课题基金 / 基金详情

A neuronal network generating flexible locomotor behaviour in a simple vertebrate: studies on function and embryonic self-assembly

A neuronal network generating flexible locomotor behaviour in a simple vertebrate: studies on function and embryonic self-assembly
在简单脊椎动物中产生灵活运动行为的神经元网络:功能和胚胎自组装的研究
批准号:
BB/G006652/1
负责人:
Stephen Soffe
金额:
$73.93万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2009
资助国家:
英国
项目状态:
已结题
起止时间:
2009 至 --

项目摘要

项目成果

Stephen Soffe的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
How do nervous systems allow animals to behave? The challenge here is immediately clear from the vast numbers of neurons (over 2 billion) in a human brain. Less obvious is the minute scale of nervous systems construction with many neurons only 0.01 mm in diameter. Problems of size and complexity have led to the study of simpler animals like snails and squid which have complex behaviour but many fewer, often larger, neurons. A further remarkable feature of nervous systems is that they must self-assemble rapidly during embryonic development to allow early responses that aid survival. How do they do this? Recent genetic work on development has emphasised fundamental features, common to animals as diverse as nematode worms, fruit flies and vertebrates like us. Detailed research on embryos has shown that vertebrate nervous systems share a common plan particularly in core parts like the spinal cord. We can therefore investigate how nervous systems develop and function in the simplest vertebrates. We study just-hatched, 2 day old frog tadpoles. While only 5 mm long and with less than 2000 neurons, they will swim when touched, struggle when grasped by a predator, and stop and attach when they bump into things: behaviour that aids survival. Exploiting the simplicity of the early tadpole nervous system and new methods that we devised, we have recorded activity from most types of neuron controlling movement and now have a uniquely detailed picture of the neuronal circuits for swimming and struggling. In collaboration with computer scientists and mathematicians, we built simplified models of these circuits and uncovered key principals of operation. This theoretical work emphasised commonality in neuronal circuits controlling movement, from snails to mammals, but revealed gaps in our knowledge. As well as asking how early neuronal circuits work we also want to know how they develop. We found that connections between tadpole neurons are not very specific. Broadly, their nerve fibres simply contact the neurons they encounter as they grow. Since neurons responding to sensory stimuli lie at the top and neurons controlling muscles lie at the bottom, those growing near the top will connect to different neurons to those growing near the bottom. Our mathematical models showed that very simple rules could direct nerve fibre growth to form neuronal circuits able to generate swimming activity when stimulated. In this study we will ask whether the ordered structure of the early tadpole nervous system allows functional neuronal circuits to self-assemble in response to 3 chemical gradients known to control growth of nerve fibres along and around the nervous system. To answer this question we need many more electrical recordings to establish exactly how swimming and struggling are initiated by different skin stimuli. We also need more detailed information on morphology for each neuron type. Our study should reveal how nervous systems 'decide' to initiate movement. Using the morphological information we will build a mathematical model of neuron growth to generate the synaptic connections that different types of neuron make with each other to self-assemble neuronal circuits. Using the physiological information we will build models where the different neurons are connected into functional circuits which we can stimulate to find how they generate the neuronal activity that produces swimming and struggling. Our ultimate aim is to see if simple growth rules can allow the self-assembly of neuronal networks which can 'decide' when and how to respond to sensory stimuli, behaving like a tadpole. By making a 'virtual tadpole' whose movements are controlled by our networks we can actually watch them producing behaviour. If successful, our study will lay a foundation for understanding the way more mature, complex nervous systems control movements and how they develop.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1371/journal.pcbi.1004702
发表时间: 2016-01
期刊: PLoS computational biology
影响因子: 4.3
作者: [Hull MJ, Soffe SR, Willshaw DJ, Roberts A]
通讯作者: Roberts A
A functional scaffold of CNS neurons for the vertebrates: the developing Xenopus laevis spinal cord.
脊椎动物中枢神经系统神经元的功能支架:正在发育的非洲爪蟾脊髓。
DOI: 10.1002/dneu.20889
发表时间: 2012
期刊: Developmental neurobiology
影响因子: 3
作者: [Roberts A]
通讯作者: Roberts A
DOI: 10.3389/fninf.2011.00020
发表时间: 2011
期刊: Frontiers in neuroinformatics
影响因子: 3.5
作者: [Borisyuk R, Al Azad AK, Conte D, Roberts A, Soffe SR]
通讯作者: Soffe SR
DOI: 10.1371/journal.pone.0089461
发表时间: 2014
期刊: PloS one
影响因子: 3.7
作者: [Borisyuk R, Al Azad AK, Conte D, Roberts A, Soffe SR]
通讯作者: Soffe SR
8
    Cross-modality integration of sensory signals leading to initiation of locomotion
    • 批准号:
      BB/L002353/1
    • 项目类别:
      Research Grant
    • 资助金额:
      $54.99万
    • 财政年份:
      2014
    • 负责人:
      Stephen Soffe
    • 依托单位:
    国内基金
    海外基金
    铜募集微纳米网片上调LOX活性稳定胶原网络促进盆底修复的研究
    • 批准号:
      82371638
    • 项目类别:
      面上项目
    • 资助金额:
      49.00万元
    • 批准年份:
      2023
    • 负责人:
      陈信良
    • 依托单位:
    GPSM1介导Ca2+循环-II型肌球蛋白网络调控脂肪产热及代谢稳态的机制研究
    • 批准号:
      82370879
    • 项目类别:
      面上项目
    • 资助金额:
      49.00万元
    • 批准年份:
      2023
    • 负责人:
      严婧
    • 依托单位:
    RagD调控mTORC2溶酶体定位的机制及功能研究
    • 批准号:
      32100578
    • 项目类别:
      青年科学基金项目(C类)
    • 资助金额:
      30.0万元
    • 批准年份:
      2021
    • 负责人:
      陈蕾
    • 依托单位:
    机械力传导的分子机制—细胞感知力与诱导基因表达的方式如何?
    • 批准号:
      32070777
    • 项目类别:
      面上项目
    • 资助金额:
      58.0万元
    • 批准年份:
      2020
    • 负责人:
      Fumihiko Nakamura
    • 依托单位: