Nature Communications · 2014 · 69 citations · 61 references
Life SciencesCardiologyPhysiologyCell SignalingMolecular PhysiologySignal TransductionApoptosis RegulationBcl-2 Family ProteinsCell Signaling NetworksReceptor RegulationSignal Transduction ModelingSignal Transduction PathwaysAdrenergic Receptor AgonistsAdrenergic Receptor SignalingBcl-2 Protein ExpressionBeta-adrenergic AgentsCell Death Signaling PathwaysCell Fate ConversionCell Fate DecisionsFeed-forward Loops
How cell fate (survival or death) is determined and whether such determination depends on the strength of stimulation has remained unclear. In this study, we discover that the cell fate of cardiomyocytes switches from survival to death with the increase of β-adrenergic receptor (β-AR) stimulation. Mathematical simulations combined with biochemical experimentation of β-AR signalling pathways show that the gradual increment of isoproterenol (a non-selective β1/β2-AR agonist) induces the switching response of Bcl-2 expression from the initial increase followed by a decrease below its basal level. The ERK1/2 and ICER-mediated feed-forward loop is the hidden design principle underlying such cell fate switching characteristics. Moreover, we find that β1-blocker treatment increases the survival effect of β-AR stimuli through the regulation of Bcl-2 expression leading to the resistance to cell death, providing new insight into the mechanism of therapeutic effects. Our systems analysis further suggests a novel potential therapeutic strategy for heart disease.
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L. F. Shampine, Mark W. Reichelt · SIAM Journal on Scientific Computing · 1997 · 3.6K citations · Full text
Natural Sciences, Computer Science, Differential Equations +9
Bcl-2 Antiapoptotic Proteins Inhibit Beclin 1-Dependent Autophagy
Sophie Pattingre, Amina Tassa, Xueping Qu et al. · Cell · 2005 · 3.5K citations · Full text