Jeffrey G. Mellott1,2*
Syllissa Duncan1Justine Busby1Laila S. Almassri1,2Alexa Wawrzyniak1Milena C. Iafrate1Andrew P. Ohl1Elizabeth A. Slabinski1Abigail M. Beaver1Diana Albaba1Brenda Vega1Amir M. Mafi3Morgan Buerke4Nick J. Tokar1
Jesse W. Young1- 1Department of Anatomy and Neurobiology, Northeast Ohio Medical University, Rootstown, OH, United States
- 2University Hospitals Hearing Research Center, Northeast Ohio Medical University, Rootstown, OH, United States
- 3The Ohio State University College of Medicine, Columbus, OH, United States
- 4Department of Psychology, Louisiana State University, Baton Rouge, LA, United States
Presbycusis is one of the most prevalent disabilities in aged populations of industrialized countries. As we age less excitation reaches the central auditory system from the periphery. To compensate, the central auditory system [e.g., the inferior colliculus (IC)], downregulates GABAergic inhibition to maintain homeostatic balance. However, the continued downregulation of GABA in the IC causes a disruption in temporal precision related to presbycusis. Many studies of age-related changes to neurotransmission in the IC have therefore focused on GABAergic systems. However, we have discovered that dense core vesicles (DCVs) are significantly upregulated with age in the IC. DCVs can carry neuropeptides, co-transmitters, neurotrophic factors, and proteins destined for the presynaptic zone to participate in synaptogenesis. We used immuno transmission electron microscopy across four age groups (3-month; 19-month; 24-month; and 28-month) of Fisher Brown Norway rats to examine the ultrastructure of DCVs in the IC. Tissue was stained post-embedding for GABA immunoreactivity. DCVs were characterized by diameter and by the neurochemical profile (GABAergic/non-GABAergic) of their location (bouton, axon, soma, and dendrite). Our data was collected across the dorsolateral to ventromedial axis of the central IC. After quantification, we had three primary findings. First, the age-related increase of DCVs occurred most robustly in non-GABAergic dendrites in the middle and low frequency regions of the central IC during middle age. Second, the likelihood of a bouton having more than one DCV increased with age. Lastly, although there was an age-related loss of terminals throughout the IC, the proportion of terminals that contained at least one DCV did not decline. We interpret this finding to mean that terminals carrying proteins packaged in DCVs are spared with age. Several recent studies have demonstrated a role for neuropeptides in the IC in defining cell types and regulating inhibitory and excitatory neurotransmission. Given the age-related increase of DCVs in the IC, it will be critical that future studies determine whether (1) specific neuropeptides are altered with age in the IC and (2) if these neuropeptides contribute to the loss of inhibition and/or increase of excitability that occurs during presbycusis and tinnitus.
1 Introduction
The auditory system plays a crucial role in our everyday lives by enabling communication, sound localization, and information processing. Conversely, auditory system dysfunction leads to impaired communication, difficulty participating in noisy social environments, and an overall decrease in quality of life. As the aging population continues to grow, there is an increased demand for understanding the mechanisms underlying hearing loss, which affects nearly three-quarters of individuals aged 70 years or older (Goman and Lin, 2016). The functional decline of the auditory system with age often begins with the degradation of the peripheral auditory system, which leads to a decrease in excitation sent to the central auditory system (Knipper et al., 2022; Rumschlag et al., 2022). The central auditory system compensates for this decreased excitation by downregulating GABAergic inhibition; this is believed to be an attempt at restoring homeostatic levels of activity (Caspary et al., 2008; Richardson et al., 2012; Caspary and Llano, 2018). Unfortunately the gradual loss of GABA into old age leads to functional deficits and increased central neural gain (Caspary et al., 2008; Auerbach et al., 2014, 2019). Age-related downregulation of GABAergic inhibition is well documented in the inferior colliculus (IC), an auditory midbrain structure that serves as the hub of the central auditory system (Wenstrup, 2005; Caspary et al., 2008; Syka, 2020). The IC is organized into three subdivisions [central (ICc), lateral cortex (IClc), and dorsal cortex (ICd)] and processes information from multiple ascending and descending auditory projections (see reviews: Oliver, 2005; Syka, 2020). Neurons and inputs within the lemniscal ICc are arranged into isofrequency lamina, which are organized tonotopically along the ventromedial (high frequencies) to dorsolateral (low frequencies) axis (Oliver and Morest, 1984; Oliver, 2005; Malmierca et al., 2008; Syka, 2020).
Considering that mammalian presbycusis is frequency specific, it is important to understand age-related molecular and ultrastructural changes in relation to the tonotopic axis (Walton et al., 1998; Cai et al., 2018; Parthasarathy et al., 2018; Koehler et al., 2023). In our ongoing investigations of the aging synaptic ultrastructure in the IC, we observed a dramatic increase of dense core vesicles (DCVs) in the aged IC. In the current study, we quantify and characterize this increase in DCVs. DCVs are membrane-bound organelles that contain dense granular cores; they are one of two types of organelles that secrete chemical signals throughout the nervous system, with classic clear synaptic vesicles being the other (Sorra et al., 2006; Persoon et al., 2018). Unlike synaptic vesicles which are found in large pools at active zones and carry classic neurotransmitters, DCVs are rarer, and they tend to package biogenic amines, neuromodulators, presynaptic machinery, neuropeptides, neurotrophic factors, and hormones (Peters et al., 1991; Michael et al., 2006; Sorra et al., 2006; Merighi, 2018). A number of important neuromodulators involved in auditory midbrain function are transported by DCVs, including serotonin, neuropeptide Y (NPY), vasoactive intestinal peptide (VIP), brain-derived neurotrophic factor (BDNF), and fibroblast growth factors (Pelletier et al., 1981; Sato et al., 2001; Dieni et al., 2012; Schofield and Hurley, 2018; Goyer et al., 2019; Silveira et al., 2020, 2023). DCVs are transported via both dendritic and axonal trafficking, where microtubule dependent kinesin-1 motors (KIF1) and motor dynein mediate trafficking into dendrites and axons (Zheng et al., 2008; Lipka et al., 2016). It is unclear whether DCVs are preferentially released at axons or dendrites (Kennedy and Ehlers, 2011; Persoon et al., 2018). To our knowledge, very little is understood about the populations of DCVs in the auditory midbrain, including what proteins they contain and their trafficking patterns.
The goal of the present study is to determine whether DCVs are upregulated in the aging ICc. Specifically, we examined three tissue blocks taken across the ventromedial-dorsolateral ICc axis. For the sake of conciseness, alignment with our previous studies, and convention as the tonotopic axis is well established, we refer to the ventromedial-most ICc block as representing the high frequency region, the middle block as representing the middle frequency region, and dorsolateral-most block as representing lower frequencies. We used immuno transmission electron microscopy to analyze DCVs in GABAergic and non-GABAergic boutons, axons, and dendrites of Fischer Brown Norway (FBN) rats across four (3–4 months “young”; 19–20 months “early middle-age”; 24 months “late middle-age”; and 28–29 months “old”) age groups. We discovered that: (1) DCVs were markedly increased in non-GABAergic dendrites during middle age. Many of these DCVs were located near postsynaptic densities. (2) The probability of a GABAergic or non-GABAergic bouton having more than one DCV increased with age. (3) Despite the age-related loss of boutons throughout the IC, the percentage of non-GABAergic and GABAergic boutons that had at least one DCV did not decline with age. We conclude that synapses lost in the IC in aging may not be synapses that co-release neuropeptides. Ultimately, it appears that the many possible proteins packaged by DCVs may have a significant role in the processing of acoustic signals in the aging IC.
2 Materials and methods
2.1 Animals
All procedures were conducted in accordance with the Northeast Ohio Medical University Institutional Animal Care and Use Committee and NIH guidelines. Results are described from 20 male FBN rats [National Institute of Aging; Bethesda, MD, USA; RRID:SCR_007317 (housed by Charles River Laboratories, Wilmington, MA, USA)] across four age groups (5 animals per age group): 3–4 months “young”; 19–20 months “early middle-age”; 24 months “late middle-age”; and 28–29 months “old” (Tables 1–3). For a details regarding ambient sound levels, please see Cai et al. (2018). Efforts were made to minimize the number of animals and their suffering.
Table 1. Summary of ICc DCV in GABA-negative profiles.
Table 2. Excitatory bouton breakdown.
Table 3. GABAergic bouton breakdown.
2.2 Perfusion and sectioning
Each animal was deeply anesthetized with isoflurane and perfused transcardially with Tyrode’s solution, followed by 250 ml of 2% glutaraldehyde and 2% paraformaldehyde [with one exception; case R79, Blocks 93,94, and 95 (Tables 1, 2) was perfused and stored with 3% glutaraldehyde and 1% paraformaldehyde] in 0.1 M phosphate buffer at a pH 7.4. The brain was removed and stored at 4°C in 2% glutaraldehyde and 2% paraformaldehyde in 0.1 M phosphate buffer. The following day the brain was prepared for processing by removing the cerebellum and cortex and blocking the remaining piece with transverse cuts posterior to the cochlear nucleus and anterior to the thalamus. The tissue was then cut into 50 μm thick transverse section with a Vibratome (VT1000S, Leica Microsystems, Buffalo Grove, IL, USA). The tissue was collected in six series. Series were processed as described below or stored in freezing buffer for future processing.
2.3 Tissue processing for EM
A series of tissue was post-fixed in 1% osmium tetroxide for 30 min, dehydrated in a series of alcohols (50%, 70%, 95%, 100% and 2× propylene oxide; each run was 10 min), embedded in Durcupan resin (Sigma-Aldrich; Millipore Sigma, Burlington, MA, USA) and flat-mounted between sheets of Aclar Embedding Film (Ted Pella, Inc., Redding, CA, USA) at 60°C for 48–72 h. Mid-rostrocaudal IC sections (between interaural levels 0.24 and 0.36 mm; Paxinos and Watson, 1998) were examined with brightfield stereomicroscopy. Trapezoidal blocks, with a 0.75 mm base and 0.5–0.6 mm height, were extracted across the ventromedial-dorsolateral axis of the ICc (Figure 1). Three “blocks” of tissue were taken from each animal processed in the study. The ventromedial-dorsomedial axis of the rat ICc, after fixation, is approximately 2 mm. To better avoid our dorsolateral-most block including lateral or dorsal cortex of the IC, the total length of tissue taken across the axis was ∼1.8 mm (0.6 mm height per block). Initial borders of the ICc were delineated according to the rat anatomical atlas of the brain (Paxinos and Watson, 1998). Osmium fixation revealing the conspicuous lateral lemniscal fibers, libraries of decarboxylase (GAD) immunoreactivity in EM prepared tissue, adjacent sections reacted for Nissl, and our experience with EM in the IC further guided our block trimming to best ensure tissue was from ICc (Nakamoto et al., 2013; Mellott et al., 2014; Mafi et al., 2022). More specific details on the trimming process can be found in Mafi et al. (2022). Tissue blocks were glued to a cylindric resin base with cyanoacrylate (Krazy Glue, Columbus, OH, USA). IC sections with removed tissue blocks were then imaged for record keeping and representative comparison between cases. We refer to the ventromedial-most ICc block as representing the high frequency region, the middle-most block representing the middle frequency region, and dorsolateral-most block representing lower frequencies (Figure 1). We did not record from the ICc; however we adopt this naming convention for the sake of conciseness, brevity, and convention as the tonotopic axis is well established.
Figure 1. Schematic illustrating three subdivisions of the inferior colliculus in the coronal plane. The black trapezoids indicate the regions of ICc across the ventromedial-dorsolateral axis where tissue was extracted from in each case. Dashed lines demonstrate the approximate borders between the three layers of the lateral cortex of the inferior colliculus (IClc). Green ovals indicate the approximate locations of the GABAergic modules that are often found and define anatomical features of the second IClc layer. D, dorsal; L, lateral; HF, high frequency region; ICc, central inferior colliculus; ICd, dorsal cortex of the IC; IClc layer I, the first layer of the lateral cortex of the IC; IClc layer II, the second layer of the IClc; IClc layer III, the third layer of the IClc; LF, low frequency region; MF, middle frequency region.
Ultrathin sections were taken at a thickness of 50 nm with an ultramicrotome (UC6 Ultramicrotome, Leica Microsystems, Buffalo Grove, IL, USA). For each block of tissue, every twelfth section was collected onto a 200 or 300-mesh Formvar coated nickel mesh grid (Electron Microscopy Science, Hatfield, PA, USA) to ensure a singular synapse was not collected across two grids and analyzed twice. A total of eight grids, each with a single ultrathin section of layer of the ICc, were collected per block of tissue. Briefly, see Nakamoto et al. (2013) and Mellott et al. (2014), sections dried for 3 h and were then placed overnight into anti-GABA antibody (rabbit anti-GABA, Sigma, St. Louis, MO, USA) diluted 1:500 in 0.05 M Tris-buffered saline with 0.1% Triton X-100, pH 7.6 (TBST), washed in TBST pH 7.6, then washed in TBST pH 8.2, and placed into a secondary antibody conjugated to 15 nm gold particles (goat anti-rabbit, diluted 1:25 in TBST pH 8.2; Ted Pella Inc., Redding, CA, USA). Lastly, sections were washed in TBST pH 7.6, washed in Nanopure water, stained with uranyl acetate (2% aqueous) and Reynold’s lead citrate (Reynolds, 1963), and dried.
2.4 EM imaging
Sixty blocks of tissue from 20 male FBN rats with superior ultrastructure were chosen for imaging and quantification. We use a 5-point scale to grade the intactness and quality of ultrastructure in each case. Only tissue with a score of 4 or 5 was quantified. Our 5-point scale reflects a combination of successful fixation, immunogold processing and absence of electron dense artifacts. Nine of the 15 cases were scored as a “5” and the remaining six cases were a “4.” Scores of 4 and 5 yield clear ultrastructure with easily identifiable profiles that are readily resolved. The distinction between a 4 and a 5 is commonly due to a fold in the tissue or excess precipitate, which we avoid when imaging. Tissue scored as a 3 yields ultrastructure that can be qualitatively analyzed; however membrane integrity is not preserved such that quantitative data can be consistently extracted. All images presented are from a case scored as a 4/5. Tissue scored as a 1 or 2 has severe defects in the pre- and postsynaptic membranes such that synaptic profiles are difficult to interpret. Ultrastructure of the ICc was imaged with a transmission electron microscope (JEM-1400Plus, JEOL, Peabody, MA, USA) at an accelerating voltage of 80 kV and at a magnification of 50,000. Based on experience, a magnification of 50,000 ensures that all inhibitory synapses in the inferior colliculus are visible. Tissue was digitally imaged and rendered with an Orius 100 keV or Rio9 side mount camera (Gatan, Pleasanton, CA, USA). Images of ultrastructure were taken with Gatan Microscopy Suite Software (GMS3, Gatan, Pleasanton, CA, USA) integrated and calibrated with SerialEM Tomography software (Mastronarde, 2003). SerialEM is a gold standard for analytical applications in biological TEM and allowed us to image and analyze and add data at higher rate of efficiency. For each tissue block, we collected 400 μm2 (22,214 × 22,214 pixels) montages across 8 grids for a total of 3,200 μm2. All attempts were made such that each montage was collected from the center of each ultrathin section. Montages were analyzed by individuals blind to the age and ICc region imaged. Adobe Photoshop (Adobe Systems, Inc., San Jose, CA, USA) was used to add scale bars, crop images, adjust intensity levels and colorize monochrome images.
2.5 Analysis of inhibitory and excitatory profiles
We recorded each DCV that was present in a bouton, axon, and dendrite. Our classification of ultrastructure is largely based on the criteria defined by Peters et al. (1991) and our previous work (Mellott et al., 2014; Nakamoto et al., 2014; Mafi et al., 2022). Briefly, boutons have a “pool” of vesicles with clear centers and generally an absence of a cytoskeleton. We never observed a bouton with a DCV without clear vesicles. Dendrites were identified through a combination of criteria (irregular contours, spines, presence of synaptic inputs, and free ribosomes). Axons were commonly myelinated, and axons do not commonly contain free ribosomes in their cytoplasm. Identifying small unmyelinated axons from small dendrites provides some difficulty (Peters et al., 1991). Generally speaking, small axons in the IC travel as bundles through the neuropil while dendrites travel in irregular patterns and are not typically in bundles. Additionally, the presence of ribosomes can help identify dendrites. When identifying a presynaptic terminal with a DCV we first note if the postsynaptic density is symmetric or asymmetric. We then classified each profile (bouton, axon, and dendrite) as non-GABAergic or GABAergic based on the accumulation of gold particles as compared to background (Nakamoto et al., 2013; Mellott et al., 2014; Mafi et al., 2022). In our previous report on the aging ultrastructure of the IC, we found that immunogold labeling was reduced in the aged tissue (Mafi et al., 2022). To maintain consistency between studies, older structures that were characterized as GABAergic had to have a density of gold particles that was at least three times greater than background. Although the goal of the current study was not synaptic analysis, when a DCV was identified in a bouton forming a synapse, we characterized the synapse as either excitatory or GABAergic for qualitative analysis. Synapses were classified by: (1) vesicle shape [pleomorphic vesicles (inhibitory) or round vesicles (excitatory)] and, (2) postsynaptic densities forming symmetric (pre- and postsynaptic membranes were of similar thickness; inhibitory) or asymmetric (postsynaptic densities were conspicuously thicker than the presynaptic densities; excitatory) junctions (Rockel and Jones, 1973; Paloff and Usunoff, 1992; Helfert et al., 1999; Nakamoto et al., 2013). Detailed descriptions characterizing IC ultrastructure with post-embedding immunogold techniques to label GABAergic profiles can be found in Nakamoto et al. (2013) and Mafi et al. (2022).
2.6 Data analysis
We examined 48,000 μm2 of ICc across five blocks of 3–4-month-old tissue, 48,000 μm2 of ICc across five blocks of 19–20-month-old tissue, 48,000 μm2 of ICc across five blocks of 24-month-old tissue, and 48,000 μm2 of ICc across five blocks of 28–29-month-old tissue with ImageJ (Schneider et al., 2012; Table 1). As boutons and synapses are known to be reduced in the aging IC, we quantified each bouton in each tissue block of each case to better understand age-related changes to the presence of DCVs in boutons (Helfert et al., 1999; Mafi et al., 2022).
Variation in number of DCVs by ultrastructural location according to age group, was analyzed using one-way analysis of variance (ANOVA) models for each region. Six separate ANOVAs were run with age as the independent variable and number of DCVs as the outcome. Tukey’s Honest Significant Difference (HSD) was run for pairwise post-hoc tests of differences between consecutive age groups (i.e., 3–4 months versus 19–20 months, 19–20 months versus 24 months, 24 months versus 28–29 months) and pairwise values were adjusted using the false discovery rate procedure (Benjamini and Hochberg, 1995), a method that simultaneously limits experiment-wise alpha inflation and minimizes the correlated loss of statistical power. All statistical tests were performed in R (version 3.6.3 for Mac OS X; R Core Team, 2020), supplemented by the add-on packages nlme compareGroups (Subirana et al., 2014).
3 Results
We examined the ultrastructural location of DCVs in non-GABAergic and GABAergic terminals, axons, and dendrites across four age groups (3–4 months, 19–20 months, 24 months, and 28–29 months) in the central inferior colliculus (ICc). We analyzed 3,811 DCVs in excitatory profiles and 1,567 DCVs in inhibitory profiles across 192,000 μm2 of tissue (Table 1). DCVs were most commonly located in non-GABAergic profiles at each age (Table 1). The most robust age-related increases of DCVs also occurred in non-GABAergic profiles (Table 1). We first describe DCV ultrastructure across the ventromedial-dorsolateral axis of the ICc. We then present data regarding age-related increases of DCVs in the dendrites of IC cells. Lastly, we qualitatively describe the frequency of DCVs in non-GABAergic and GABAergic boutons in the aging IC.
3.1 DCVs can be found across the ICc, regardless of age
Regardless of age and ventromedial-dorsolateral location, DCVs were found in dendrites, terminals, and axons in the ICc (Figure 2). We observed DCVs in both GABAergic and non-GABAergic presynaptic terminals in the ICc (Figures 2A, C, H, J–L). DCVs were also found in GABAergic and non-GABAergic dendrites (Figures 2D–G, I). Often, DCVs located in dendrites were near the postsynaptic density (Figures 2D, F, G, I). We did not observe DCVs at dendrodendritic synapses; it appears that dendrodendritic synapses in the rat IC are rare. At 28–29 months DCVs were found in presynaptic terminals forming non-prototypical synapses [e.g., GABAergic synapse forming an apparent asymmetric synapse (Figure 2J), non-GABAergic synapse with a subsynaptic body (Figure 2L)]. However, it was rare to observe a DCV bound to the pre- or postsynaptic membrane (Figure 2).
Figure 2. Electron micrographs across four age groups showing dense core vesicle (DCV) ultrastructure across the ventromedial-dorsolateral axis of the central inferior colliculus (ICc). GABAergic presynaptic (Pre G+) terminals are pseudocolored green. GABAergic postsynaptic targets are pseudocolored red. GABA-negative presynaptic (Pre G–) terminals are pseudocolored yellow. GABA-negative postsynaptic targets are pseudocolored blue. Black dots demonstrate immunogold labeling of GABA. Synapses are indicated by pairs of white arrows. (A–C) Electron micrographs showing examples of DCVs in 3–4 month old tissue across the ventromedial-dorsolateral axis of the ICc. (D–F) Electron micrographs showing examples DCVs in 19–20 month old tissue across the ventromedial-dorsolateral axis of the ICc. (G–I) Electron micrographs showing examples DCVs in 24 month old tissue across the ventromedial-dorsolateral axis of the ICc. (J–L) Electron micrographs showing examples DCVs in 28 month old tissue across the ventromedial-dorsolateral axis of the ICc. DCVs are circled in red. LD, large dendrite; MD, medium dendrite; SD, small dendrite. Scale bars, 500 nm.
3.2 DCVs increase with age in non-GABAergic dendrites in low- and middle-frequency areas of the ICc
The total number of DCVs in non-GABAergic dendrites at 3–4 months across the high (ventromedial), middle and low (dorsolateral) frequency regions was 84, 83, and 81, respectively (Table 1). By 19–20 months these values doubled across the IC and increased further at 24 months (Table 1). When DCVs were observed in dendrites, they were typically singular and not near other DCVs. However at older ages in the low and middle frequency regions, while still uncommon, we observed DCVs near each other (Figure 3). In the low frequency region, the number of DCVs significantly increased from 83 to 226 at 24 months (*p = 0.004; Figure 4A). In the middle frequency region, the number of DCVs significantly increased from 83 to 255 at 24 months (*p = 0.025; Figure 4A). However the age-related increase of DCVs was not found to be significant at 19–20 months and 28–29 months (Figure 4A). In the high frequency region, despite an increase in the number of DCVs with age, our models did not detect a significant increase with age (Figure 4A).
Figure 3. Electron micrographs at 24 months showing dense core vesicle (DCV) ultrastructure in the middle and low frequency regions of the central inferior colliculus (ICc). GABA-negative dendrites are pseudocolored blue. A GABA-negative presynaptic (Pre G–) terminal is pseudocolored yellow. Black dots demonstrate immunogold labeling of GABA. Synapses are indicated by pairs of white arrows. (A) Electron micrograph showing a group of DCVs in a non-GABAergic dendrite at 24 months in the middle frequency region of the ICc. (B) Electron micrograph showing a group of DCVs in a non-GABAergic dendrite at 24 months in the low frequency region of the ICc. DCVs are circled in red. MD, medium dendrite. Scale bars, 500 nm.
Figure 4. Bar graphs summarizing the number of DCVs found in non-GABAergic and GABAergic dendrites. (A) Pairwise differences demonstrated a significant increase of DCVs in non-GABAergic dendrites in the middle frequency region between 3–4 and 24 months (*p = 0.025). Pairwise differences also revealed a significant increase of DCVs in non-GABAergic dendrites in the low frequency region at 24 months (*p = 0.004). (B) Pairwise differences demonstrated no significant age-related differences in the number of DCVs from 3 to 4 months across GABAergic dendrites in the high frequency region (19–20 months, p = 0.98; 24 months, p = 0.96; 28–29 months, p = 0.79), middle frequency region (19–20 months, p = 0.87; 24 months, p = 0.233; 28–29 months, p = 0.65), and low frequency region (19–20 months, p = 0.97; 24 months, p = 0.76; 28–29 months, [p = 0.71]). Each age group had five cases.
3.3 DCVs do not significantly increase with age in GABAergic dendrites in the ICc
Although the total raw number of DCVs increased at older ages in the GABAergic dendrites, we found no significant change from 3 to 4 months in the high frequency region, middle frequency region and low frequency region (Figure 4B). A contributing factor to the non-significant findings appears to be the variability of DCV pools in the aging GABAergic dendrites. During aging we observed a few aged GABAergic dendrites in cross-section with dozens of DCVs (Figure 5). Thus, it appears that a few select neurons in the ICc may retrogradely transport neurotrophins and/or neuropeptides at great quantities during aging.
Figure 5. Electron micrograph of a medium sized GABAergic dendrite at 24-months from the ventromedial (high frequency region) of the central IC with over 40 DCVs. Although rare, GABAergic dendrites packed with DCVs could be found in the aged IC. Black dots demonstrate immunogold labeling of GABA. mito, mitochondria; ?, likely DCV. Scale bar, 500 nm.
3.4 Non-GABAergic boutons with DCVs are more likely to be spared in aging
Approximately 6% of non-GABAergic boutons had one or more DCVs at 3–4 months of age (Table 2). The majority of these boutons had just one DCV, regardless of location in the ICc (Figure 6 and Table 2). At later ages, it became more common to find non-GABAergic boutons with at least one DCV, and boutons with multiple DCVs also increased (Figures 6, 7 and Table 2). These boutons with multiple DCVs commonly made synapses onto non-GABAergic dendrites (Figure 7). The most conspicuous increase of DCVs occurred in the high frequency ICc at 19–20 months, and the high and middle frequency regions at 24 months (Figure 6 and Table 2). At 3–4 months of age, the low frequency ICc had the greatest raw number (100) of DCVs (Table 2). However, by 19–20 months the number of DCVs in the high frequency/ventromedial region had more than doubled (75–162), and the percentage of non-GABAergic boutons with at least one DCV increased from 5.24% to 11.2% (Table 2). At 24 months, the number of DCVs in the middle frequency region of the ICc doubled (68–160), and the percentage of boutons with at least one DCV increased from 6.6% to 10.5% (Table 2). Increases in the number of DCVs in the low frequency region were less robust between 3–4 months and 24/28–29 months (100–133), and the percentage of boutons having at least one DCV between 3–4 months and 28 months increased slightly (6.8%–8.7%; Table 2). Overall, these increases were largely driven by an increasing population of non-GABAergic boutons having four or more DCVs (Figure 7 and Table 2).
Figure 6. Pie charts showing the distribution of non-GABAergic boutons that had at least one DCV across four age groups from tissue representing the high, middle, and low frequency regions of the ICc. Regardless of ICc region, when a bouton had a DCV at 3–4 months, having just one was the most common (blue). We did not observe a 3–4 month non-GABAergic bouton with five or more. At the three later ages it became more common for non-GABAergic boutons that had a DCV to have three (green), four (yellow), five (orange), or more (red). The n’s represent the number of boutons that had at least one DCV. HF, high frequency; MF, middle frequency; LF, low frequency.
Figure 7. Electron micrograph of a non-GABAergic terminal from the dorsolateral (low frequency region) of the ICc at 28–29 months with at least four DCVs forming an asymmetric synapse onto a non-GABAergic medium dendrite. DCVs are circled in red. Scale bar, 500 nm.
As boutons and synapses are known to be downregulated in the aging IC, we quantified each non-GABAergic bouton in our experiments to better understand what proportion of boutons contain DCVs during aging. At 3–4 months we found a consistent number of boutons across the ventromedial-dorsolateral axis of the ICc (high-1,067; middle-1,031; low-1,096: Table 2). In the high frequency region at 19–20 month, 24 months, and 28–29 months there was a 9.1%, 23.8%, and 29.7% reduction of non-GABAergic boutons, respectively (Table 2). In the middle frequency region at 19–20 months, 24 months, and 28–29 months there was a 7.4%, 20.9%, and 24.8% reduction of non-GABAergic boutons, respectively (Table 2). Lastly, in the low frequency region at 19–20 months, 24 months, and 28–29 months there was a 8.0%, 15.8%, and 17.6% reduction of non-GABAergic boutons, respectively (Table 2). Taken together with the data mentioned above, our findings suggest that non-GABAergic cells/boutons that package DCVs are more likely to be spared during aging than non-GABAergic cells/boutons that do not package DCVs.
3.5 GABAergic boutons with DCVs are more likely to be spared in aging
Similar to non-GABAergic boutons, at any age and/or ICc location GABAergic boutons that contained DCVs typically had just one (Figure 8). GABAergic boutons with multiple DCVs occurred more routinely during aging in the middle and low frequency regions (Figure 8). However, at older ages, the proportion of GABAergic boutons with just one DCV increased in the high frequency ICc (Figure 8). As with the non-GABAergic population, during aging there was a greater raw number of DCVs in GABAergic boutons and a higher number of GABAergic boutons with at least one DCV in the high and middle frequency regions of the ICc (Figure 8 and Table 3). The raw number of DCVs in GABAergic boutons and number of GABAergic boutons with at least one DCV peaked at 24 months, but was lowest at 28 months (Figure 8 and Table 3).
Figure 8. Pie charts showing the distribution of GABAergic boutons that had at least one DCV across four age groups from tissue representing the high, middle, and low frequency regions of the ICc. Regardless of ICc region, when a bouton had a DCV at 3–4 months, having just one was the most common (blue). We did not observe a 3–4 month GABAergic bouton with five or more. At the three later ages there was a slight increase in the number of GABAergic boutons with four (yellow) or more (orange and red) DCVs. The n’s represent the number of boutons that had at least one DCV. HF, high frequency; MF, middle frequency; LF, low frequency.
We also quantified each GABAergic bouton in our experiments. Unsurprisingly, there was an overall reduction of GABAergic boutons at each age and at each ICc region (Table 3). The percentage of GABAergic boutons across the ICc with a DCV was only ∼4% at 3–4 months and increased during aging, with greater variability in the low frequency ICc (Table 3). Taken together we come to the same conclusion as we have with the non-GABAergic population: GABAergic cells/boutons that package DCVs are more likely to be spared during aging than GABAergic cells/boutons that do not package DCVs.
4 Discussion
The current study describes populations of DCVs in the aging ICc. Our findings demonstrate that DCVs are infrequent in the young rat ICc. This agrees with studies conducted in cat (Paloff and Usunoff, 1992). However, our data demonstrate that DCVs increase with aging in the rat ICc. Specifically we found the greatest increase of DCVs at 24 months in non-GABAergic dendrites throughout the middle and dorsolateral portions of the ICc’s ventromedial-dorsolateral tonotopic axis (corresponding to mid- and low-frequency representation). This is interesting as the FBN rat has been shown to lose low frequency hearing around 24 months of age (Keithley et al., 1992; Caspary et al., 2005; Cai et al., 2018). While the raw number of DCVs in boutons did not significantly change during aging, there was (1) an increase in the number of boutons with multiple DCVs, and (2) the percentage of all boutons that had at least one DCV increased with age. Given that we broadly found a ∼25% loss of boutons across the ICc, which reflects findings by Helfert et al. (1999), we interpret our data to imply that presynaptic boutons in the ICc which are lost with age are not likely releasing contents that would be packaged by a DCV. As this is the first report of age-related changes to DCVs in the IC, future studies will hopefully determine what neuropeptides, neurotrophins and/or presynaptic proteins are undergoing age-related changes in the IC.
4.1 Technical considerations
The FBN rat is a recommended aging model by the National Institute on Aging as it has a longer median lifespan than other strains of mice and rats (Lipman et al., 1996; Lipman, 1997). Of note, the FBN rat is routinely used as a characterized model for aging, in particular for studies of the central auditory system (Caspary et al., 2008; Cai et al., 2018; Caspary and Llano, 2018; Robinson et al., 2019; Mafi et al., 2020, 2021, 2022; Kommajosyula et al., 2021). We have chosen to use four age groups in this study. Our 3–4 month and 28–29 month groups are standard ages for “young” and “old,” when there are no hearing deficits and very well characterized hearing loss, respectively. The use of two middle ages, a 19–20 month group and 24 month group, reflect ages when hearing deficits are not commonly reported and when hearing thresholds are significantly elevated, respectively (Cai et al., 2018). However, we acknowledge that the hearing thresholds of the FBN rats in the current study were not measured and we do not know if a 19 month old rat had perfect hearing or if a 24 month old rat had poor hearing.
In the current study we equate parts of the ICc with tonotopic regions (e.g., low-frequency region). We did not characterize IC cells with electrophysiological techniques in the current study. We took the ventromedial-dorsomedial axis of the ICc tissue and divided it into thirds. While we do not know the characteristic frequencies represented in each tissue block, as the tonotopic axis of the IC is well established, we have no reason to believe that our ventromedial most block does not represent higher frequencies compared to the other two blocks; and the dorsolateral most block would represent the lowest frequencies. Another consideration in the interpretation of our data is that, although a common view of the IC’s tonotopic map is one of a continuous gradient, the rat IC tonotopic map may be organized in a stepwise manner (Malmierca et al., 2008). Thus, our middle-most ICc blocks may represent frequencies closer to one end of the tonotopic map than the other.
We only immunolabeled for GABA, thus we cannot know the neurochemical profile of boutons that were not GABAergic. In terms of non-GABAergic boutons that formed symmetric synapses, we presume these are in part glycinergic. That said, the IC receives input from many neuromodulators, and the morphology of their postsynaptic densities are not well classified (Schofield and Hurley, 2018). We hope that this study will serve as a foundation to examine the ultrastructure of neuromodulators and neurotransmitters that are packaged by DCVs in the aging IC.
4.2 DCVs in the inferior colliculus
The first ultrastructural description of DCVs in the IC was in cat (Jones and Rockel, 1973; Rockel and Jones, 1973; Paloff et al., 1989). Decades later, boutons containing DCVs were characterized in greater detail and defined a unique type of ICc bouton (Paloff and Usunoff, 1992). The current study broadly agrees with the findings from these original studies: (1) DCVs occurred in boutons with pools of smaller clear vesicles, (2) DCVs were not clustered toward the synapse or membrane, (3) boutons with DCVs commonly had 0–1 mitochondria, (4) DCVs are not uniformly found throughout the ICc, and (5) DCVs are generally uncommon in the ICc (Paloff and Usunoff, 1992). Our findings are further in line with Paloff and Usunoff (1992) in that we found presynaptic terminals with a DCV(s) terminating on a soma to be exceedingly rare (observed only once in our analysis of 192,000 μm2 of tissue). However, Rockel and Jones (1973) found that boutons carrying DCVs more routinely terminate on cell bodies.
The current study (in rat) differs from the previous studies (in cat) in two ways. First, work in the cat has demonstrated that when DCVs are present in presynaptic boutons, there may be over one to two dozen (Rockel and Jones, 1973; Paloff and Usunoff, 1992). The current study in rats, and mice (unpublished observations), rarely revealed more than three DCVs in a single bouton. Previous reports of the rat IC ultrastructure also imply that DCVs, let alone pools of them, are rare (Ribak and Roberts, 1986; Roberts and Ribak, 1987). Even though Roberts and Ribak revealed and described the rat IC ultrastructure in considerable detail, only one DCV is visible throughout their images (Ribak and Roberts, 1986; Roberts and Ribak, 1987). Our data also appears to be in agreement with prior studies in rat hippocampus that quantified DCVs, as presynaptic terminals containing DCVs commonly had only a few (Sorra et al., 2006; Tao et al., 2018). Taken together, we believe that the pool size of DCVs in presynaptic terminals is likely species dependent.
Second, we found that the number of DCVs found in dendrites was nearly equal to the number of DCVs found in axons/boutons at young age (Table 1). Furthermore, specifically during middle-age in the dorsolateral half of the ICc, there was a significant age-related increase of DCVs in the ICc dendrites. Previous reports focus on DCVs pools in the IC do not describe a consistent population of DCVs throughout the dendrites of the ICc (Rockel and Jones, 1973; Paloff and Usunoff, 1992). It is unknown if these reports simply did not analyze dendrites for DCVs or if there is a species difference between cats and the current studies that largely utilize rodent and cell culture. However, in the mammalian central nervous system, DCVs pools can be found equally distributed between the dendrites and axons/terminals of a given cell (Persoon et al., 2018). However, DCVs in the axons and boutons are often focused on as their release probability is much higher than the ones in the dendrites (Persoon, et al., 2018). It is important to note DCV fusion events in dendrites are not as tightly time locked to a cell firing and require sustained Ca2+ (Xia et al., 2009). Fusion mechanism aside, dendritic exocytosis is a critical function for retrograde signaling, synapse growth and plasticity, and cellular morphology and DCVs play a prominent role in the dendritic release of many neuropeptides and neurotrophins (Regehr et al., 2009; Kennedy and Ehlers, 2011; Ramamoorthy et al., 2011).
A major finding of the current study was that while there was a loss (∼25%) of boutons at old age, the percentage of boutons with DCVs did not change with age. Similar to the dendritic population, the more robust increases occurred in the GABA-negative boutons. We found that non-GABAergic and GABAergic boutons with DCVs made synapses onto both GABAergic and excitatory dendrites (we presume non-GABAergic dendrites in the IC are excitatory as only GABAergic and glutamatergic cells have been demonstrated in the IC, Merchán et al., 2005; Oliver, 2005) at any age. Thus, the contents of DCVs in the aging IC are likely affecting both inhibitory and excitatory circuits.
4.3 Functional implications
Broadly, DCVs are divided into small (∼40–80 nm) and large (∼90–200 nm) groups (Peters et al., 1991; Paloff and Usunoff, 1992; Edwards, 1998; Sorra et al., 2006; Trueta and De-Miguel, 2012; Merighi, 2018; Tao et al., 2018). Smaller DCVs tend to package biogenic amines, neuromodulators, and presynaptic machinery, while larger DCVs tend to package neuropeptides, hormones and neurotrophic factors (Peters et al., 1991; Michael et al., 2006; Sorra et al., 2006; Merighi, 2018). The exact diameter that defines a small versus a large DCV appears to be a sliding scale based on location (peripheral or central nervous system) and species, and what ultimately determines the size of a DCV is not well known (Merighi, 2018; Lin et al., 2022). Regardless of diameter, there appears to be considerable differences in the locations, releasing mechanisms, stimulation rates for release, and packaged content of DCVs between the peripheral and central nervous systems, nuclei within in the central nervous system, and between cultured and in vivo studies (Hökfelt, 2010; Kennedy and Ehlers, 2011; Persoon et al., 2018). In the central nervous system, much of our knowledge regarding DCVs is obtained from the hippocampus, hypothalamus, and neuromodulatory nuclei (e.g. Raphe and Locus Coeruleus: Sorra et al., 2006; Trueta and De-Miguel, 2012). As this is the first report on the aging DCV population in the IC, further studies are needed to reveal the functional relevance of our data. That said, we would like to comment on a few functions that an age-related increase of DCVs may reflect.
4.3.1 Hearing loss and neuromodulation
GABAergic inhibition is reduced in the aging IC (Caspary et al., 2008; Syka, 2020). This downregulation of GABA may be a compensatory homeostatic response to the loss of peripheral excitation (Caspary et al., 2008; Richardson et al., 2012; Caspary and Llano, 2018). Later in life the ongoing decline in GABAergic neurotransmission likely contributes to disrupted temporal precision and increases in central gain that underlie conditions such as presbycusis, tinnitus, and hyperacusis (Palombi and Caspary, 1996; Frisina, 2001; Brozoski et al., 2002; Walton et al., 2002; Norena, 2011; Parthasarathy and Bartlett, 2011; Auerbach et al., 2019).
Although a number of neuromodulators are released in the IC (e.g., serotonin, dopamine, acetylcholine, and noradrenaline), their roles in the aging IC across middle and old ages have not been thoroughly explored (Klepper and Herbert, 1991; Paloff and Usunoff, 2000; Hurley and Pollak, 2005a; Motts and Schofield, 2009; Hurley and Sullivan, 2012; Schofield and Hurley, 2018; Noftz et al., 2020, 2021). In the context of the current study, serotonin neurotransmission may be a promising avenue to pursue in future studies. First, serotonin is known to be packaged in DCVs in the central nervous system (Bruns et al., 2000; Trueta and De-Miguel, 2012; Kim et al., 2021). Second, serotonin has a myriad of functions in the IC (Hurley and Pollak, 1999, 2001; 2005b; Hurley et al., 2002). Third, it is known that aging and hearing loss affects serotonergic neurotransmission (Tadros et al., 2007; Hall et al., 2012; Shim et al., 2012). It is notable that in each of these studies, serotonin and its receptors increased in the aging IC and during hearing loss. Perhaps the increase of DCVs is correlated with increases of serotonin neurotransmission in the aging IC.
Recent studies in the IC have identified a novel class of GABAergic cells that express the neuropeptide/neuromodulator NPY (Silveira et al., 2020, 2023; Anair et al., 2022). Generally speaking, NPY in the brain provides neuroprotective effects during healthy and pathological aging (Chen et al., 2019; Pain et al., 2022). Interestingly, NPY can be trafficked down dendrites, released postsynaptically, and act on presynaptic and postsynaptic receptors (Ramamoorthy et al., 2011; Yi et al., 2018). Future studies will use immunoEM to determine if NPY is also trafficked by DCVs in the dendrites of GABAergic IC cells. Given that NPY significantly regulates local excitation in the IC, it will be critical to determine how the balance of excitation and inhibition is affected by NPY neurotransmission in the aging IC. Our data show increased DCVs in middle and low frequency IC in a model of presbycusis, so it will be interesting to determine whether serotonin or NPY effects change across the tonotopic axis.
4.3.2 Brain-derived growth factor and plasticity
Another potential peptide contained in IC DCVs is BDNF, a neurotrophin released by DCVs throughout the brain to regulate functions such as synaptic transmission, plasticity, neurite growth, and gene regulation (Kennedy and Ehlers, 2011; Dieni et al., 2012). In the auditory system, BDNF is critical for development and normal acoustic function (Wissel et al., 2006; Singer et al., 2014; Chumak et al., 2016). In the IC, BDNF has been tied to development, acoustic trauma, and dendritic integrity (Hafidi et al., 1996; Sato et al., 2001; Sharma et al., 2009; Meltser and Canlon, 2010). Further studies will need to determine if BDNF DCVs are trafficked to IC axons, dendrites or both as the cellular location of BDNF DCVs differ across reports (Dean et al., 2009; Matsuda et al., 2009; Kennedy and Ehlers, 2011; Dieni et al., 2012; Persoon et al., 2018).
Fibroblast growth factors are another likely protein packaged by IC DCVs. Compellingly, levels of fibroblast growth factor receptor 2 (FGF-2) spike during middle age when hearing deficits are not common, and while there is a decrease at old age, FGF-2 levels are still elevated compared to young brains (Sato et al., 2001). This pattern is very similar to trends in the current study, where DCVs in excitatory dendrites maximally increase at middle age and then decline into old age, yet are still more numerous than at young age. Given that (1) FGF-2 contributes to dendritic arborization and synaptic plasticity, (2) DCVs often carry contents such growth factors that play a role in synaptogenesis, and (3) the aged IC has a loss of dendrites and synapses, the IC may undergo a number of plastic events during middle age (Helfert et al., 1999; Sorra et al., 2006; Li et al., 2020). Further supporting the theory of increased plasticity with aging in the IC, perineuronal nets (organized extracellular matrix that have substantial roles in neural plasticity) increase with aging in the IC (Fader et al., 2016; Bosiacki et al., 2019; Mafi et al., 2020, 2021; Almassri et al., 2023). Taken altogether, the increase of DCVs in the aging IC may contribute to elements of dendritic and synaptic plasticity.
Data availability statement
The original contributions presented in this study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.
Ethics statement
The animal study was approved by the Northeast Ohio Medical University Institutional Animal Care and Use Committee. The study was conducted in accordance with the local legislation and institutional requirements.
Author contributions
JM: Conceptualization, Data curation, Funding acquisition, Investigation, Methodology, Project administration, Resources, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. SD: Data curation, Formal analysis, Investigation, Writing – review & editing. JB: Data curation, Formal analysis, Investigation, Writing – review & editing. LA: Writing – original draft, Writing – review & editing. AW: Data curation, Formal analysis, Investigation, Supervision, Writing – review & editing. MI: Formal analysis, Investigation, Writing – review & editing. AO: Investigation, Methodology, Supervision, Writing – review & editing. ES: Data curation, Formal analysis, Investigation, Writing – review & editing. AB: Data curation, Investigation, Writing – review & editing. DA: Data curation, Investigation, Writing – review & editing. BV: Data curation, Investigation, Writing – review & editing. AM: Data curation, Formal analysis, Investigation, Methodology, Writing – review & editing. MB: Data curation, Formal analysis, Investigation, Methodology, Software, Writing – review & editing. NT: Investigation, Project administration, Supervision, Writing – review & editing. JY: Data curation, Formal analysis, Software, Supervision, Writing – review & editing.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the NIH/NIDCD grant R01 DC017708 and National Institute on Aging rodent colony.
Acknowledgments
We gratefully acknowledge Dr. Nichole Beebe for critical feedback on an earlier draft of the manuscript.
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.
Abbreviations
DCV, dense core vesicle; FBN, Fischer Brown Norway; GABA, gamma-aminobutyric acid; GAD, glutamic acid decarboxylase; IC, inferior colliculus; ICc, central nucleus of the inferior colliculus; ICd, dorsal cortex of the inferior colliculus; IClc, lateral cortex of the inferior colliculus; LD, large dendrite; MD, medium dendrite; SD, small dendrite.
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Keywords: inferior colliculus, GABA, synapse, aging, dense core vesicles
Citation: Mellott JG, Duncan S, Busby J, Almassri LS, Wawrzyniak A, Iafrate MC, Ohl AP, Slabinski EA, Beaver AM, Albaba D, Vega B, Mafi AM, Buerke M, Tokar NJ and Young JW (2024) Age-related upregulation of dense core vesicles in the central inferior colliculus. Front. Cell. Neurosci. 18:1396387. doi: 10.3389/fncel.2024.1396387
Received: 05 March 2024; Accepted: 11 April 2024;
Published: 01 May 2024.
Edited by:
Christian Keine, University of Oldenburg, GermanyReviewed by:
Tara Sankar Roy, North DMC Medical College and Hindu Rao Hospital, IndiaAaron Benson Wong, Erasmus University Medical Center, Netherlands
Copyright © 2024 Mellott, Duncan, Busby, Almassri, Wawrzyniak, Iafrate, Ohl, Slabinski, Beaver, Albaba, Vega, Mafi, Buerke, Tokar and Young. 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: Jeffrey G. Mellott, am1lbGxvdHRAbmVvbWVkLmVkdQ==