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耳蜗损伤后巨噬细胞的有害与有益功能

The Detrimental and Beneficial Functions of Macrophages After Cochlear Injury.

作者信息

Zhang Yuan, Li Yiyuan, Fu Xiaolong, Wang Pengjun, Wang Qin, Meng Wei, Wang Tian, Yang Jianming, Chai Renjie

机构信息

MOE Key Laboratory for Developmental Genes and Human Disease, Jiangsu Province High-Tech Key Laboratory for Bio-Medical Research, School of Life Sciences and Technology, Southeast University, Nanjing, China.

Department of Otolaryngology Head and Neck, Nanjing Tongren Hospital, School of Medicine, Southeast University, Nanjing, China.

出版信息

Front Cell Dev Biol. 2021 Aug 11;9:631904. doi: 10.3389/fcell.2021.631904. eCollection 2021.

DOI:10.3389/fcell.2021.631904
PMID:34458249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8385413/
Abstract

Macrophages are the main intrinsic immune cells in the cochlea; they can be activated and play a complicated role after cochlear injury. Many studies have shown that the number of macrophages and their morphological characteristics within the major cochlear partitions undergo significant changes under various pathological conditions including acoustic trauma, ototoxic drug treatment, age-related cochlear degeneration, selective hair cell (HC) and spiral ganglion neuron (SGN) elimination, and surgery. However, the exact role of these macrophages after cochlear injury is still unclear. Regulating the migration and activity of macrophages may be a therapeutic approach to reduce the risk or magnitude of trauma-induced hearing loss, and this review highlights the role of macrophages on the peripheral auditory structures of the cochlea and elucidate the mechanisms of macrophage injury and the strategies to reduce the injury by regulating macrophage.

摘要

巨噬细胞是耳蜗内主要的固有免疫细胞;在耳蜗损伤后,它们可被激活并发挥复杂的作用。许多研究表明,在包括声创伤、耳毒性药物治疗、年龄相关性耳蜗退变、选择性毛细胞(HC)和螺旋神经节神经元(SGN)消除以及手术等各种病理条件下,主要耳蜗分区内巨噬细胞的数量及其形态特征会发生显著变化。然而,这些巨噬细胞在耳蜗损伤后的具体作用仍不清楚。调节巨噬细胞的迁移和活性可能是一种降低创伤性听力损失风险或程度的治疗方法,本综述重点介绍了巨噬细胞在耳蜗外周听觉结构上的作用,并阐明了巨噬细胞损伤的机制以及通过调节巨噬细胞来减轻损伤的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fe2/8385413/2be0cc6046ca/fcell-09-631904-g005.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fe2/8385413/2be0cc6046ca/fcell-09-631904-g005.jpg

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J Clin Med. 2020 Jun 2;9(6):1711. doi: 10.3390/jcm9061711.
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The Distribution and Prevalence of Macrophages in the Cochlea Following Cochlear Implantation in the Human: An Immunohistochemical Study Using Anti-Iba1 Antibody.人内耳植入后巨噬细胞的分布和流行:抗 Iba1 抗体的免疫组织化学研究。
Otol Neurotol. 2020 Mar;41(3):e304-e316. doi: 10.1097/MAO.0000000000002495.
3
Inflammation associated with noise-induced hearing loss.
肿瘤坏死因子-α预处理的骨髓间充质干细胞来源的外泌体减轻顺铂诱导的小鼠耳毒性。
Int J Med Sci. 2025 Feb 18;22(5):1215-1222. doi: 10.7150/ijms.104121. eCollection 2025.
4
Wnt signalling facilitates neuronal differentiation of cochlear Frizzled10-positive cells in mouse cochlea via glypican 6 modulation.Wnt信号通路通过调节磷脂酰肌醇蛋白聚糖6促进小鼠耳蜗中卷曲蛋白10阳性细胞的神经元分化。
Cell Commun Signal. 2025 Jan 27;23(1):50. doi: 10.1186/s12964-025-02039-9.
5
Bioinformatics approach reveals the critical role of inflammation-related genes in age-related hearing loss.生物信息学方法揭示了炎症相关基因在年龄相关性听力损失中的关键作用。
Sci Rep. 2025 Jan 21;15(1):2687. doi: 10.1038/s41598-024-83428-x.
6
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Antiinflamm Antiallergy Agents Med Chem. 2024;23(2):85-104. doi: 10.2174/0118715230294413240415054610.
7
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