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圆窗膜反复经微针穿刺的解剖学、生理学及蛋白质组学后果

Anatomic, physiologic, and proteomic consequences of repeated microneedle-mediated perforations of the round window membrane.

作者信息

Leong Stephen, Aksit Aykut, Szeto Betsy, Feng Sharon J, Ji Xiang, Soni Rajesh K, Olson Elizabeth S, Kysar Jeffrey W, Lalwani Anil K

机构信息

Vagelos College of Physicians & Surgeons, Columbia University Irving Medical Center, New York, NY, United States.

Department of Mechanical Engineering, Columbia University, New York, NY, United States.

出版信息

Hear Res. 2023 May;432:108739. doi: 10.1016/j.heares.2023.108739. Epub 2023 Mar 14.

Abstract

BACKGROUND

We have developed 3D-printed microneedle technology for diagnostic aspiration of perilymph and intracochlear delivery of therapeutic agents. Single microneedle-mediated round window membrane (RWM) perforation does not cause hearing loss, heals within 48-72 h, and yields sufficient perilymph for proteomic analysis. In this study, we investigate the anatomic, physiologic, and proteomic consequences of repeated microneedle-mediated perforations of the same RWM at different timepoints.

METHODS

100-μm-diameter hollow microneedles were fabricated using two-photon polymerization (2PP) lithography. The tympanic bullae of Hartley guinea pigs (n = 8) were opened with adequate exposure of the RWM. Distortion product otoacoustic emissions (DPOAE) and compound action potential (CAP) were recorded to assess hearing. The hollow microneedle was introduced into the bulla and the RWM was perforated; 1 μL of perilymph was aspirated from the cochlea over the course of 45 s. 72 h later, the above procedure was repeated with aspiration of an additional 1 μL of perilymph. 72 h after the second perforation, RWMs were harvested for confocal imaging. Perilymph proteomic analysis was completed using liquid chromatography-tandem mass spectrometry (LC-MS/MS).

RESULTS

Two perforations and aspirations were performed in 8 guinea pigs. In six, CAP, DPOAE, and proteomic analysis were obtained; in one, only CAP and DPOAE results were obtained; and in one, only proteomics results were obtained. Hearing tests demonstrated mild hearing loss at 1-4 kHz and 28 kHz, most consistent with conductive hearing loss. Confocal microscopy demonstrated complete healing of all perforations with full reconstitution of the RWM. Perilymph proteomic analysis identified 1855 proteins across 14 samples. The inner ear protein cochlin was observed in all samples, indicating successful aspiration of perilymph. Non-adjusted paired t-tests with p < 0.01 revealed significant changes in 13 of 1855 identified proteins (0.7%) between the first and second aspirations.

CONCLUSIONS

We demonstrate that repeated microneedle perforation of the RWM is feasible, allows for complete healing of the RWM, and minimally changes the proteomic expression profile. Thus, microneedle-mediated repeated aspirations in a single animal can be used to monitor the response to inner ear treatments over time.

摘要

背景

我们已经开发出用于外淋巴诊断性抽吸和治疗药物耳蜗内递送的3D打印微针技术。单根微针介导的圆窗膜(RWM)穿孔不会导致听力损失,在48 - 72小时内愈合,并能获取足够的外淋巴用于蛋白质组学分析。在本研究中,我们调查了在不同时间点对同一RWM进行重复微针介导穿孔的解剖学、生理学和蛋白质组学后果。

方法

使用双光子聚合(2PP)光刻法制造直径为100μm的空心微针。打开哈特利豚鼠(n = 8)的鼓泡,充分暴露RWM。记录畸变产物耳声发射(DPOAE)和复合动作电位(CAP)以评估听力。将空心微针插入鼓泡并刺穿RWM;在45秒内从耳蜗抽吸1μL外淋巴。72小时后,重复上述操作,再抽吸1μL外淋巴。第二次穿孔72小时后,收获RWM用于共聚焦成像。使用液相色谱 - 串联质谱(LC - MS/MS)完成外淋巴蛋白质组学分析。

结果

对8只豚鼠进行了两次穿孔和抽吸。6只获得了CAP、DPOAE和蛋白质组学分析结果;1只仅获得了CAP和DPOAE结果;1只仅获得了蛋白质组学结果。听力测试显示在1 - 4kHz和28kHz处有轻度听力损失,最符合传导性听力损失。共聚焦显微镜显示所有穿孔完全愈合,RWM完全重建。外淋巴蛋白质组学分析在14个样本中鉴定出1855种蛋白质。在所有样本中均观察到内耳蛋白耳蜗素,表明成功抽吸了外淋巴。未调整的配对t检验(p < 0.01)显示,在第一次和第二次抽吸之间,1855种已鉴定蛋白质中有13种(0.7%)发生了显著变化。

结论

我们证明对RWM进行重复微针穿孔是可行的,能使RWM完全愈合,并且对蛋白质组表达谱的改变最小。因此,在单只动物中进行微针介导的重复抽吸可用于随时间监测内耳治疗的反应。

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