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Impaired Hearing and Altered Subplate Circuits During the First and Second Postnatal Weeks of Otoferlin-Deficient Mice

机译:耳铁蛋白缺陷小鼠出生后第一周和第二周的听力受损和底板电路改变

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Sensory deprivation from the periphery impacts cortical development. Otoferlin deficiency leads to impaired cochlear synaptic transmission and is associated with progressive hearing loss in adults. However, it remains elusive how sensory deprivation due to otoferlin deficiency impacts the early development of the auditory cortex (ACX) especially before the onset of low threshold hearing. To test that, we performed in vivo imaging of the ACX in awake mice lacking otoferlin (Otof(-/-)) during the first and second postnatal weeks and found that spontaneous and sound-driven cortical activity were progressively impaired. We then characterized the effects on developing auditory cortical circuits by performing in vitro recordings from subplate neurons (SPN), the first primary targets of thalamocortical inputs. We found that in Otof(-/-) pups, SPNs received exuberant connections from excitatory and inhibitory neurons. Moreover, as a population, SPNs showed higher similarity with respect to their circuit topology in the absence of otoferlin. Together, our results show that otoferlin deficiency results in impaired hearing and has a powerful influence on cortical connections and spontaneous activity in early development even before complete deafness. Therefore, peripheral activity has the potential to sculpt cortical structures from the earliest ages, even before hearing impairment is diagnosed.
机译:外周的感觉剥夺会影响皮质发育。耳铁蛋白缺乏导致耳蜗突触传递受损,并与成人进行性听力损失有关。然而,由于耳铁蛋白缺乏导致的感觉剥夺如何影响听觉皮层 (ACX) 的早期发育,尤其是在低阈值听力发作之前,仍然难以捉摸。为了测试这一点,我们在出生后第一周和第二周对缺乏奥托铁蛋白(Otof(-/-))的清醒小鼠进行了ACX的体内成像,发现自发和声音驱动的皮质活动逐渐受损。然后,我们通过从亚板神经元 (SPN) 进行体外记录来表征对发育听觉皮层回路的影响,SPN 是丘脑皮质输入的第一个主要目标。我们发现,在 Otof(-/-) 幼崽中,SPN 接收到来自兴奋性和抑制性神经元的旺盛连接。此外,作为一个群体,在没有奥托铁蛋白的情况下,SPNs在电路拓扑方面表现出更高的相似性。总之,我们的结果表明,耳铁蛋白缺乏会导致听力受损,并且对早期发育中的皮质连接和自发活动有强大的影响,甚至在完全耳聋之前。因此,外周活动有可能从最早的年龄开始塑造皮质结构,甚至在诊断出听力障碍之前。

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