Targeting the NLRP3 inflammasome in cochlear macrophages protects against hearing loss in chronic suppurative otitis media

IF 9.3 1区 医学 Q1 IMMUNOLOGY Journal of Neuroinflammation Pub Date : 2024-09-14 DOI:10.1186/s12974-024-03212-6
Viktoria Schiel, Ritwija Bhattacharya, Ankur Gupta, Kourosh Eftekharian, Anping Xia, Peter L Santa Maria
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Abstract

The activation of the NLRP3 inflammasome has been linked to several inflammatory and autoinflammatory diseases. Despite cases of potential hearing improvement in immune-mediated diseases, direct evidence of the efficacy of targeting this mechanism in the inner ear is still lacking. Previously, we discovered that macrophages are associated with Sensorineural Hearing loss (SNHL) in Chronic Suppurative Otitis Media (CSOM), the leading cause of this permanent hearing loss in the developing world and incurring costs of $4 to $11 billion dollars in the United States. However, the underlying mechanism remained unknown. Here, we investigate how macrophages drive permanent hearing loss in CSOM. We first confirmed the occurrence of NLRP3 inflammasome activation in cochlear macrophages in CSOM. We then revealed that Outer Hair Cells (OHCs) were protected in CSOM by macrophage depletion and subsequently confirmed the same protection in the NLRP3 knockout condition. Furthermore, we showed that therapeutic inhibition of NLRP3 inflammasome activation and downstream inhibition of IL-1β protects OHCs in CSOM. Collectively, our data demonstrates that the main driver for hearing loss in CSOM is NLRP3 inflammasome activation in cochlear macrophages and this is therapeutically targetable, leading the way for the development of interventions to prevent the leading cause of permanent hearing loss and a costly disease in the developed world.
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靶向耳蜗巨噬细胞中的 NLRP3 炎性体可预防慢性化脓性中耳炎患者的听力损失
NLRP3 炎性体的激活与多种炎症和自身炎症疾病有关。尽管在免疫介导的疾病中存在潜在的听力改善病例,但仍缺乏直接证据证明针对内耳中这一机制的疗效。在此之前,我们发现巨噬细胞与慢性化脓性中耳炎(CSOM)中的感音神经性听力损失(SNHL)有关,慢性化脓性中耳炎是发展中国家造成这种永久性听力损失的主要原因,在美国造成的损失高达 40 亿至 110 亿美元。然而,其潜在机制仍不为人知。在此,我们研究了巨噬细胞是如何驱动 CSOM 出现永久性听力损失的。我们首先证实了 CSOM 中的耳蜗巨噬细胞发生了 NLRP3 炎性体激活。然后,我们发现外耳道毛细胞(OHC)在CSOM中受到巨噬细胞消耗的保护,随后又证实了在NLRP3基因敲除条件下也受到了同样的保护。此外,我们还发现,治疗性抑制 NLRP3 炎性体活化和下游抑制 IL-1β 可保护 CSOM 中的外耳道细胞。总之,我们的数据表明,CSOM听力损失的主要驱动因素是耳蜗巨噬细胞中NLRP3炎性体的活化,而这是可治疗的靶点,这为开发干预措施以预防永久性听力损失的主要原因和发达国家的昂贵疾病开辟了道路。
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来源期刊
Journal of Neuroinflammation
Journal of Neuroinflammation 医学-神经科学
CiteScore
15.90
自引率
3.20%
发文量
276
审稿时长
1 months
期刊介绍: The Journal of Neuroinflammation is a peer-reviewed, open access publication that emphasizes the interaction between the immune system, particularly the innate immune system, and the nervous system. It covers various aspects, including the involvement of CNS immune mediators like microglia and astrocytes, the cytokines and chemokines they produce, and the influence of peripheral neuro-immune interactions, T cells, monocytes, complement proteins, acute phase proteins, oxidative injury, and related molecular processes. Neuroinflammation is a rapidly expanding field that has significantly enhanced our knowledge of chronic neurological diseases. It attracts researchers from diverse disciplines such as pathology, biochemistry, molecular biology, genetics, clinical medicine, and epidemiology. Substantial contributions to this field have been made through studies involving populations, patients, postmortem tissues, animal models, and in vitro systems. The Journal of Neuroinflammation consolidates research that centers around common pathogenic processes. It serves as a platform for integrative reviews and commentaries in this field.
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