Intratympanic injection of MSC-derived small extracellular vesicles protects spiral ganglion neurons from degeneration

螺旋神经节 标记法 神经突 再生(生物学) 神经保护 细胞生物学 神经科学 生物 细胞凋亡 内耳 生物化学 体外
作者
Anning Chen,Jiaxi Qu,Yunyou You,Jing Pan,Verena Scheper,Yongdong Lin,Xuexin Tian,Fan Shu,Yanjing Luo,Jie Tang,Hongzheng Zhang
出处
期刊:Biomedicine & Pharmacotherapy [Elsevier BV]
卷期号:179: 117392-117392
标识
DOI:10.1016/j.biopha.2024.117392
摘要

Sensorineural hearing loss is one of the most prevalent sensory deficits. Spiral ganglion neurons (SGNs) exhibit very limited regeneration capacity and their degeneration leads to profound hearing loss. Mesenchymal stem cell-derived small extracellular vesicles (MSC-sEV) have been demonstrated to repair tissue damage in various degenerative diseases. However, the effects of MSC-sEV on SGN degeneration remain unclear. In this study, we investigated the efficacy of MSC-sEV for protection against ouabain-induced SGN degeneration. MSC-sEV were derived from rat bone marrow and their components related to neuron growth were determined by proteomic analysis. In primary culture SGNs, MSC-sEV significantly promoted neurite growth and growth cone development. The RNA-Seq analysis of SGNs showed that enriched pathways include neuron development and axon regeneration, consistent with proteomics. In ouabain induced SGN degeneration rat model, MSC-sEV administration via intratympanic injection significantly enhanced SGN survival and mitigated hearing loss. Furthermore, after ouabain treatment, SGNs displayed evident signs of apoptosis, including nuclei condensation and fragmentation, with numerous cells exhibiting TUNEL-positive. However, administration of MSC-sEV effectively decreased the number of TUNEL-positive cells and reduced caspase-3 activation. In conclusion, our findings demonstrate the potential of MSC-sEV in preventing SGN degeneration and promoting neural growth, suggesting intratympanic injection of MSC-sEV is a specific and efficient strategy for neural hearing loss.
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