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通过枕部途径移植人角膜缘间充质基质细胞可改善动物听觉神经病的听力。

Transplantation of human limbus-derived mesenchymal stromal cells via occipital approach improves hearing in animal auditory neuropathy.

作者信息

Chen Hsin-Chien, Liang Chang-Min, Wang Chih-Hung, Huang Ming-Yuan, Lin Yuan-Yung, Shih Cheng-Ping, Kuo Chao-Yin, Lin Yi-Chun, Chen Hang-Kang

机构信息

Department of Otolaryngology-Head and Neck Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei, 114, Taiwan.

Department of Ophthalmology, Tri-Service General Hospital, National Defense Medical Center, Taipei, 114, Taiwan; Graduate Institute of Aerospace and Undersea Medicine, National Defense Medical Center, Taipei, 114, Taiwan.

出版信息

Int J Pediatr Otorhinolaryngol. 2019 Feb;117:67-72. doi: 10.1016/j.ijporl.2018.11.018. Epub 2018 Nov 15.

Abstract

OBJECTIVE

To develop a surgical approach for cell transplantation into mouse cochlear nerves via an intracranial route and investigate whether transplantation of human limbus-derived mesenchymal stromal cells (HL-MSCs) can improve hearing in this model of auditory neuropathy.

METHODS

We used 8-week-old CBA/CaJ male mice and created ouabain-induced auditory neuropathy. The surgical approach passed through the cerebellum to reveal the superior semicircular canal and brainstem, allowing access to the auditory nerve. Then HL-MSCs were injected around the cochlear nerve trunk using a micropipette driven by a micropump. Hearing thresholds in the mice were determined by auditory brainstem responses (ABRs) and distortion product otoacoustic emissions (DPOAEs).

RESULTS

We produced ouabain-induced neuropathy in mice with an elevated hearing threshold but normal DPOAE. Using immunohistological staining, we detected HL-MSCs were localized in the cochlear nerve trunk 2 days after cell transplantation via this occipital approach. More spiral ganglion neurons were detected in ouabain-treated cochleae 3 months after HL-MSCs transplantation compared to those without HL-MSCs transplantation. The ABR showed significant hearing improvement 3 months after HL-MSCs transplantation.

CONCLUSIONS

We successfully established a mouse model for cell transplantation into the intracranial cochlear nerve trunk and showed that HL-MSCs potentially can be applied as cell therapy to treat sensorineural hearing loss.

摘要

目的

开发一种通过颅内途径将细胞移植到小鼠耳蜗神经的手术方法,并研究人角膜缘间充质基质细胞(HL-MSCs)移植是否能改善这种听觉神经病变模型中的听力。

方法

我们使用8周龄的CBA/CaJ雄性小鼠,制造哇巴因诱导的听觉神经病变。手术路径穿过小脑以暴露上半规管和脑干,从而能够接近听神经。然后使用由微量泵驱动的微量移液器将HL-MSCs注射到耳蜗神经干周围。通过听性脑干反应(ABR)和畸变产物耳声发射(DPOAE)测定小鼠的听力阈值。

结果

我们在小鼠中制造了哇巴因诱导的神经病变,其听力阈值升高但DPOAE正常。使用免疫组织化学染色,我们发现在通过这种枕部途径进行细胞移植后2天,HL-MSCs定位于耳蜗神经干。与未进行HL-MSCs移植的小鼠相比,在HL-MSCs移植后3个月,在哇巴因处理的耳蜗中检测到更多的螺旋神经节神经元。HL-MSCs移植后3个月,ABR显示听力有显著改善。

结论

我们成功建立了一种将细胞移植到颅内耳蜗神经干的小鼠模型,并表明HL-MSCs有可能作为细胞疗法用于治疗感音神经性听力损失。

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