Department of Otolaryngology Head & Neck Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, 510282, China.
Ear Research Institute, Zhujiang Hospital, Southern Medical University, Guangzhou, 510282, China.
Commun Biol. 2024 Sep 2;7(1):1078. doi: 10.1038/s42003-024-06768-4.
Macrophages serve as the primary immune cell population and assume a pivotal role in the immune response within the damaged cochleae. Yet, the origin and role of macrophages in response to noise exposure remain controversial. Here, we take advantage of Ccr2 Cx3cr1 dual-reporter mice to identify the infiltrated and tissue-resident macrophages. After noise exposure, we reveal that activated resident macrophages change in morphology, increase in abundance, and migrate to the region of hair cells, leading to the loss of outer hair cells and the damage of ribbon synapses. Meanwhile, peripheral monocytes are not implicated in the noise-induced hair cell insults. These noise-induced activities of macrophages are abolished by inhibiting TLR4 signaling, resulting in alleviated insults of hair cells and partial recovery of hearing. Our findings indicate cochlear resident macrophages are pro-inflammatory and detrimental players in acoustic trauma and introduce a potential therapeutic target in noise-induced hearing loss.
巨噬细胞作为主要的免疫细胞群,在受损耳蜗的免疫反应中发挥关键作用。然而,巨噬细胞在噪声暴露中的起源和作用仍存在争议。在这里,我们利用 Ccr2 Cx3cr1 双重报告小鼠来鉴定浸润和组织驻留巨噬细胞。在噪声暴露后,我们发现活化的驻留巨噬细胞形态发生变化,数量增加,并迁移到毛细胞区域,导致外毛细胞丢失和连接突触损伤。同时,外周单核细胞不参与噪声诱导的毛细胞损伤。通过抑制 TLR4 信号通路,抑制了巨噬细胞的这些噪声诱导活性,减轻了毛细胞的损伤,并部分恢复了听力。我们的研究结果表明,耳蜗驻留巨噬细胞在声创伤中是促炎和有害的,为噪声性听力损失提供了一个潜在的治疗靶点。