Bionics Institute, Australia; Department of Medical Bionics, The University of Melbourne, Australia.
Bionics Institute, Australia.
J Control Release. 2015 Jan 28;198:26-34. doi: 10.1016/j.jconrel.2014.11.026. Epub 2014 Dec 4.
The cochlear implant provides auditory cues to profoundly deaf patients by electrically stimulating the primary auditory neurons (ANs) of the cochlea. However, ANs degenerate in deafness; the preservation of a robust AN target population, in combination with advances in cochlear implant technology, may provide improved hearing outcomes for cochlear implant patients. The exogenous delivery of neurotrophins such as brain-derived neurotrophic factor (BDNF) and neurotrophin-3 is well known to support AN survival in deafness, and cell-based therapies provide a potential clinically viable option for delivering neurotrophins into the deaf cochlea. This study utilized cells that were genetically modified to express BDNF and encapsulated in alginate microspheres, and investigated AN survival in the deaf guinea pig following (a) cell-based neurotrophin treatment in conjunction with chronic electrical stimulation from a cochlear implant, and (b) long-term cell-based neurotrophin delivery. In comparison to deafened controls, there was significantly greater AN survival following the cell-based neurotrophin treatment, and there were ongoing survival effects for at least six months. In addition, functional benefits were observed following cell-based neurotrophin treatment and chronic electrical stimulation, with a statistically significant decrease in electrically evoked auditory brainstem response thresholds observed during the experimental period. This study demonstrates that cell-based therapies, in conjunction with a cochlear implant, shows potential as a clinically transferable means of providing neurotrophin treatment to support AN survival in deafness. This technology also has the potential to deliver other therapeutic agents, and to be used in conjunction with other biomedical devices for the treatment of a variety of neurodegenerative conditions.
人工耳蜗通过电刺激耳蜗内的初级听觉神经元(ANs)为极重度聋患者提供听觉线索。然而,在耳聋中 ANs 会退化;保留一个强大的 AN 靶细胞群体,结合人工耳蜗技术的进步,可能为人工耳蜗患者提供更好的听力效果。外源性给予神经营养因子,如脑源性神经营养因子(BDNF)和神经营养因子-3,已被证实可支持耳聋中 ANs 的存活,并且基于细胞的疗法为将神经营养因子递送至聋的耳蜗提供了一种潜在的临床可行的选择。本研究利用经基因修饰表达 BDNF 并包被在藻酸盐微球中的细胞,研究了在(a)细胞神经营养因子治疗结合人工耳蜗的慢性电刺激,和(b)长期细胞神经营养因子递送至聋的豚鼠后,ANs 的存活情况。与耳聋对照组相比,细胞神经营养因子治疗后 ANs 的存活明显增加,并且至少有六个月的持续存活效应。此外,在细胞神经营养因子治疗和慢性电刺激后观察到了功能益处,在实验期间观察到电诱发听觉脑干反应阈值有统计学意义的降低。本研究表明,细胞疗法结合人工耳蜗作为一种有潜力的临床可转化手段,可提供神经营养因子治疗以支持耳聋中的 ANs 存活。该技术还有潜力递送至其他治疗剂,并与其他生物医学设备联合用于治疗各种神经退行性疾病。