Abstract
The central nucleus of the inferior colliculus (IC) is the site of convergence for nearly all ascending monaural and binaural projections. Several of these inputs, including inhibitory connections from the dorsal nucleus of the lateral lemniscus (DNLL), are highly ordered and organized into series of afferent bands or patches. Although inputs to the IC from the contralateral DNLL are present in the rat by birth [postnatal day 0 (P0)], the earliest indications of band formation are not evident until P4. Subsequently, the initially diffuse projection segregates into a pattern of bands and interband spaces, and by P12 adult-like, afferent-dense patches are established (Gabriele et al., 2000). To determine the role of the auditory periphery in the development of bands and patches before the onset of hearing (P12/P13), unilateral cochlear ablations were performed at P2 (before any evidence of banding). Rat pups were reared to P12, at which time glass pins coated with 1,1′-dioctodecyl-3,3,3′,3′-tetramethylindocarbocyanine perchlorate were placed in fixed tissue in the commissure of Probst where DNLL fibers cross the midline. The results indicate that a unilateral cochlear ablation disrupts the normal development of afferent patches in the IC. Although the crossed DNLL projections labeled via commissural dye placement always mirrored each other in P12 controls, ablation cases exhibited a consistent, bilateral asymmetry in pattern formation and relative density of the labeled projections. Possible developmental mechanisms likely to be involved in the establishment of afferent bands and patches before the onset of hearing are discussed.
- afferent patterns
- inferior colliculus
- DNLL
- cochlear ablation
- auditory midbrain
- commissure of Probst
- carbocyanine dye
- bands
- patches
- rat
The inferior colliculus (IC) is the site of convergence for nearly all ascending and descending auditory pathways. Based on regional variations in cellular anatomy, neuropil, and afferent and efferent connectivity, the auditory midbrain can be broken down into nuclear subdivisions (Morest and Oliver, 1984; Oliver and Morest, 1984), each with its distinct hierarchy of organization. The central nucleus of the IC (see Fig. 1) receives inputs from essentially all ascending pathways en route to higher auditory centers of thalamus and cortex. The majority of neurons residing within the central nucleus exhibit disk-shaped dendritic arbors that are oriented parallel to the numerous afferent fibers. The arrangement of incoming lemniscal fibers as afferent layers and their association with the underlying cellular architecture of the central nucleus together constitute fibrodendritic laminae (Oliver and Morest, 1984; Faye-Lund and Osen, 1985; Oliver et al., 1991; Malmierca et al., 1993). This laminar organization preserves the frequency order of the cochlea (Clopton and Winfield, 1973; Merzenich and Reid, 1974; Semple and Aitkin, 1979; Huang and Fex, 1986; Ryan et al., 1988; Kelly et al., 1998). Several inputs terminate primarily within alternating sublayers of neighboring lamina, thereby giving the projection distribution a banded or patchy appearance.
Recently, we described the normal development of a banded afferent projection to the IC arising from the dorsal nucleus of the lateral lemniscus (DNLL) (Gabriele and Henkel, 1999; Gabriele et al., 2000). Although the DNLL sends inhibitory, GABAergic projections bilaterally to the IC (Beyerl, 1978; Adams, 1979; Brunso-Bechtold et al., 1981;Kudo, 1981; Adams and Mugnaini, 1984; Thompson et al., 1985; Coleman and Clerici, 1987; Roberts and Ribak, 1987; Glendenning and Baker, 1988; Shneiderman et al., 1988, 1993; Shneiderman and Oliver, 1989;Hutson et al., 1991; Bajo et al., 1993; Merchán et al., 1994; van Adel et al., 1999), a preparation was designed to specifically examine the development of the crossed projection. Dye placement in the commissure of Probst where DNLL fibers cross the midline invariably resulted in equivalent, bilaterally labeled bands in the IC (Gabriele et al., 2000). The results of this recent study in prenatal and postnatal rats indicated that mature afferent bands and patches are established before the onset of hearing [postnatal day 12/13 (P12/13) in rat] (Jewett and Romano, 1972; Puel and Uziel, 1987), suggesting that evoked activity may not be required for the initial organization of patterned projections in the ascending auditory pathway.
Despite considerable debate (for review, see Hübener and Bonhoeffer, 1999), it appears that both endogenously generated patterns of activity and molecular gradients contribute to the initial patterning that occurs in the absence of visual experience (i.e., thalamic eye-specific layers and cortical ocular dominance columns) (Stryker and Harris, 1986; Shatz and Stryker, 1988; Sretavan et al., 1988; Katz and Shatz, 1996; Penn et al., 1998; Crowley and Katz, 1999;Donoghue and Rakic, 1999; Miyashita-Lin et al., 1999; Rubenstein et al., 1999). It may be that these same developmental mechanisms are also influential in guiding the formation of projection patterns in the auditory system before experience. Mounting evidence suggests that spontaneous rhythmic discharges similar to those first described in the retina (Galli and Maffei, 1988; Meister et al., 1991; Wong et al., 1993; Feller et al., 1996, 1997) are present at various levels of the developing auditory system before the onset of hearing (Romand and Ehret, 1990; Rübsamen and Schäfer, 1990; Gummer and Mark, 1994; Lippe, 1994, 1995; Kotak and Sanes, 1995; Kros et al., 1998;Jones and Jones, 2000). Findings in the embryonic chick (Lippe, 1994,1995) suggest that the synchronous and rhythmic firing observed in the auditory nerve and brainstem is generated peripherally because it is abolished after cochlear removal or injection of tetrodotoxin into the perilymph (Koerber et al., 1966; Born and Rubel, 1988; Born et al., 1991; Lippe, 1994).
To determine the role of the sensory epithelia in pattern formation in the absence of auditory experience, we performed unilateral cochlear ablations on P2 rats, before segregation of the crossed DNLL projection (see Fig. 2). The results suggest that the density of the projection is determined by the target environment (IC), whereas pattern formation within the target depends on the activity of the afferent source (DNLL).
Preliminary findings have been published previously (Gabriele and Henkel, 2000).
MATERIALS AND METHODS
Experimental design and cochlear surgery. All procedures were approved by the institution's Animal Care and Use Committee and conform to National Institutes of Health standards. Data compiled from a total of 26 postnatal Sprague Dawley rats were included in the results of the present study (Table1). To test the influence of the auditory periphery on formation of afferent patterns in the IC (Fig.1), unilateral cochlear ablations were performed on P2, before the appearance of afferent banding (Fig.2). Rat pups were anesthetized by hypothermia, and an incision was made just inferior and ventral to the left pinna. The external auditory canal was identified and followed to the tympanic membrane. The middle ear cavity was exposed and cleared of mesenchyme, and the ossicles were identified. At this stage, surgical control animals were sutured and placed on a heating pad until consciousness was regained. In the ablation cases, the footplate of the stapes was carefully removed and access to the cochlear spaces was gained through the oval window. Exposure of the round window was also achieved in several of the cases. In an effort to disrupt the delicate ionic composition of the scalae, distilled water was perfused through the cochlea. Using a pulled Pasteur pipette, remaining cochlear contents were aspirated. The animals were sutured and placed on a heating pad. After recovery, pups were returned as a group to the litter and reared to P12.
Fixation, tracer placement, and sectioning. At P12, pups (control, surgical control, and experimental groups) were given an overdose of ketamine (100 mg/kg) and xylazine (12 mg/kg) and perfused through the heart with 4% paraformaldehyde fixative. The brains were subsequently removed from the skull, blocked in the coronal plane just rostral to the superior colliculus, and embedded in an egg yolk/gelatin mixture (5 ml 8% gelatin in dH2O/10 ml egg yolk). Coronal sections (50–75 μm) were cut on a vibratome from rostral to caudal through the block of tissue until the rostral boundary of the commissure of Probst was identified. The commissure was completely severed in the remaining block of tissue, and glass pins coated with crystals of the lipophilic dye 1,1′-dioctodecyl-3,3,3′,3′-tetramethylindocarbocyanine perchlorate (DiI) (Molecular Probes, Eugene, OR) were positioned in the midline (Fig. 3) [see Gabriele et al. (2000) for a more detailed description of the technique, DiI properties, and tracer limitations]. After dye placement, the block was placed in fresh 4% paraformaldehyde fixative and incubated at 37°C in the dark for 2–3 months. Fixative was changed monthly during the incubation period. Coronal sections were then cut (75 μm), mounted onto charged slides, and coverslipped while still wet with 0.1 mphosphate buffer, pH 7.4. Immediately after data collection, the temporary coverslips were removed, and the sections were remounted onto gelatin-subbed slides for Nissl staining with cresyl violet. Slides were then permanently coverslipped with Cytoseal (Stephens Scientific, Riverdale, NJ).
Fluorescence microscopy and image acquisition. Sections were viewed with an epifluorescent microscope (Nikon) equipped with a rhodamine filter set (ChromaTechnology, Brattleboro, VT). Because of the unstable nature of the fluorescent dye after sectioning, data collection was performed immediately and was completed within 48 hr. Images of all sections containing the DNLL and IC were video-captured and digitized using the public domain NIH Image program [developed at National Institutes of Health and available on the internet athttp://rsb.info.nih.gov/nih-image/; modified by Scion Corp. (Frederick, MD) for Windows system]. To qualitatively assess changes in the development of the projection pattern within the IC, comparable levels of the central nucleus (standardized region comprising the caudal extent of the rostral third of the central nucleus where banding was most evident in P12 controls) were determined on the two sides, and 35 mm photographs were taken. The midpoint of the DNLL along the rostrocaudal axis was also determined and photographed for each case to facilitate comparisons with the contralateral DNLL. Negatives were digitized using an AGFA DuoScan (Brockton, MA). Scanned images then were cropped in Adobe Photoshop (Adobe Systems Inc., San Jose, CA), and only the brightness and contrast were modified. The minimal image processing was standardized, such that minor manipulations in brightness and contrast were uniform for all digitized images.
Quantification of afferent bands in the IC. Digitized images of representative sections of the DiI-labeled DNLL projections to the central nucleus of the IC were processed and analyzed similar to that described previously for quantification of ocular dominance columns (Cabelli et al., 1995; Finney and Shatz, 1998). Briefly, images were smoothed with a low-pass Fourier filter (20% filter size and transition width) using NIH Image software (Scion Corp.). A brightness profile was derived along a line drawn from ventromedial to dorsolateral orthogonal to the axonal layers. Gray levels were normalized by the mean level for each profile. Peaks and troughs in the brightness profiles were identified and (1) band amplitude (peak-to-trough), (2) periodicity of banding (peak-to-peak), and (3) band width (at 50% maximal height) were determined. The mean and SD were calculated for each parameter. The data for the right and left side in unilateral ablation cases and controls were compared using a Student's t test, two-tailed. The data were also processed using a nonlinear regression to best fit a sine wave (GraphPad Prism, San Diego, CA) to the brightness profiles. Coefficient of determination (R2) values within the range 0.5 to 1.0 suggest periodicity of the labeled afferent pattern.
In addition, an index of the overall density (integrated density/unit area) of the projections in the central nucleus of the IC was measured (Scion Image Software) by determining the integrated density for an outlined selection of the central nucleus. In this way, overall density of the labeled projections on each side could be compared in the control and experimental groups.
Histology and data analysis. An essential part of any manipulation study is verification that the desired manipulation was accomplished. Thus, histological preparations of the cochlear nuclei and temporal bones containing the cochleas were assessed for each case.
It has been well documented in the literature that cochlear ablations result in a marked reduction in cochlear nucleus (CN) volume on the side of the ablation (Trune, 1982; Nordeen et al., 1983; Moore and Kowalchuk, 1988; Hashisaki and Rubel, 1989; Hardie and Shepherd, 1999). Using Neurolucida software (Microbrightfield, Colchester, VT), CN areas were traced directly from alternating Nissl sections. The total volume of each CN was estimated from the compiled data using Neuroexplorer (part of the Neurolucida software package). Volumetric comparisons were then calculated for individual cases (percentage reduction; left CN relative to right CN; positive percentages reflect a left CN volume reduction), and means for the three experimental groups were compared using statistical tests.
Temporal bone histology was performed to assess the degree of cochlear damage. Briefly, temporal bones containing the cochleas were harvested for each case after fixation and brain removal. Temporal bones were decalcified in 1% nitric acid in 10% formalin for 2 weeks, dehydrated, embedded in celloidin, and serially sectioned at 20 μm. Sections were then stained with hematoxylin and eosin, mounted, and coverslipped with Solvent-100 medium (IMEB, Inc., San Marcos, CA). Cochlear assessments were performed blindly, and determination of a compromised periphery was made on the basis of several factors (i.e., gross physical disruption or presence of blood in scalae, integrity of the Organ of Corti, presence of hair cells and spiral ganglion neurons, appearance of the stria vascularis).
Cochlear ablation cases (n = 7) were defined on the basis of two criteria: (1) cases showing a 20% or greater reduction in cochlear nucleus volume on the side of the ablation, and (2) cases exhibiting some degree of cochlear damage on the left side as evidenced by the temporal bone histology. Cases that failed to meet both criteria (n = 5) were not considered unilateral cochlear ablations and were included with surgical controls.
RESULTS
DiI labeling of the crossed DNLL projections to the IC
In each of the 26 cases, dye placement in paraformaldehyde-fixed tissue from P12 rat pups was consistently centered in the commissure of Probst. Given the relative isolation of decussating DNLL fibers from other ascending inputs to the IC, the midline commissure was severed to ensure complete labeling of the projections of interest. Labeling in every case yielded detectable axonal labeling that spanned the entire frequency-axis of the central nucleus, as well as retrogradely labeled cells present throughout DNLL isofrequency contours (Tanaka et al., 1985; Merchán et al., 1994; Bajo et al., 1999; Saint-Marie et al., 1999). Importantly, examination of retrogradely filled DNLL cells under high magnification revealed no evidence of collaterals to the ipsilateral IC. In addition, examination of cochlear nuclear subdivisions and the superior olivary complex revealed no retrogradely labeled cells in these hindbrain sources of afferent projections to the IC. Such observations not only provided confidence that the entirety of the crossed DNLL projections was labeled, but also excluded the possibility of partial labeling of other pathways known to send banded inputs to the IC (Kudo, 1981; Oliver, 1987; Shneiderman and Henkel, 1987; Shneiderman et al., 1988; Bajo et al., 1993; Oliver et al., 1997).
Control cases
In all P12 control cases (both normal and surgical controls), dye placement in the midline commissure resulted in symmetrical labeling (Fig. 4). The density and organization of labeled afferents within the IC in normal animals (Fig.4A,B), as well as retrograde filling of their cells of origin within the DNLL (Fig.4C,D), were always equivalent on the two sides. Despite unavoidable differences in the depth of pin placement and the amount of DiI that diffused into the DNLL commissure, the relative density of labeled afferent patterns and retrogradely labeled cells was remarkably consistent across controls. A quantitative index of the density of labeled fibers in the central nucleus of the IC (integrated density/unit area) when compared for the left and right sides varied <5%, thus supporting the qualitative observations.
Despite the absence of auditory experience during this early postnatal period, each of the labeled DNLL projections had segregated from a homogeneous distribution into an unmistakable pattern of afferent bands and patches that encompassed the entire frequency-axis of the central nucleus. The dense region of axonal labeling within the central nucleus was distinguished by fibers running parallel to the presumed fibrodendritic laminae. In all cases, these parallel afferent fibers appeared to terminate most heavily within alternating sublayers, thereby creating a pattern of afferent bands. Regions along bands that exhibited the heaviest labeling were termed afferent patches. An isolated band of fibers was consistently observed ending lateral to the central nucleus, confirming the presence of a crossed projection from the DNLL to deep layers of the external cortex of the IC [see Gabriele et al. (2000), their Fig. 8, for further detail]. Such reliable symmetry in the density, nuclear distribution, and patterns on the two sides provided an ideal model system for comparison of labeling from equivalent tracer placements in unilaterally lesioned animals.
Unilateral ablation cases
After unilateral cochlear ablation at P2, commissural dye placement at P12 revealed significant changes in the development of the crossed DNLL inputs to the IC. In contrast to the symmetry of anterograde and retrograde labeling observed in controls, each of the seven ablation cases exhibited notable differences in the density and pattern of afferents within the IC on the two sides, as well as in the densities of labeled cells in the DNLLs (Fig.5). A qualitative index of projection density (density/unit area) supports the qualitative observations of asymmetry in that the density of labeling on the left side (ipsilateral to the ablation) was at least five times greater than on the right side (contralateral to ablation) in the experimental group.
Differences in the amount and relative organization of labeled fibers within the ICs were most striking (Fig.5A,B). Considerably more afferent fibers were apparent within the ipsilateral IC (input from DNLL on the intact side) compared with the contralateral IC (input from the DNLL on the affected side). However, in no experimental case did either of these labeled projections appear as dense as the DNLL projections labeled in control cases (compare with Fig. 4). In addition to differences in the relative density of labeled afferent fibers, the two sides also displayed obvious differences in projection pattern. Although the bulk of labeling for each projection appeared to occupy the appropriate target area (normal DNLL patch location) within the central nucleus, a normal projection pattern within the IC ipsilateral to the ablation was no longer apparent (Fig. 5A). Bands and patches either failed to segregate within the central nucleus or were obscured by increased branching within intervening spaces. Although the normal banding pattern was not observed in the IC on the side of the ablation, the sparsely labeled projection in the opposite IC was clearly segregated (Fig. 5B), resembling the organization described in control cases. Like P12 controls, the thickness of bands and patches (ventromedial–dorsolateral dimension) within the contralateral IC measured ∼75 μm after unilateral cochlear ablation.
Asymmetric labeling also was apparent in retrograde filling of the DNLLs (Fig. 5C,D). Qualitatively fewer cells were observed in the DNLL contralateral to the ablation. This asymmetric distribution of labeled cells between the ipsilateral and contralateral DNLL was observed in all experimental cases. Although the differences in apparent number of retrogradely filled cells between the ipsilateral and contralateral DNLL was greater in some cases than in others, there were always more labeled cells in the DNLL ipsilateral to the ablation. Although the number of labeled cells appeared to be greater on the side receiving excitatory drive from the intact ear, morphometric analysis indicated no differences in either the volume of the ipsilateral and contralateral DNLL or the mean cell size (data not shown).
Experimental analyses
Quantification of DNLL afferent banding
To quantify the described effects of unilateral cochlear ablation on the establishment of DNLL bands and patches within the central nucleus of the IC, brightness profiles were generated from acquired images of standardized sections (see Materials and Methods). Brightness profiles of a representative control (Fig.6A) and an experimental case (Fig. 6B) illustrate the presence or absence of periodicity for the crossed DNLL projections. A regular sinusoidal periodicity was apparent for the left and right profiles of the control case (Fig. 6A, stippled and solid curves, respectively) as well as for the right profile of the experimental case (Fig. 6B, solid curve), whereas the left profile of the experimental case exhibited no periodicity (Fig. 6B, stippled curve). As a measure of sinusoidal periodicity, nonlinear regressions were performed to best fit a sine wave to each of the individual brightness profiles (offsets of Fig. 6, A and B; see Materials and Methods for significance of nonlinear regressions andR2 values). The meanR2 values for controls and experimental right sides suggest a regular periodicity and were not considered different (0.56 and 0.52, respectively), but the meanR2 value for experimental left sides was significantly different (0.09). Such a low meanR2 value supports the qualitative assessment that the labeled projection distributions for the crossed DNLL inputs terminating within the IC ipsilateral to the ablation were not periodic.
In addition, peaks and troughs in the afferent pattern were identified from the brightness profiles, and peak-to-trough amplitude, period length, and band width were measured. Means and SDs are shown in Table2. The banding parameters were not different between the left and right sides of any controls. In all experimental cases, left side values were significantly different from controls, whereas right side values were not significantly different from controls. Although the period and band width appeared to decrease on the left side relative to controls, it should be emphasized that these measures were not actually periodic based on best sine wave curve fit (Fig. 6B). Therefore, these parameters cannot be compared directly in the experimental cases. It should also be noted that when comparing the amplitudes the data were normalized by the mean in each sample. Thus, the relative change in density of labeling between the peaks and troughs for the right side in the experimental group is not different from controls, but the absolute values of amplitude are greatly reduced given that overall density (integrated density/unit area) is at least five times less than the left side or control density.
Cochlear nucleus degeneration
Unilateral cochlear ablation resulted in a significant reduction in cochlear nucleus volume on the side of the lesion (Fig.7). Although different divisions of the CN appeared to be affected to varying degrees as previously described (Trune, 1982; Moore and Kowalchuk, 1988), percentages reflect reductions in total volume. In experimental animals, reduction in volume of the left CN relative to the right CN ranged from 20 to 57%, with a mean value of 42%. The extent of volume reduction appeared to correlate with the severity of the cochlear lesion.
Large reductions in CN volume determined by quantitative measurements were evident qualitatively as well, especially in the anteroventral division of the cochlear nucleus (AVCN). Coronal sections through comparable regions of the AVCN are shown for a control and an ablation case (Fig. 8). In the control case, the left and right AVCN appeared similar (Fig.8A,B), whereas the AVCN ipsilateral to the cochlear ablation (Fig. 8C) appeared much smaller than the AVCN on the normal side (Fig. 8D).
Cochlear assessment
Cochlear damage was determined based on the overall physical appearance of the structure, including the relative integrity of the Organ of Corti, the presence or lack of hair cells and spiral ganglion neurons, and the appearance of the stria vascularis. Examination of temporal bone histology revealed evidence of cochlear damage on the operated side (left) in each of the ablation cases. Disruption of cochlear spaces, substantial hair cell loss, and a compromised stria vascularis were common indications of an affected cochlea (Fig.9). Although there was considerable variation in the extent of cochlear damage among cases, the disruption in each case was sufficient not only to cause a substantial reduction in CN volume on the affected side, but also to result in significant reorganization of the developing DNLL circuitry within the auditory midbrain. It is noteworthy that the spiral ganglion appeared unaffected on the ablated side in a few cases, despite evidence of widespread hair cell loss (Fig. 9C). These cases provided confidence that the observed changes were not simply caused by transneuronal degeneration.
DISCUSSION
The results of these experiments in control and unilaterally ablated postnatal rats indicate considerable plasticity in the development of DNLL afferent patterns within the IC. This plasticity suggests that the auditory periphery influences the development of afferent patterns within the IC before the onset of hearing. Although DiI placements in the commissure of Probst in P12 control rats resulted in symmetrical labeling of the DNLL afferent projections, such a balance was altered dramatically after unilateral cochlear ablation (Fig. 10). Specifically, the relative amplitude, periodicity, and band width that were quantitatively assessed from brightness profiles of the labeled afferent projections were significantly asymmetric in experimental animals (Fig. 6, Table2). These results support the possibility that segregation of this binaural projection into bands and patches before the onset of hearing is dependent on a balance of cochlear activity. To further test this notion, future experiments are planned to examine the development of afferent bands and patches in the central nucleus of the IC after bilateral cochlear ablation.
Band and patch formation: what guides them?
The initial, diffuse arrangement of DNLL fibers and subsequent segregation into afferent bands previously described (Gabriele et al., 2000), together with the present findings, suggest that developmental factors influence the establishment of projection domains before the onset of experience. For an afferent fiber to project to the appropriate domain within the IC, it not only must identify the appropriate sublayer (afferent bands) of a given fibrodendritic lamina, it also must determine the specific population of neurons within the target sublayer with which to form connections (afferent patches).
In adult cats, it has been shown that injections in matched frequency regions of the dorsal cochlear nucleus and the lateral superior olive (LSO) that are driven by the same ear produced labeled bands of afferent fibers that appeared to terminate within the same sublayer of the contralateral IC (Oliver et al., 1997). Despite being driven by the same ear and occupying the same sublayers, the distribution of these two inputs was shown to preferentially target spatially distinct regions of specific sublayers. These data suggest that laterality of input may guide afferents to their appropriate sublayers, whereas the establishment of patches within sublayers may follow a nucleotopic order that is determined by origin of inputs.
Potential role of the auditory periphery
DNLL bands and patches form before the onset of evoked auditory experience in rat (Gabriele et al., 2000), and the banded pattern of afferents within IC appears to be related to the laterality of inputs. These observations, paired with the present data demonstrating considerable developmental plasticity after unilateral cochlear ablation, suggest that the auditory periphery plays a role in the development of afferent patterns within the IC. Although the rat cochlea is still immature during the first 2 postnatal weeks and compound action potentials recorded at the round window do not appear until between P12 and P13 (Uziel et al., 1981; Rybak et al., 1992), there is rhythmic endogenous activity within the ascending system of various species before hearing onset that is thought to be generated peripherally (Koerber et al., 1966; Born and Rubel, 1988; Romand and Ehret, 1990; Rübsamen and Schäfer, 1990; Born et al., 1991;Gummer and Mark, 1994; Lippe, 1994, 1995; Kotak and Sanes, 1995; Kros et al., 1998; Jones and Jones, 2000). If such endogenous activity conveys meaningful representations of correlated, peripheral events to the IC, then the segregation of afferents within the central nucleus into ear-specific sublayers (i.e., formation of afferent bands within sublayers based on laterality) may involve activity-dependent mechanisms.
Segregation of afferents into appropriate sublayers then may be conceptualized as a pattern of “aural dominance bands,” analogous to ocular dominance columns in the visual cortex (for review, see Katz and Shatz, 1996). In the formation of these aural dominance bands, it is possible that any of the full complement of afferent projections in the interband spaces driven by the opposite ear actively compete with crossed DNLL projections for synaptic space. A number of bilaterally projecting inputs to the IC, including those from the DNLL, distribute endings within parallel interdigitating bands or sublayers (Shneiderman and Henkel, 1987; Oliver et al., 1997; Gabriele et al., 2000). Competition with the uncrossed DNLL projections would be analogous to competitive interactions of pathways from right and left eyes in eye-specific layers in thalamus or ocular dominance columns in visual cortex. Nevertheless, the present data do not provide sufficient information about the potential players in the competitive process to conclude the specific role of competition in forming aural dominance bands.
Results from our experimental animals suggest that segregation of the DNLL input into aural dominance bands depends in some manner on the activity originating in the cochlea. Considering both excitatory and inhibitory ascending auditory circuits, predictions can be made regarding the net effect that a unilateral cochlear ablation has on the activity level in specific auditory nuclei (Fig.11). For example, both DNLL and IC receive most of their excitatory drive contralaterally, whereas ipsilaterally driven inputs are mostly inhibitory in nature (Clopton and Winfield, 1974; Silverman and Clopton, 1977; Beyerl, 1978; Semple and Aitkin, 1979; Brunso-Bechtold et al., 1981; Glendenning et al., 1981; Markovitz and Pollak, 1994; Wu and Kelly, 1995a,b, 1996; Kelly and Li, 1997; Pollak, 1997). The local environments of the DNLL and the IC opposite the lesion, therefore, theoretically will be deprived, because ipsilateral suppression is unaffected, and contralateral excitation is compromised by the ablation. The opposite is true for the DNLL and the IC on the side of the ablation. Decreased inhibition coupled with intact excitatory pathways should result in activity levels that are likely to be enhanced relative to normal.
Segregation of the crossed projection from the deprived DNLL into distinct bands after cochlear ablation was invariably less evident than in control animals, whereas fibers arising from the DNLL receiving excitatory input from the intact ear consistently separated into bands within the contralateral IC (Fig. 11). A brain slice study performed in neonatal gerbils (Sanes and Takács, 1993) is particularly relevant to these findings (specifically the projection arising from the deprived DNLL), because it demonstrated activity-dependent refinement of another inhibitory brainstem circuit early in auditory development. After cochlear removal in P7 gerbils, individual axons arising from the functionally denervated medial nucleus of the trapezoid body failed to restrict their terminal arbors into isofrequency bands (Henkel and Gabriele, 1999) within the target LSO as previously described (Sanes and Siverls, 1991). The effect of cochlear removal on the LSO environment is analogous to that hypothesized for the IC ipsilateral to the ablation in our study. Similarly, the inhibitory connections from the denervated medial nucleus of the trapezoid body can be likened to the crossed projection from the deprived DNLL. Despite an absence of change in total arbor length and bouton number, Sanes and Takács (1993) reported a significant increase in the number of branch points after denervation of the fibers, perhaps indicative of de novo sprouting. Increased branching and lack of refinement of the crossed projection from the deprived DNLL may contribute to the lack of evident banding within the IC on the side of the ablation. Similar brain slice studies looking at single DNLL axons will be needed to confirm this hypothesis.
Mechanisms of pattern formation before onset of hearing
As described previously, there is considerable evidence that correlated patterns of spontaneous neural activity are present at various levels of the ascending auditory system long before the onset of hearing. These patterns of activity that are thought to be of peripheral origin may direct activity-dependent development of aural dominance bands in the central nucleus of IC. To address appropriately the potential role of activity in early circuit formation, interpretation of the results should not simply consider the amount of afferent activity but rather focus on the correlation between presynaptic and postsynaptic activity. Segregation of the labeled projections within the IC into afferent bands after unilateral cochlear ablation appeared to be dependent on presynaptic activity (activity of DNLL fibers). Fibers arising from the nondeprived DNLL clearly were able to segregate, whereas axons arising from the deprived DNLL failed to form distinct bands within the target. Interestingly, the amount of afferent activity appeared to be unimportant for determining the density of the projection distribution within the target. Instead, the results suggest that the postsynaptic environment (activity of IC cells) determines the relative density of the projection within the target (Fig. 11).
Differential mechanisms for presynaptic and postsynaptic activity might explain the present findings that the denser projection arises from the deprived DNLL with qualitatively fewer retrogradely labeled cells, whereas the sparser projection arises from the nondeprived DNLL exhibiting more retrogradely labeled cells. Terminal arbors from the few cells in the deprived DNLL do not segregate clearly, presumably because of the decrease in afferent activity, yet they appear to elaborate extensively within their target. The relative density of this input likely reflects target conditions favorable for axon elaboration, i.e., normal or enhanced levels of excitation and presumably a normal trophic environment. Conversely, the projection from the nondeprived DNLL likely encounters a target unfavorable for elaboration, i.e., loss of excitation and presumably a decrease in trophic support. Thus, despite being an active input, it fails to display a normal degree of axon elaboration. A recent study in the visual system reported evidence that the differential effects of activity of the afferent axons in comparison with the activity of the target cells regulate the growth and retraction of geniculocortical fibers (Hata et al., 1999). Such findings suggest that it is not merely the amount of activity in afferent fibers but rather the correlation between presynaptic and postsynaptic activity that is important for different aspects of afferent organization.
Although segregation into afferent bands and the relative density of the crossed DNLL projections appeared to be contingent on activity levels of the afferent fibers and the target cells, the ability of these projections to recognize appropriate terminal zones (i.e., DNLL patch location) appeared to be unaffected by cochlear ablation. In all experimental cases, the area along the frequency-axis of the central nucleus with the heaviest label was consistent with the patch location for the crossed DNLL input defined in P12 controls (Gabriele et al., 2000). It may be that the auditory periphery exerts no influence over the nucleotopic ordering of afferents within the central nucleus of the IC. Instead, signaling between presynaptic and postsynaptic elements, including receptor/ligand interactions and/or molecular cues (i.e., neurotrophic or extracellular matrix gradients), may provide sufficient instruction for the organization of afferents based on origin of input. Future experiments are planned to further assess what developmental mechanisms drive circuit formation in the ascending auditory system before experience.
Footnotes
This work was supported by National Institutes of Health (National Institute on Deafness and Other Communication Disorders) Grant DC000813. We thank Dr. David Riddle and Dr. John McHaffie for their helpful comments during the preparation of this manuscript. Technical assistance for temporal bone histology provided by Stephanie Evans and Joan Schnute was invaluable.
Correspondence should be addressed to Dr. Mark L. Gabriele, Department of Neurobiology and Anatomy, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1010. E-mail:gabriele{at}wfubmc.edu.