Network Crosstalk Dynamically Changes during Neutrophil Polarization

被引:42
作者
Ku, Chin-Jen [1 ]
Wang, Yanqin [1 ]
Weiner, Orion D. [2 ,3 ]
Altschuler, Steven J. [1 ]
Wu, Lani F. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Pharmacol, Green Ctr Syst Biol, Simmons Canc Ctr, Dallas, TX 75390 USA
[2] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Dept Biochem, San Francisco, CA 94158 USA
关键词
RHOA ACTIVITY; POLARITY; MICROTUBULES; CHEMOTAXIS; ACTIVATION; TALK; ADAPTATION; FEEDBACK; CALCIUM; SIGNALS;
D O I
10.1016/j.cell.2012.03.044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
How complex signaling networks shape highly coordinated, multistep cellular responses is poorly understood. Here, we made use of a network-perturbation approach to investigate causal influences, or "crosstalk,'' among signaling modules involved in the cytoskeletal response of neutrophils to chemoattractant. We quantified the intensity and polarity of cytoskeletal marker proteins over time to characterize stereotyped cellular responses. Analyzing the effects of network disruptions revealed that, not only does crosstalk evolve rapidly during polarization, but also that intensity and polarity responses are influenced by different patterns of crosstalk. Interestingly, persistent crosstalk is arranged in a surprisingly simple circuit: a linear cascade from front to back to microtubules influences intensities, and a feed-forward network in the reverse direction influences polarity. Our approach provided a rational strategy for decomposing a complex, dynamically evolving signaling system and revealed evolving paths of causal influence that shape the neutrophil polarization response.
引用
收藏
页码:1073 / 1083
页数:11
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