Department of Otolaryngology and Head and Neck Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Department of Neurology, Feinberg School of Medicine, Northwestern University, Chicago IL 60611, USA.
Acta Biomater. 2020 May;108:111-127. doi: 10.1016/j.actbio.2020.03.007. Epub 2020 Mar 7.
Although the application of human embryonic stem cells (hESCs) in stem cell-replacement therapy remains promising, its potential is hindered by a low cell survival rate in post-transplantation within the inner ear. Here, we aim to enhance the in vitro and in vivo survival rate and neuronal differentiation of otic neuronal progenitors (ONPs) by generating an artificial stem cell niche consisting of three-dimensional (3D) hESC-derived ONP spheroids with a nanofibrillar cellulose hydrogel and a sustained-release brain-derivative neurotrophic factor delivery system. Our results demonstrated that the transplanted hESC-derived ONP spheroids survived and neuronally differentiated into otic neuronal lineages in vitro and in vivo and also extended neurites toward the bony wall of the cochlea 90 days after the transplantation without the use of immunosuppressant medication. Our data in vitro and in vivo presented here provide sufficient evidence that we have established a robust, reproducible protocol for in vivo transplantation of hESC-derived ONPs to the inner ear. Using our protocol to create an artificial stem cell niche in the inner ear, it is now possible to work on integrating transplanted hESC-derived ONPs further and also to work toward achieving functional auditory neurons generated from hESCs. Our findings suggest that the provision of an artificial stem cell niche can be a future approach to stem cell-replacement therapy for inner-ear regeneration. STATEMENT OF SIGNIFICANCE: Inner ear regeneration utilizing human embryonic stem cell-derived otic neuronal progenitors (hESC-derived ONPs) has remarkable potential for treating sensorineural hearing loss. However, the local environment of the inner ear requires a suitable stem cell niche to allow hESC-derived ONP engraftment as well as neuronal differentiation. To overcome this obstacle, we utilized three-dimensional spheroid formation (direct contact), nanofibrillar cellulose hydrogel (extracellular matrix), and a neurotrophic factor delivery system to artificially create a stem cell niche in vitro and in vivo. Our in vitro and in vivo data presented here provide sufficient evidence that we have established a robust, reproducible protocol for in vivo transplantation of hESC-derived ONPs to the inner ear.
虽然人胚胎干细胞(hESC)在干细胞替代疗法中的应用具有广阔的前景,但由于其在内耳移植后的细胞存活率低,其应用潜力受到了限制。在这里,我们旨在通过生成由三维(3D)hESC 来源的耳神经元祖细胞(ONP)球体、纳米纤维纤维素水凝胶和持续释放脑源性神经营养因子输送系统组成的人工干细胞龛,来提高体外和体内的耳神经元祖细胞的存活率和向神经元分化的能力。我们的结果表明,移植的 hESC 来源的 ONP 球体在体外和体内存活并向耳神经元谱系分化,并在移植后 90 天向耳蜗的骨壁延伸轴突,而无需使用免疫抑制剂药物。我们的体内外数据提供了充分的证据,证明我们已经建立了一个强大的、可重复的方案,用于将 hESC 来源的 ONP 移植到内耳。利用我们的方案在内耳中创建一个人工干细胞龛,现在可以进一步整合移植的 hESC 来源的 ONP,并致力于从 hESC 中生成功能性听觉神经元。我们的研究结果表明,提供人工干细胞龛可以作为内耳再生的干细胞替代疗法的未来方法。