Functional cooperation between two otoconial proteins Oc90 and Nox3

2.1 Animals

Generation of Oc90 null mice has been previously described [28]. Nox3 null mice were obtained from the Jackson Laboratory (stock # 002557, Bar Harbor, ME, USA). The Nox3 mutant strain has an endogenous retroviral insertion in intron 12, resulting in aberrant splicing that renders absent expression of the gene and is therefore functional null [17].

Both Oc90 and Nox3 mice have been backcrossed to and maintained in the C57BL/6J (as C57) genetic background. The backcrossed lines were used to generate the Oc90 heterozygous (Oc90 het) and Nox3 heterozygous (Nox3 het) mice, or crossed to each other to generate double heterozygous (Oc90/Nox3 D-het) and double homozygous (Oc90/Nox3 D-null) mice. Oc90/Nox3 D-null mice were screened by PCR genotyping using the primer sets described in Zhao et al and Flaherty et al. [5, 28]. For Oc90 mutation, the PCR primer sequences were 5^′-TCTAACATCCCATTGCCCAGAGGA-3^′, 5^′-CCAGCCTGACCTGTTCCTTTGTT-3^′ and 5^′-AATATCACGGGTAGCCAACGCTATGTC-3^′. For Nox3 mutation, the PCR primer sequences were 5’-GTTCTGGAGCACCACCTTGT-3’, 5’-CCCATAGGGAGCCAAGAAAT-3’ and 5’-TGTCAAGCTGACTCCACCAG-3’. All animal procedures were ap-proved by the Institutional Animal Care and Use Committee at the Boys Town National Research Hospital (BTNRH) and/or the University of Nebraska at Lincoln in accordance with federal and international guidelines on the ethical use of animals.

2.2 Rotarod test

A four-lane rotarod (Rotamex-5, Columbus Instruments, Columbus, OH, USA) was used in our experiments. Age-matched mice (2∼3 months old, 9 to 16 mice for each genotype) were tested for five consecutive days with three trials a day. All tests were carried out within the same time window of the day (between 1 and 4 pm) to control for possible variations introduced by circadian rhythms. Prior to the test each day, a single training session was done during which each mouse was placed on the rotarod at a constant speed (5 rpm) for 60 seconds. Then the mice were tested on the accelerating rod (5– 20 rpm over 3 min) for three consecutive sessions, separated by 10-minute resting periods. A laser sensor detected if the animal fell from the rod and the time and speed of rotation at falling were recorded. After the rotation speed reached 20 rpm, animals which remained on the rotarod were allowed to stay on for another 5 min at a constant speed of 20 rpm. The average latency of fall (time the mice remained on the rotating rotarod) was calculated and plotted for each trial and each genotype. One way ANOVA with Bonferroni correction was used to compare differences between groups.

2.3 Measurement of vestibular sensory evoked potentials (VsEPs)

Animals were anesthetized by intraperitoneal injection with a mixture of ketamine (180 mg/kg body weight)/xylazine (20 mg/kg body weight). Depth of anesthesia was monitored and maintenance doses of anesthetic were administered as needed during physiological recording. Body core temperature was maintained at 37.0±0.2°C using a homeothermic heating blanket and rectal thermocouple (FHC, Inc., Bowdoin, ME).

VsEPs recording methods were as published previously [6, 20] and are briefly described here. Vestibular stimuli were delivered by securing the head using non-invasive spring clip to a voltage-controlled mechanical shaker. Linear acceleration pulses (17 pulses/s, 2 ms duration) ranged from + 6 dB to – 18 dB re: 1.0 g/ms (where 1 g = 9.8 m/s²) adjusted in 3 dB steps were presented along the naso-occipital cranial axis. Needle electrodes were placed posterior to the left pinna and at the ventral neck or hip (inverting and ground electrodes, respectively). Stainless-steel wire was placed subcutaneously at the nuchal crest served as noninverting electrode. Ongoing electroencephalographic activity was amplified (200,000x), filtered (300– 3000 Hz, – 6 dB amplitude points) and digitized (1024 points, 10μs/pt). 256 primary responses were averaged and replicated for each VsEP waveform. VsEP intensity series were collected beginning at the maximum stimulus level (i.e., + 6dB re:1.0 g/ms) with and without acoustic masking, then descending in 3dB steps to -18 dB re:1.0 g/ms. A broad-band forward masker (50– 50,000 Hz, 97dB SPL) was presented during VsEP measurements to verify absence of cochlear responses [8]. The first three positive and negative response peaks were scored for VsEPs. Response peak latencies (P1, N1, P2, measured in milliseconds), peak-to-peak amplitudes (P1-N1 and P2-N1, measured in microvolts) and thresholds (measured in dB re: 1.0 g/ms) were quantified.

Multivariate analysis of variance (MANOVA) with Bonferroni correction was used to compare response peak latencies amplitudes and thresholds of VsEPs between genotypes.

2.4 Scanning electron microscopy (SEM)

Animals were anesthetized using ketamine (200 mg/kg) and xylazine (5 mg/kg), followed by decapitation. Whole inner ears were fixed in 3% glutaraldehyde in 0.1 M sodium cacodylate buffer (pH 7.2) containing 3 mM CaCl₂ overnight at 4°C. Fine dissection was then performed in artificial endolymph (125 mM KCl, 25 mM KHCO₃, 5 mM HEPES, 2 mM CaCl₂, 1 mM NaCl) to separate the utricle and saccule. The “roof” of the utricle and saccule was gently removed to expose the otoconia, and otoconia were removed in some samples to expose the sensory epithelia. Tissues were washed three times in artificial endolymph, and post-fixed in 1% osmium tetroxide in 0.1 M sodium cacodylate buffer for 1 h. Samples were then washed three times in artificial endolymph, dehydrated, critical point dried in CO₂, mounted, sputter coated with gold palladium and viewed on a FEI Quanta 200 SEM at 15– 20 KV.

2.5 Phalloidin staining

Mouse inner ears were dissected and fixed in 4% paraformaldehyde for 4 hrs at 4°C. The utricle and saccule were then dissected out of the inner ear in 1X PBS, decalcified in 0.25 M EDTA prepared in 1X PBS for 2 hrs at 4°C, washed three times with 1X PBS, followed by an incubation with a 25μg/ml FITC-conjugated phalloidin solution (Cat# P5282, Sigma-Aldrich, St. Louis, MO, USA) containing 0.1% Triton X-100 for 1 hr at room temperature in the dark. Unbound conjugated phalloidin was washed off with 1X PBS, and tissues were mounted and viewed using a Zeiss LSM 510 confocal microscope.

2.6 Construction of expression vectors

Full-length Oc90 and Nox3 transcripts were amplified by RT-PCR of postnatal mouse inner ear tissues and unidirectionally cloned into pTracer-EF/V5-His(C) (pOc90) and pcDNA3.1 (pNox3). The RT-PCR primers were 5’-ggaattcATGATTATGCTGCTCATGGTCGGT-3’ and 5’-gctcgagTTTCCCACCGAGGGGTCTGGCCC-3’ for Oc90, and 5’-acagaattcATGCAACGCACAGGCTCAAATG-3’ and 5’-acactcgagAGTGCATTGACTGTACCC-3’ for Nox3. Nucleotides in lower cases were non-endo-genous sequences to create restriction sites for cloning, and restriction enzymes used were EcoR I (Cat# R0101, NEB, Ipswich, MA) and Xho I (R0146, NEB) for both Oc90 and Nox3. Constructs were confirmed by DNA sequencing and correct protein expression was confirmed by Western blotting.

2.7 Cell culture and stable transfection

NIH/3T3 cells were cultured in Dulbecco’s Modified Eagle’s Medium containing 4.5 g/l glucose, 4 mM L-glutamine, 100 U/ml penicillin and 10% fetal bovine serum. Conventional culture condition was used at 37°C in a humidified incubator supplemented with 5% CO_2 .  The cells were transfected with pTracer-Oc90 (pOc90) and pcDNA3.1-Nox3 (pNox3), alone or together, and with the empty vector pcDNA3.1 or pTracer using FuGENE^® HD (Cat# 4709705001, Roche Applied Science, Indianapolis, IN). Stably transfected clones were selected over a two-week period using 400μg/ml Zeocin (Cat# R25001, Invitrogen, San Diego, CA) for pOc90, or 800μg/ml G418 (Cat# 11811023, Invitrogen, San Diego, CA) for pNox3. Selected clones were then expanded and analyzed for calcification potential as described below.

2.8 Induction of extracellular matrix (ECM) calcification

To induce ECM mineralization, stable NIH/3T3 clones expressing pOc90, pNox3, pOc90 + pNox3, pcDNA3.1 (empty vector) were treated with 0.5 mM Ca^2 + (CaCl₂) and 2 mM Pi (Na₂HPO₄) in growth media to provide a source of inorganic components for mineralization [24, 26]. Phosphate, instead of carbonate, was used so as not to alter the optimal pH and CO₂ content. On the sixth day, cells were fixed with 4% paraformaldehyde, and stained with Alizarin Red S (ARS) (Cat# A5533, Sigma-Aldrich). Calcification nodules and total cells were photographed and counted for each 20x view field under an inverted microscope (approximately 1.2 mm²); averaged ratios of nodules/total cells were compared among transfectants and the empty vector using one way ANOVA with Bonferroni correction.

2.9 Data analysis

Reported data represent the mean values±stan-dard deviation. Statistical significance was determined by ANOVA or MANOVA with Bonferroni correction, as described at the end of each procedure. Significance was set at the level of p < 0.05. P values are expressed as ^* or ^$p < 0.05, ^**p < 0.01, and ^***, ^# # # or ^$$$p < 0.001.

3.1 Oc90/Nox3 double mutant mice had severe balance deficits

The balance function of Oc90 and Nox3 single and double mutants, along with age-matched wild-type (WT), was examined by rotarod tests. While deficits in other systems (such as the central nervous system and neuromuscular system) can also influence rotarod performance, only inner ear deficits are known to exist in these two lines of mutant mice as Oc90 and Nox3 genes are reported to be primarily expressed in the inner ear [2, 28]. All double null and single null mice stayed on the rotarod for a significantly shorter time than WT mice in all trials, with Oc90/Nox3 double null and Nox3 single null mice as the worst performers (Fig. 1, p < 0.01 between double mutants and WT, as well as between single mutants and WT). The order of best to worst performers was WT (n = 14), Oc90 null (n = 16), Oc90/Nox3 D-het (n = 12), Nox3 single null (n = 9) and Oc90/Nox3 D-null (n = 11). Single heterozygous mice have normal balance function and normal inner ear histology [27, 28]. Surprisingly, double heterozygous mice could stay on the rotarod for significantly less time than the WT mice (p < 0.01). The difference between double null and double heterozygous mice was also significant (p < 0.05 except Day1). Such poor rotarod performance of Oc90/Nox3 double mutants is indicative of the severe balance deficits which caused them to fall from the rod much easier than the WT mice.

OPEN IN VIEWER

Fig. 1

Severe balance deficits of Oc90/Nox3 double mutant mice by rotarod tests (all mice were 1.5 months old). Oc90/Nox3 D-het mice (n = 12) could stay on the accelerating rotarod for a significantly shorter time than WT mice (n = 14, p < 0.001). The latencies of Oc90/Nox3 D-null mice (n = 11) were even shorter (p < 0.01 vs. D-hets, p < 0.05 vs. Oc90 null mice (n = 16) , and p < 0.001 vs. WT) and were similar to that of Nox3 null mice (n = 9).

Interestingly, the difference between the mutants and WT mice became even greater with each subsequent trial, as the WT mice improved their performance much more over time. Double null and Nox3 single null mice did not improve their performance over time. The slope of improvement ranked the same order as their balance functions stated above, with a nearly four-fold increase in latencies on the rotarod on day 5 as compared with day 1 for WT mice (p < 0.001).

The vestibular function of Oc90/Nox3 double mutant mice was further evaluated by measuring the vestibular evoked potentials (VsEPs). As shown in Table 1, Oc90/Nox3 D-het mice (n = 8) showed significantly elevated VsEP thresholds, longer latencies, and smaller peak-to-peak amplitudes than those of age-matched C57 mice (n = 4, p < 0.05 vs. C57). The VsEP responses in Oc90/Nox3 D-nulls (n = 6) were completely absent.

Linear VsEPs are compound action potentials generated by the vestibular nerve and its central relays in response to linear acceleration. They depend critically on the utricle and saccule, and provide a direct measure of the functional status of those two organs [6, 9]. Thus, the significantly changed VsEPs recordings reflect the impaired gravity receptor function in Oc90/Nox3 D-het and D-null mice.

As with Nox3 null mice, otoconia were completely absent in the utricle and saccule in Oc90/Nox3 D-null mice [Fig. 2C, all mice were postnatal day 14 (P14)], which may explain their extremely poor rotarod performance shown in Fig. 1. While the D-het mice had otoconia, the crystal morphology was abnormal as shown by scanning electron microscopy in Fig. 2. In WT mice, the crystals had barrel-shaped bodies and tri-planar facets at each end, and had smooth surfaces (Fig. 2A). In comparison, most of the otoconia in Oc90/Nox3 D-het mice had fissured surface and irregular shape, and some were fused (Fig. 2B). The percentage of otoconia with rugged surface was much higher in the D-het mice than that in the WT mice (92.9% vs. 3.3%, n = 5, p < 0.001, Fig. 2D).

OPEN IN VIEWER

Fig. 2

Abnormal otoconia morphology in the Oc90/Nox3 double heterozygous mice by scanning electron microscopy. (A) Otoconia crystals in WT mice have normal barrel-shaped bodies and tri-planar facets at the ends with smooth surfaces. (B) Crystals in Oc90/Nox3 D-het mice have irregular shapes and fissured surfaces. (C) No otoconial crystal is found in Oc90/Nox3 D-null mice. (D) The percentage of otoconia with rugged surface is much higher in the D-het mice than that in the WT mice (92.9% vs. 3.3%, n = 5, ^*** indicates p < 0.001). P14 utricles are shown.

Whole-mount phalloidin staining was performed to examine the gross morphology of hair bundles in the vestibule of WT and mutant mice. Phalloidin staining of F-actin in hair bundles showed that Oc90/Nox3 D-null mice had some loss of hair bundles in the utricle and saccule at 3 months (3M) of age (Fig. 3B vs. 3A; the saccule is shown). At this age, there were approximately 2.8 bundles per 100μm² in the WT saccule, whereas D-null only had 1.8 bundles per 100μm² (n = 6, p < 0.001). No gross abnormality was apparent in hair bundles in D-null mice at perinatal ages (data not shown), suggesting that the bundle loss occurred at later ages and likely arose from accelerated degeneration. D-het mice had normal-appearing hair bundles similar to those in WT mice (data not shown).

OPEN IN VIEWER

Fig. 3

Accelerated hair bundle degeneration in Oc90/Nox3 D-mutant mice as shown by phalloidin staining. (B) Loss of hair bundles in Oc90/Nox3 D-null mice in comparison with age-matched WT mice (A) (saccules are shown). (C). Numbers of hair bundles per 100μm² in WT and D-null saccules (n = 6, ^*** indicates p < 0.001). Scale bars: A & B, 20μm. 3 M, aged 3 months old.

Our previous studies have shown that the presence of Oc90 can augment ECM calcification in cell culture [24, 26]. In this study, the pro-calcification efficiency of Oc90 and Nox3 in cultured cells was compared by a similar induction system. NIH/3T3 cells stably transfected with the empty vector, pOc90 and/or pNox3 were cultured for 5 days in media supplemented with 0.5 mM Ca^2 + and 2 mM Pi as calcification-inducing condition. Inorganic calcium deposits were then visualized with Alizarin Red S (ARS) staining and imaged on the 6^th day. Averaged percentages of cells covered with calcified nodules over total cells in each sample were calculated and plotted. As shown in Fig. 4, Nox3 slightly but significantly increased calcification when compared with cells transfected with the empty vector (^**p < 0.01), and Oc90 had a much greater effect than Nox3 (^# # #p < 0.001, n = 9 in each group). Co-transfection of Oc90 and Nox3 drastically increased matrix calcification under the same inducing conditions, when compared with the empty vector, Oc90 or Nox3 single transfection (p = 4.75×10^–13, 5.96×10^–13 and 1.23×10^–7, respectively, n = 9 each). These data demonstrate the functional synergy between Oc90 and Nox3 in promoting matrix calcification in vitro.

OPEN IN VIEWER

Fig. 4

Synergy between Oc90 and Nox3 in promoting extracellular matrix calcification. NIH/3T3 cells stably transfected with empty vector (A), pNox3 (B), pOc90 (C) and pOc90 + pNox3 (D) were cultured in media supplied with 0.5 mM Ca^2 + and 2 mM Pi for 5 days. Extracellular matrix calcium deposits were visualized with Alizarin Red S staining on the 6^th day, and averaged percentages of cells covered with calcified nodules over total cells were calculated and plotted (E). ^** and ^*** indicates p < 0.01 and 0.001 vs. empty vector, respectively; ### indicates p < 0.001 vs. pNox3; $$$ indicates p < 0.001 vs. pOc90, n = 9 each.