Patterns of Unilateral and Bilateral Projections From Layers 5 and 6 of the Auditory Cortex to the Inferior Colliculus in Mouse
Nathiya Vaithiyalingam Chandra Sekaran1,2† 
Meena S. Deshpande1,2† 
Baher A. Ibrahim1,2 
Gang Xiao1,2 Yoshitaka Shinagawa1,2 
Daniel A. Llano1,2,3*- 1Department of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign, Champaign, IL, United States
- 2Beckman Institute for Advanced Science and Technology, Urbana, IL, United States
- 3Carle Illinois College of Medicine, Urbana, IL, United States
The auditory cortex sends massive projections to the inferior colliculus, but the organization of this pathway is not yet well understood. Previous work has shown that the corticocollicular projection emanates from both layers 5 and 6 of the auditory cortex and that neurons in these layers have different morphological and physiological properties. It is not yet known in the mouse if both layer 5 and layer 6 project bilaterally, nor is it known if the projection patterns differ based on projection location. Using targeted injections of Fluorogold into either the lateral cortex or dorsal cortex of the inferior colliculus, we quantified retrogradely labeled neurons in both the left and right lemniscal regions of the auditory cortex, as delineated using parvalbumin immunostaining. After dorsal cortex injections, we observed that approximately 18–20% of labeled cells were in layer 6 and that this proportion was similar bilaterally. After lateral cortex injections, only ipsilateral cells were observed in the auditory cortex, and they were found in both layer 5 and layer 6. The ratio of layer 5:layer 6 cells after lateral cortex injection was similar to that seen after dorsal cortex injection. Finally, injections of different tracers were made into the two inferior colliculi, and an average of 15–17% of cells in the auditory cortex were double-labeled, and these proportions were similar in layers 5 and 6. These data suggest that (1) only the dorsal cortex of the inferior colliculus receives bilateral projections from the auditory cortex, (2) both the dorsal and lateral cortex of the inferior colliculus receive similar layer 5 and layer 6 auditory cortical input, and (3) a subpopulation of individual neurons in both layers 5 and 6 branch to innervate both dorsal cortices of the inferior colliculus.
Introduction
The auditory corticocollicular system consists of a large set of descending projections from the auditory cortex (AC) to the inferior colliculus (IC), which is the midbrain integration center (Suga, 2008; Malmierca and Ryugo, 2011; Bajo and King, 2012; Stebbings et al., 2014). The projection primarily targets the non-lemniscal nuclei of the IC: the dorsal cortex (DC) and lateral cortex (LC) (Saldaña et al., 1996; Winer et al., 1998; Torii et al., 2013). Stimulation and inactivation of AC inputs have been shown to have prominent effects upon the response properties of IC cells with respect to sound frequency and intensity, cues for spatial sound localization, and plastic changes in the IC (Jen et al., 1998; Yan and Suga, 1998; Popelář et al., 2003; Yan et al., 2005; Sun et al., 2007; Bajo et al., 2010; Asokan et al., 2018). The corticocollicular system is also heterogeneous and has been shown to emanate from two distinct layers of the AC: a large projection from layer 5 and a smaller (25% of the total in mice) projection from lower layer 6 (Schofield, 2009; Slater et al., 2019). Previous work has shown that neurons in these layers have different physiological properties, receive different cortical and thalamic inputs, and have different termination sizes in the IC (Slater et al., 2013, 2019; Yudintsev et al., 2019). Although the functional impact of layer 5 vs. layer 6 projections onto IC neurons is not yet known, in other corticofugal systems such as the corticothalamic projection, layer 5 and layer 6 neurons have different impacts on their synaptic targets, and likely have different roles in sensory processing (Ojima, 1994; Reichova and Sherman, 2004; Takayanagi and Ojima, 2006; Theyel et al., 2010; Williamson and Polley, 2019).
The corticocollicular system is one of multiple auditory corticofugal pathways that have cascading connectivity to ultimately influence auditory processing at the level of the auditory periphery (Xiao and Suga, 2002; Perrot et al., 2006; León et al., 2012; Terreros and Délano, 2015). Although these corticofugal systems appear to have many common organizational properties, one way in which they appear to differ is in the degree to which the projections are bilateral. Corticothalamic projections from AC to the medial geniculate body appear to be unilateral, whereas AC projections to the cochlear nucleus appear to be bilateral, but with an ipsilateral bias (Weedman and Ryugo, 1996; Jacomme et al., 2003; Schofield and Coomes, 2005). Studies have shown that corticocollicular neurons have a bilateral component in opossums, guinea pigs, and hedgehogs (Willard and Martin, 1984; Künzle, 1995; Saldaña et al., 1996; Coomes et al., 2005), with the majority of the projection being ipsilateral.
Despite the anatomical differences between layer 5 and layer 6 projections to the IC, many questions remain about the functional organization of this projection. For example, it is unknown in the mouse if both layer 5 and layer 6 project to both the DC and LC of the IC, and if so, if they project in equal proportions. In addition, it is unknown if both layer 5 and layer 6 project to both ICs in the mouse, and if so, if individual neurons branch to project to both sides. Therefore, in the current study, we injected a sensitive retrograde tracer, Fluorogold, unilaterally into either the DC or the LC of the mouse and determined the extent to which the projection was in the ipsi- vs. contralateral lemniscal AC fields. To determine if the bilaterality of the projection was due to individual neurons that branch to both ICs, or comprise separate ipsi- and contralateral projections, different tracers were placed in each IC, and examination was done for double-labeled cells in the AC. We found that while both LC and DC received layer 5 and layer 6 AC inputs in similar proportions, only the DC received bilateral inputs from the AC. In addition, we observed that after injections of different tracers to the two different ICs, double-labeled cells were observed in both layers 5 and 6, suggesting that a subset of cells from each layer branch to innervate each DC.
Materials and Methods
Animals
Experiments were performed in adult CBA/CaJ (Jackson Labs, 000654) or Swiss Webster (Envigo, Hsd:ND4) mice of both sexes ranging from ages 4 to 6 months. Swiss Webster mice were only used for the three injections involving red retrobeads. Thirteen mice were used in the quantitative analysis of this study, and their data are summarized in Tables 1, 2. Eight additional animals were excluded due to poor injection sites and were not included in the analysis. All procedures were approved by the Institutional Animal Care and Use Committee at the University of Illinois. Animals were housed in care facilities approved by the Association for Assessment and Accreditation of Laboratory Animal Care International. Every attempt was made to minimize the number of animals used and to reduce suffering at all stages of the study.
Table 1. All animals used for unilateral injections in this study, with numbers of cells counted per animal.
Table 2. All animals used for bilateral injections in this study, with numbers of cells counted per animal.
Tracer Injection
Sterile instruments and aseptic techniques were used for all surgical procedures. Mice were anesthetized intraperitoneally with a mixture of ketamine hydrochloride (100 mg/kg) and xylazine (3 mg/kg) and acepromazine (3 mg/kg). The mouse was placed into a Kopf Model 940 Small Animal Stereotaxic Instrument with digital readout. The head was shaved and disinfected with Povidone–iodide and 70% ethanol. An incision was made in the scalp and the surrounding skin was injected with lidocaine (2% Covetrus, United States) intradermally as local anesthetic and carprofen (3 mg/kg, Henry Schein Melville, NY, United States) was given subcutaneously for post-operative pain management. Moisture Eyes ophthalmic ointment was applied to each eye to protect the cornea from drying. A small craniotomy was made over the IC using a surgical drill, and a small glass micropipette (tip size approximately 10 microns) was filled with Fluorogold (Fluorochrome, LLC, Denver, CO, United States), 1% in phosphate-buffered saline (PBS) for unilateral injections, and 0.1 acetate buffer (pH 3.3) for the bilateral injections. The left side was chosen for consistency, given left–right differences that have been described in the mouse auditory system (Oviedo et al., 2010; Levy et al., 2019). For bilateral injections, the right IC was injected with either Cholera Toxin B conjugated to Alexa-Fluor 555 (CTB-555, Invitrogen Cat# C34776) at 1% in PBS, Lumafluor red retrobeads (RB, diluted 1:1.5 in PBS), or unconjugated CTB (Listlabs #104, 2 mg/mL in PBS). In all cases, tracers were pressure injected into the IC using a WPI Nanoliter 2010 injector and Micro4 pump controller at 10–20 nl per min. Volumes of injectates varied and are shown in Tables 1, 2. After awakening from surgery, animals were returned to their home cages and to their vivarium until euthanized.
Tissue Processing
Following a 7-day survival period, animals were anesthetized with overdose of ketamine and xylazine (200 mg/kg, 6 mg/kg) and perfused transcardially with 4% paraformaldehyde (PFA) in PBS at pH 7.4. Brains were removed and post fixed overnight in the PFA solution. After being cryoprotected in an ascending series of sucrose solutions, each brain was embedded and cut into 40–50-μm-thick coronal sections on a cryostat that were collected serially in two sets.
Immunostaining
Parvalbumin (PV) immunostaining was done to delineate the borders of the lemniscal regions of the AC [primary AC and anterior auditory field (Molinari et al., 1995; Kosaki et al., 1997; Cruikshank et al., 2001; Llano and Sherman, 2008)]. Sections were microwaved for 15 s and then incubated for 30 min in a solution of 0.3% Triton X-100 in PBS to enhance membrane permeability. The sections were then transferred to a blocking solution consisting of 0.3% Triton X-100 and 3% goat serum in PBS and incubated for 30 min. The primary antibody solution consisted of 1:500 monoclonal anti-PV raised in mouse (P 3088, Sigma Aldrich) in the blocking solution. Sections were incubated in this solution overnight and rinsed in three changes of the Triton X-100 in PBS solution the following day. The sections were then transferred to a secondary antibody solution and incubated at room temperature for 2 h. This solution consisted of 1:100 Alexa Fluor 568-conjugated goat anti-mouse secondary antibody (catalog #A-11004, Invitrogen). Following a final series of washes in PBS, the sections were mounted on gelatin-coated slides and coverslipped with an anti-fade solution (Vectashield; Vector Laboratories). For immunostaining of CTB, after blocking with 3% donkey serum in 0.3% Triton X-100, sections were incubated with 1:10,000 anti-CTB antibody in blocking solution (#703 Listlabs) overnight at 4°C. After washing, sections were incubated with 1:200 solution of Donkey anti-Goat IgG (H + L) Cross-Adsorbed Secondary Antibody conjugated to Alexa Fluor 555 (Invitrogen # A-21432) diluted in blocking buffer with a 1:200 dilution.
Imaging and Analysis
Sections were imaged with a Leica SP8 laser scanning confocal microscope and LAS X control software or with an Olympus IX71 inverted epifluorescence microscope. For confocal images, each IC tissue section containing retrograde label, 40 × mosaic Z-stacks were taken throughout the entire depth and x–y plane of the IC. The stacks were collapsed into 2D maximum intensity projections and tiled into a single image using LAS X software. ImageJ software was used to adjust the color balance and to draw masks around the edge of the tissue to remove the embedding medium.
Data Quantification and Statistics
PV immunostaining was used to mark the borders of the lemniscal portions of the AC. For counting Fluorogold-labeled cells in the AC, neurons from six non-consecutive sections were selected. These sections were distributed across the anterior–posterior dimension of the AC. The labeled cells in AC within the PV-enriched zone were counted using ImageJ software. For counting double-labeled cells, to ensure that areas of maximum overlap were examined, only sections where at least 20 cells per tracer type were present were analyzed. Given the small numbers of animals (n = 4 in each injection location for unilateral injections, n = 5 for bilateral tracer injections), normality was not assumed and non-parametric statistics were used throughout with a threshold for significance of p < 0.05. Data are presented as median ± standard deviation.
Results
Thirteen adult (4–6 months old) male and female mice were used in this study. Four were injected with Fluorogold into the left LC, four were injected into the left DC, and five were injected into both ICs. For both DC and LC injection sites, there tended to be some spillover into the central nucleus of the IC (CNIC). See Tables 1, 2 for a listing of all mice used for quantitative analysis in this study. For the mice injected into either DC or LC, PV immunostaining was done to delineate the lemniscal regions of the AC. An example of a DC injection site as well as images from both ACs demonstrating layer 5 and layer 6 retrograde label, and the corresponding PV images are shown in Figure 1.
Figure 1. Coronal images showing an example DC injection site (inset), and the corresponding contralateral Fluorogold label (B), ipsilateral Fluorogold label (C), and PV immunostaining pattern (A,D). Scale bar = 250 μm. L5 = layer 5, L6 = layer 6, AUDv, ventral auditory region.
Distributions of Ipsi- vs. Contralateral Cells in Auditory Cortex After Dorsal Cortex or Lateral Cortex Tracer Injection
The total number of cells in the lemniscal regions of the ipsilateral and contralateral AC were counted and compared. In all cases of DC injections (n = 4), there were significantly greater numbers of retrogradely labeled cells in the ipsilateral cortex (p = 0.02, Wilcoxon signed-rank test), with a median ipsilateral:contralateral ratio = 6.63 ± 2.18, indicating that approximately 85% of all labeled cells were ipsilateral. After injection into the LC (n = 4), 100% of all labeled cells in all animals were found in the ipsilateral AC.
Distribution of Layer 5 vs. Layer 6 Corticocollicular Cells in Ipsi- vs. Contralateral Dorsal Cortex Injection
After DC injection, the proportions of layer 5 vs. layer 6 corticocollicular cells in the lemniscal AC were compared using a within-animal comparison. Although the total number of cells was significantly greater on the ipsilateral side, there was no difference in the proportion of layer 6 cells on the two sides (ipsilateral: 20.83 ± 4.96% vs. contralateral: 17.09 ± 3.36%, p = 0.69, Wilcoxon signed-rank test, Figure 2). Although LC injections did not produce any contralateral label, the retrogradely labeled cells in the ipsilateral lemniscal AC contained substantial layer 6 label. We compared the proportion of ipsilateral layer 6 label after DC compared to LC injections and found no significant difference between the two (DC 20.83 ± 4.96%, LC 18.72 ± 7.11%, p = 0.49, Mann–Whitney).
Figure 2. Comparison of the layer 6 percent of total cells located ipsilaterally and contralaterally of the lemniscal AC between each mouse (n = 4) with injection site in DC. p-value calculated using Wilcoxon Signed Rank Test. See Table 1 for actual values. n = 4 mice. Each color corresponds to a different mouse.
Double-Retrograde Injection Into Left and Right Lateral Cortex
CTB-555, unconjugated CTB, or RB were injected into the right IC and Fluorogold was injected into the left IC, and images containing cells stained with each tracer were overlaid. Similar to previous findings (Coomes et al., 2005), we found three cell labeling types in each layer: CTB- or RB-only labeled cells, Fluorogold-only labeled cells, and cells labeling with both a red tracer and Fluorogold. All three cell types were found in both layer 5 and layer 6 (Figure 3), suggesting the presence of branching cells in each layer. The numbers of single- and double-labeled cells in each layer were counted and summarized in Table 2. The proportions of double-labeled cells ranged from 2.6 to 34.2% per layer per animal. The mean proportion of double-labeled cells was similar in layer 5 compared to layer 6 (15.7 ± 12.5 [SD]% in layer 5 vs. 16.6 ± 6.1 [SD]% in layer 6, n = 5 mice, p = 0.686, Wilcoxon Signed Rank, see Figure 4).
Figure 3. Coronal sections showing double injection site of Fluorogold (FG) on the left and CTB-555 on the right IC. (A) Grayscale image showing contralateral CTB-555-labeled cells. (B) Grayscale image showing ipsilateral FG-labeled cells. (C) Overlay between panel (A) and panel (B), showing single-labeled (red or green) and double-labeled (yellow) cells in each layer in insets. Scale bar = 100 μm.
Figure 4. Comparison of the proportion of double-labeled cells found in each layer after injection of different tracers into the left and right IC. See Table 2 for actual values. n = 5 mice. p-value calculated using Wilcoxon Signed Rank Test. Each color corresponds to a different mouse.
Discussion
In this report, we used single- and double-retrograde tracing methods in the mouse to investigate patterns of unilateral vs. bilateral input from AC layers 5 and 6 to the IC. We report three main findings: (1) only the DC receives bilateral projections from the AC, (2) both the DC and LC receive similar proportions of layer 5 and layer 6 auditory cortical input, and (3) a subset of individual neurons in both layers 5 and 6 branch to innervate the DC bilaterally. These findings are summarized in the model shown in Figure 5. Below, we discuss the implications of these findings.
Figure 5. Model depicting the unilateral and projections from layers 5 and 6 of the AC. CNIC, central nucleus of the IC.
Technical Considerations
Cortical areas in this study were defined using PV immunostaining, which has been established to distinguish lemniscal auditory areas (primary AC and anterior auditory field) from non-lemniscal areas (Molinari et al., 1995; Kosaki et al., 1997; Cruikshank et al., 2001). Thus, we have not attempted to differentiate primary AC vs. anterior auditory field proportions of either layer 5 or layer 6, although we consistently see similar proportions of each cell type throughout the anterior–posterior extent of the PV-enriched zone. Future work using in vivo mapping of auditory fields prior to the injection of tracers may be helpful to determine if differences exist in the layer 5 vs. 6 projections from primary AC or anterior auditory field to the IC, or in the non-lemniscal regions of the auditory cortex.
The proportion of cells found to be double-labeled after injection of different tracers into different sides was found to be relatively low (range = 2.6–34.2%). Previous work has shown that this approach is susceptible to significant undercounting (Doucet et al., 2003; Coomes et al., 2005; Schofield et al., 2007). For example, when co-injecting mixed tracers of different chemical entities, one of which being synthetic beads (similar to the current study) into the same location of the IC, a range of 4–70.1% of AC cells were double-labeled (Schofield et al., 2007). The undercounting occurs because the two injections may not be matched in terms of their projection fields and because of differential efficiency of the two labels. We attempted to make our sites large enough to encompass major portions of the DC bilaterally, but without being so large as to risk entering neighboring structures, such as superior colliculus. Thus, we assume that the percentage of cells that branch to innervate both colliculi is higher than the proportion of double-labeled cells reported here.
Implications
The results of this study suggest that both the DC and LC receive similar proportions of layer 5 and layer 6 input, but that only DC receives input from the contralateral AC. These results differ somewhat from those of Schofield (2009), who did not observe contralateral corticocollicular projections from layer 6 in guinea pig. The differences may be related to the different species or tracer used. Although layer 6 projections to the IC have been identified in multiple species including mice, rats, gerbils, ferrets, and hedgehog tenrec (Games and Winer, 1988; Künzle, 1995; Doucet et al., 2003; Bajo and Moore, 2005; Bajo et al., 2007), the relative proportions of those projections may differ. In the case of guinea pigs, approximately 10.2% of the total cell population was determined to come from layer 6 using a variety of tracers excluding Fluorogold. However, the current study and a previous study have established that this number is roughly 20–25% in mice using Fluorogold, which is a very sensitive retrograde tracer (Schofield, 2008). This difference in the tracers, and the approximately sixfold greater ipsilateral- vs. contralateral-projecting corticocollicular cells than contralateral-projecting cells, coupled with a smaller proportion of layer 6 cells in guinea pigs, suggest that the observation of the lack of layer 6 contralateral-projecting cells in guinea pig was due to a threshold effect.
We also observed that a small proportion of cells branched to innervate both ICs (15.7% in layer 5 and 16.6% in layer 6). These values are higher than those seen in the guinea pig layer 5 [range = 2.5–11.9% (Coomes et al., 2005)]. However, given the uncertainties regarding the precise values of double-labeled cells as outlined by several authors previously (Doucet et al., 2003; Coomes et al., 2005; Schofield et al., 2007) as well as the species and tracer differences in this study, it is not clear that the differences between our study and the Coomes et al. (2005) study represent real biological differences in branching patterns. However, both studies do indicate that bilateral coordination of IC modulation is an important feature in a subset of the corticocollicular projection, and the current report extends this finding to layer 6.
The implications of having bilateral projections from AC to portions of the IC are not yet known. The IC receives bilateral projections from the auditory brainstem (Coleman and Clerici, 1987; Cant and Benson, 2006, 2008) and receives inputs from the superior olive (Kelly et al., 1998; Loftus et al., 2004), which itself gets bilateral input. Therefore, it is unlikely that a bilateral descending projection is required to produce sensitivity to sounds from both ears. The layer 5 corticofugal system has been hypothesized to serve as a system that drives rapid escape behaviors (Xiong et al., 2015; Li et al., 2021). In addition, the layer 5 corticofugal projections in other sensory systems appear to be widely branching to multiple sensory and motor regions (Deschênes et al., 1994; Bourassa and Deschenes, 1995; Bourassa et al., 1995; Kita and Kita, 2012; Guo et al., 2017; Prasad et al., 2020). Therefore, it is not surprising to find a bilateral projection system to the inferior colliculi, which also project to motor structures to mediate escape responses (Kawamura, 1975; Aitkin and Boyd, 1978; Edwards et al., 1979; Cadusseau and Roger, 1985; Appell and Behan, 1990; Huffman and Henson, 1990; Lesicko and Llano, 2020). The presence of a bilateral layer 6 system, which we have previously speculated to serve a modulatory role (Yudintsev et al., 2019; Asilador and Llano, 2020), was less expected, but may suggest that the dual functions of layer 5 and layer 6 are necessary for the potential escape function of the layer 5 corticofugal projections. The absence, then, of a bilateral projection to the LC may suggest that this region is less likely to be involved in rapid motor escape behaviors than DC. Future work comparing the corticofugal response properties of cortical-recipient cells in LC or DC will help to clarify their separate roles in acoustic behavior.
Summary and Conclusion
In this study, we observed that lemniscal regions of the AC send bilateral projections from layers 5 and 6 to the DC of both inferior colliculi, with the majority being ipsilateral. We also observed that the LC receives only an ipsilateral projection from the AC and that this projection is derived from both layers 5 and 6. The proportion of layer 6 cells projecting to the IC is approximately 18–20% and does not differ based on IC target. Finally, we observed that the bilateral projection to the DC comprises, at least in part, individual neurons in both layers 5 and 6 that branch to innervate both DCs. Understanding the implications of these findings requires further investigation but may relate to the suspected roles of corticofugal projections in rapid acoustic escape behaviors.
Data Availability Statement
The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.
Ethics Statement
The animal study was reviewed and approved by Illinois Institutional Animal Care and Use Committee (IACUC).
Author Contributions
NV, MD, and DL analyzed the data and co-wrote the manuscript. BI performed stereotactic injections. GX and YS processed the tissue sections. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by R01DC013073 and R01DC016599 to DL and an award from the Benjamin R. and Elinor W. Bullock and Edwin E. and Jeanne Bullock Professorial Scholar fund to DL.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
Aitkin, L., and Boyd, J. (1978). Acoustic input to the lateral pontine nuclei. Hear. Res. 1, 67–77. doi: 10.1016/0378-5955(78)90010-2
Appell, P. P., and Behan, M. (1990). Sources of subcortical GABAergic projections to the superior colliculus in the cat. J. Comp. Neurol. 302, 143–158. doi: 10.1002/cne.903020111
Asilador, A., and Llano, D. A. (2020). Top-down inference in the auditory system: potential roles for corticofugal projections. Front. Neural Circuits 14:615259.
Asokan, M. M., Williamson, R. S., Hancock, K. E., and Polley, D. B. (2018). Sensory overamplification in layer 5 auditory corticofugal projection neurons following cochlear nerve synaptic damage. Nat. Commun. 9:2468.
Bajo, V. M., and King, A. J. (2012). Cortical modulation of auditory processing in the midbrain. Front. Neural Circuits 6:114.
Bajo, V. M., and Moore, D. R. (2005). Descending projections from the auditory cortex to the inferior colliculus in the gerbil, Meriones unguiculatus. J. Comp. Neurol. 486, 101–116. doi: 10.1002/cne.20542
Bajo, V. M., Nodal, F. R., Bizley, J. K., Moore, D. R., and King, A. J. (2007). The ferret auditory cortex: descending projections to the inferior colliculus. Cereb. Cortex 17, 475–491. doi: 10.1093/cercor/bhj164
Bajo, V. M., Nodal, F. R., Moore, D. R., and King, A. J. (2010). The descending corticocollicular pathway mediates learning-induced auditory plasticity. Nat. Neurosci. 13, 253–260. doi: 10.1038/nn.2466
Bourassa, J., and Deschenes, M. (1995). Corticothalamic projections from the primary visual cortex in rats: a single fiber study using biocytin as an anterograde tracer. Neuroscience 66, 253–263. doi: 10.1016/0306-4522(95)00009-8
Bourassa, J., Pinault, D., and Deschenes, M. (1995). Corticothalamic projections from the cortical barrel field to the somatosensory thalamus in rats: a single-fibre study using biocytin as an anterograde tracer. Eur. J. Neurosci. 7, 19–30. doi: 10.1111/j.1460-9568.1995.tb01016.x
Cadusseau, J., and Roger, M. (1985). Afferent projections to the superior colliculus in the rat, with special attention to the deep layers. J. fur Hirnforschung 26, 667–681.
Cant, N. B., and Benson, C. G. (2006). Organization of the inferior colliculus of the gerbil (Meriones unguiculatus): differences in distribution of projections from the cochlear nuclei and the superior olivary complex. J. Comp. Neurol. 495, 511–528. doi: 10.1002/cne.20888
Cant, N. B., and Benson, C. G. (2008). Organization of the inferior colliculus of the gerbil (Meriones unguiculatus): projections from the cochlear nucleus. Neuroscience 154, 206–217. doi: 10.1016/j.neuroscience.2008.02.015
Coleman, J. R., and Clerici, W. J. (1987). Sources of projections to subdivisions of the inferior colliculus in the rat. J. Comp. Neurol. 262, 215–226. doi: 10.1002/cne.902620204
Coomes, D. L., Schofield, R. M., and Schofield, B. R. (2005). Unilateral and bilateral projections from cortical cells to the inferior colliculus in guinea pigs. Brain Res. 1042, 62–72. doi: 10.1016/j.brainres.2005.02.015
Cruikshank, S. J., Killackey, H. P., and Metherate, R. (2001). Parvalbumin and calbindin are differentially distributed within primary and secondary subregions of the mouse auditory forebrain. Neuroscience 105, 553–569. doi: 10.1016/s0306-4522(01)00226-3
Deschênes, M., Bourassa, J., and Pinault, D. (1994). Corticothalamic projections from layer V cells in rat are collaterals of long-range corticofugal axons. Brain Res. 664, 215–219. doi: 10.1016/0006-8993(94)91974-7
Doucet, J., Molavi, D., and Ryugo, D. (2003). The source of corticocollicular and corticobulbar projections in area Te1 of the rat. Exp. Brain Res. 153, 461–466. doi: 10.1007/s00221-003-1604-4
Edwards, S. B., Ginsburgh, C. L., Henkel, C. K., and Stein, B. E. (1979). Sources of subcortical projections to the superior colliculus in the cat. J. Comp. Neurol. 184, 309–329. doi: 10.1002/cne.901840207
Games, K. D., and Winer, J. A. (1988). Layer V in rat auditory cortex: projections to the inferior colliculus and contralateral cortex. Hear. Res. 34, 1–25. doi: 10.1016/0378-5955(88)90047-0
Guo, C., Peng, J., Zhang, Y., Li, A., Li, Y., Yuan, J., et al. (2017). Single-axon level morphological analysis of corticofugal projection neurons in mouse barrel field. Sci. Rep. 7:2846.
Huffman, R. F., and Henson, O. (1990). The descending auditory pathway and acousticomotor systems: connections with the inferior colliculus. Brain Res. Rev. 15, 295–323. doi: 10.1016/0165-0173(90)90005-9
Jacomme, A.-V., Nodal, F., Bajo, V., Manunta, Y., Edeline, J.-M., Babalian, A., et al. (2003). The projection from auditory cortex to cochlear nucleus in guinea pigs: an in vivo anatomical and in vitro electrophysiological study. Exp. Brain Res. 153, 467–476. doi: 10.1007/s00221-003-1606-2
Jen, P.-S., Chen, Q., and Sun, X. (1998). Corticofugal regulation of auditory sensitivity in the bat inferior colliculus. J. Comp. Physiol. A 183, 683–697. doi: 10.1007/s003590050291
Kawamura, K. (1975). The pontine projection from the inferior colliculus in the cat. an experimental anatomical study. Brain Res. 95, 309–322. doi: 10.1016/0006-8993(75)90109-2
Kelly, J. B., Liscum, A., Van Adel, B., and Ito, M. (1998). Projections from the superior olive and lateral lemniscus to tonotopic regions of the rat’s inferior colliculus. Hear. Res. 116, 43–54.
Kita, T., and Kita, H. (2012). The subthalamic nucleus is one of multiple innervation sites for long-range corticofugal axons: a single-axon tracing study in the rat. J. Neurosci. 32, 5990–5999. doi: 10.1523/jneurosci.5717-11.2012
Kosaki, H., Hashikawa, T., He, J., and Jones, E. (1997). Tonotopic organization of auditory cortical fields delineated by parvalbumin immunoreactivity in macaque monkeys. J. Comp. Neurol. 386, 304–316. doi: 10.1002/(sici)1096-9861(19970922)386:2<304::aid-cne10>3.0.co;2-k
Künzle, H. (1995). Regional and laminar distribution of cortical neurons projecting to either superior or inferior colliculus in the hedgehog tenrec. Cereb. Cortex 5, 338–352. doi: 10.1093/cercor/5.4.338
León, A., Elgueda, D., Silva, M. A., Hamamé, C. M., and Délano, P. H. (2012). Auditory cortex basal activity modulates cochlear responses in chinchillas. PLoS One 7:e36203. doi: 10.1371/journal.pone.0036203
Lesicko, A. M., and Llano, D. A. (2020). Circuit mechanisms underlying the segregation and integration of parallel processing streams in the inferior colliculus. J. Neurosci. 40, 6328–6344. doi: 10.1523/jneurosci.0646-20.2020
Levy, R. B., Marquarding, T., Reid, A. P., Pun, C. M., Renier, N., and Oviedo, H. V. (2019). Circuit asymmetries underlie functional lateralization in the mouse auditory cortex. Nat. Commun. 10:2783.
Li, Z., Wei, J.-X., Zhang, G.-W., Huang, J. J., Zingg, B., Wang, X., et al. (2021). Corticostriatal control of defense behavior in mice induced by auditory looming cues. Nat. Commun. 12:1040.
Llano, D. A., and Sherman, S. M. (2008). Evidence for nonreciprocal organization of the mouse auditory thalamocortical-corticothalamic projection systems. J. Comp. Neurol. 507, 1209–1227. doi: 10.1002/cne.21602
Loftus, W. C., Bishop, D. C., Saint Marie, R. L., and Oliver, D. L. (2004). Organization of binaural excitatory and inhibitory inputs to the inferior colliculus from the superior olive. J. Comp. Neurol. 472, 330–344. doi: 10.1002/cne.20070
Malmierca, M. S., and Ryugo, D. K. (2011). “Descending connections of auditory cortex to the midbrain and brain stem,” in The Auditory Cortex, eds J. A. Winer and C. E. Schreiner (Berlin: Springer), 189–208. doi: 10.1007/978-1-4419-0074-6_9
Molinari, M., Dell’anna, M., Rausell, E., Leggio, M., Hashikawa, T., and Jones, E. (1995). Auditory thalamocortical pathways defined in monkeys by calcium-binding protein immunoreactivity. J. Comp. Neurol. 362, 171–194. doi: 10.1002/cne.903620203
Ojima, H. (1994). Terminal morphology and distribution of corticothalamic fibers originating from layers 5 and 6 of cat primary auditory cortex. Cereb. Cortex 4, 646–663. doi: 10.1093/cercor/4.6.646
Oviedo, H. V., Bureau, I., Svoboda, K., and Zador, A. M. (2010). The functional asymmetry of auditory cortex is reflected in the organization of local cortical circuits. Nat. Neurosci. 13, 1413–1420. doi: 10.1038/nn.2659
Perrot, X., Ryvlin, P., Isnard, J., Guènot, M., Catenoix, H., Fischer, C., et al. (2006). Evidence for corticofugal modulation of peripheral auditory activity in humans. Cereb. Cortex 16, 941–948. doi: 10.1093/cercor/bhj035
Popelář, J., Nwabueze-Ogbo, F., and Syka, J. (2003). Changes in neuronal activity of the inferior colliculus in rat after temporal inactivation of the auditory cortex. Physiol. Res. 52, 615–628.
Prasad, J. A., Carroll, B. J., and Sherman, S. M. (2020). Layer 5 corticofugal projections from diverse cortical areas: variations on a pattern of thalamic and extrathalamic targets. J. Neurosci. 40, 5785–5796. doi: 10.1523/jneurosci.0529-20.2020
Reichova, I., and Sherman, S. M. (2004). Somatosensory corticothalamic projections: distinguishing drivers from modulators. J. Neurophysiol. 92, 2185–2197. doi: 10.1152/jn.00322.2004
Saldaña, E., Feliciano, M., and Mugnaini, E. (1996). Distribution of descending projections from primary auditory neocortex to inferior colliculus mimics the topography of intracollicular projections. J. Comp. Neurol. 371, 15–40. doi: 10.1002/(sici)1096-9861(19960715)371:1<15::aid-cne2>3.0.co;2-o
Schofield, B. R. (2008). Retrograde axonal tracing with fluorescent markers. Curr. Protoc. Neurosci. Chapter 1:Unit 1.17. doi: 10.1002/0471142301.ns0117s43
Schofield, B. R. (2009). Projections to the inferior colliculus from layer VI cells of auditory cortex. Neuroscience 159, 246–258. doi: 10.1016/j.neuroscience.2008.11.013
Schofield, B. R., and Coomes, D. L. (2005). Auditory cortical projections to the cochlear nucleus in guinea pigs. Hear. Res. 199, 89–102. doi: 10.1016/j.heares.2004.08.003
Schofield, B. R., Schofield, R. M., Sorensen, K. A., and Motts, S. D. (2007). On the use of retrograde tracers for identification of axon collaterals with multiple fluorescent retrograde tracers. Neuroscience 146, 773–783. doi: 10.1016/j.neuroscience.2007.02.026
Slater, B. J., Sons, S. K., Yudintsev, G., Lee, C. M., and Llano, D. A. (2019). Thalamocortical and intracortical inputs differentiate layer-specific mouse auditory corticocollicular neurons. J. Neurosci. 39, 256–270. doi: 10.1523/jneurosci.3352-17.2018
Slater, B. J., Willis, A. M., and Llano, D. A. (2013). Evidence for layer-specific differences in auditory corticocollicular neurons. Neuroscience 229, 144–154. doi: 10.1016/j.neuroscience.2012.10.053
Stebbings, K. A., Lesicko, A. M., and Llano, D. A. (2014). The auditory corticocollicular system: Molecular and circuit-level considerations. Hear. Res. 314, 51–59. doi: 10.1016/j.heares.2014.05.004
Suga, N. (2008). Role of corticofugal feedback in hearing. J. Comp. Physiol. A 194, 169–183. doi: 10.1007/s00359-007-0274-2
Sun, X., Xia, Q., Lai, C. H., Shum, D. K. Y., Chan, Y. S., and He, J. (2007). Corticofugal modulation of acoustically induced Fos expression in the rat auditory pathway. J. Comp. Neurol. 501, 509–525. doi: 10.1002/cne.21249
Takayanagi, M., and Ojima, H. (2006). Microtopography of the dual corticothalamic projections originating from domains along the frequency axis of the cat primary auditory cortex. Neuroscience 142, 769–780. doi: 10.1016/j.neuroscience.2006.06.048
Terreros, G., and Délano, P. H. (2015). Corticofugal modulation of peripheral auditory responses. Front. Syst. Neurosci. 9:134.
Theyel, B. B., Llano, D. A., and Sherman, S. M. (2010). The corticothalamocortical circuit drives higher-order cortex in the mouse. Nat. Neurosci. 13, 84–88. doi: 10.1038/nn.2449
Torii, M., Hackett, T. A., Rakic, P., Levitt, P., and Polley, D. B. (2013). EphA signaling impacts development of topographic connectivity in auditory corticofugal systems. Cereb. Cortex 23, 775–785. doi: 10.1093/cercor/bhs066
Weedman, D. L., and Ryugo, D. K. (1996). Projections from auditory cortex to the cochlear nucleus in rats: synapses on granule cell dendrites. J. Comp. Neurol. 371, 311–324. doi: 10.1002/(sici)1096-9861(19960722)371:2<311::aid-cne10>3.0.co;2-v
Willard, F., and Martin, G. (1984). Collateral innervation of the inferior colliculus in the North American opossum: a study using fluorescent markers in a double-labeling paradigm. Brain Res. 303, 171–182. doi: 10.1016/0006-8993(84)90225-7
Williamson, R. S., and Polley, D. B. (2019). Parallel pathways for sound processing and functional connectivity among layer 5 and 6 auditory corticofugal neurons. Elife 8:e42974.
Winer, J. A., Larue, D. T., Diehl, J. J., and Hefti, B. J. (1998). Auditory cortical projections to the cat inferior colliculus. J. Comp. Neurol. 400, 147–174. doi: 10.1002/(sici)1096-9861(19981019)400:2<147::aid-cne1>3.0.co;2-9
Xiao, Z., and Suga, N. (2002). Modulation of cochlear hair cells by the auditory cortex in the mustached bat. Nat. Neurosci. 5, 57–63. doi: 10.1038/nn786
Xiong, X. R., Liang, F., Zingg, B., Ji, X.-Y., Ibrahim, L. A., Tao, H. W., et al. (2015). Auditory cortex controls sound-driven innate defense behaviour through corticofugal projections to inferior colliculus. Nat. Commun. 6:7224.
Yan, J., Zhang, Y., and Ehret, G. (2005). Corticofugal shaping of frequency tuning curves in the central nucleus of the inferior colliculus of mice. J. Neurophysiol. 93, 71–83. doi: 10.1152/jn.00348.2004
Yan, W., and Suga, N. (1998). Corticofugal modulation of the midbrain frequency map in the bat auditory system. Nat. Neurosci. 1, 54–58. doi: 10.1038/255
Keywords: auditory cortex, inferior colliculus, corticocollicular, corticotectal, auditory midbrain, Fluorogold, cholera toxin B, retrobeads
Citation: Vaithiyalingam Chandra Sekaran N, Deshpande MS, Ibrahim BA, Xiao G, Shinagawa Y and Llano DA (2021) Patterns of Unilateral and Bilateral Projections From Layers 5 and 6 of the Auditory Cortex to the Inferior Colliculus in Mouse. Front. Syst. Neurosci. 15:674098. doi: 10.3389/fnsys.2021.674098
Received: 28 February 2021; Accepted: 19 August 2021;
Published: 21 October 2021.
Edited by:
David K. Ryugo, Garvan Institute of Medical Research, AustraliaReviewed by:
Stephen Lomber, McGill University, CanadaManuel S. Malmierca, University of Salamanca, Spain
Copyright © 2021 Vaithiyalingam Chandra Sekaran, Deshpande, Ibrahim, Xiao, Shinagawa and Llano. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Daniel A. Llano, llano@life.illinois.edu
†These authors have contributed equally to this work