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CRCNS: Deciphering the Dynamical Multi-Scale Structure-Function Relation of Dendritic Spines

CRCNS: Deciphering the Dynamical Multi-Scale Structure-Function Relation of Dendritic Spines
CRCNS:破译树突棘的动态多尺度结构-功能关系
批准号:
9100682
负责人:
Mark H Ellisman
金额:
$17.65万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-07-01 至 2019-06-30

项目摘要

项目成果

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中文摘要
翻译
描述(由申请人提供):我们储存和保留新信息的能力依赖于大脑巨大的可塑性。实验证据表明,单个树突棘的形态化学修饰可能有助于学习和记忆,但我们缺乏对棘功能的定量和机制理解。为了解决这一缺陷,该项目旨在探索树突棘的超结构三维结构如何塑造其电化学信号转导以及结构变化如何改变转导从而影响突触效能。最先进的三维电子显微镜(EM)重建赋予精确的离子化受体动力学和精确的生物物理模型将用于构建纳米分辨率的树突棘模型。为了在如此复杂的多尺度环境中模拟电化学动力学,将采用有限元离散化和快速多级求解等先进的数值方法。通过在硅中进行详细的实验,将确定影响刺中离子电流传导的主要因素
英文摘要
DESCRIPTION (provided by applicant): Our ability to store and retain new information rests upon the brain's immense plastic capabilities. Experimental evidence suggests that morpho-chemical modifications at the level of single dendritic spines may contribute to learning and memory but we lack both a quantitative and a mechanistic understanding of how spines function. To address this deficit, the proposed project aims to explore how the ultra-structural three-dimensional architecture of dendritic spines shapes their electro-chemical signal transduction and how structural changes alter the transduction and thus affect synaptic efficacy. State-of-the-art 3D electron microscope (EM) reconstructions endowed with precise ionotropic receptor kinetics and accurate biophysical models will be used to construct a nanometer-resolution model for dendritic spines. To simulate the electro-chemical dynamics within such a complex multi-scale environment, advanced numeric schemes such as finite-element discretization and fast multi-level solvers will be employed. By performing detailed experiments in silico, the primary factors that influence ionic current conduction in spines will be identified and then used to systematically derive a low-dimensional spine model amenable to exact mathematical analysis. Both, the full and the reduced model will allow the consortium to study the sub-cellular information-processing capabilities of single spines, and to compare the results with in vivo and in vitro data. The models will enable researchers to develop and test spine-related experimental hypotheses and to interpret data recorded in healthy and disease-modified tissue within a unified framework. Objective 1: Reconstruct Dendritic Spines in 3D at Nanometer Resolution; Objective 2: Establish a Biophysically Realistic Nanometer-Resolution Spine Model; Objective 3: Develop High-Performance Numerical Methods to Simulate the Spine Model; Objective 4: Use Simulations and Theory to Study the Computations of Dendritic Spines. The project aims to relate the multi-scale biological organization of dendritic spines to possible functional consequences at the macroscopic and systems level. In the era of ever-increasing super-computing capabilities, any mechanistic model of synaptic transmission and postsynaptic integration should start with a clear insight into precisely how biophysics orchestrates the signal transduction at the smallest scales. Deciphering the impact of micro-structural features on spine dynamics will be a stepping-stone towards understanding neural signal propagation and synaptic plasticity, and likely reveal novel sub-cellular computational principles. The findings wil deepen our understanding of neural information processing in healthy and disease-modified brains and may lead to new designs for neuromorphic devices. Alterations in spine morphology are seen in various brain diseases [1] including Down's syndrome and fragile X syndrome [2]. Similarly, changes of the intra-spine calcium dynamics and homeostasis have been documented for Alzheimer's disease [3]. Developing new cures and therapies for these diseases will profit from a better understanding of the relation between the dynamical structure and the function of dendritic spines. To reach this goal, in continuation of past NSF-supported projects, we will recruit and train young scientists to meet the interdisciplinary challenges of modern multi-scale and multi-modal data-driven biology, where progess is driven not only by neuroscience, but also engineering, mathematics and physical sciences, computational science and neuroinformatics The planned collaboration between the three laboratories in the US and Germany will generate international training opportunities for graduate students and postdoctoral researchers, and the participation of researchers in programs that encourage underrepresented minorities to pursue career paths in STEM disciplines.
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200keV, Energy Filtered, Intermediate-High Voltage Transmission Electron Microscope(IVEM)"
Scalable electron tomography for connectomics
  • 批准号:
    10410742
  • 项目类别:
  • 资助金额:
    $291.62万
  • 财政年份:
    2022
  • 负责人:
    Mark H Ellisman
  • 依托单位:
Reversing Microglial Inflammarafts and Mitochondrial Dysfunction in Alzheimer's Disease
National Center for Microscopy and Imaging Research: A BRAIN Technology Integration and Dissemination Resource
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