4-TG mice affects their hearing 347
function after stress and accelerates the progress of NIHL. We exposed anesthetized, 5-week-old 348
NOX4-TG and control mice to intense noise with an intensity of 110 dB SPL for 1 h (Fig. 3D), 349
which is known to induce a permanent threshold shift in the hearing level of WT mice (Yamaguchi 350
et al. 2017). ABR threshold shifts (in dB SPL) were highest immediately after NE at day 0 and 351
gradually decreased in the 14-day period after the injury, being more remarkable when tested at 352
higher (12 and 20 kHz) than at low frequencies (4 kHz) (Fig. 3A). At day 0, the ABR threshold 353
shifts of NOX4-TG mice were comparable to those of control mice (Fig. 3A). However, at day 5, 354
the threshold shifts at high frequencies (12 and 20 kHz), but not at 4 kHz, became significantly 355
higher in NOX4-TG mice (49.0 ± 1.9 and 61.0 ± 3.3, for 12 and 20 kHz, respectively) than in 356
control mice (34.0 ± 3.4 and 44.0 ± 3.3, for 12 and 20 kHz, respectively; Fig. 3A). At 20 kHz at 357
days 7 and 14, the ABR threshold shifts were significantly higher in NOX4-TG mice (59.0 ± 2.4 358
at day 7 and 53.0 ± 5.1 at day 14) than in control mice (36.9 ± 3.8 at day 7 and 32.1 ± 5.3 at day 359
14) (Fig. 3A). 360
We also examined the morphology of the basal, middle, and apical turns of the cochlea at day 361
14. A few OHCs were missing in the basal and middle turns, but not in the apical turn, in control 362
mice, consistent with a permanent ABR threshold shift at high frequencies (Fig. 3B). The 363
remaining OHCs were significantly less at the basal turn of the cochlea in NOX4-TG mice (71.4 ± 364
5.4% in NOX4-TG mice and 93.3 ± 0.6% in control mice; Fig. 3B and C), in line with the 365
significantly increased ABR threshold, observed specifically at 20 kHz. We did not observe a loss 366
of IHCs in either NOX4-TG or control mice (Fig. 3C), consistent with previous studies reporting 367
18
that OHCs are mainly damaged in NIHL (Harding et al. 2005, Yang et al. 2015b, Yamaguchi et al. 368
2017). These results suggest that the greater OHC loss is one of the main causes of the increased 369
threshold shift in NOX4-TG mice in the NE experiment. 370
371
Rescue of hearing vulnerability in NOX4-TG mice by the antioxidant Tempol 372
To confirm that the exacerbated NIHL in NOX4-TG mice was caused by ROS, we applied the 373
antioxidant Tempol (300 mg/kg) twice intraperitoneally; immediately before and 24 h after NE 374
(Fig. 3D). Tempol functions by metabolizing superoxide to H2O2 (termed as superoxide dismutase 375
[SOD]-mimetic action) and by catalytically and stoichiometrically metabolizing H2O2 (catalase-376
like action) (Wilcox & Pearlman 2008). As expected, the NIHL observed in the NOX4-TG group 377
was rescued by treatment with Tempol. At day 1, the ABR threshold shifts were significantly lower 378
in the Tempol-treated NOX4-TG (NOX4-TG + Tempol; 48.3 ± 3.3 at 12 kHz and 53.3 ± 3.3 at 20 379
kHz) than in the untreated control group (66.6 ± 1.7 at 12 kHz and 65.0 ± 2.9 at 20 kHz). At day 380
14, the ABR threshold shifts in the NOX4-TG + Tempol group (15.0 ± 2.9 at 4 kHz, 25.0 ± 2.9 at 381
12 kHz, and 38.3 ± 3.3 at 20 kHz) were decreased to the levels observed in WT control mice (Fig. 382
4A, see 3A). Thus, the threshold shifts at high-frequencies (12 and 20 kHz), but not at 4 kHz, were 383
significantly lower in the group treated with Tempol than in the untreated group during the entire 384
14-day period (Fig. 4A). Loss of OHCs at day 14 was also decreased in the NOX4-TG + Tempol 385
group compared with the untreated control NOX4-TG group, most apparently in the basal turn of 386
the cochlea (Fig. 4B). The percentage of remaining OHCs in the basal cochlear turn was 387
significantly larger in the NOX4-TG + Tempol group (95.3 ± 1.8 %) than in the control NOX4-TG 388
group (78.3 ± 5.5 %; Fig. 4B, right). These results strongly suggest that the exacerbated NIHL 389
observed in NOX4-TG mice is due to the increased levels of ROS. 390
391
19
Increased HSP47 protein levels due to ROS 392
Although our results suggested the involvement of ROS in NIHL progression in NOX4-TG 393
mice, their hearing function was maintained under baseline conditions, suggesting chronic 394
activation of signaling pathways that protect against oxidative stress. To explore these putative 395
pathways, we attempted to identify proteins that bind to and function with NOX4, by means of 396
immunoprecipitation assays. We used lysates of HEK293 cells that were stably transfected with 397
3xFLAG-NOX4 (HEKFLAG-NOX4) or 3xFLAG-CMV(10) (HEKcont) and incubated then with 398
magnetic-bead-conjugated anti-FLAG monoclonal Ab. Immunoblotting analysis confirmed the 399
expression of 3xFLAG-NOX4 protein, as well as increased levels of the endogenous NOX4- 400
heterodimerizing p22phox protein, in HEKFLAG-NOX4 but not in HEKcont cells (Fig. 5A). Using mass 401
spectrometry, we then identified six proteins that potentially form a complex with NOX4; heat 402
shock protein 47 (HSP47, also called SERPINH1), calnexin, glucose-regulated protein 78, 403
apoptosis-inducing factor, nucleolin, and lipoprotein lipase. Among these, we focused on HSP47, 404
a collagen-specific molecular chaperone that has been reportedly involved in cell survival 405
(Kawasaki et al. 2015, Franco et al. 2016). Therefore, we investigated whether HSP47 can form a 406
complex with NOX4, using immunoprecipitation. Unexpectedly, we failed to detect HSP47 in 407
immunoprecipitates of HEKFLAG-NOX4 lysates, indicating that HSP47 does not bind to NOX4. 408
Instead, immunoblotting using whole cell lysates showed significantly increased HSP47 protein 409
levels in HEKFLAG-NOX4 cells than in HEKcont cells (Fig. 5B). Increased HSP47 protein levels were 410
also confirmed in cells transfected with untagged NOX4 or 3xFLAG-NOX4, but not in those 411
transfected with mock plasmid or NOX4(1-305) (Fig. 5C). Furthermore, HSP47 protein levels in 412
HEK293 cells increased after treatment with H2O2 in a dose-dependent manner; this increase was 413
statistically significant after treatment with 100 (P = 0.011) but not 10 (P = 0.680) M H2O2 (Fig. 414
5D). These results suggest that ROS produced by NOX4 increase HSP47 protein levels. 415
20
416
Increased Hsp47 protein levels in the cochlea of NOX4-TG mice 417
Finally, we examined Hsp47 protein levels in the cochlea of NOX4-TG mice. In the cochlea 418
of adult control mice, we detected Hsp47 immunoreactivity in OHCs, the SL, spiral limbus (LB), 419
and spiral ganglion (SG); the SV was weakly positive. The immunoreactivity of Hsp47 at these 420
regions was significantly more intense in NOX4-TG than in age-matched control mice (Fig. 6A). 421
To confirm the increased protein levels of Hsp47 in the cochlea of NOX4-TG mice, we performed 422
immunoblotting. Indeed, Hsp47 protein levels were significantly increased in NOX4-TG above 423
those in control mice, as early as by the first postnatal week (Fig. 6B). In addition, we found that 424
immunoreactivity of Hsp47 in the heart was also significantly stronger in adult NOX4-TG mice 425
than in age-matched control mice (Fig. 6C). This result was also confirmed by immunoblotting 426
analysis of Hsp47 levels in the heart (Fig. 6D). These results suggest that the NOX4-ROS-Hsp47 427
pathway is present and functions in many different tissues, organs, and cells. In contrast, we could 428
not detect any Hsp47 protein upregulation in the cochlea 2 days after NE by 429
immunohistochemistry in either WT or NOX4-TG mice at 2 weeks of age (data not shown). 430
21
Discussion 431
Establishment of a transgenic ROS overproduction mouse model 432
Gene-targeted mouse models are useful tools for studying the mechanism of ROS involvement 433
in various types of organ failure, including SNHL. Several mouse models with genetic 434
modifications of ROS metabolism have been reported to show increased cochlear damage. For 435
example, mice with deletion of superoxide dismutase 1 (Sod1), a major antioxidant molecule, show 436
increased vulnerability to age-related hearing loss (McFadden et al. 1999). Several KO mouse 437
lines with deficiencies in other major antioxidants or their regulators, such as Sod2 (Tuerdi et al. 438
2017), glutathione peroxidase 1 (Ohlemiller et al. 2000), and nuclear factor erythroid-2 related 439
factor 2 (Nrf2) (Honkura et al. 2016), show vulnerability to NIHL. Moreover, pejvakin KO mice, 440
which have disturbed peroxisome antioxidant activity, show a similar phenotype (Delmaghani et 441
al. 2015). Unlike these strains, this newly established NOX4-TG mouse line is a genetic model of 442
increased ROS production and is thus more suitable for studying the direct effects of ROS exposure 443
on various organs. The auditory phenotype that we observed in NOX4-TG mice is the accelerated 444
NIHL, which is limited to high-frequency sounds. This is consistent with the results from previous 445
defense-failure models, indicating that a common pathology is induced in the cochlea, either by 446
failure of defense against or overload of ROS. NOX4 is a constitutively active NOX, localized at 447
internal cell membranes, and mainly produces H2O2 (H2O2 and superoxide are approximately 90% 448
and 10%, respectively) (Leto et al. 2009, Takac et al. 2011, Nisimoto et al. 2014). In contrast, NOX 449
members, other than Nox4 and Duox-s, primarily produce superoxide and probably have a 450
different subcellular localization (Leto et al. 2009, Nisimoto et al. 2014, Ueyama et al. 2015). 451
Hence, although superoxide is spontaneously converted to H2O2 (Winterbourn 2017), the different 452
effects of ROS in NIHL observed in Nox3 KO mice (Lavinsky et al. 2015) and our NOX4-TG mice 453
could be explained by the different effect of H2O2, produced by NOX4, and of superoxide, 454
22
produced by NOX3. 455
456
Hearing phenotype in NOX4-TG mice under baseline conditions and after NE 457
Infusion of chemicals, which are known to generate H2O2, superoxide, or hydroxyl radicals, 458
into the perilymphatic space, cause a significant increase in the threshold of compound action 459
potentials of the cochlear nerve (Clerici & Yang 1996). Paraquat, for example, enhances 460
superoxide production in a reaction catalyzed by NADPH oxidase. When delivered into the 461
perilymph through the round window, paraquat induces hearing loss and HC loss (Bielefeld et al. 462
2005). Moreover, H2O2 treatment of cultured OCs isolated from P3 WT mice causes HC death in 463
a concentration-dependent manner (Baker & Staecker 2012). 464
NOX4-TG mice; however, have no baseline cochlear damage. One possible explanation for 465
this is the insufficient ROS overproduction. An early study reported that NE causes a permanent 466
hearing threshold shift by producing 4-fold higher ROS levels in the cochlea (Ohlemiller et al. 467
1999). However, a more recent report suggested that even lower levels of ROS can cause 468
irreversible damage to the cochlea. Furthermore, cisplatin treatment, which increases ROS 469
production by 1.8–2.2 folds, decreases cell viability in HEI-OC1 cells, an auditory cell line (Kim 470
et al. 2010, Chang et al. 2014). In cultured OCs, cisplatin treatment causes a 1.19-fold higher ROS 471
production, leading to increased loss of HCs (Kikkawa et al. 2014). Moreover, a 2.05-fold increase 472
in ROS induced by NE was reported to cause permanent hearing loss, as confirmed by ABR in 473
vivo (Wilson et al. 2014). These data suggest that the 1.7-fold higher levels of ROS seen in NOX4-474
TG mice should be sufficient to affect baseline hearing function. 475
Another plausible explanation of this contradiction is that chronic exposure to excessive ROS 476
in a genetically engineered model, such as NOX4-TG mice, may result in a reduced effect on 477
cochlear function as compared to acute exposure. Indeed, NOX4-TG mice show a hearing 478
23
vulnerability upon NE that is induced by ROS, as confirmed by the compensation observed after 479
the antioxidant treatment. Mouse models with antioxidant-defense failure reportedly have normal 480
hearing (Tuerdi et al. 2017, Honkura et al. 2016) or only subtle hearing loss (Ohlemiller et al. 2000, 481
Delmaghani et al. 2015) under baseline conditions, but show exacerbated NIHL and OHC loss 482
after NE. For example, mice lacking Nrf2, which is a transcription factor regulating the major 483
antioxidant response elements (Loboda et al. 2016), have normal hearing but increased 484
susceptibility to NE (Honkura et al. 2016). Interestingly, the expression of Nrf2-targeted genes is 485
not altered in Nrf2 KO mice, suggesting the presence of other antioxidant signaling molecules and 486
pathways activated in the chronic phase of ROS/antioxidant imbalance. Considering the above, 487
the hypothetical modified redox signaling(s), probably mediated by antioxidants and induced by 488
chronic ROS exposure, is insufficient to prevent the irreversible damage caused by an acute 489
increase of ROS. 490
With respect to the lesions, we found that OHC is mainly affected by the acutely increased 491
ROS levels; however, other regions, including the SL, SV, LB, and SG could also be involved in 492
the pathology of NOX4-TG mice. The SL and SV were also reported to be affected by NE (Sha & 493
Schacht 2017), and our 4-HNE immunostaining showed increased ROS production in these 494
structures. Indeed, although we detected a larger threshold shift in NOX4-TG mice at 12 kHz, 495
particularly at day 5, we observed a significantly higher OHC loss specifically in the basal turn of 496
the cochlea 14 days after NE. 497
498
Potential role of HSP47 in hearing protection 499
In the present study, we identified Hsp47 as a novel signaling molecule that is upregulated in 500
the cochlea upon NOX4-induced ROS stress. Hsp47 is a collagen-specific molecular chaperone 501
and plays an important role in the biosynthesis, structural assembly, and homeostasis of collagen 502
24
(Nagata et al. 1988, Ito & Nagata 2017). It was reported to have cytoprotective effects against 503
oxidative stress, since it could inhibit the H2O2-induced apoptosis in the lymphoma U937 cell line, 504
when added to the cells (Franco et al. 2016). Previous studies have shown that NOX4 is involved 505
in the development of fibrosis in several organs, including lung (Hecker et al. 2009), kidney 506
(Barnes & Gorin 2011), and liver (Jiang et al. 2012). Knockdown of Hsp47 by siRNA was shown 507
to decrease Nox4 levels both in vitro and in vivo in fibrosis models (Morry et al. 2015). These 508
findings support our hypothesis that both NOX4 and Hsp47 are involved in a common signaling 509
pathway, while, our data further demonstrate the opposite regulation of Hsp47 by NOX4 and 510
suggest that NOX4ROSHsp47 signaling is regulated in an interdependent manner. Altogether, 511
these data indicate that Hsp47 is an attractive candidate as a hearing-protective molecule against 512
chronic ROS overexposure. In contrast, Hsp47 protein levels were not increased in the cochlea 513
after NE, suggesting that upregulation of Hsp47 in vivo is not induced in the acute phase after ROS 514
exposure, consistent with a previous report (Gong et al. 2012). It is thus possible that sufficient 515
amounts of Hsp47, administered in the acute phase, may contribute to reducing cochlear damage. 516
Further studies are required to explore the functional mechanism and potential therapeutic effect 517
of HSP47 on NIHL. 518
In summary, NOX4-TG mice have normal hearing, but show hearing vulnerability after intense 519
NE, suggesting that antioxidant pathways are induced/activated in chronic ROS overexposure. 520
These results also suggest that ROS have different effects on functional and damaged tissue, 521
depending on chronic or acute exposure. Hsp47 protein levels are upregulated in the cochlea of 522
NOX4-TG mice, suggesting that HSP47 may be an endogenous antioxidant factor compensating 523
for chronic ROS overexposure. 524
25
Acknowledgement 525
We thank Dr. Ken-ichi Yoshino (Biosignal Research Center, Kobe University) for analysis of MS 526
experiments. This study was supported by grants from the JSPS KAKENHI program, #17H04042 527
to TU and #17H0432 to NS; and by a grant from the joint research program of the Biosignal 528
Research Center, Kobe University, #281005 to HS. 529
530
Author disclosure statement 531
No competing financial interests exist. 532
533
Author contributions 534
TU planned the project. SM, TU, HS, and TN performed the molecular and cellular biology 535
experiments. SM, YN, and HM performed the histological experiments and analysis. TY and KO 536
performed noise exposure experiments and analysis. SM, TU, HS, YH, and NS analyzed the data. 537
SM, HS, and TU wrote the manuscript. 538
26
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Figure legends 708
Fig. 1. Generation of NOX4-TG mice: a model of ROS overproduction in the cochlea. 709
(A) Illustration of the linearized expression plasmid used for injection into fertilized eggs. The 710
cassette contains the CAG promoter, the 3xFLAG-tagged NOX4, and the rabbit -globin poly A 711
sequence. (B) ROS production, measured using a luminol-based chemiluminescence (CL) method, 712
in HEK293 cells transfected with mock, NOX4, 3xFLAG-tagged NOX4, or NOX4(1-305) plasmids. 713
No significant difference is detected between NOX4 and 3xFLAG-tagged NOX4 (n = 4; P = 714
0.2841; Student’s t-test). (C) Immunoblotting analysis using anti-FLAG and anti-actin-β (used as 715
loading control) antibodies. Expression of FLAG-tagged NOX4 protein is confirmed in the cochlea 716
and heart of NOX4-TG mice at P7 (right panels) but not in control mice (left panels). Multiple 717
bands marked by arrowheads, probably correspond to glycosylated forms of NOX4 (predicted MW 718
= 66.5 kDa). FLAG-NOX4 levels are much higher in the heart, even with much lower protein 719
loaded, as evident by actin-β bands. n = 4. (D) ROS production assessment in cochlear lysates 720
obtained from P7 mice, using a luminol-based CL method. Overproduction of ROS in the cochleae 721
of NOX4-TG mice is suppressed to control levels by Tempol or DPI; n = 4; P = 0.016 [control vs 722
TG], P = 0.010 [TG vs TG+Tempol], and P = 0.013 [TG vs TG+DPI]). *, P <0.05; one-way 723
ANOVA with Bonferroni’s post-hoc test. (E) Representative sections of cochleae from P14 control 724
and NOX4-TG mice stained with anti-4-HNE antibody. Rectangles in the upper panels (scale bars, 725
50 m) indicate the magnified areas shown in the lower panels (scale bars, 25 m). The asterisk 726
and black dot indicate Corti’s tunnel and Nuel’s space, respectively. Graph on the right is showing 727
the quantification of 4-HNE immunoreactivity in outer hair cells (OHCs; P = 0.045), spiral 728
ligament (SL; P = 0.001), and stria vascularis (SV; P = 0.045). n = 5; *, P <0.05; **, P <0.001; 729
Student’s t-test. 730
731
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Fig. 2. Normal hearing and morphology of the organ of Corti (OC) in NOX4-TG mice. 732
(A) ABR thresholds (dB SPL) tested with clicks and pure-tone bursts at 4, 12, and 20 kHz in 5- 733
and 24-week-old control (n = 4) and NOX4-TG mice (n = 4 and 6 at 5 and 24 weeks, respectively). 734
No statistically significant difference is observed between control and NOX4-TG mice. (B) 735
Representative histochemical images of the OC at the three cochlear turns (apical, middle, and 736
basal) of control and NOX4-TG mice at 5 weeks of age. Sections were stained using Alexa Fluor 737
488-labeled phalloidin. No significant difference is observed between the two groups. IHC, inner 738
hair cell; OHC, outer hair cell. Scale bars, 25 m. 739
740
Fig. 3. NE causes vulnerability of hearing and OHC loss in NOX4-TG mice. 741
(A) Five-week-old mice were exposed to intense noise (110 dB) for 1 h. ABR threshold shifts (dB 742
SPL) between pre- and post-NE, were tested at 4, 12, and 20 kHz and monitored immediately after 743
NE (day 0) and for the next 14 days. A significant difference is observed at 12 kHz at day 5 (*, P 744
= 0.041) and at 20 kHz at days 5, 7, and 14 (*, P = 0.033, 0.022, and 0.028, respectively). n = 7 in 745
control and n = 5 in NOX4-TG mice; two-way ANOVA with Bonferroni’s post-hoc test. (B) 746
Representative histochemical images showing HCs at the three cochlear turns (apical, middle, and 747
basal) of the OC, in sections obtained from control and NOX4-TG mice at day 14 and stained using 748
Alexa Fluor 488-labeled phalloidin. OHC loss is most prominent in the basal turn, which is 749
responsive to high-frequency tones, and is more severe in NOX4-TG than in control mice. White 750
dots indicate missing OHCs. The quantification of the percentage of OHCs remaining in the apical, 751
middle, and basal turn is shown in C (n = 7 in control mice and 8 in NOX4-TG mice; **, P = 0.002 752
in the basal turn; Student’s t-test). Scale bars, 25 m. (D) Chart showing the timings of ABR 753
measurements under baseline conditions and in NE experiments. Bf, immediately before NE; Af, 754
immediately after NE. 755
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756
Fig. 4. Tempol reduces the NE-induced hearing vulnerability and OHC loss in NOX4-TG 757
mice. 758
(A) Intense noise (110 dB) was applied to 5-week-old NOX4-TG mice for 1 h, with or without 759
combined pre- and post-treatment with Tempol (300 mg/kg, i.p.). ABR threshold shifts at 4, 12, 760
and 20 kHz were monitored immediately after NE (day 0) and for the next 14 days. At 12 kHz, P 761
= 0.029 at day 1, 0.025 at day 2, 0.021 at day 5, 0.016 at day 7, and 0.014 at day 14. At 20 kHz, P 762
= 0.026 at day 1, 0.010 at day 2, 0.026 at day 5, 0.005 at day 7, and 0.004 at day 14. n = 3; *, P 763
<0.05; **, P <0.01; ***, P <0.001; two-way ANOVA with Bonferroni’s post-hoc test. (B) 764
Representative sections stained using Alexa Fluor 488-labeled phalloidin, showing OHCs at the 765
basal turn of the OC at day 14 (left). White dots indicate missing OHCs. Graph on the right is 766
showing the percentage of OHCs remaining in the basal turn (n = 6 in control and 5 in NOX4-TG 767
mice; *, P = 0.031; Student’s t-test). Scale bars, 25 m. 768
769
Fig. 5. Upregulated protein levels of HSP47 by NOX4 and ROS in HEK293 cells. 770
(A) Immunoblotting analysis of FLAG-NOX4 and endogenous p22phox proteins in HEKFLAG-NOX4 771
cells using anti-FLAG and anti-p22phox antibodies, respectively, and anti-tubulin as a loading 772
control. Graph is showing the quantification of p22phox expression levels (n = 3; ***, P= 0.0007; 773
Student’s t-test). (B) Immunoprecipitation (IP) of HEKcont and HEKFLAG-NOX4 cell lysates, using 774
FLAG antibody-conjugated magnetic beads, followed by immunoblotting (IB) using an anti-775
HSP47 antibody. Binding of FLAG-NOX4 to HSP47 is not detected; however, significantly higher 776
levels of HSP47 protein are detected in HEKFLAG-NOX4 compared to HEKcont lysates. Quantification 777
of the immunoreactive bands in the first two lanes over GAPDH, used as a loading control, is 778
shown in the graph (n = 5; ***, P = 0.0009; Student’s t-test). (C) Immunoblotting analysis of 779
35
HEK293 cell lysates 48 hours after transfection with mock, NOX4, FLAG-NOX4, or NOX4(1-305) 780
plasmid. Blots were incubated with an anti-HSP47 antibody and actin-β, used as a loading control. 781
Graph is showing the quantification of HSP47 protein levels. HSP47 protein levels are 782
significantly increased in NOX4- and FLAG-NOX4-transfected HEK293 cells (P = 0.0034 and 783
0.0009, respectively, but are unchanged in mock- and NOX4(1-305)-transfected cells (P = 0.007 784
for NOX4 vs. NOX4(1-305) and P = 0.002 for FLAG-NOX4 vs. NOX4(1-305); n = 5; one-way 785
ANOVA with Bonferroni’s post-hoc test). **, P <0.01; ***, P <0.001. (D) Immunoblotting 786
analysis of HEK293 cell lysates after treatment with H2O2 for 24 h (10 M or 100 M), using anti-787
HSP47 and anti-actin-β antibodies, the latter used as a loading control. H2O2 increases HSP47 788
protein levels in a concentration-dependent manner (n = 3; *, P = 0.011; one-way ANOVA with 789
Bonferroni’s post-hoc test). 790
791
Fig. 6. Upregulation of Hsp47 protein levels in NOX4-TG mice. 792
(A) Representative sections of the cochleae from adult control and NOX4-TG mice stained with 793
an anti-HSP47 antibody. Rectangles in the upper panels (scale bars, 100 m) indicate the 794
magnified areas shown in the lower panels (scale bars, 25 m). Magnified images show sensory 795
regions of the OC, containing OHCs. The asterisk and black dot indicate Corti’s tunnel and Nuel’s 796
space, respectively. Graph is showing the quantification of Hsp47 immunoreactivity at OHCs (P 797
= 0.014), SL (P = 0.005), SV (P = 0.004), LB (P = 0.0006), and SG (P = 0.045). n = 3; *, P <0.05; 798
**, P <0.01; ***, P <0.001; Student’s t-test. (B) Immunoblotting analysis of Hsp47 protein levels 799
in membranous cochleae obtained from control and NOX4-TG mice at P4–P6, using an HSP47 800
antibody. Tubulin was used as a loading control. Graph is showing the quantification of the 801
immunoreactive bands (n = 3; *, P = 0.015; Student’s t-test). (C) Representative sections of the 802
heart from adult control and NOX4-TG mice, immunostained with an anti-HSP47 antibody. Graph 803
36
is showing the quantification of Hsp47 immunoreactivity (n = 4; *, P = 0.003; Student’s t-test). 804
Scale bars, 200 m. (D) Immunoblotting analysis of heart lysates obtained from adult control and 805
NOX4-TG mice, using an anti-HSP47 antibody and anti-GAPDH, used as a loading control. Graph 806
is showing the quantification of Hsp47 protein levels (n = 3; *, P = 0.017; Student’s t-test). 807
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