共 85 条
Understanding the temporal codes of intra-cellular signals
被引:130
作者:

Behar, Marcelo
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机构: Univ Calif San Diego, Signaling Syst Lab, BioCircuits Inst, La Jolla, CA 92093 USA

Hoffmann, Alexander
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机构:
Univ Calif San Diego, Signaling Syst Lab, BioCircuits Inst, La Jolla, CA 92093 USA Univ Calif San Diego, Signaling Syst Lab, BioCircuits Inst, La Jolla, CA 92093 USA
机构:
[1] Univ Calif San Diego, Signaling Syst Lab, BioCircuits Inst, La Jolla, CA 92093 USA
关键词:
NF-KAPPA-B;
GONADOTROPIN-RELEASING-HORMONE;
EARLY GENE-PRODUCTS;
CALCIUM OSCILLATIONS;
DIFFERENTIAL REGULATION;
FEEDBACK INHIBITION;
FUNCTIONAL MODULES;
CYTOSOLIC CALCIUM;
C-FOS;
SPECIFICITY;
D O I:
10.1016/j.gde.2010.09.007
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The health of organisms and cells depends on appropriate responses to diverse internal and external cues, stimuli, or challenges, such as changes in hormone or cytokine levels, or exposure to a pathogen. Cellular responses must be tailored to the identity and intensity of the stimulus and therefore intracellular signals must carry information about both. However, signaling mediators often form intricate networks that react to multiple stimuli yet manage to produce stimulus-specific responses. The multi-functionality ('functional pleiotropism') of signaling nodes suggests that biological networks have evolved ways of passing physiologically relevant stimulus information through shared channels. Increasing evidence supports the notion that this is achieved in part through temporal regulation of signaling mediators' activities. The present challenge is to identify the features of temporal activity profile that represent information about a given stimulus and understand how cells read the temporal codes to control their responses.
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页码:684 / 693
页数:10
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