Department of Otorhinolaryngology, Hannover Medical School, Hannover, Germany.
Lower Saxony Centre for Biomedical Engineering, Implant Research and Development (NIFE), Hannover Medical School, Hannover, Germany.
PLoS One. 2024 Jul 26;19(7):e0307973. doi: 10.1371/journal.pone.0307973. eCollection 2024.
Although cochlear implants have become a well-established method for patients with sensory neural hearing loss, clinical results indicate that in some cases, corrosion of electrode contacts leads to high impedance that interferes with successful stimulation of the auditory nerve. As it is unclear whether corrosion products induce cell damage, we focused on cell culture models of the organ of Corti cell line (HEI-OC1), rat spiral ganglion cells (SGC) and rat organ of Corti explant (OCex) cultivated from neonatal rat cochleae to characterize the cytotoxicity of sodium hexachloroplatinate (IV) (Na2(PtCl6)). The oxidative activity in HEI-OC1 cells decreased with increasing Na2(PtCl6) concentrations between 8 and 16 ng/μl, and live cell staining with Calcein acetoxymethyl/Ethidium homodimer III revealed an increasing number of cells with disrupted membranes. Ultrastructural evidence of mitophagy followed by necroptosis was detected. Additionally, exposure of the SGC to 15-35 ng/μl Na2(PtCl6) dose-dependently reduced neuronal survival and neuritogenesis, as determined by neurofilament antigen staining. In parallel, staining glial cells and fibroblasts with specific antibodies confirmed the dose-dependent induction of cell death by Na2(PtCl6). Exposure of the OCex to 25-45 ng/μl Na2(PtCl6) resulted in severe concentration-dependent hair cell loss. Our data show for the first time that Na2(PtCl6) induces cell death in a concentration-dependent manner in inner ear cell types and tissues.
尽管人工耳蜗已成为感音神经性听力损失患者的一种成熟方法,但临床结果表明,在某些情况下,电极接触腐蚀会导致高阻抗,从而干扰听神经的成功刺激。由于尚不清楚腐蚀产物是否会引起细胞损伤,我们专注于耳蜗组织细胞系(HEI-OC1)、大鼠螺旋神经节细胞(SGC)和大鼠耳蜗组织外植体(OCex)的细胞培养模型,这些模型是从新生大鼠耳蜗培养而来的,用于表征六氯铂酸钠(IV)(Na2(PtCl6))的细胞毒性。在 8 至 16 ng/μl 之间,HEI-OC1 细胞中的氧化活性随着 Na2(PtCl6)浓度的增加而降低,用 Calcein 乙氧甲酯/Ethidium homodimer III 进行活细胞染色显示出越来越多的细胞膜破裂的细胞。随后检测到自噬导致的细胞坏死。此外,SGC 暴露于 15-35 ng/μl Na2(PtCl6)中,神经元存活率和神经突生成呈剂量依赖性降低,这通过神经丝抗原染色来确定。同时,用特异性抗体对神经胶质细胞和成纤维细胞进行染色证实了 Na2(PtCl6)诱导细胞死亡的剂量依赖性。OCex 暴露于 25-45 ng/μl Na2(PtCl6)中会导致严重的、浓度依赖性的毛细胞丧失。我们的数据首次表明,Na2(PtCl6)以浓度依赖的方式诱导内耳细胞类型和组织中的细胞死亡。