Soares Vitor Y R, Atai Nadia A, Fujita Takeshi, Dilwali Sonam, Sivaraman Sarada, Landegger Lukas D, Hochberg Fred H, Oliveira Carlos A P C, Bahmad Fayez, Breakefield Xandra O, Stankovic Konstantina M
Department of Otolaryngology, Eaton Peabody Laboratories, Massachusetts Eye and Ear, Boston, Massachusetts (V.Y.R.S., T.F., S.D., L.D.L., K.M.S.); Department of Otology and Laryngology, Harvard Medical School, Boston, Massachusetts (V.Y.R.S., T.F., L.D.L., K.M.S.); Health Science Program and Department of Otolaryngology, University of Brasilia, Brasília, Distrito Federal, Brazil (V.Y.R.S., C.A.P.C.O., F.B.); University of Amsterdam, Amsterdam, the Netherlands (N.A.A.); Department of Neurology and Radiology, Massachusetts General Hospital and Program in Neuroscience, Harvard Medical School, Charlestown, Massachusetts (N.A.A., S.S., X.O.B.); Harvard-MIT Program in Speech and Hearing Bioscience and Technology, Boston, Massachusetts (S.D., K.M.S); Department of Neurosurgery, University of California at San Diego, San Diego, California (F.H.H.).
Neuro Oncol. 2016 Nov;18(11):1498-1507. doi: 10.1093/neuonc/now099. Epub 2016 May 18.
Vestibular schwannoma (VS) is a tumor of the vestibular nerve that transmits balance information from the inner ear to the brain. Sensorineural hearing loss occurs in 95% of patients with these tumors, but the cause of this loss is not well understood. We posit a role of VS-secreted extracellular vesicles (EVs) as a major contributing factor in cochlear nerve damage.
Using differential centrifugation, we isolated EVs from VS cell line HEI-193 and primary cultured human VS cells from patients with good hearing or poor hearing. The EVs were characterized using a Nanosight device and transmission electron microscopy and by extracting their RNA content. The EVs' effects on cultured murine spiral ganglion cells and organotypic cochlear cultures were studied using a transwell dual-culture system and by direct labeling of EVs with PKH-67 dye. EV-induced changes in cochlear cells were quantified using confocal immunohistochemistry. Transfection of VS cells with a green fluorescent protein-containing plasmid was confirmed with reverse transcription PCR.
Human VS cells, from patients with poor hearing, produced EVs that could damage both cultured murine cochlear sensory cells and neurons. In contrast, EVs derived from VS cells from patients with good hearing did not damage the cultured cochlear cells.
This is the first report on EVs derived from VSs and on the capacity of EVs from VSs from patients with hearing loss to selectively damage cochlear cells, thereby identifying a potential novel mechanism of VS-associated sensorineural hearing loss.
前庭神经鞘瘤(VS)是一种前庭神经肿瘤,该神经负责将内耳的平衡信息传递至大脑。95%的此类肿瘤患者会出现感音神经性听力损失,但其病因尚不清楚。我们认为VS分泌的细胞外囊泡(EVs)是导致耳蜗神经损伤的主要因素。
我们采用差速离心法,从VS细胞系HEI - 193以及听力正常或听力受损患者的原代培养人VS细胞中分离出EVs。使用纳米可视分析仪、透射电子显微镜并提取其RNA含量对EVs进行表征。利用Transwell共培养系统以及用PKH - 67染料直接标记EVs,研究了EVs对培养的小鼠螺旋神经节细胞和耳蜗器官型培养物的影响。使用共聚焦免疫组织化学法定量分析了EVs诱导的耳蜗细胞变化。通过逆转录PCR证实了用含绿色荧光蛋白的质粒转染VS细胞。
听力受损患者的人VS细胞产生的EVs可损害培养的小鼠耳蜗感觉细胞和神经元。相比之下,听力正常患者的VS细胞来源的EVs不会损害培养的耳蜗细胞。
这是关于VS来源的EVs以及听力损失患者的VS来源的EVs选择性损害耳蜗细胞能力的首份报告,从而确定了VS相关感音神经性听力损失的一种潜在新机制。