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Regulatory mechanisms in biological systems in response to compound environmental changes

Regulatory mechanisms in biological systems in response to compound environmental changes
生物系统响应复合环境变化的调节机制
批准号:
EP/G007446/1
负责人:
Reiko Tanaka
金额:
$65.94万
依托单位:
依托单位国家:
英国
项目类别:
Fellowship
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

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中文摘要
翻译
生物系统中的所有活动都受到不同层面(如细胞、生理和个体层面)内和跨层面的广泛调控网络的控制。从这个意义上说,控制是任何生命活动的表现,它的揭示是理解生命奥秘的关键。在这里,控制被认为是生物有机体为实现其目标而使用的一种基于物理成分的机制。本研究的最终目的是建立生物控制理论,从控制的角度(重新)捕捉生物系统中的各种现象,揭示不同水平和不同物种的生物控制系统的共同设计原则。虽然控制长期以来一直是生命科学领域的一个重要主题,但生命科学中控制的研究已经在不同的层面上独立发展:生理层面的稳态,物种层面的控制论,以及细胞层面的调节生物学和最近的系统生物学。然而,复杂的生物调控机制是从细胞资源严格受限的原始单细胞生物进化而来的,这一事实表明,调控机制的基本组成部分可能在不同水平上具有共同特征。因此,我认为,在生命科学的新时代,寻找一种统一的生物防治理论是很自然的,这种理论可以提供一种观点,以提高我们对生物调控的基本理解。这样的理论不仅在学术界至关重要,而且对于动态变化的疾病状态的准确评估和有效治疗也是必要的。它应该为下一代医疗保健的实际临床治疗提供必要的信息。与人造控制系统相比,生物控制系统的显著特点之一是能够改变其结构和/或功能以适应情况。这种可塑性使生物有机体能够适应几乎任何环境变化并采取适当的行动。根据时间尺度的不同,可塑性表现为进化、分化或学习。人造系统使用与环境变化相对应的特定调节机制,而资源有限的生物系统必须在一种调节机制下表现出广泛的灵活行动,以应对各种各样的环境变化。本研究的重点是这一特征,旨在通过发展一种可以解释生物控制潜在机制的数学理论,揭示生物控制在不同水平上实现这种可塑性的基本要素。特别是,我将从复合控制的角度探讨潜在的调控机制,其基本思想是复杂的生物调控是由简单的同质计算介质的空间和时间组合产生的,例如不同分子之间的相互作用用于细胞控制,神经元放电用于大脑控制,对应于各种复合环境变化。我将首先关注细胞水平生物控制的理论基础的发展,然后是免疫系统,它使用细胞和生理水平的控制。在细胞水平上对遗传和代谢系统的基础研究以及对免疫系统的应用研究,都是基于复合控制的思想,应该揭示生物控制系统的基本设计原则。
英文摘要
All actions in biological systems are controlled by extensive regulatory networks within and across different levels, such as cellular, physiological, and individual levels. In this sense, control is the manifestation of any life activity, and its revelation is the key to understanding the mystery of life . Here, control is considered to be a physical-components-based mechanism used by biological organisms to attain their objectives. The ultimate aim of the proposed research is to establish a theory for biological control, to (re)capture the various phenomena in biological systems from the viewpoint of control, and to reveal the design principles that are common to biological control systems across different levels and different species.Although control has been an essential theme in the field of life sciences for a long time, research on control in life sciences has been developed independently at different levels: homeostasis at the physiological level, cybernetics at the species level, and regulatory biology and more recently systems biology at the cellular level. However, the fact that complex biological regulatory mechanisms have developed through evolution from primitive single-cell organisms with strictly constrained cellular resources suggests that the essential components of regulatory mechanisms might have common features across different levels. I believe that it is thus natural to search for a unified theory of biological control that can provide a viewpoint that will improve our essential understanding of biological regulations in the new era of life sciences. Such a theory is not only crucial in academia but also necessary for accurate assessment and effective treatment of dynamically changing disease states. It should provide essential information for practical clinical treatment towards next-generation healthcare.One of the salient features of biological control systems, compared to man-made ones, is their ability to change their structures and/or functions to match the situation. This plasticity enables biological organisms to adapt to almost any environmental change and to take appropriate actions. Plasticity appears, depending on the time scale, as evolution, differentiation, or learning. Whereas man-made systems use specific regulatory mechanisms corresponding to the environmental change, biological systems, with their limited resources, have to exhibit a broad range of flexible actions with one regulatory mechanism in response to a wide variety of environmental changes. The proposed research focuses on this characteristic and aims to reveal the essential elements of biological control across different levels that attain such plasticity by developing a mathematical theory that can explain the underlying mechanisms of biological control. In particular, I will pursue the underlying regulatory mechanisms from the viewpoint of compound control, the basic idea of which is that complex biological regulations result from spatial and temporal combinations of simple homogeneous computational media, such as interactions among different molecules for cellular control and neuron firings for cerebral control, corresponding to various compound environmental changes. I will focus on the development of a theoretical basis for biological control at the cellular level first and then that in immune systems, which use both cellular- and physiological-level controls. The basic studies at the cellular level on genetic and metabolic systems, together with applied studies on immune systems, both based on the idea of compound control, should reveal the essential design principles of biological control systems.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1098/rsta.2016.0285
发表时间: 2017-06-28
期刊: Philosophical transactions. Series A, Mathematical, physical, and engineering sciences
影响因子: --
作者: [Christodoulides P, Hirata Y, Domínguez-Hüttinger E, Danby SG, Cork MJ, Williams HC, Aihara K, Tanaka RJ]
通讯作者: Tanaka RJ
DOI: 10.3389/fphys.2017.00115
发表时间: 2017
期刊: Frontiers in physiology
影响因子: 4
作者: [Domínguez-Hüttinger E, Boon NJ, Clarke TB, Tanaka RJ]
通讯作者: Tanaka RJ
DOI: 10.1098/rsfs.2012.0090
发表时间: 2013-04-06
期刊: Interface focus
影响因子: 4.4
作者: [Domínguez-Hüttinger E, Ono M, Barahona M, Tanaka RJ]
通讯作者: Tanaka RJ
Model Predictive Control for Designing Proactive Therapy of Atopic Dermatitis
设计特应性皮炎主动治疗的模型预测控制
DOI: 10.23919/ecc.2018.8550380
发表时间: 2018
期刊:
影响因子: --
作者: [Giannari A]
通讯作者: Giannari A
国内基金
海外基金
Exploring the Intrinsic Mechanisms of CEO Turnover and Market
  • 批准号:
    --
  • 项目类别:
    外国学者研究基金
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    HAOFEI Z
  • 依托单位:
Exploring the Intrinsic Mechanisms of CEO Turnover and Market Reaction: An Explanation Based on Information Asymmetry
  • 批准号:
    W2433169
  • 项目类别:
    外国学者研究基金项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    HAOFEI ZHANG
  • 依托单位:
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  • 批准号:
    82371255
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    曹立
  • 依托单位:
Foxc2介导Syap1/Akt信号通路调控破骨/成骨细胞分化促进颞下颌关节骨关节炎的机制研究
  • 批准号:
    82370979
  • 项目类别:
    面上项目
  • 资助金额:
    48.00万元
  • 批准年份:
    2023
  • 负责人:
    张善勇
  • 依托单位: