Actin cytoskeleton: Regulation through protein interactions and epigenetic re-programming
肌动蛋白细胞骨架:通过蛋白质相互作用和表观遗传重编程进行调节
基本信息
- 批准号:RGPIN-2020-05388
- 负责人:
- 金额:$ 3.64万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Discovery Grants Program - Individual
- 财政年份:2021
- 资助国家:加拿大
- 起止时间:2021-01-01 至 2022-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The shape of each cell in the human body is determined by an internal structure called the cytoskeleton, which is a network of interconnected proteins that provides a "load-bearing" structure that enables movement and provides protection from potentially damaging external forces. Two of the most important cytoskeleton proteins are actin and myosin. Individual actin molecules can be joined together to form long fibres. Myosin is a large protein complex, composed of 2 heavy chains, 2 essential light chains and 2 regulatory light chains. Actin fibres and myosin complexes bind to each other, and when myosin is activated it pulls on the actin fibres they are bound to, shortening the length of actin-myosin fibres and leading to tension in the cytoskeleton network. Since the cytoskeleton is responsible for protecting cells from damaging external forces, it is important for cells to adjust the physical strength of their cytoskeleton to adapt to changing environments. An important way that cells reinforce their cytoskeleton is to activate the myosin complex to shrink the length of actin-myosin fibres. This actin-myosin fibre shortening produces cytoskeleton tension that makes cells physically stiffer. In addition to myosin activation, there may be changes in the collection of proteins that are associated with the cytoskeleton. In this proposal, we will identify the proteins that are part of the cytoskeleton when it is relaxed, and discover how the collection of associated proteins changes when the cytoskeleton becomes tense. If the environment undergoes long term changes in how it exerts pressure on cells, cells may compensate by rapidly changing how specific genes are expressed, and even by modifying their DNA to alter the long-term expression of genes that contribute to the cytoskeleton's physical strength. In this proposal, we will determine if cells "re-wire" their DNA to change gene expression patterns if cytoskeleton tension is prolonged, and we will identify the cytoskeleton-related genes that are expressed differently as a result of these DNA alterations. The experiments in this proposal will be the first to systematically examine how the complex of proteins in the cytoskeleton changes between the relaxed and contracted states, and how sustained cytoskeleton contraction alters the expression of genes encoding for proteins related to cytoskeleton organization and function. The proposed research will benefit Canadians by: 1) Leading to novel discoveries in cell biology and cytoskeleton regulation that will enhance Canada's scientific reputation and innovation potential; 2) Training of highly-qualified personnel to expand their career perspectives and increase future employability in academic or industrial biomedical research so that they may contribute to Canada's knowledge economy; 3) Development of novel multi-disciplinary approaches and generation of unique biological research tools that will be shared with the Canadian research community.
人体中每个细胞的形状由称为细胞骨架的内部结构决定,细胞骨架是一种相互连接的蛋白质网络,它提供了一种“承重”结构,使运动成为可能,并提供保护,免受潜在的破坏性外力的影响。两种最重要的细胞骨架蛋白是肌动蛋白和肌球蛋白。单个肌动蛋白分子可以连接在一起形成长纤维。肌球蛋白是一种大型蛋白质复合物,由2条重链、2条必需轻链和2条调节轻链组成。肌动蛋白纤维和肌球蛋白复合物相互结合,当肌球蛋白被激活时,它会拉动它们所结合的肌动蛋白纤维,缩短肌动蛋白-肌球蛋白纤维的长度,并导致细胞骨架网络的张力。由于细胞骨架负责保护细胞免受破坏性外力的影响,因此细胞调整其细胞骨架的物理强度以适应不断变化的环境非常重要。细胞强化其细胞骨架的一个重要方式是激活肌球蛋白复合物以缩短肌动蛋白-肌球蛋白纤维的长度。这种肌动蛋白-肌球蛋白纤维缩短产生细胞骨架张力,使细胞物理上更僵硬。除了肌球蛋白活化,与细胞骨架相关的蛋白质集合也可能发生变化。在这个提议中,我们将确定当细胞骨架放松时作为细胞骨架一部分的蛋白质,并发现当细胞骨架变得紧张时相关蛋白质的集合如何变化。如果环境对细胞施加压力的方式发生长期变化,细胞可能会通过快速改变特定基因的表达方式来补偿,甚至通过修改它们的DNA来改变有助于细胞骨架物理强度的基因的长期表达。在这个提议中,我们将确定如果细胞骨架张力延长,细胞是否会“重新连接”它们的DNA以改变基因表达模式,并且我们将鉴定由于这些DNA改变而表达不同的细胞因子相关基因。该提案中的实验将首次系统地研究细胞骨架中的蛋白质复合物如何在松弛和收缩状态之间变化,以及持续的细胞骨架收缩如何改变编码与细胞骨架组织和功能相关的蛋白质的基因表达。拟议的研究将使加拿大人受益:(1)导致细胞生物学和细胞骨架调节方面的新发现,这将提高加拿大的科学声誉和创新潜力;(2)培训高素质的人员,以扩大他们的职业前景,提高他们未来在学术或工业生物医学研究中的就业能力,使他们能够为加拿大的知识经济做出贡献; 3)开发新的多学科方法,并产生独特的生物研究工具,将与加拿大研究界分享。
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Olson, Michael其他文献
Flexion-relaxation response to gravity
- DOI:
10.1016/j.jbiomech.2005.09.009 - 发表时间:
2006-01-01 - 期刊:
- 影响因子:2.4
- 作者:
Olson, Michael;Solomonow, Moshe;Li, Li - 通讯作者:
Li, Li
Succeeding in Rural Mental Health Practice: Being Sensitive to Culture by Fitting in and Collaborating
- DOI:
10.1007/s10591-013-9287-x - 发表时间:
2014-03-01 - 期刊:
- 影响因子:1.3
- 作者:
Bischoff, Richard J.;Reisbig, Allison M. J.;Olson, Michael - 通讯作者:
Olson, Michael
Genomic Study on Blood Culture Isolates From Patients With Staphylococcus Infection-associated Glomerulonephritis.
- DOI:
10.1016/j.ekir.2022.07.010 - 发表时间:
2022-10 - 期刊:
- 影响因子:6
- 作者:
Rana, Pranav S. J. B.;Aljabban, Jihad;Prarat, Melanie;Pancholi, Preeti;Balada-Llasat, Joan Miquel;Stephens, Julie;Webb, Amy;Chen, Liang;Brodsky, Sergey, V;Nadasdy, Tibor;Zhang, Yan;Parikh, Samir, V;Wozniak, Daniel J.;Wang, Shu-Hua;Olson, Michael;Satoskar, Anjali A. - 通讯作者:
Satoskar, Anjali A.
On the relationship between automatic attitudes and self-reported sexual assault in men.
- DOI:
10.1007/s10508-012-9970-2 - 发表时间:
2013-07 - 期刊:
- 影响因子:3.8
- 作者:
Widman, Laura;Olson, Michael - 通讯作者:
Olson, Michael
Olson, Michael的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Olson, Michael', 18)}}的其他基金
Actin cytoskeleton: Regulation through protein interactions and epigenetic re-programming
肌动蛋白细胞骨架:通过蛋白质相互作用和表观遗传重编程进行调节
- 批准号:
RGPIN-2020-05388 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别:
Discovery Grants Program - Individual
Actin cytoskeleton: Regulation through protein interactions and epigenetic re-programming
肌动蛋白细胞骨架:通过蛋白质相互作用和表观遗传重编程进行调节
- 批准号:
RGPIN-2020-05388 - 财政年份:2020
- 资助金额:
$ 3.64万 - 项目类别:
Discovery Grants Program - Individual
embedded systems
嵌入式系统
- 批准号:
529724-2018 - 财政年份:2018
- 资助金额:
$ 3.64万 - 项目类别:
Experience Awards (previously Industrial Undergraduate Student Research Awards)
Reinforcement Pulps & Pulp and Paper Products
增强纸浆
- 批准号:
468917-2014 - 财政年份:2014
- 资助金额:
$ 3.64万 - 项目类别:
Experience Awards (previously Industrial Undergraduate Student Research Awards)
相似国自然基金
Piezo1/Cytoskeleton介导的YAP核易位在4D仿生骨膜修复骨缺损中的作用及机制研究
- 批准号:
- 批准年份:2022
- 资助金额:30 万元
- 项目类别:青年科学基金项目
胚体类器官研究Wnt-PCP通路介导基底膜定向分泌与运输的分子机制
- 批准号:32000553
- 批准年份:2020
- 资助金额:24.0 万元
- 项目类别:青年科学基金项目
上皮层形态发生过程中远程机械力传导的分子作用机制
- 批准号:31900563
- 批准年份:2019
- 资助金额:26.0 万元
- 项目类别:青年科学基金项目
Dysbindin蛋白通过PI3K-AKT-Ezrin通路诱导胰腺癌单细胞极性促进远处转移定植的作用及其机制研究
- 批准号:31900566
- 批准年份:2019
- 资助金额:26.0 万元
- 项目类别:青年科学基金项目
泛素连接酶TRIM65通过RhoGAP调控Rho活性促进结直肠癌侵袭转移的分子机制
- 批准号:31970703
- 批准年份:2019
- 资助金额:50.0 万元
- 项目类别:面上项目
细胞迁移受体蛋白MIG-13/LRP12区域性活化的机制研究
- 批准号:31900535
- 批准年份:2019
- 资助金额:15.0 万元
- 项目类别:青年科学基金项目
ALG-2调控纤毛发生的分子机制研究
- 批准号:31900538
- 批准年份:2019
- 资助金额:25.0 万元
- 项目类别:青年科学基金项目
EB1的翻译后修饰对细胞行为的影响
- 批准号:31771542
- 批准年份:2017
- 资助金额:61.0 万元
- 项目类别:面上项目
HDAC6调控巨噬细胞和中性粒细胞向炎症部位浸润的分子机理研究
- 批准号:31701216
- 批准年份:2017
- 资助金额:25.0 万元
- 项目类别:青年科学基金项目
PEAK1通过FAK-CTTN-Arp2/3信号调控细胞迁移的分子机制研究
- 批准号:31701218
- 批准年份:2017
- 资助金额:25.0 万元
- 项目类别:青年科学基金项目
相似海外基金
Regulation of GluN2B-NMDA Receptors by Interactions with the Actin Cytoskeleton
通过与肌动蛋白细胞骨架相互作用调节 GluN2B-NMDA 受体
- 批准号:
10606121 - 财政年份:2023
- 资助金额:
$ 3.64万 - 项目类别:
Actin Regulation of Dendritic Spine Development and Plasticity
树突棘发育和可塑性的肌动蛋白调节
- 批准号:
10608784 - 财政年份:2023
- 资助金额:
$ 3.64万 - 项目类别:
Regulation of structural plasticity and actin cytoskeleton by plasma membrane cholesterol turnover in dendritic spines
树突棘质膜胆固醇周转对结构可塑性和肌动蛋白细胞骨架的调节
- 批准号:
RGPIN-2018-05562 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别:
Discovery Grants Program - Individual
Regulation of dynamic actin networks during epithelial morphogenesis
上皮形态发生过程中动态肌动蛋白网络的调节
- 批准号:
10617348 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别:
Mechanisms of regulation of lymphocyte migration by actin cytoskeletal effectors
肌动蛋白细胞骨架效应器调节淋巴细胞迁移的机制
- 批准号:
10709904 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别:
Actin cytoskeleton: Regulation through protein interactions and epigenetic re-programming
肌动蛋白细胞骨架:通过蛋白质相互作用和表观遗传重编程进行调节
- 批准号:
RGPIN-2020-05388 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别:
Discovery Grants Program - Individual
Regulation of dynamic actin networks during epithelial morphogenesis
上皮形态发生过程中动态肌动蛋白网络的调节
- 批准号:
10797655 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别:
Mechanisms of regulation of lymphocyte migration by actin cytoskeletal effectors
肌动蛋白细胞骨架效应器调节淋巴细胞迁移的机制
- 批准号:
10583309 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别:
Regulation of the adaptive actin response by force-dependent bonds
通过力依赖性键调节适应性肌动蛋白反应
- 批准号:
10537442 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别:
Regulation of the adaptive actin response by force-dependent bonds
通过力依赖性键调节适应性肌动蛋白反应
- 批准号:
10689699 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别: