BDNF-enriched small extracellular vesicles protect against noise-induced hearing loss in mice

毛细胞 脑源性神经营养因子 听力损失 噪声性听力损失 神经营养因子 螺旋神经节 耳蜗 神经科学 细胞生物学 医学 生物 内科学 听力学 噪声暴露 受体
作者
Xin Min,Xiaohui Deng,Huilin Lao,Zicong Wu,Yi Chen,Yuelian Luo,Haoyang Wu,Junbo Wang,Qing‐Ling Fu,Hao Xiong
出处
期刊:Journal of Controlled Release [Elsevier BV]
卷期号:364: 546-561 被引量:39
标识
DOI:10.1016/j.jconrel.2023.11.007
摘要

Noise-induced hearing loss (NIHL) is one of the most prevalent acquired sensorineural hearing loss etiologies and is characterized by the loss of cochlear hair cells, synapses, and nerve terminals. Currently, there are no agents available for the treatment of NIHL because drug delivery to the inner ear is greatly limited by the blood–labyrinth barrier. In this study, we used mesenchymal stem cell-derived small extracellular vesicles (MSC-sEVs) as nanoscale vehicles to deliver brain-derived neurotrophic factor (BDNF) and evaluated their protective effects in a mouse model of NIHL. Following intravenous administration, BDNF-loaded sEVs (BDNF-sEVs) efficiently increased the expression of BDNF protein in the cochlea. Systemic application of sEVs and BDNF-sEVs significantly attenuated noise-induced cochlear hair cell loss and NIHL in CBA/J mice. BDNF-sEVs also alleviated noise-induced loss of inner hair cell ribbon synapses and cochlear nerve terminals. In cochlear explants, sEVs and BDNF-sEVs effectively protected hair cells against H2O2-induced cell loss. Additionally, BDNF-sEVs remarkably ameliorated H2O2-induced oxidative stress, cell apoptosis, and cochlear nerve terminal degeneration. Transcriptomic analysis revealed that many mRNAs and miRNAs were involved in the protective actions of BDNF-sEVs against oxidative stress. Collectively, our findings reveal a novel therapeutic strategy of MSC-sEVs-mediated BDNF delivery for the treatment of NIHL.
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