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通过上调GDF15/SIRT1轴,过表达生长分化因子6的间充质干细胞对年龄相关性听力损失的治疗作用

Therapeutic Effects of GDF6-Overexpressing Mesenchymal Stem Cells through Upregulation of the GDF15/SIRT1 Axis in Age-Related Hearing Loss.

作者信息

Liu Jiali, Peng Haisen, Liu Yuehui, Li Chunhua, Xie Wen

机构信息

Department of Otolaryngology, Head and Neck Surgery, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, 330006 Nanchang, Jiangxi, China.

出版信息

Front Biosci (Landmark Ed). 2025 Jan 15;30(1):26179. doi: 10.31083/FBL26179.

Abstract

BACKGROUND

It has been reported the therapeutic effects of mesenchymal stem cells (MSCs) on hearing loss. This study explored the therapeutic effects of growth differentiation factor 6 (GDF6) overexpression-induced MSCs (MSCs-GDF6) on age-related hearing loss (ARHL) and its underlying mechanisms.

METHODS

Reverse transcription-quantitative PCR and western blotting were used to evaluate gene expression. Flow cytometry and immunofluorescence assays were performed for the detection of apoptosis and autophagy, respectively. Hearing function and loss of outer hair cells (HCs) in ARHL rats were measured using the auditory brainstem response and cochlear silver nitrate staining, respectively. MSC proliferation was evaluated with the Cell Counting Kit-8 assay.

RESULTS

Growth differentiation factor 15 (GDF15) and sirtuin 1 (SIRT1) expression was significantly decreased in hydrogen peroxide (HO)-induced House Ear Institute-Organ of Corti 1 (HEI-OC1) cells and the cochlea of ARHL rats. Elevated apoptosis and blocked autophagic flux were uncovered in HO-induced HEI-OC1 cells and ARHL rats. GDF15 overexpression inhibited apoptosis and restored autophagic flux and . Meanwhile, GDF15 positively regulated SIRT1 protein expression. MSCs-GDF6 not only upregulated GDF15 and SIRT1 expression but also suppressed apoptosis and restored autophagic flux to reduce loss of HCs and hearing loss in ARHL rats.

CONCLUSIONS

MSCs-GDF6 prevented loss of HCs to relieve ARHL by inhibiting apoptosis and restoring autophagic flux, likely in association with upregulation of the GDF15/SIRT1 axis.

摘要

背景

已有报道间充质干细胞(MSCs)对听力损失具有治疗作用。本研究探讨生长分化因子6(GDF6)过表达诱导的间充质干细胞(MSCs-GDF6)对年龄相关性听力损失(ARHL)的治疗作用及其潜在机制。

方法

采用逆转录定量PCR和蛋白质印迹法评估基因表达。分别通过流式细胞术和免疫荧光测定法检测细胞凋亡和自噬。分别使用听觉脑干反应和耳蜗硝酸银染色测量ARHL大鼠的听力功能和外毛细胞(HCs)损失。用细胞计数试剂盒-8法评估间充质干细胞增殖。

结果

在过氧化氢(HO)诱导的耳科研究所-柯蒂器1(HEI-OC1)细胞和ARHL大鼠的耳蜗中,生长分化因子15(GDF15)和沉默调节蛋白1(SIRT1)的表达显著降低。在HO诱导的HEI-OC1细胞和ARHL大鼠中发现细胞凋亡增加和自噬流受阻。GDF15过表达抑制细胞凋亡并恢复自噬流。同时,GDF15正向调节SIRT1蛋白表达。MSCs-GDF6不仅上调GDF15和SIRT1的表达,还抑制细胞凋亡并恢复自噬流,以减少ARHL大鼠的HCs损失和听力损失。

结论

MSCs-GDF6可能通过上调GDF15/SIRT1轴,抑制细胞凋亡并恢复自噬流,从而防止HCs损失,减轻ARHL。

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