Dendritic patterning by interacting extrinsic cues
通过相互作用的外部线索形成树突图案
基本信息
- 批准号:10006606
- 负责人:
- 金额:$ 34.64万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2008
- 资助国家:美国
- 起止时间:2008-04-01 至 2023-08-31
- 项目状态:已结题
- 来源:
- 关键词:AblationAdhesionsAffectAfferent NeuronsAutomobile DrivingAxonBehaviorBehavioralCell CommunicationCellsCuesDataDendritesDevelopmentDevelopmental ProcessDrosophila genusEnsureExcisionFinancial compensationImageIndividualLeadLightMediatingModalityModelingMolecularMorphogenesisMorphologyMotor outputNerveNervous System PhysiologyNervous system structureNeuraxisNeuronsNeuropilNociceptionNociceptorsOutputPathway interactionsPatternPeripheral Nervous SystemPositioning AttributePresynaptic TerminalsProcessReceptor ActivationResolutionRoleSensorySignal TransductionSorting - Cell MovementSpecific qualifier valueSpecificityStimulusSynapsesSystemTestingTouch sensationbehavioral responsecohesioncohortdesigndevelopmental diseaseflyinsightnervous system developmentnervous system disorderneural circuitnovelreceptorrelating to nervous systemresponsesegregationsensory inputsomatosensory
项目摘要
Project Summary
The targeting of axons and dendrites is essential for proper wiring of the nervous system and the expression of
behavior. To understand how the nervous system is wired during development we focus on cell-cell
interactions that underlie specificity in wiring the somatosensory system. Somatosensation is important for
sensing touch and noxious stimuli, and for driving distinct and appropriate behavioral responses. We focus on
the influence of local axon-axon interactions in circuit organization, function, and behavior. The somatosensory
system of Drosophila is an excellent model to probe the cellular and molecular basis for neural circuit wiring
and function. Here we focus on the developmental mechanisms that ensure robust axon segregation to
different parts of the nervous system and how these patterns ensure appropriate neural circuit functioning.
Many of the developmental processes under study, including axon-axon adhesion, repulsion, refinement, axon
target selection, and the control of these processes by molecular cues and neural activity, are central to
nervous system development in other species. We find that the positioning of somatosensory axons is highly
ordered in the Drosophila central nervous system. This precise ordering appears to ensure that different
qualities of sensory information are passed to correct downstream circuits and lead to appropriate behavioral
responses. We propose that developing axons that are responsible for sensing different modalities engage in
interactions that ensure separation of connections and distinct behaviors in response to sensory stimulation.
By contrast we propose that axons of the same modality may engage in positive attractive interactions that
ensure cohesion during wiring. We aim to test the developmental mechanisms that enforce the normally robust
and distinct relationships between sensory input and motor output. We propose that at least part of the
mechanism lies in a hierarchy of developmental axon-axon interactions between different sensory modalities
and that understanding how this orderly wiring emerges will provide insights into the mechanisms by which
nervous systems are patterned more generally, and how patterning might be disrupted in developmental
disorders of the nervous system.
项目摘要
轴突和树突的靶向对于神经系统的正确布线和神经元的表达是必不可少的。
行为为了了解神经系统在发育过程中是如何连接的,我们专注于细胞-细胞
在连接躯体感觉系统的特异性基础上的相互作用。躯体感觉对于
感知触摸和有害刺激,并驱动不同的和适当的行为反应。我们专注于
局部轴突-轴突相互作用对回路组织、功能和行为的影响。体感
果蝇的神经元系统是研究神经回路连接的细胞和分子基础的极好模型
和功能在这里,我们专注于发展机制,确保强大的轴突分离,
神经系统的不同部分以及这些模式如何确保适当的神经回路功能。
许多正在研究的发育过程,包括轴突-轴突粘附,排斥,细化,轴突
目标选择,以及分子线索和神经活动对这些过程的控制,
其他物种的神经系统发育。我们发现,躯体感觉轴突的定位是高度
在果蝇的中枢神经系统中。这种精确的排序似乎确保了不同的
感官信息的质量被传递到正确的下游电路,并导致适当的行为
应答我们认为,负责感知不同模式的发育中的轴突参与
确保对感官刺激做出反应的连接和不同行为的分离的相互作用。
相比之下,我们提出,相同形态的轴突可能参与积极的吸引力相互作用,
确保接线时的粘合力。我们的目标是测试执行通常强大的发展机制,
以及感觉输入和运动输出之间的独特关系。我们建议,至少部分
其机制在于不同感觉方式之间的发育轴突-轴突相互作用的层次结构
了解这种有序的连接是如何出现的,将有助于深入了解
神经系统更普遍地形成模式,以及在发育过程中模式如何被破坏。
神经系统紊乱。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Wesley B Grueber其他文献
Wesley B Grueber的其他文献
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{{ truncateString('Wesley B Grueber', 18)}}的其他基金
Neuron-macrophage interactions in models of chemotherapy-induced peripheral neuropathy
化疗引起的周围神经病变模型中神经元-巨噬细胞的相互作用
- 批准号:
10511496 - 财政年份:2022
- 资助金额:
$ 34.64万 - 项目类别:
Neuron-macrophage interactions in models of chemotherapy-induced peripheral neuropathy
化疗引起的周围神经病变模型中神经元-巨噬细胞的相互作用
- 批准号:
10673851 - 财政年份:2022
- 资助金额:
$ 34.64万 - 项目类别:
CADRE Program for Postbaccalaureate Training in the Neurosciences
神经科学学士后培训 CADRE 计划
- 批准号:
10611758 - 财政年份:2022
- 资助金额:
$ 34.64万 - 项目类别:
Dendritic patterning by interacting extrinsic cues
通过相互作用的外部线索形成树突图案
- 批准号:
10527168 - 财政年份:2021
- 资助金额:
$ 34.64万 - 项目类别:
Summer Program for Undergraduate Rising Stars (SPURS), a Columbia University biomedical sciences pipeline program
本科生新星暑期项目 (SPURS),哥伦比亚大学生物医学科学管道项目
- 批准号:
10594256 - 财政年份:2012
- 资助金额:
$ 34.64万 - 项目类别:
Dendritic patterning by interacting extrinsic cues
通过相互作用的外部线索形成树突图案
- 批准号:
8505789 - 财政年份:2008
- 资助金额:
$ 34.64万 - 项目类别:
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