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

IF 3.1 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in bioscience (Landmark edition) Pub Date : 2025-01-15 DOI:10.31083/FBL26179
Jiali Liu, Haisen Peng, Yuehui Liu, Chunhua Li, Wen Xie
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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 (H2O2)-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 H2O2-induced HEI-OC1 cells and ARHL rats. GDF15 overexpression inhibited apoptosis and restored autophagic flux in vitro and in vivo. 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.

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过表达gdf6的间充质干细胞通过上调GDF15/SIRT1轴对年龄相关性听力损失的治疗作用
背景:间充质干细胞(MSCs)对听力损失的治疗作用已有报道。本研究探讨生长分化因子6 (GDF6)过表达诱导间充质干细胞(MSCs-GDF6)对年龄相关性听力损失(ARHL)的治疗作用及其机制。方法:采用逆转录-定量PCR和免疫印迹法检测基因表达。流式细胞术检测细胞凋亡,免疫荧光法检测细胞自噬。采用听觉脑干反应法和耳蜗硝酸银染色法分别测定ARHL大鼠的听力功能和外毛细胞损失情况。用细胞计数试剂盒-8检测MSC增殖。结果:过氧化氢(H2O2)诱导的House Ear Institute-Organ of Corti 1 (HEI-OC1)细胞和ARHL大鼠耳蜗中生长分化因子15 (GDF15)和sirtuin 1 (SIRT1)表达显著降低。在h2o2诱导的HEI-OC1细胞和ARHL大鼠中发现凋亡升高和自噬通量阻滞。GDF15过表达抑制细胞凋亡,恢复细胞自噬通量。同时,GDF15正调控SIRT1蛋白的表达。MSCs-GDF6不仅能上调GDF15和SIRT1的表达,还能抑制细胞凋亡,恢复自噬通量,从而减轻ARHL大鼠的hc损失和听力损失。结论:MSCs-GDF6通过抑制细胞凋亡和恢复自噬通量来阻止hc的丢失,从而缓解ARHL,这可能与GDF15/SIRT1轴的上调有关。
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