不同的抑制性神经元以不同方式形成听觉皮层中声音强度的神经元编码。

IF 4.4 2区 医学 Q1 NEUROSCIENCES Journal of Neuroscience Pub Date : 2024-11-08 DOI:10.1523/JNEUROSCI.1502-23.2024
Melanie Tobin, Janaki Sheth, Katherine C Wood, Erin K Michel, Maria N Geffen
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引用次数: 0

摘要

大脑皮层回路包含多种类型的抑制性神经元,它们决定了神经元网络内的信息处理方式。在这里,我们探讨了表达体生长抑素(SST)和表达血管活性肠肽(VIP)的抑制性神经元是否会对神经元群对不同强度噪声脉冲的反应产生不同的影响。我们对 SST 或 VIP 神经元进行了光遗传刺激,同时测量了头部固定的雌雄清醒小鼠听皮层中数百个神经元群对声音的钙离子反应。当 SST 神经元被激活时,不同强度水平的噪声脉冲表征变得更加离散,这依赖于细胞的特性而非强度。相比之下,VIP神经元激活后,不同强度水平的噪声脉冲会激活重叠的神经元群,尽管反应强度不同。在单细胞水平上,SST 和 VIP 神经元激活对单调和非单调神经元的反应水平曲线有不同的调节作用。SST 神经元激活效应与神经元群反应转向更局部的编码一致,不同细胞对不同强度的声音做出反应。与此相反,VIP 神经元激活则使反应转向更分散的代码,其中不同强度水平的声音被编码在类似细胞群的相对反应中。这些结果描述了听觉皮层中不同的抑制性神经元是如何动态控制皮层群体代码的。在不同的行为需求下,不同的抑制性神经元群可能会被招募,这取决于分类表征或不变表征对任务是否有利。皮层神经元群由多种类型的兴奋性和抑制性神经元组成。在这里,我们发现激活不同类型的抑制性神经元会对群体神经元表征产生不同的控制作用,其中一种抑制性神经元会增加被招募来表征不同声音的细胞身份的差异,而另一种抑制性神经元类型则会改变重叠神经元群体的相对活动水平。这种转变可能有利于不同类型的听觉行为,表明这些不同类型的抑制性神经元可能是在优化声音神经元表征的不同行为限制条件下被招募的。
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Distinct inhibitory neurons differently shape neuronal codes for sound intensity in the auditory cortex.

Cortical circuits contain multiple types of inhibitory neurons which shape how information is processed within neuronal networks. Here, we asked whether somatostatin-expressing (SST) and vasoactive intestinal peptide-expressing (VIP) inhibitory neurons have distinct effects on population neuronal responses to noise bursts of varying intensities. We optogenetically stimulated SST or VIP neurons while simultaneously measuring the calcium responses of populations of hundreds of neurons in the auditory cortex of male and female awake, head-fixed mice to sounds. Upon SST neuronal activation, noise bursts representations became more discrete for different intensity levels, relying on cell identity rather than strength. By contrast, upon VIP neuronal activation, noise bursts of different intensity level activated overlapping neuronal populations, albeit at different response strengths. At the single-cell level, SST and VIP neuronal activation differentially modulated the response-level curves of monotonic and nonmonotonic neurons. SST neuronal activation effects were consistent with a shift of the neuronal population responses toward a more localist code with different cells responding to sounds of different intensity. By contrast, VIP neuronal activation shifted responses towards a more distributed code, in which sounds of different intensity level are encoded in the relative response of similar populations of cells. These results delineate how distinct inhibitory neurons in the auditory cortex dynamically control cortical population codes. Different inhibitory neuronal populations may be recruited under different behavioral demands, depending on whether categorical or invariant representations are advantageous for the task.Significance Statement Information about sounds is represented in the auditory cortex by neuronal population activity that has a characteristic sparse structure. Cortical neuronal populations comprise multiple types of excitatory and inhibitory neurons. Here, we find that activating different types of inhibitory neurons differentially controls population neuronal representations, with one type of inhibitory neurons increasing the differences in the identity of the cells recruited to represent the different sounds, and another inhibitory neuron type changing the relative activity level of overlapping neuronal populations. Such transformations may be beneficial for different types of auditory behaviors, suggesting that these different types of inhibitory neurons may be recruited under different behavioral constraints in optimizing neuronal representations of sounds.

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来源期刊
Journal of Neuroscience
Journal of Neuroscience 医学-神经科学
CiteScore
9.30
自引率
3.80%
发文量
1164
审稿时长
12 months
期刊介绍: JNeurosci (ISSN 0270-6474) is an official journal of the Society for Neuroscience. It is published weekly by the Society, fifty weeks a year, one volume a year. JNeurosci publishes papers on a broad range of topics of general interest to those working on the nervous system. Authors now have an Open Choice option for their published articles
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