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Astrocyte-Neuron Network Activity During In Vivo Brain Stimulation

Astrocyte-Neuron Network Activity During In Vivo Brain Stimulation
体内脑刺激期间星形胶质细胞-神经元网络活动
批准号:
10537479
负责人:
Kevin Stieger
金额:
$4.68万
依托单位国家:
美国
项目类别:
财政年份:
2022
资助国家:
美国
项目状态:
未结题
起止时间:
2022-09-20 至 2025-09-19

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中文摘要
翻译
项目总结 皮层内微刺激(ICMS)是基础神经科学研究的主要组成部分 神经假体中感觉恢复或感觉反馈的巨大潜力。尽管电力的广泛使用 神经假体中的刺激和干预措施,如脊髓刺激和脑深部刺激 (DBS),定义治疗效果的基本生理和机械特性仍然很差 明白了。例如,目前还不清楚哪些类型的细胞被激活,它们在治疗中扮演什么角色 结果,以及如何调整刺激参数以选择性地在这些细胞类型中诱导相关活动 感觉恢复。特别令人感兴趣的是非神经元细胞,如星形胶质细胞的贡献。星形胶质细胞 在感觉处理过程中成为调节神经元活动的重要细胞,在这一过程中 反应神经递质与钙升高导致神经活性物质释放调节 突触功能(即神经胶质传递)。重要的是,星形胶质细胞调节神经元和 突触活性与ICMS诱导的神经活性一致。正是因为这些最近受到赞赏的角色 关于星形胶质细胞-神经元的通讯,星形胶质细胞被认为是大脑的重要组成部分 刺激。然而,目前尚不清楚星形胶质细胞对临床相关刺激参数的反应。 网络水平,以及这种激活随后如何调节清醒动物的神经元活动。致信地址 在这种认识上的差距,这一建议将首先量化大脑皮质星形胶质细胞中的钙活性,并跨越更大的 具有不同频率和时间模式的ICMS诱导的网络具有差异治疗 使用双光子显微镜和中尺度成像的效果。接下来,该提案将量化ICMS如何- 当星形胶质细胞钙活性选择性增加时,诱导的神经元活动被调节(光遗传学)或 降低(质膜钙泵的病毒转导)以确定星形胶质细胞如何调节 ICMS期间的神经元网络活动。因为星形胶质细胞的钙活动调节这些重要细胞如何 调节神经元活动,这一建议的累积结果将为基础研究提供有价值的见解 神经科学研究和刺激范例的设计以诱导与感觉相关的星形胶质细胞活动 修复。
英文摘要
PROJECT SUMMARY Intracortical microstimulation (ICMS) is a primary component of fundamental neuroscience research and holds great potential for sensory restoration or sensory feedback in neuroprosthetics. Despite the wide use of electrical stimulation in neuroprosthetics and interventions such as spinal cord stimulation and deep brain stimulation (DBS), the fundamental physiological and mechanistic properties defining therapeutic efficacy remain poorly understood. For example, it is still unclear which cell types are activated, what role they play in therapeutic outcomes, and how to tune stimulation parameters to selectively elicit relevant activity in those cell types for sensory restoration. Of particular interest is the contribution of non-neuronal cells such as astrocytes. Astrocytes are emerging as important cells in the modulation of neuronal activity during sensory processing in which they respond to neurotransmitters with calcium elevations leading to the release of neuroactive substances to regulate synaptic function (i.e., gliotransmission). Importantly, the time scale in which astrocytes modulate neuronal and synaptic activity is consistent with ICMS-induced neural activity. It is because of these recently appreciated roles regarding astrocyte-neuron communication that astrocytes have been suggested as a vital component to brain stimulation. However, it is unclear how astrocytes respond to clinically relevant stimulation parameters on a network level and how that activation subsequently modulates neuronal activity in an awake animal. To address this gap in knowledge, this proposal will first quantify the calcium activity in cortical astrocytes and across a larger network induced by ICMS with different frequencies and temporal patterns known to have differential therapeutic efficacy using both two-photon microscopy and mesoscale imaging. Next, this proposal will quantify how ICMS- induced neuronal activity is modulated when astrocyte calcium activity is selectively increased (optogenetics) or decreased (viral transduction of a plasma membrane calcium pump) to determine how astrocytes regulate neuronal network activity during ICMS. Because astrocyte calcium activity regulates how these important cells modulate neuronal activity, the cumulative results of this proposal will provide valuable insight for fundamental neuroscience research and the design of stimulation paradigms to elicit astrocyte activity relevant to sensory restoration.
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Astrocyte-Neuron Network Activity During In Vivo Brain Stimulation
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