On the emergence of polarization and motility responses from chemotactic networks
On the emergence of polarization and motility responses from chemotactic networks
批准号:
8848168
负责人:
STEVEN J ALTSCHULER
金额:
$30.18万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-07-01 至 2015-05-31
中文摘要
描述(由申请人提供):许多真核细胞类型可以响应于化学引诱物的外部梯度而增殖。建立指向精确方向的内部指南针的能力对于酵母细胞交配,轴突在发育中的神经系统中找到方向以及先天免疫系统中的细胞找到并杀死入侵病原体至关重要。细胞迁移的失调与人类疾病如动脉粥样硬化和癌症转移密切相关。了解生物网络如何动态控制趋化反应是在病理条件下开发有针对性的干预措施的关键一步。中性粒细胞趋化网络中的许多成分和相互作用已经被确定。然而,目前还不知道如何从这些网络的详细分子描述中出现趋化性的基本属性。我们的长期目标是了解:1)信号网络如何产生动态极化反应; 2)极性的哪些特性对于指导有效的运动至关重要; 3)在不同的运动细胞中采用哪些一般机制来调节精确和有效的运动。在这里,我们建议研究如何动态极化和运动反应产生的信号网络在人类中性粒细胞。我们的具体目标是:1.确定控制极化动力学的趋化性网络内的相互作用; 2.模拟极化过程;以及3.确定指导有效运动所需的关键极性表型。
英文摘要
DESCRIPTION (provided by applicant): Many eukaryotic cell types can polarize in response to an external gradient of chemoattractant. The ability to establish an internal compass that points in a precise direction is essential for yeast cells to mate, axons to find their way in the developing nervous system, and cells in the innate immune system to find and kill invading pathogens. Misregulation of cell migration is intimately involved in human disease, such as atherosclerosis and cancer metastasis. Understanding how biological networks dynamically control chemotactic responses is a key step towards developing targeted interventions in pathological conditions. Many of the components and interactions within neutrophil chemotaxis networks have been identified. However, it is not known how basic properties of chemotaxis emerge from detailed molecular descriptions of these networks. Our long term goals are to understand: 1) how dynamic polarization responses are generated by signaling networks; 2) which properties of polarity are essential for guiding efficient motility; 3) what general mechanisms are employed in diverse motile cells to regulate precise and efficient motility. Here, we propose to study how dynamic polarization and motility responses are generated by signaling networks in human neutrophils. Our specific aims are to: 1. Identify interactions within the chemotaxis network that control polarization dynamics; 2. Model the polarization process; and 3. Identify key polarity phenotypes that are required for guiding efficient motility.
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Rapid analysis and exploration of fluorescence microscopy images.
荧光显微镜图像的快速分析和探索。
DOI:
10.3791/51280
发表时间:
2014
期刊:
Journal of visualized experiments : JoVE
影响因子:
--
作者:
[Pavie,Benjamin, Rajaram,Satwik, Ouyang,Austin, Altschuler,JasonM, Steininger3rd,RobertJ, Wu,LaniF, Altschuler,StevenJ]
通讯作者:
Altschuler,StevenJ
Envisioning migration: mathematics in both experimental analysis and modeling of cell behavior.
设想迁移:实验分析和细胞行为建模中的数学。
DOI:
10.1016/j.ceb.2013.04.004
发表时间:
2013
期刊:
Current opinion in cell biology
影响因子:
7.5
作者:
[Zhang,ElizabethR, Wu,LaniF, Altschuler,StevenJ]
通讯作者:
Altschuler,StevenJ
DOI:
10.1038/nature07119
发表时间:
2008-08-14
期刊:
NATURE
影响因子:
64.8
作者:
[Altschuler, Steven J., Angenent, Sigurd B., Wang, Yanqin, Wu, Lani F.]
通讯作者:
Wu, Lani F.
Identifying network motifs that buffer front-to-back signaling in polarized neutrophils.
识别缓冲极化中性粒细胞中前后信号传导的网络基序。
DOI:
10.1016/j.celrep.2013.04.009
发表时间:
2013
期刊:
Cell reports
影响因子:
8.8
作者:
[Wang,Yanqin, Ku,Chin-Jen, Zhang,ElizabethR, Artyukhin,AlexanderB, Weiner,OrionD, Wu,LaniF, Altschuler,StevenJ]
通讯作者:
Altschuler,StevenJ
DOI:
10.1109/isbi.2010.5490165
发表时间:
2010-04-01
期刊:
Proceedings. IEEE International Symposium on Biomedical Imaging
影响因子:
--
作者:
[Ku CJ, Wang Y, Pavie B, Altschuler SJ, Wu LF]
通讯作者:
Wu LF
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