Hackelberg Sandra, Tuck Samuel J, He Long, Rastogi Arjun, White Christina, Liu Liqian, Prieskorn Diane M, Miller Ryan J, Chan Che, Loomis Benjamin R, Corey Joseph M, Miller Josef M, Duncan R Keith
Kresge Hearing Research Institute, Department of Otolaryngology-Head & Neck Surgery, University of Michigan, Ann Arbor, MI, United States of America.
Geriatrics Research, Education, and Clinical Center (GRECC), VA Ann Arbor Healthcare Center (VAAAHC), Ann Arbor, MI, United States of America.
PLoS One. 2017 Jul 3;12(7):e0180427. doi: 10.1371/journal.pone.0180427. eCollection 2017.
Impairment of spiral ganglion neurons (SGNs) of the auditory nerve is a major cause for hearing loss occurring independently or in addition to sensory hair cell damage. Unfortunately, mammalian SGNs lack the potential for autonomous regeneration. Stem cell based therapy is a promising approach for auditory nerve regeneration, but proper integration of exogenous cells into the auditory circuit remains a fundamental challenge. Here, we present novel nanofibrous scaffolds designed to guide the integration of human stem cell-derived neurons in the internal auditory meatus (IAM), the foramen allowing passage of the spiral ganglion to the auditory brainstem. Human embryonic stem cells (hESC) were differentiated into neural precursor cells (NPCs) and seeded onto aligned nanofiber mats. The NPCs terminally differentiated into glutamatergic neurons with high efficiency, and neurite projections aligned with nanofibers in vitro. Scaffolds were assembled by seeding GFP-labeled NPCs on nanofibers integrated in a polymer sheath. Biocompatibility and functionality of the NPC-seeded scaffolds were evaluated in vivo in deafened guinea pigs (Cavia porcellus). To this end, we established an ouabain-based deafening procedure that depleted an average 72% of SGNs from apex to base of the cochleae and caused profound hearing loss. Further, we developed a surgical procedure to implant seeded scaffolds directly into the guinea pig IAM. No evidence of an inflammatory response was observed, but post-surgery tissue repair appeared to be facilitated by infiltrating Schwann cells. While NPC survival was found to be poor, both subjects implanted with NPC-seeded and cell-free control scaffolds showed partial recovery of electrically-evoked auditory brainstem thresholds. Thus, while future studies must address cell survival, nanofibrous scaffolds pose a promising strategy for auditory nerve regeneration.
听神经螺旋神经节神经元(SGNs)受损是导致听力丧失的主要原因,其可独立发生,也可在感觉毛细胞损伤之外出现。遗憾的是,哺乳动物的SGNs缺乏自主再生的潜力。基于干细胞的疗法是一种有前景的听神经再生方法,但将外源细胞正确整合到听觉回路中仍然是一个根本性挑战。在此,我们展示了一种新型纳米纤维支架,其设计目的是引导人干细胞衍生的神经元在内耳道(IAM)中整合,内耳道是允许螺旋神经节通向听觉脑干的孔道。人胚胎干细胞(hESC)被分化为神经前体细胞(NPCs),并接种到排列好的纳米纤维垫上。NPCs高效地终末分化为谷氨酸能神经元,并且在体外其神经突投射与纳米纤维对齐。通过将绿色荧光蛋白(GFP)标记的NPCs接种到整合在聚合物鞘中的纳米纤维上来组装支架。在致聋的豚鼠(豚鼠)体内评估接种NPCs的支架的生物相容性和功能。为此,我们建立了一种基于哇巴因的致聋程序,该程序使耳蜗从顶部到基部平均72%的SGNs减少,并导致严重的听力损失。此外,我们开发了一种外科手术程序,将接种好的支架直接植入豚鼠的IAM。未观察到炎症反应的迹象,但术后组织修复似乎因施万细胞的浸润而得到促进。虽然发现NPC的存活率较低,但植入接种NPCs的支架和无细胞对照支架的两个实验对象均显示出电诱发听觉脑干阈值的部分恢复。因此,虽然未来的研究必须解决细胞存活问题,但纳米纤维支架是一种有前景的听神经再生策略。