Schulze Jennifer, Kaiser Odett, Paasche Gerrit, Lamm Hans, Pich Andreas, Hoffmann Andrea, Lenarz Thomas, Warnecke Athanasia
Department of Otorhinolaryngology, Head and Neck Surgery, Hannover Medical School, Hannover, Germany.
Cluster of Excellence "Hearing4all", Hannover, Germany.
PLoS One. 2017 May 23;12(5):e0178182. doi: 10.1371/journal.pone.0178182. eCollection 2017.
Hyperbaric oxygen therapy (HBOT) is a noninvasive widely applied treatment that increases the oxygen pressure in tissues. In cochlear implant (CI) research, intracochlear application of neurotrophic factors (NTFs) is able to improve survival of spiral ganglion neurons (SGN) after deafness. Cell-based delivery of NTFs such as brain-derived neurotrophic factor (BDNF) may be realized by cell-coating of the surface of the CI electrode. Human mesenchymal stem cells (MSC) secrete a variety of different neurotrophic factors and may be used for the development of a biohybrid electrode in order to release endogenously-derived neuroprotective factors for the protection of residual SGN and for a guided outgrowth of dendrites in the direction of the CI electrode. HBOT could be used to influence cell behaviour after transplantation to the inner ear. The aim of this study was to investigate the effect of HBOT on the proliferation, BDNF-release and secretion of neuroprotective factors. Thus, model cells (an immortalized fibroblast cell line (NIH3T3)-native and genetically modified) and MSCs were repeatedly (3 x - 10 x) exposed to 100% oxygen at different pressures. The effects of HBO on cell proliferation were investigated in relation to normoxic and normobaric conditions (NOR). Moreover, the neuroprotective and neuroregenerative effects of HBO-treated cells were analysed by cultivation of SGN in conditioned medium. Both, the genetically modified NIH3T3/BDNF and native NIH3T3 fibroblasts, showed a highly significant increased proliferation after five days of HBOT in comparison to normoxic controls. By contrast, the number of MSCs was decreased in MSCs treated with 2.0 bar of HBO. Treating SGN cultures with supernatants of fibroblasts and MSCs significantly increased the survival rate of SGN. HBO treatment did not influence (increase / reduce) this effect. Secretome analysis showed that HBO treatment altered the protein expression pattern in MSCs.
高压氧疗法(HBOT)是一种广泛应用的非侵入性治疗方法,可增加组织中的氧分压。在人工耳蜗(CI)研究中,耳蜗内应用神经营养因子(NTFs)能够提高耳聋后螺旋神经节神经元(SGN)的存活率。基于细胞的神经营养因子递送,如脑源性神经营养因子(BDNF),可通过人工耳蜗电极表面的细胞包被来实现。人骨髓间充质干细胞(MSC)分泌多种不同的神经营养因子,可用于开发生物混合电极,以释放内源性神经保护因子,保护残余的螺旋神经节神经元,并引导树突向人工耳蜗电极方向生长。高压氧疗法可用于影响内耳移植后的细胞行为。本研究的目的是探讨高压氧疗法对细胞增殖、BDNF释放和神经保护因子分泌 的影响。因此,将模型细胞(永生化成纤维细胞系(NIH3T3)——天然的和基因改造的)和骨髓间充质干细胞在不同压力下反复(3次 - 10次)暴露于100%氧气中。研究了高压氧对细胞增殖的影响,并与常氧和常压条件(NOR)进行了比较。此外,通过在条件培养基中培养螺旋神经节神经元,分析了高压氧处理细胞的神经保护和神经再生作用。与常氧对照组相比,基因改造的NIH3T3/BDNF和天然NIH3T3成纤维细胞在高压氧疗法治疗五天后均显示出高度显著的增殖增加。相比之下,用2.0巴高压氧处理的骨髓间充质干细胞数量减少。用成纤维细胞和骨髓间充质干细胞的上清液处理螺旋神经节神经元培养物可显著提高螺旋神经节神经元的存活率。高压氧疗法治疗不影响(增加/降低)这种效果。分泌组分析表明,高压氧疗法治疗改变了骨髓间充质干细胞中的蛋白质表达模式。