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本文引用的文献

1
Ancestral Adeno-Associated Virus Vector Delivery of Opsins to Spiral Ganglion Neurons: Implications for Optogenetic Cochlear Implants.祖源腺相关病毒载体向螺旋神经节神经元传递视蛋白:光遗传学人工耳蜗的启示。
Mol Ther. 2018 Aug 1;26(8):1931-1939. doi: 10.1016/j.ymthe.2018.05.023. Epub 2018 Jul 13.
2
Optogenetic stimulation of cochlear neurons activates the auditory pathway and restores auditory-driven behavior in deaf adult gerbils.光遗传学刺激耳蜗神经元激活听觉通路,并恢复聋成年沙鼠的听觉驱动行为。
Sci Transl Med. 2018 Jul 11;10(449). doi: 10.1126/scitranslmed.aao0540.
3
High frequency neural spiking and auditory signaling by ultrafast red-shifted optogenetics.超快红移光遗传学的高频神经尖峰和听觉信号。
Nat Commun. 2018 May 1;9(1):1750. doi: 10.1038/s41467-018-04146-3.
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Precise multimodal optical control of neural ensemble activity.对神经集群活动进行精确的多模态光学控制。
Nat Neurosci. 2018 Jun;21(6):881-893. doi: 10.1038/s41593-018-0139-8. Epub 2018 Apr 30.
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Cochlear implant - state of the art.人工耳蜗——最新技术水平
GMS Curr Top Otorhinolaryngol Head Neck Surg. 2018 Feb 19;16:Doc04. doi: 10.3205/cto000143. eCollection 2017.
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Challenges in Improving Cochlear Implant Performance and Accessibility.改善人工耳蜗性能与可及性面临的挑战。
IEEE Trans Biomed Eng. 2017 Aug;64(8):1662-1664. doi: 10.1109/TBME.2017.2718939. Epub 2017 Jun 22.
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Integration of optogenetics with complementary methodologies in systems neuroscience.光遗传学与系统神经科学中互补方法的整合。
Nat Rev Neurosci. 2017 Mar 17;18(4):222-235. doi: 10.1038/nrn.2017.15.
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Cre-dependent selection yields AAV variants for widespread gene transfer to the adult brain.Cre依赖性筛选产生用于广泛基因转移至成年大脑的腺相关病毒(AAV)变体。
Nat Biotechnol. 2016 Feb;34(2):204-9. doi: 10.1038/nbt.3440. Epub 2016 Feb 1.
9
Disruption of adaptor protein 2μ (AP-2μ) in cochlear hair cells impairs vesicle reloading of synaptic release sites and hearing.耳蜗毛细胞中衔接蛋白2μ(AP-2μ)的破坏会损害突触释放位点的囊泡再装载及听力。
EMBO J. 2015 Nov 3;34(21):2686-702. doi: 10.15252/embj.201591885. Epub 2015 Oct 7.
10
Optogenetics: 10 years after ChR2 in neurons--views from the community.光遗传学:ChR2应用于神经元研究十年后——学界观点
Nat Neurosci. 2015 Sep;18(9):1202-12. doi: 10.1038/nn.4106.

靶向优化 Chronos 实现听觉通路的超快光遗传学刺激。

Ultrafast optogenetic stimulation of the auditory pathway by targeting-optimized Chronos.

机构信息

Institute for Auditory Neuroscience and InnerEarLab, University Medical Center Göttingen, Göttingen, Germany.

Göttingen Graduate School for Neurosciences and Molecular Biosciences, University of Göttingen, Göttingen, Germany.

出版信息

EMBO J. 2018 Dec 14;37(24). doi: 10.15252/embj.201899649. Epub 2018 Nov 5.

DOI:10.15252/embj.201899649
PMID:30396994
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6293277/
Abstract

Optogenetic tools, providing non-invasive control over selected cells, have the potential to revolutionize sensory prostheses for humans. Optogenetic stimulation of spiral ganglion neurons (SGNs) in the ear provides a future alternative to electrical stimulation used in cochlear implants. However, most channelrhodopsins do not support the high temporal fidelity pertinent to auditory coding because they require milliseconds to close after light-off. Here, we biophysically characterized the fast channelrhodopsin Chronos and revealed a deactivation time constant of less than a millisecond at body temperature. In order to enhance neural expression, we improved its trafficking to the plasma membrane (Chronos-ES/TS). Following efficient transduction of SGNs using early postnatal injection of the adeno-associated virus AAV-PHPB into the mouse cochlea, fiber-based optical stimulation elicited optical auditory brainstem responses (oABR) with minimal latencies of 1 ms, thresholds of 5 μJ and 100 μs per pulse, and sizable amplitudes even at 1,000 Hz of stimulation. Recordings from single SGNs demonstrated good temporal precision of light-evoked spiking. In conclusion, efficient virus-mediated expression of targeting-optimized Chronos-ES/TS achieves ultrafast optogenetic control of neurons.

摘要

光遗传学工具提供了对选定细胞的非侵入性控制,有可能彻底改变人类的感觉假体。对耳朵中的螺旋神经节神经元 (SGN) 的光遗传学刺激为耳蜗植入中使用的电刺激提供了未来的替代方案。然而,大多数通道蛋白不支持与听觉编码相关的高时间保真度,因为它们在关闭后需要几毫秒才能关闭。在这里,我们对快速通道蛋白 Chronos 进行了生物物理特性表征,并在体温下发现其失活时间常数小于一毫秒。为了增强神经表达,我们改进了其向质膜的运输(Chronos-ES/TS)。通过在早期产后将腺相关病毒 AAV-PHPB 注射到小鼠耳蜗中进行 SGN 的有效转导后,基于纤维的光刺激引发了具有最小潜伏期为 1ms 的光听觉脑干反应 (oABR),阈值为 5μJ 和 100μs 脉冲,即使在 1000Hz 的刺激下也具有可观的振幅。单个 SGN 的记录表明光诱发的尖峰具有良好的时间精度。总之,靶向优化的 Chronos-ES/TS 的高效病毒介导表达实现了神经元的超快光遗传学控制。