Abstract
Introduction:
Macrophages are essential immune cells in the cochlea that contribute to inflammation, tissue repair, and homeostasis. They also play an important role in local cochlear immunity. The developmental immigration and maturation of macrophages in the cochlea have been investigated and are considered essential for normal hearing acquisition. Most of our current knowledge regarding cochlear development is based on rodent models because of the ethical challenges of using human fetal samples for research. However, inter-species differences between rodents and humans have been reported. In this study, we used a primate animal model to investigate the distributions of macrophages in the developing cochlea. The common marmoset (Callithrix jacchus), a small monkey species that inhabits the New World, was used as the model.
Methods:
We investigated the distribution of macrophages in the developing cochlea of the common marmoset by performing immunohistochemical analyses of cochlear tissue from common marmoset embryos at different development stages.
Results:
We revealed detailed distribution changes in the macrophages of a primate animal model cochlea. This observation indicates that most of the changes in the general distribution of macrophages were well preserved between rodents and this primate. The distribution changes observed in the common marmoset were also compatible with observations in the human fetus; although, observations in the human fetus are limited. Our observations in this study also revealed several differences between common marmosets and rodents.
Conclusion:
The time course of immunological development and maturations established in this study will aid in the study of the primate-specific developmental biology of the inner ear. These observations may eventually lead to new therapeutic strategies for hearing loss in humans. In addition, understanding the immunological steady-state of the cochlea may help in the study of age- and genetic-induced hearing loss and in the design of regenerative therapies.
1 Introduction
The inner ear is a sensory organ essential for hearing, balance, and the perception of acceleration. The inner ear of mammals comprises several parts, and the cochlea acts as an organ for hearing perception. In the cochlea, the vibrations produced by sound waves are converted into electrical pulses in hair cells. This mechanoelectrical transmission is essential for hearing, and the electrical pulses generated in these steps are perceived in the brain as sound.
Immunological studies of the cochlea have received considerable attention, especially from the viewpoint of hearing disorders mediated by ototoxic drugs (1, 2) and noise-induced hearing loss (3–5). Moreover, a relationship between the immunological state of the cochlea and age-related hearing loss has been suggested (6, 7). There are several cells that plays immunologically important roles in the cochlea including T cells, B cells, and neutrophils. Between these cells, macrophages are the most abundant and thought to be essential immune cells in the cochlea (8). Macrophages contribute to inflammation, tissue repair, and homeostasis and are critical in the cochlea (9). In response to acute cochlear damage, macrophages will significantly modify their distribution, phenotype, and number. This observation supports the hypothesis that macrophages are vital in the cochlear response to acoustic trauma. Macrophages prevent the loss of spiral ganglion neurons after cochlear injury (10). Moreover, macrophages promote the repair of inner hair cell ribbon synapses after noise-induced cochlear synaptopathy (11).
The immigration and maturation of macrophages in the cochlea is essential for normal hearing (12–15). Most studies investigated rodent models because of restrictions on the use of human fetal temporal bone samples, and only a few reports have addressed human cochlear macrophage development (16, 17). In addition, cochlear development in humans is not fully understood because it occurs in the late phases of gestation (18–20). Moreover, ethical regulations have prevented the study of late-stage fetal human samples. As yet, several inter-species differences in the cochlear development of primates and rodents have been reported. Therefore, it has been suggested that our knowledge based on rodent models cannot always be directly applied to humans (19). To overcome this the common marmoset (Callithrix jacchus), a small primate, has been used to understand cochlear development(21–25), as well as genetic and age-related hearing loss (26). A similar approach has been applied in investigations on the brain (27).
We previously reported on cochlear development in the common marmoset, highlighting basic anatomical staging of the developing cochlea, and comparisons with that in humans and mice. We further revealed several differences between rodents and marmosets in the development of the organ of Corti, spiral ganglion neurons, and the stria vascularis. Moreover, we demonstrated similarities with human developmental processes, indicating that this primate is a promising animal model (21, 22, 24). Nevertheless, researchers have not yet examined the cochlear development of the common marmoset from an immunological viewpoint.
In this study, the development of the cochlea was investigated from an immunological viewpoint, and the distribution of macrophages in the developing cochlea of a non-human primate animal model was examined. The present study provides valuable insights on the process of macrophage invasion and the role of macrophages in cochlear development in this animal model. This study aims to contribute to the development of feasible treatment methods to modulate macrophage activity in sensorineural hearing loss or hearing loss caused by noise or ototoxic agents.
2 Materials and methods
Cadaverous temporal bone samples from common marmoset fetuses at E70 (n = 4), E77 (n = 2), E87 (n = 4), E96 (n = 3), E109 (n = 3), E120 (n = 3), P0 (n = 3), and young adults (n = 3) were used in this study, as described in our previous reports (21, 22, 24). Adult animals were anesthetized via isoflurane inhalation (1.5–4%). Caesarion section was performed as previously described (28). Embryos were anesthetized on ice and deeply dissected in phosphate-buffered saline (PBS). Finally, the temporal bones containing cochlea were removed from the skull. Part of the tissue samples in this study were those prepared and used in our previous studies. Animal experiments were approved by the Animal Experiment Committee of Keio University (approval numbers: 11006, 08020). All animal experiments were performed in accordance with the guidelines of the National Institutes of Health and the Ministry of Education, Culture, Sports, Science, and Technology of Japan.
2.1 Tissue preparation
The temporal bones were dissected immediately after euthanasia. The samples were fixed overnight in 4% paraformaldehyde in PBS overnight. The specimens were embedded in Tissue-Tek O.C.T. compound (Sakura Fine Technical Co., Ltd., Tokyo, Japan) for cross-sectioning. P0 specimens were embedded in Tissue-Tek O.C.T. compound after decalcification in Decalcifying Solution B (Wako, Osaka, Japan) for one week, as described in our previous reports (21, 24, 29). Sections (7 µm) were used for immunohistochemical analysis.
2.2 Antibodies
The following primary antibodies were used in this study: Anti-ionized calcium binding adapter molecule 1 (IBA1; Rabbit IgG; ab5076, Abcam, Cambridge, UK, 1:500), anti-POU domain class 3 transcription factor 4 (POU3F4; HPA; HPA031984, Atlas Antibodies, Bromma, Sweden; 1:500), anti-SRY-box transcription factor 10 (SOX10; Mouse IgG1; 365692, Santa Cruz Biotechnology, Santa Cruz, CA, USA; 1:200), anti-cochlin (COCH; Rabbit IgG; HPA050122, Atlas Antibodies; 1:200), anti-SRY-box transcription factor (SOX2; Rabbit IgG; ab92494, Abcam; 1:200), anti- myosin 7A (MYO7A; Mouse IgG1; 138-1-s, DSHB, GeneTex, Irvine, CA, USA; 1:30), anti-MYO7A (Rabbit IgG; 25-6790, Proteus Biosciences, Ramona, CA, USA; 1:500), anti-human leukocyte antigen (HLA) DQ/DR/DP (Mouse IgG1; CR3/43, NB120-17101, Novus, St. Charies, MO, USA; 1:50), anti-neurofilament heavy chain (NEFH; Chick IgY; ab4680, Abcam, 1:1000), anti-S100 calcium-binding protein B (S100B; Rabbit IgG; ab52642, Abcam; 1:200), anti-myelin protein zero (MPZ; Rabbit IgG; ab31851, Abcam, Cambridge, UK; 1:200), anti-tubulin beta 3 (TUBB3; Mouse IgG2b; GTX631836, DSHB, GeneTex, 1:1000), anti-melan A (MLANA; Rabbit IgG; NBP1-30151, Novus; 1:500), anti-sodium/potassium-transporting ATPase subunit alpha-1 (ATP1A1; Mouse IgG2a; a6F, DSHB, Iowa City, IA, USA; 1:500), anti-actin alpha 2 (ACTA2; Mouse IgG2a; A2547, SIGMA, Saint Louis, MO, USA; 1:200), anti-solute carrier family 2 member 1 (SLC2A; Rabbit IgG; ab115730, Abcam; 1:500), anti-cluster of differentiation 163 (CD163; Rabbit IgG; ab182522, Abcam; 1:200).
The following secondary antibodies were used in this study: Donkey anti-goat IgG (Alexa Fluor Plus 647; A32814, Invitrogen, Waltham, MA, USA; 1:500), donkey anti-rabbit IgG (Alexa Fluor Plus 555; A32794, Invitrogen; 1:500), donkey anti-rabbit IgG, (Fluor Plus 647; A32795, Invitrogen; 1:500), donkey anti-mouse IgG (Alexa Fluor Plus 555; A32773, Invitrogen; 1:500), donkey anti-mouse IgG (Alexa Fluor Plus 647; A32787, Invitrogen; 1:500), and donkey anti-chicken IgY (Alexa Fluor 647; 703-605-155, Jackson Immuno-Research, West Grove, PA, USA; 1:500).
2.3 Immunohistochemistry
The tissue sections were heated (80°C) in 10 µM citrate buffer (pH 6) for 15 min, after a brief wash with PBS. Then, the sections were pre-blocked in PBS containing 10% normal serum for one hour at room temperature. Next, the sections were incubated with the relevant primary antibodies overnight at 4°C. Finally, the sections were incubated with Alexa Fluor-conjugated secondary antibodies for 60 min at room temperature. The nuclei were counterstained with Hoechst 33258.
3 Results
3.1 Distributions of macrophages in the developing cochlea of the common marmoset
First, IBA1 expression was examined in the developing cochlea of the common marmoset. IBA1 encodes the ionized calcium-binding adapter molecule 1, an established macrophage marker in the cochlea of both rodents (30, 31) and humans (32–34). IBA1 has also been used as a macrophage marker in common marmosets (35). Abundant cells expressing IBA1 were observed as early as E70 surrounding the cochlear duct. At this stage, IBA1-positive cells were localized to POU3F4-positive developing periotic mesenchymal cells (Figures 1A, B). Notably, several IBA1-positive cells that integrated into the cochlea were observed at this stage (indicated by arrows in Figure 1B). At E77 and E87, abundant IBA1-positive cells surrounded the SOX10-positive cochlear epithelium and were present among periotic mesenchymal cells (Figures 1C–E). At E96, IBA1-positive cells were observed mainly among periotic mesenchymal cells, especially in the fibrocytes of the developing lateral wall (Figures 1F, G). As late as E96, relatively abundant IBA1-positive cells were observed in the developing cochlea. After E109, the number of IBA1-positive cells gradually decreased; especially between E96 and E109, the decrease in IBA1-positive cells was prominent (Figures 1H, I). At P0, a small number of IBA-1 positive cells were observed in the cochlea, including lateral wall fibrocytes, stria vascularis, and organs of Corti (Figure 1J).
Figure 1
3.2 Distributions of macrophages in the sensory epithelium of the common marmoset
Next, we examined the infiltration of IBA1-positive cells into the sensory epithelium of the cochlear duct. As early as E87, a small number of IBA1-positive cells were integrated into the SOX10-positive cochlear epithelium (Figures 2A, B). Except for infiltrations into the stria vascularis, the infiltration of macrophages was observed only in the modiolar half of the cochlear duct. After E92, macrophage infiltration was observed in SOX2-negative cells (Figures 2C–F). Macrophage infiltration into SOX10-positive cochlear epithelium was observed as late as E120. At E109 and E120, macrophage integration into epithelial cells was observed in the epithelium covering the spiral limbus (Figures 2G–J). At P0, macrophages were observed in the organ of Corti, whereas no IBA1-expression was observed until E120 in the SOX2-positive developing organ of Corti (Figure 3). Most macrophages in the organ of Corti were observed around Deiters’ cells and Hensen’s cells beneath the outer hair cells.
Figure 2
Figure 3
3.3 Distributions of macrophages in the spiral ganglion of the common marmoset
Next, the localization of macrophages in the ganglion neurons was examined. As early as E87, macrophages infiltrated spiral ganglion neurons (Figures 4A, B). Throughout the development of spiral ganglion neurons, infiltrating macrophages were observed among NEFH-positive spiral ganglion neurons and S100B-positive developing glial cells (Figures 4C–H). Macrophage infiltration into spiral ganglion neurons was also observed at the time of MPZ-positive myelin formation in glial cells (Figures 4I, J). Macrophages were also observed among the neurons in the osseous spiral lamina as late as E96 (Figures 4F, H, J). At P0, Macrophages were observed in the spiral ganglion located between the NEFH-positive neural cells and MPZ-positive glial cells (Figures 4K, L).
Figure 4
3.4 Distributions of macrophages in the stria vascularis of the common marmoset
Next, we examined macrophage infiltration into the stria vascularis. Infiltration of intermediate cells marked with MLANA into marginal cells marked with ATP1A1 has been reported in the developing stria vascularis (24). In this study, we analyzed the migration of IBA1-positive macrophages by comparing intermediate and marginal cell development. At E87, the infiltration of IBA1-positive cells between ATP1A1-positive cochlear epithelia was observed (Figures 5A, B). In contrast, as previously reported (24), no MLANA-positive cell infiltration was detected; MLANA-positive cells were located next to the marginal cells. At E96, both intermediate cells and macrophages were integrated between ATP1A1-positive marginal cells (Figures 5C, D). At E101, when the marginal and intermediate cells formed complicated cell-cell contacts, macrophages were also embedded between these cells (Figures 5E, F). At E109 and E120, a decrease in the number of macrophages between the incorporated marginal and intermediate cells was observed, whereas small numbers of macrophages were observed in this space (Figures 5G–I). At P0, only a few perivascular macrophages (PVMs) were located in the perivascular spaces (Figures 5J–M), as previously reported in rodents (36). At this stage, PVMs had arms that held small vessels in the stria vascularis. A schematic representation of macrophage infiltration into the stria vascularis is shown in Figure 6.
Figure 5
Figure 6
3.5 Localization of macrophage subpopulations in the developing cochlea of the common marmoset
Next, to estimate the localization of macrophage subpopulations in the developing primate cochlea, the expression of CD163 was examined. CD163 is a protein encoded by the CD163 gene. CD163 is a high-affinity scavenger receptor for the hemoglobin-haptoglobin complex (37). It is also a marker of cells of the monocyte/macrophage lineage and acts as an innate immune sensor for Gram-positive and Gram-negative bacteria. CD163 expression in the developing and adult cochlea in humans has been previously reported (17, 32, 33, 38).
In the common marmoset, CD163 expression in macrophages was observed as early as E77 (Figure 7A). At this stage, abundant CD163-positive cells were observed among periotic mesenchymal cells, and most IBA1-positive cells expressed CD163. After E87, a gradual decrease in CD163-positive macrophages was observed (Figures 7B–D). At E120, only a few IBA1-positive cells expressed CD163 (Figure 7E). At P0, no CD163 expression was detected in the sensory epithelium (Figure 7F). The distribution of CD163-positive cells in spiral ganglion neurons was also examined. In the developing spiral ganglion, some IBA1-positive cells exhibited CD163 expression as early as E87 (Figure 8A). Some macrophages in the spiral ganglion continued to express CD163 expression until E120 (Figures 8B–D), whereas no CD163 expression was detected in the P0 spiral ganglion (Figure 8E).
Figure 7
Figure 8
3.6 Expression patterns of Class II MHC components in the developing cochlea of the common marmoset
Finally, expression patterns of class II major histocompatibility complex (MHC) components were investigated. Class II MHC is a characteristic marker of macrophages, which is essential for antigen presentation and functions as a key regulator of adaptive immune responses (39). MHC class II proteins are expressed in macrophages, B cells, monocytes, and dendritic cells and comprises HLA DR/DP/DQ. In the developing cochlea of the common marmoset, HLA DR/DP/DQ expression was not observed in macrophages in the developing cochlea as late as E120 (Figures 9A, B). At P0, some macrophages expressed HLA-DR/DP/DQ (Figure 9C), including macrophages in the organs of Corti (Figure 9D). In contrast, no HLA DR/DP/DQ expression was observed in the PVMs of the stria vascularis at this stage (Figure 9E). However, HLA DR/DP/DQ expression in PVMs was detected in the postnatal stages (Figure 9F), as reported in human PVMs (33).
Figure 9
4 Discussion
To the best of our knowledge, this is the first report describing macrophage distribution in the developing cochlea of a primate animal model (Figure 10). A previous study showed dynamic changes in the distribution of resident macrophages depending on the cochlear tissue area or developmental stage (13, 14), in mice as well as in humans (17). In mice, the density of cochlear macrophages increases as the mice grow, it peaks around the neonatal stages, and decreases from P3 onward (14). Similar dynamic changes were also observed in the developing cochlea of the common marmoset, although its peak was observed around E77–87 and decreases in the macrophages in the cochlea were prominent after E109 (Figure 1). Combined with a previous observation that P0 in mice is the morphological equivalent of E101 in the marmoset (21), changes in the distribution of macrophages in the common marmoset and rodents are conserved, except for the relative timing of birth.
Figure 10
After birth, the immunological circumstances rapidly change. The outer and middle ears are not sterile at the time of birth, and these changes cannot be underestimated in the immunological state of the inner ear. However, in primates, our observations indicate that changes in the distribution of macrophages do not depend on delivery. This preservation also indicates that developmental rather than environmental changes control the changes in immunological conditions in the cochlea.
While it has been reported that the mature organ of Corti in mice lacks tissue macrophages (3, 30, 40), the developing postnatal organ of Corti contains macrophages (13). In rodents, macrophages were transiently observed beneath the organ of Corti around postnatal day 7 (13). Likewise, in the present study, we observed macrophages beneath the organ of Corti at P0, although in early stages of development, no infiltration of macrophages was observed in SOX2-positive regions, except at E87 when broad SOX2 expression was observed (Figures 2, 3). To date, no observation of macrophage infiltration of the organ of Corti in the developing human cochlea has been reported, and no infiltration of macrophages into the organ of Corti was observed in a previous report examining the cochlea of human fetuses in the 9th to 17th week of gestation (17). Considering our previous observation that the developing cochlea of the P0 common marmoset is equivalent to approximately 24 gestational weeks in human fetuses (21), macrophage infiltration may occur at the late stages in human fetuses. However, in most cases, late human fetal sampling is unethical. From this point of view, the common marmoset is a suitable alternative to a human fetus for studying the developmental roles of macrophages in the organs of Corti in primates.
Previous reports showed important roles of cochlear macrophages in the refinement of connections between spiral ganglion neurons and hair cells, both in normal development (13, 41) and after noise trauma (11). Based on previous observations in rodents, macrophages were suspected to facilitate the formation or pruning of cochlear ribbon synapses during cochlear development (41). Although the pruning of the spiral ganglion neurons occurs between E115 and P0 in the common marmoset (22), an increase in the number of macrophages in the spiral ganglion neuron or the osseous spiral lamina was not observed at this stage. Macrophage infiltration in the spiral ganglion neurons was observed in the early stages, and no obvious increase in spiral ganglion neurons was detected (Figure 4). This observation indicated a limited number of macrophages regarding this pruning in the primate cochlea. Moreover, it has been suggested that macrophages are also related to the myelination of spiral ganglion neurons in rodents (12). However, macrophages in spiral ganglion neurons in the primate cochlea are observed much earlier than those in the myelination of spiral ganglion neurons, which was first observed at E115 (22). These observations, in which the infiltration of macrophages occurred much earlier than that in neural pruning or myelination, suggest other developmental roles for cochlear macrophages in the primate cochlea. Hence, to determine the exact role of cochlear macrophages, further studies on these animals are warranted.
Several previous studies in rodents have shown macrophage infiltration into the stria vascularis and the subsequent development of these macrophages into PVMs (36, 42). Observations in the present study also demonstrated that PVMs in the stria vascularis originate from infiltrating macrophages (Figure 5). In addition, this study benefits from the species-specific trait that the primate cochlea develops three times slower than that of other species (21) and the detailed infiltration of macrophages can be studied by comparing the integration of MLANA-positive intermediate cells into marginal cells in the stria vascularis. In primates, macrophage integration into the stria vascularis was detected in the early phases of cochlear development, just before the integration of MLANA-positive cells was observed. As MLANA-positive cell integration proceeds, macrophage infiltration becomes obvious.
Based on a previous study using rodent models, PVMs and MLANA-positive cells were believed to have the same origin (36). However, a recent study suggested that PVMs in the stria vascularis have a different origin than melanin-positive intermediate cells (43); therefore, the relationship between PVMs and intermediate cells in rodents remains unclear (42). During the development of the stria vascularis in this study’s animal, IBA1-positive and MLANA-positive macrophages could be clearly distinguished (Figure 5). This observation indicates that, at least in this primate, intermediate cells and PVMs develop from different precursor cells. Simultaneously, the present study showed that initial integrations of macrophages and intermediate cells proceed in parallel. This observation suggests a cooperative mechanism such as the existence of chemoattractants between the intermediate cells and macrophages in the stria vascularis. Therefore, further studies are required to confirm this conjecture.
Previous studies on rodents and humans have shown that macrophages in the developing cochlea have several subgroups (17). Our study also indicated subgroups in the developing primate animal model cochlea: at least CD163-positive and -negative macrophages (Figures 7, 8), as observed in human fetuses (17). To date, two different lineages of macrophages have been identified in the developing cochlea of rodents: yolk sac macrophages and fetal liver lineages (14). Although we still do not know whether the expression patterns of CD163 in macrophages affect their characteristics as macrophages or indicate lineage differences, our observations showed the possibility of several subgroups in developing cochlear macrophages in this primate animal model.
Antigen presentation plays an essential role in macrophages. In particular, the MHC Class II-mediated presentation of extracellular antigens and subsequent stimulation of CD4+ T cells is essential for antigen-specific adaptive immune responses. The present study showed that most IBA1-positive macrophages in the developing cochlea did not express MHC Class II (Figure 9). This indicated that the macrophages were not activated for antigen presentation via MHC Class II, at least in the steady state. In contrast, as previously reported in the human cochlea (33), IBA1-positive macrophages in the postnatal cochlea showed MHC Class II expression in common marmosets. Whether these differences in MHC Class II expression between the developing and postnatal cochlea are caused by the maturation status of macrophages or by several mechanisms that downregulate the expression of MHC II (44) has not been clarified. However, our observations suggest that developing cochlear macrophages do not have antigen-presenting activity and may be more engaged in other macrophage functions, such as phagocytosis, which removes cellular debris created during development.
In this study, the distribution of macrophages in the developing cochlea of the common marmoset was examined. Although our previous studies have revealed general cochlear developmental courses of the common marmoset, including hair cells and supporting cells, spiral ganglion neurons, and the stria vascularis (21–24), no detailed examinations from the immunological viewpoint have been performed. In this study, the immunological state of the developing cochlea in the common marmoset was investigated for the first time. Combined with our previous developmental study, we revealed the relationships between generally important developmental stages of the cochlea, such as hair cell differentiation, pruning of spiral ganglion neurons, and the distribution of macrophages (Figure 10). This observation is important for understanding the steady immunological state of the developing cochlea in this primate. Recently, cochlear immunological changes have received considerable attention due to their protective and insulating functions (32). Therefore, this study would be useful not only for future studies targeting fetal immunology in the cochlea of this primate, but also for investigations of the damaged cochlea model, including noise-induced hearing loss and ototoxicity in this animal.
In this study, we investigated the distribution of macrophages in the developing cochlea of the common marmoset; however, other immune cells’ distribution and infiltrations have not been examined in this primate. Therefore, future studies can explore this to further understand the immunological steady state of the primate’s cochlear development.
5 Conclusion
In the present study, we showed detailed distribution changes of the macrophages in the cochlea using a primate animal model. This observation indicates that most of the changes in the general distribution of macrophages were well preserved between rodents and primates. The distribution changes observed in the common marmoset were also compatible with observations in the human fetus; although, observations in the human fetus are limited. Our observations in this study also revealed several differences between common marmosets and rodents. The study will help researchers understand the primate-specific immunological development of the cochlea and facilitate studies that manipulate the immunological state of the cochlea, especially those focusing on noise trauma or ototoxicity.
Statements
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.
Ethics statement
The animal study was approved by the Animal Experiment Committee of Keio University. The study was conducted in accordance with the local legislation and institutional requirements.
Author contributions
MH, TK, MS, TN, NO, HOk, and HOz, conceived and designed the experiments. MH, TK, and MS, wrote the manuscript. MH performed most of the experiments. MH, TK, and MS analyzed the data. All authors read and approved the final version of the manuscript.
Funding
MH was supported by a grant from the Japanese government, MEXT KAKENHI (Grant-in-Aid for Scientific Research (B) 20H03836, Grant-in-Aid for Challenging Research (Exploratory) 21K19581, Grant-in-Aid for Scientific Research (C) 23K08973, the Keio Medical Association and Keio University Medical Science Fund, the Takeda Science Foundation, and Keio Gijuku Academic Development Funds. MS was supported by a grant from the Japanese government, MEXT KAKENHI (23K08972).
Acknowledgments
We thank Saki Ninomiya for providing technical support. Moreover, we thank Ayako Y. Murayama, Sho Yoshimatsu, and Junko Okahara for providing materials.
Conflict of interest
HOk is a founding scientist and a paid scientific advisory board member of San Bio Co., Ltd and K Pharma Inc. MH was part of the founding scientists of Otolink Inc.
The remaining 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
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Summary
Keywords
cochlea development, macrophages, marmoset, primate model, immune cells
Citation
Hosoya M, Kitama T, Shimanuki MN, Nishiyama T, Oishi N, Okano H and Ozawa H (2023) Distribution of macrophages in the developing cochlea of the common marmoset, a primate model animal. Front. Immunol. 14:1229414. doi: 10.3389/fimmu.2023.1229414
Received
26 May 2023
Accepted
04 August 2023
Published
22 August 2023
Volume
14 - 2023
Edited by
Sabyasachi Das, Emory University, United States
Reviewed by
Akil Akhtar, Emory University, United States; Iram Maqsood, Shaheed Benazir Bhutto Women University, Pakistan
Updates
Copyright
© 2023 Hosoya, Kitama, Shimanuki, Nishiyama, Oishi, Okano and Ozawa.
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: Makoto Hosoya, mhosoya1985@keio.jp
Disclaimer
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