CRCNS: Mechanistic Modeling and Inference of Neuronal Synaptic Transmission
CRCNS:神经元突触传递的机制建模和推断
基本信息
- 批准号:10426127
- 负责人:
- 金额:$ 11.1万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2020
- 资助国家:美国
- 起止时间:2020-07-01 至 2025-06-30
- 项目状态:未结题
- 来源:
- 关键词:Action PotentialsAcuteAddressAdolescentAgeAuditoryAuditory systemBiological ModelsBiological ProcessBrainBrain StemCellsCentral Auditory Processing DisorderCommunicationComputer ModelsCoupledDataDerivation procedureDevelopmentDockingElectrophysiology (science)EngineeringEventFrequenciesGeneticGoalsHearingHippocampus (Brain)HybridsInstructionInterneuronsInvestigationJointsKnowledgeLiteratureMathematicsMembrane PotentialsMethodsModelingMusNamesNeuronsNeurotransmittersNoisePharmacologyPlayProcessProtocols documentationRecoveryResearchRoleSensoryShapesSliceSound LocalizationSourceSynapsesSynaptic TransmissionSynaptic VesiclesSystemTimeTrainingVariantVesicleWorkbasedata exchangeexperimental studyhearing impairmentinformation processinginterdisciplinary approachmathematical modelneurotransmissionneurotransmitter releaseneurotransmitter uptakenovelpatch clamppostsynaptic neuronspresynaptic neuronsresponsesocioeconomicssynaptic depressiontooluptakevesicular release
项目摘要
Action potential-triggered transmitter release forms a hallmark of interneuronal communication. The
release is critically impacted by diverse noise mechanisms, such as random arrival of action potentials,
probabilistic vesicle release, and random replenishment of vesicle pools. How these noise mechanisms
combine to impact fidelity of interneuronal communication is an intriguing fundamental problem. A key
focus of this project is to use the mathematical formalism of Stochastic Hybrid Systems (SHS) that
combine continuous dynamics with discrete random events for modeling synaptic transmission. The
SHS-based formalism will be used to derive analytical results connecting synaptic noise mechanisms to
randomness in the neurotransmitter levels, and its impact on temporal precision of the responses in the
postsynaptic neuron. The project will also develop novel inference methods for inferring
neurotransmission parameters from whole-cell patch-clamp recordings in acute brain slices of juvenile
mice. Integration of mathematical models with experimental data on long-lasting high-frequency activation
of input neurons will be used to characterize neurotransmission at various auditory and non-auditory
synapse types. This interdisciplinary approach--coupled with genetic and pharmacological manipulation of
neurotransmitter release, re-uptake, and vesicle replenishment--will systematically uncover the role of
these processes in information processing at the single-cell level and how auditory brainstem synapses
achieve exquisitely high fidelity during prolonged stimulation. Altogether, the project will reveal the
extraordinary capabilities of auditory synapses and thus form a basis for a better understanding of central
auditory processing disorders.
RELEVANCE (See instructions):
Hearing impairment is the most prevalent sensory deficit, with major socioeconomic impact. In order to
understand how hearing happens, we must obtain a comprehensive knowledge about neuronal
information processing in the central auditory system. The project will thoroughly address synaptic
processes involved in sound localization by combining empirical work with computational modeling, and
we will achieve hitherto unreached synergistic effects towards our goal.
动作电位触发的递质释放形成了神经元间交流的标志。这
释放受到多种噪声机制的严重影响,例如动作电位的随机到达,
概率囊泡释放和囊泡池的随机补充。这些噪音机制如何
结合起来影响神经元间交流的保真度是一个有趣的基本问题。一把钥匙
该项目的重点是使用随机混合系统(SHS)的数学形式
将连续动态与离散随机事件相结合来建模突触传递。这
基于 SHS 的形式主义将用于导出将突触噪声机制与
神经递质水平的随机性及其对反应时间精度的影响
突触后神经元。该项目还将开发新的推理方法来推断
青少年急性脑切片全细胞膜片钳记录的神经传递参数
老鼠。将数学模型与持久高频激活的实验数据相结合
输入神经元的数量将用于表征各种听觉和非听觉的神经传递
突触类型。这种跨学科的方法——结合遗传和药理学操作
神经递质释放、再摄取和囊泡补充——将系统地揭示
单细胞水平信息处理的这些过程以及听觉脑干突触如何
在长时间的刺激过程中实现极高的保真度。总而言之,该项目将揭示
听觉突触的非凡能力,从而为更好地理解中枢奠定了基础
听觉处理障碍。
相关性(参见说明):
听力障碍是最普遍的感觉缺陷,具有重大的社会经济影响。为了
了解听觉是如何发生的,我们必须获得关于神经元的全面知识
中枢听觉系统的信息处理。该项目将彻底解决突触问题
通过将经验工作与计算模型相结合来参与声音定位的过程,以及
我们将在实现我们的目标方面实现前所未有的协同效应。
项目成果
期刊论文数量(3)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Glycinergic Transmission in the Presence and Absence of Functional GlyT2: Lessons From the Auditory Brainstem.
存在和不存在功能性 GlyT2 时的甘氨酸能传递:来自听觉脑干的教训。
- DOI:
- 发表时间:2020
- 期刊:
- 影响因子:0
- 作者:Brill, Sina E;Maraslioglu, Ayse;Kurz, Catharina;Kramer, Florian;Fuhr, Martin F;Singh, Abhyudai;Friauf, Eckhard
- 通讯作者:Friauf, Eckhard
Considerable differences between auditory medulla, auditory midbrain, and hippocampal synapses during sustained high-frequency stimulation: Exceptional vesicle replenishment restricted to sound localization circuit.
在持续高频刺激期间,听觉延髓、听觉中脑和海马突触之间存在相当大的差异:异常的囊泡补充仅限于声音定位电路。
- DOI:
- 发表时间:2019
- 期刊:
- 影响因子:2.8
- 作者:Brill, Sina E;Janz, Katrin;Singh, Abhyudai;Friauf, Eckhard
- 通讯作者:Friauf, Eckhard
Characterizing the role of autaptic feedback in enhancing precision of neuronal firing times.
表征自动反馈在提高神经元放电时间精度方面的作用。
- DOI:
- 发表时间:2023-10-09
- 期刊:
- 影响因子:0
- 作者:Vahdat Z;Gambrell O;Singh A
- 通讯作者:Singh A
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Abhyudai Singh其他文献
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{{ truncateString('Abhyudai Singh', 18)}}的其他基金
Generalized fluctuation test for deciphering phenotypic switching within cell populations
破译细胞群内表型转换的广义波动测试
- 批准号:
10552300 - 财政年份:2023
- 资助金额:
$ 11.1万 - 项目类别:
CRCNS: Mechanistic Modeling and Inference of Neuronal Synaptic Transmission
CRCNS:神经元突触传递的机制建模和推断
- 批准号:
10206091 - 财政年份:2020
- 资助金额:
$ 11.1万 - 项目类别:
Stochastic hybrid systems approach to uncovering cell-size control mechanisms
揭示细胞大小控制机制的随机混合系统方法
- 批准号:
9460644 - 财政年份:2017
- 资助金额:
$ 11.1万 - 项目类别:
Consequences and Control of Randomness in Timing of Intracellular
细胞内时间随机性的后果和控制
- 批准号:
9754192 - 财政年份:2017
- 资助金额:
$ 11.1万 - 项目类别:
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