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Unlike the structural and mechanical role of bone crystals, the inertial mass of otoconia crystals provides a shearing force to stimulate the mechanoreceptors of the utricle and saccule (the gravity receptor organ) under the stimuli of linear motion. It is not clear whether otoconia, composed primarily of CaCO3 and glycoproteins, go through similar calcification processes as bone. We have recently shown that otoconin-90 (Oc90) regulates the growth of otoconia crystals as osteopontin does bone crystals. Here, we analyzed the role of this non-collagenous bone matrix protein, osteopontin, in otoconia formation and balance function utilizing its knockout mice, whose inner ear phenotype has not been examined. Despite the presence of the protein in wild-type otoconia and vestibular hair cells, morphological, ultrastructural, and protein and calcium composition analyses of osteopontin null otoconia show that the protein is not needed for crystal formation, and no evidence of compensatory protein deposition is found. Employment of a wide spectrum of balance behavioral tests demonstrates that the protein is not critical for balance function either, which is confirmed by the normal function of the gravity receptor organ directly measured with linear vestibular-evoked potentials (VsEPs). When compared with findings on other otoconins, the data manifest a hierarchy of importance of proteins in crystallization and indicate mechanistic similarities and differences between bone and otoconia calcification.
In humans, otoconia and other vestibular disorders are prevalent and severely interfere with daily life. It is estimated that 50% of those at age 65 years or older will develop positional vertigo, whose most common cause is otoconia dislocation. Otoconia degeneration and abnormalities worsen with exposure to ototoxic drugs, infection of the vestibular labyrinth, certain genetic mutations, and in the elderly (Preston et al. 1975; Ross et al. 1976; Lim 1984; Zhang et al. 1996; Balsamo et al. 2000), although accurate statistics are not available. To develop effective treatments, it is imperative to identify the necessary and sufficient components for crystal regeneration or prevention of degeneration.
We have recently demonstrated that, during the formative stage, otoconia matrix particles (the organic framework upon which inorganic CaCO3 crystals are deposited) and crystals exhibit a striking ultrastructural resemblance to bone matrix vesicles and crystals, respectively, (Zhao et al. 2007) despite the fact that bone crystals contain calcium phosphate (apatite), and otoconia crystals contain calcium carbonate (calcite). Furthermore, the organic components of otoconia are either the same or belong to the same family of bone matrix proteins. Both types of matrices contain sulfated glycosaminoglycans (as GAGs or proteoglycans), osteopontin (OPN), fetuin-A, and members of the collagen X family (collagen X in bone and otolin in otoconia; Lundberg et al. 2006; Zhao et al. 2007). The fourth known otoconia component protein, Oc90, is the predominant otoconial matrix protein (Wang et al. 1998; Verpy et al. 1999) whose role in bone formation has yet to be studied.
Of the few otoconial proteins that are also present in bone, OPN is a non-collagenous bone matrix protein involved in ossification. Similar to the essential role of Oc90 in forming the otoconia matrix and regulating crystal growth (Zhao et al. 2007), OPN limits bone crystal sizes and mineral content (Boskey et al. 1993; Hunter et al. 1994; Shapses et al. 2003). In the vestibule, OPN is detected in otoconia and expressed in vestibular hair cells, dark cells, and the endolymph sac (Takemura et al. 1994; Sakagami 2000). The gene is expressed in a number of nervous tissues including the hindbrain, cerebellum, brainstem, spinal cord, and some parts of the peripheral nervous system (Mark et al. 1988; Shin et al. 1999; Ichikawa et al. 2000; Ju et al. 2000; Lee et al. 2001; Marsh et al. 2007). The neuronal phenotype of OPN null mice has not been thoroughly examined, but the lung, heart and kidney of mutant mice show increased fibrosis and apoptosis (Ophascharoensuk et al. 1999; Berman et al. 2004; Zohar et al. 2004). The inner ear phenotype of the null mice has not been examined either. In this study, we analyzed the function of OPN in otoconia calcification utilizing OPN knockout mice that are maintained as Spp1 (secreted phosphoprotein 1, the current official name for OPN). Our working hypothesis is that otoconia component proteins (collectively called otoconins) regulate crystal growth and morphology. Establishment of a mechanistic link between bone and otoconia calcification will greatly benefit studies of otoconia development and vestibular cell biology due to the availability of a wealth of data on bone biology.
Mice and histology Osteopontin null (as OPNspp1) mice were obtained from The Jackson Laboratory (Bar Harbor, ME, USA) and maintained in the C57BL/6J (as C57) genetic background by the supplier. Some experiments also included the otoconia-deficient strain Otopetrin1tlt (as Otop1tlt) that are known to show imbalance behaviors (Ornitz et al. 1998; Jones et al. 2004; Zhao et al. 2008). The Otop1tlt mice were also maintained in the C57 genetic background by The Jackson Laboratory. The mice were maintained by homozygous inbreeding in the laboratory. Unless otherwise indicated, the acronyms OPNspp1 and Otop1tlt refer to homozygous mutants throughout the report. Animals were euthanized by CO2 asphyxiation before tissue harvesting, and all animal procedures were approved by the Institutional Animal Care and Use Committee at the Boys Town National Research Hospital in accordance with federal guidelines.
For histological examination, inner ears were dissected and fixed in paraformaldehyde (4%). After decalcification in 0.1 M EDTA (pH 7.4) overnight, tissues were embedded in paraffin for sectioning at 6 μm.
Alizarin red complexone staining To visualize the degree of otoconia calcification, fixed whole-mount vestibular tissues were stained with 1:50 dilutions [(in phosphate buffered saline (PBS)] of 0.5% alizarin red complexone (ARC; Sigma, St. Louis, MO, USA), a reagent that stains calcium deposits, for 2 h or overnight at room temperature. After washing off excess staining reagents, tissues were viewed using a Zeiss LSM 510 confocal microscope.
Phalloidin staining Fixed and decalcified vestibules were permeabilized with 0.1% Triton X-100 in PBS for 30 min, washed with PBS and stained with a 50 μg/ml FITC-conjugated phalloidin solution (Sigma) for 40 min at room temperature. Unbound conjugated phalloidin was washed off with PBS, and tissues were viewed using a Zeiss LSM 510 confocal microscope.
Scanning electron microscopy Animals were anesthetized using a sublethal dose of ketamine (167 mg/kg) and xylazine (2 mg/kg), perfused through the left ventricle with artificial endolymph (125 mM KCl, 25 mM KHCO3, 5 mM HEPES, 2 mM CaCl2, 1 mM NaCl), followed by 20–30 ml 4% paraformaldehyde + 2.5% glutaraldehyde + 3 mM CaCl2 in 0.1 M sodium cacodylate (pH 7.2). Utricles and saccules were dissected out of the inner ear in the fixative, and openings were made by gently breaking the bony capsules at the “roof” of the utricle and saccule. Tissues were immersion-fixed for 24 h in the same fixative, washed three times with artificial endolymph, and postfixed in 1% osmium tetroxide in 0.1 M sodium cacodylate (pH 7.2) for 1 h. Samples were then dehydrated, critical point dried in CO2, mounted, sputter coated with gold palladium, and viewed on a Jeol (JSM-848) scanning electron microscope (SEM) at 15 kV.
Otoconia dissection and protein assays A detailed description of crystal dissection and stringent washes to clean off the filaments and membranes was provided previously (Zhao et al. 2007). The crystals were decalcified, and proteins were extracted with 10 μl of buffer (40 mM Tris, 4% CHAPS (3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate), 8 M urea, 10 mg/ml dithiothreitol (DTT), 0.15 M EDTA) at 4°C overnight. The buffer was used to dissolve any EDTA-insoluble component of otoconia crystals as was reported for fish otoliths (Murayama et al. 2004). After removal of EDTA and salts using a Centricon column (Millipore, Billerica, MA, USA), protein concentrations and total protein contents were determined using a Micro-BCA (bicinchoninic acid) Protein Assay Kit (Pierce, Rockford, IL, USA) following the manufacturer’s protocol. Briefly, 100 μl of each diluted bovine serum albumin standards and protein samples were added into microplate wells; 100 μl of freshly prepared working reagent (A:B:C at 25:24:1) was added into each well and mixed gently. The reaction was incubated at 37°C for 2 h with rocking, and the absorbance was measured at 562 nm on a Quant MQX200 plate reader (Bio-Tek Instruments, Inc. Winooski, VT, USA). Protein concentrations were calculated according to standard curves.
Western blotting Extraction of otoconial proteins and determination of protein concentrations were carried out in the same way as above. An aliquot of each sample containing an equal amount of total protein was mixed with 2× sample loading buffer (0.13 M Tris–HCl, 20% glycerol, 46 mg/ml sodium dodecyl sulfate (SDS), 0.2 mg/ml bromophenol blue, 20 mg/ml DTT), boiled for 5 min, loaded onto a 4–15% gradient Tris–SDS gel (Bio-Rad, Hercules, CA, USA), electrophoresed at 200 V in running buffer (25 mM Tris pH 8.3, 192 mM glycine, 0.1% SDS) for 2 h, and transferred to a PVDF membrane (Millipore) at 100 V for 1 h. The blot was washed once with Tris buffer containing salt and Tween (TBST) (50 mM Tris, 150 mM NaCl, 0.1% Tween-20) and treated with 3% blocking buffer (Roche Applied Science, Indianapolis, IN, USA) overnight at room temperature. The membrane was incubated with an antibody against the N-terminal 15 amino acids of Oc90 (Zhao et al. 2007) at 1:1,000 dilution for 3 h followed by three washes in TBST buffer and incubated with a peroxidase-conjugated goat anti-rabbit IgG secondary antibody (1:10,000; Sigma) for another 3 h. After three washes, detection solution was added for 1 min, and the blot was exposed to a Kodak X-ray film. Blots were imaged using the Canoscan 8400F imaging station, and protein band intensities were analyzed using the ImageJ software (http://rsb.info.nih.gov/ij/).
Ratiometric calcium measurement Otoconia crystals were dissected, and CaCO3 was dissolved in 0.05 N HCl. Serial dilutions (150×–200×) in Ca2+-free calibration buffer were made for neutralization and quantification purposes and [Ca2+] was measured using the ratiometric dye, Fura-2 (Molecular Probes, Eugene, OR, USA). After adding Fura-2 (100 μM), an aliquot of test solution was placed in a sealed glass pipette and imaged using a cooled CCD camera (SensiCam, Cooke Corp., La Jolla, CA, USA) on an upright fixed stage microscope (Nikon E600FN, Garden City, NY, USA). Axon Imaging Workbench (AIW 2.2, Axon Instruments) was used to control the camera, filter wheel (Lambda 10–2, Sutter Instruments, Novato, CA, USA), and image acquisition. [Ca2+] was calculated from the ratio of light emitted at 510 nm during alternate excitation by 340 and 380 nm light (Grynkiewicz et al. 1985). Calibration constants (standard curve) were determined using a series of highly buffered Ca2+ test solutions (Molecular Probes), and Ca2+ concentrations in the resolved otoconia were determined using the standard curve.
The following complementary tests are commonly used to detect balance deficits manifested in postural control, spatial orientation, and sensorimotor function and coordination (Trune and Lim 1983; Sondag et al. 1995, 1996, 1998, 1999; Ying et al. 1999; Jones et al. 2004; Walton et al. 2005; Rampello and Drago 1999; Hamm 2001; Sajdel-Sulkowska et al. 2005). Severe abnormalities in the gravity receptor organ often lead to abnormal air-righting reflexes, irregular and wider gaits, compromised ability to swim, or shortened stay on the rotorod (Trune and Lim 1983; Ying et al. 1999; Rampello and Drago 1999; Hamm 2001; Jones et al. 2004). Details of the methods are described in Zhao et al. 2008 and are briefly summarized below. We assessed the grip strengths of the animals to rule out neuromuscular weakness as a possible secondary outcome of the vestibular sensory deficits. Furthermore, we directly measured the input to the peripheral gravity receptor organ using vestibular evoked potential (VsEP) recordings. The age, genotype, and number of mice tested are summarized in the corresponding tables presented in the “Results” section.
The air-righting reflex was tested on pups three times in a row on each day from P9 to P11. The position with which the pups landed and the time they took to right their body positions were recorded. Reaching response was recorded by observing the reaction of the limbs and head-bobbing behaviors when animals were suspended by their tails. Animals that extend their forelimbs and try to reach a surface are normal, whereas animals with vestibular deficits either clasp their forelimbs or have head-bobbing behavior. Both adults (2–6 months old) and pups (2–3 weeks old) were tested. Regularity of animals’ gaits was observed on a white paper after applying India ink to the paws. The stride length and width were compared between null and age-matched C57 controls using previously published methods (Klapdor et al. 1997; Clarke and Still 1999) and adapted from a standard protocol used by the Charles River Laboratories (Wilmington, MA, USA). Findings with P20 pups are reported in this paper.
Swimming test Swimming behavior of adult mice (2–6 months old) was observed for 15–30 s. The test was repeated three times on different days, and the following scoring system was used: 0, the animal was totally submerged, could not maintain orientation at the surface of the water, and required immediate rescue. 1, the animal could swim to the surface if submerged, but did not maintain a horizontal body line at the surface and may re-submerge briefly. 2, the animal stayed at the surface but hesitated for a few seconds before swimming almost normally. 3, the animal swam at the surface immediately and maintained horizontal body position at the surface. Due to some ambiguity of scores 2 and 3, we categorized the mice as poor (score 0), intermediate (score 1), or good swimmers (score 2 and 3).
Rotorod test Adult animals between the ages of 2–6 months old were placed on a 2-cm-diameter stationary and then on a rotating rod (Rotamex-5, Columbus Instruments, Columbus, OH, USA). The rotation was initially set at a constant speed of 5 rpm/min as a test run. Once each mouse was able to maintain balance for 1 min in each trial, it was then tested on the accelerating rod (5–20 rpm over 3 min) for three consecutive trials per day for four consecutive days. At the end of each trial, animals that stayed on the rod were left on until they fell. A laser sensor detected if the animal fell from the rod, and the time and speed of rotation at falling were recorded. The average time the mice remained on the rotorod (mean latency) was calculated from five to eight animals and plotted for each trial, each genotype, and each age group. The mean values of all mice in one genotype were compared with those of C57 controls in the same trial using Student’s t test assuming similar variances. All tests were carried out within the same time window of the day (between 2 and 4 p.m.) to control for possible variations introduced by circadian rhythms.
Beam-crossing A round wood bar of 2.5 cm in diameter was attached to two Styrofoam platforms at the ends, and the length of the bar to be crossed is adjustable at the ends. Before the test, adult mice (2–6 months old) were fasted for a maximum of 4 h (water was provided ad libitum) to use food (rodent chow) as an effective incentive for the animals to cross the beam. Pretraining of mice on the bar at 5 cm long was performed first, followed by three trials of crossing the bar at 30 cm long in a row. As wild-type (wt) mice often paused on the beam to explore at some point, time spent in crossing the bar at 30 cm was not used for quantitative purposes. Rather, the posture (i.e., lowered body position) and behavior (i.e., reluctance, nervousness) on the beam were observed.
Grip-strength test Mutant and control mice were made to hang in a supine position on an inverted metal meshwork, and the length of time the animal remained on the meshwork was recorded.
Data analysis Data are presented as mean±standard deviation (SD) where applicable. Balance behaviors (except rotorod tests) of mutant strains were compared to C57 controls using Chi-square analysis. Latencies before falling off the rotorod were compared as described above. P values less than 0.05 were considered statistically significant.
Animal preparation The use of animals for vestibular-evoked potentials (VsEPs) was also approved at East Carolina University. Mice were anesthetized with a ketamine (120 mg/kg) and xylazine (13 mg/kg) solution, and core body temperature was maintained at 37.0±0.1°C using a homeothermic heating blanket system (FHC, Inc.). VsEPs were measured from 5-month-old mice.
Vestibular stimulus coupling and recording parameters VsEP recording procedures followed methods previously published (Jones et al. 1999, 2002, 2004; Jones and Jones 1999). Herein, we used a noninvasive method (a spring clip) to couple the head to the voltage-controlled mechanical shaker that delivered the motion stimuli. Linear acceleration pulses (17 pulses/s, 2 ms duration) were presented to the cranium in the naso-occipital axis using two stimulus polarities, normal and inverted. Stimulus amplitude ranged from +6 dB to −18 dB re: 1.0 g/ms (where 1 g=9.8 m/s2) adjusted in 3 dB steps.
Ongoing electroencephalographic activity was amplified (200,000×), filtered (300 to 3,000 Hz, −6 dB amplitude points), and digitized (1,024 points, 10 μs/pt). Primary responses, 256, were averaged and replicated for each VsEP waveform. VsEP recordings began at the maximum stimulus intensity (i.e., +6 dB re: 1.0 g/ms) with and without acoustic masking (broadband forward masker 50 to 50,000 Hz at 97 dB SPL), then intensity was dropped to −18 dB and raised in 3 dB steps to complete an intensity profile. The masker was used to verify absence of cochlear responses (Jones and Jones 1999).
Data analysis The first positive and negative response peaks were scored for VsEPs, as this initial response peak is generated by the peripheral eighth nerve. Peak latencies (measured in milliseconds, ms), peak-to-peak amplitude (measured in microvolts, μV) and thresholds (measured in dB re: 1.0 g/ms) were quantified. Descriptive statistics were generated, and independent sample t test was used to compare VsEP response parameters between OPNspp1 and C57 mice.
The similar effects of Oc90 and OPN on crystal formation suggest that OPN may regulate otoconia calcification. In the present study, we tested this hypothesis by analyzing the otoconia phenotype of the OPNspp1 null mice. Deletion of OPN protein in the null mice was previously validated (Liaw et al. 1998) and was confirmed in the present study by Western blotting of otoconia extracts (data not shown). With Oc90 comprising nearly 90% of the otoconial protein content (Pote and Ross 1986; Wang et al. 1998; Ornitz et al. 1998), OPN is present at only a low level in wt otoconia (Takemura et al. 1994; Sakagami 2000; Zhao et al. 2007).
No abnormality was found in the overall appearance of the end organ of the OPNspp1 null mice. Shown in Figure 1 is hematoxylin-and-eosin (H&E)-stained 6 μm sections of the utricule and saccule. All structures, including hair/supporting cells and the otoconia layer, were apparently normal. SEM observation of otoconia crystals revealed normal sizes and morphology when compared to those of C57 mice (Fig. 2A, B and Table 1). Averaged measurements of lengths and midsection widths are shown in Table 1. There was no significant difference in the averaged measurements of lengths×widths of otoconia crystals in representative areas sampled in C57 and OPNspp1 mice: above the peripheral utricular macula, above the central utricular macula, and all over the saccule. Similar to those in C57 mice, the saccular otoconia of the OPNspp1 mice were more homogeneous in sizes and were much smaller than the utricular ones. The ratio of length versus width was about 2:1 for both utricular and saccular crystals in both strains of mice. Unlike the Oc90 null mice (Zhao et al. 2007), there was no reduction in the otoconial membranes (OM) of the OPNspp1 utricle and saccule (Fig. 2C, D). In Figure 2C and D, the whole-mount tissues were partially decalcified to expose some parts of the OM for observation and at the same time to leave some overlying crystals to minimize mechanic tearing of the OM. Only the OM of the striola region is shown in the figure. OM in the peripheral region of the utricle and saccule of the OPNspp1 vestibule has smaller holes than the striola region, similar to those in C57 (data not shown). Staining of inorganic CaCO3 deposits with ARC showed similar degrees of otoconia calcification in the OPNspp1 and C57 mice (Fig. 2E, F), which was confirmed by fura-2 ratiometric Ca2+ measurements of equal masses (0.24 mg) of otoconia dissolved in equal volumes of 0.05 N HCl (10 μl each; Fig. 3A). In Figure 3A, the Ca2+ concentrations were similar between OPNspp1 and C57 mice (p=0.4).
To identify potential compensatory events, if any, that may have led to the normal otoconia phenotype, we analyzed the total protein content and composition of OPNspp1 null otoconia (1 month old). The null crystals contained 4.5±0.52 μg total protein/mg otoconia mass, compared to 4.2±0.65 μg total protein/mg otoconia mass for age-matched C57 otoconia (p=0.40, n=4) (Fig. 3A). Western blotting of protein extracts from OPNspp1 and C57 otoconia showed similar levels of Oc90 (Fig. 3B; p>0.05). The p value was obtained by the Student’s t test of the products of the intensity (pixels)×area of Oc90 bands of null and control blots. The small difference in the total protein loaded in the gel (3.9 μg for C57 and 4.2 μg for OPNspp1) was taken into account in the calculation. The migratory property of Oc90 was also unaltered in the null mice, suggesting normal posttranslational modification. The unmodified theoretical mass of secreted murine Oc90 is 50 kDa, and the size of the predominant glycosylated form is approximately 80 kDa (Ignatova et al. 2004; Zhao et al. 2007). These unchanged measurements exclude significant deposition of ectopic compensatory proteins that are normally foreign to otoconia. Although the data do not directly exclude possible deposition of another compensatory minor protein, the increased mineral content in bone crystals of OPN nulls argues against such a possibility (Boskey et al. 1993; Hunter et al. 1994; Shapses et al. 2003). Thus, OPN is not likely to play a significant role in otoconia morphogenesis or calcification. It is possible that the protein may not be an integral part of otoconia but only adheres to the crystals, which is also suggested by its presence in Oc90 null otoconia that lack any organic matrix (Zhao et al. 2007).
Next, we examined the vestibular morphology and ultrastructure of OPNspp1 null mice to gain insight into the role of the protein in vestibular development and function. In addition to the normal utricular and saccular structures shown in Figure 1, the density and organization of hair cells and stereocilia were similar between the null and C57 utricle and saccule, as visualized by phalloidin-staining of hair bundles in decalcified whole-mount tissues (Fig. 4). High magnification SEM showed no abnormality in hair bundle sizes or organization in the OPNspp1 vestibule (insets in Fig. 4). Thus, absence of OPN does not affect the morphological development of the gravity receptor organ.
Given the expression patterns of OPN in vestibular hair cells and other nervous tissues, the OPNspp1 mice may have molecular deficits in the sensory cells, ganglia, or other nervous tissues despite the unaffected morphology. Such deficits may lead to imbalance of the animals. We performed a series of balance tests to test this hypothesis. Several issues may make it difficult to pinpoint the source of balance deficits, if any, in the null mice. First of all, behavioral tests assess coordinated functions of the peripheral and central nervous systems (PNS and CNS) and the neuromuscular system. Potential effects, if any, of OPN deletion on the nervous system are likely diverse, with both beneficial and adverse outcomes (see “Discussion” section for more details). In addition, mild deficits may elude detection due to behavioral adaptation. Nevertheless, when interpreted with other types of data including reports of CNS and PNS analyses of the mice, the wide spectrum of balance tests performed on a number of mice should provide an indication of vestibular function despite the limitation of each test alone.
OPNspp1 null pups showed normal development of the air-righting reflex (Table 2). Between P9–11, null mice, like their C57 controls, could instantly right their body positions (<0.8 s on average at P9) and land in an upright position when held by their tails and suspended to make a backward somersault. In comparison, 91–100% of Otop1tlt mice often landed in a supine position rather than the normal prone position and took >3 s on average to right their body positions. All the OPNspp1 null pups and adults had normal reaching responses (Table 2), posture, and gaits (Fig. 5A, B). The mice manifested no unusual home cage behavior, nor did they circle, tilt their heads, move slowly, or become confused. All the OPNspp1 mice swam normally (score 3; Table 2) and crossed the beam just like the controls. The mice had normal grip strengths as well, indicating an absence of neuromuscular weakness.
In addition, the OPNspp1 mice performed well on the rotorod (Fig. 5C): The latencies of their stay on the accelerating rotorod had no significant differences compared to those for age-matched C57 controls on all days (day 1–4; p>0.05, 2–6 months old). In contrast, age-matched Otop1tlt mice stayed on two to three times shorter than either C57 mice or OPNspp1 (p<0.05; Zhao et al. 2008). Like the C57 mice, the OPNspp1 mice demonstrated remarkable learned behavioral adaptation of vestibular functions and stayed longer with the progressing of each trial. There was a nearly fourfold increase in latencies on the rotorod on day 4 compared to day 1 (p<0.001), demonstrating normal synaptic potentiation of vestibular neurons, proprioceptors, or locomotor control centers. Although central compensation can potentially mask peripheral deficits (Rampello and Drago 1999; Dubois et al. 2002; Besson et al. 2005; Bothe et al. 2005), concurrent tests with otoconia mutants show that the learned improvement actually differentiates further the normal and imbalance behaviors because the mutants improved less after training (Zhao et al. 2008). Furthermore, the normal balance behaviors are consistent with the normal morphology and ultrastructure of otoconia and vestibular sensory epithelia. Therefore, OPN is not critical for balance functions.
To confirm the conclusion from behavioral assessments, we directly measured the afferent function of the gravity receptor organ under the stimuli of linear motion. Figure Figure6A6A shows VsEP thresholds for OPNspp1 null and C57 control mice. On average, OPNspp1 mice had VsEP thresholds similar to the controls (−9.5±3.1 dB re: 1.0 g/ms for OPNspp1, −9.7±2.1 dB re: 1.0 g/ms for C57). VsEP response peak amplitudes (data not shown) and latencies (Fig. 6B) were also similar between the two strains of mice. Therefore, absence of OPN does not alter the sensory input or the functional status of the gravity receptor organ.
Despite the prevalence of otoconia-related balance problems in humans, the underlying molecular etiology is completely unknown. In recent years, a number of otoconins have been identified, but the roles of most of these proteins in crystal formation remain unclear. Dissecting the importance of each otoconial protein in otoconia development will help in designing rational treatments for otoconial lesion and for prevention and regeneration purposes.
The absence of any changes in the ultrastructure, protein and calcium content of OPNspp1 null otoconia strongly suggests that the protein is not critical for otoconia formation and that compensation by another unidentified factor is unlikely. The normal balance behaviors, morphology and ultrastructure of the null utricle and saccule indicate that the protein is also not critical for the morphogenesis or function of the gravity receptor organ, which is confirmed by the presence of normal VsEPs.
Both Oc90 and OPN are non-collagenous matrix proteins that, together with collagen, form the organic framework upon which the inorganic crystals are deposited (Rana-Chavez and Nanci 2001; Laboux et al. 2003; Zhao et al. 2007). Both limit the growth of the mineral crystals, but neither is involved in the initial mineral accretion (Shapses et al. 2003; Zhao et al. 2007). The effect of OPN on bone mineral deposition is a combination of a direct involvement of the protein as a hydroxyapatite-binding matrix protein and as a signaling molecule that recruits osteoclasts (Shapses et al. 2003). Oc90 is required to form the otoconia matrix by specifically recruiting other matrix components (Zhao et al. 2007). It has not been examined whether Oc90 has other indirect effects on otoconia formation.
Interestingly, OPN and Oc90 are co-expressed in vestibular dark cells and the endolymphatic sac, with the onset of Oc90 expression being much earlier than that for OPN (Verpy et al. 1999; Sakagami 2000; Ignatova et al. 2004). Given the negligible role of OPN in otoconia formation, such cellular co-localization may be coincidental or may merely reflect cellular activities in secretion and/or ion fluxes, two processes that may provide some components for otoconia formation or maintain homeostasis of the endolymph. A calcium pump, plasma membrane-bound calcium ATPase (PMCA2), is also expressed in dark cells, in addition to hair cells, and mice with mutant PMCA2 have absent otoconia (Kozel et al. 1998). Unlike the bone environment, Ca2+ concentration in the endolymph is low. The Ca2+-binding otoconial proteins and sulfated GAGs may be co-secreted with Ca2+ or may sequester Ca2+ and efficiently raise the local Ca2+ level in the matrix and/or in the otoconial membranes for calcification. As the functions of these molecules in Ca2+-sequestration may be redundant, it is possible that deletion of a minor component like OPN is buffered by other multiple components without the need to increase their expression levels.
It is not clear what kind of effect OPN may have on sensorimotor neurons. The potential impact (if any) of OPN on the CNS and PNS to affect balance and coordination likely involve both positive and negative effects. At the cellular level, the protein has pro-adhesive, chemotactic and cytokine-like properties, and is involved in a number of physiologic and pathologic events including angiogenesis, apoptosis, inflammation, oxidative stress, remyelination, wound healing, bone remodeling, cell migration and tumorigenesis (Chakraborty et al. 2006; El-Tanani et al. 2006; Pagano and Haurani 2006). As some of these events lead to neurodegeneration (Maetzler et al. 2007; Wung et al. 2007) whereas others to neuroprotection (Meller et al. 2005; Schroeter et al. 2006), the overall outcome in sensorimotor neurons may have been neutralized in the null deletion.
In summary, we demonstrate that OPN is not critical for otoconia formation or balance functions. When interpreted with previous findings, the data show a hierarchy of importance of otoconins in crystallization. Given the critical role of OPN in bone crystal growth, the present study indicates molecular differences between otoconia and bone calcification.
Part of the work was supported by grants from the National Institute on Deafness and Other Communication Disorders (DC008603 to YWL and DC006443 to SMJ) and the National Center for Research Resources (1P20RR018788 to YWL). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute on Deafness and Other Communication Disorders or the National Institutes of Health.