Context-specific network modeling identifies new crosstalk in [beta]-adrenergic cardiac hypertrophy
Cardiac hypertrophy is a context-dependent phenomenon wherein a myriad of biochemical and biomechanical factors regulate myocardial growth through a complex large-scale signaling network. Although numerous studies have investigated hypertrophic signaling pathways, less is known about hypertrophy sig...
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description | Cardiac hypertrophy is a context-dependent phenomenon wherein a myriad of biochemical and biomechanical factors regulate myocardial growth through a complex large-scale signaling network. Although numerous studies have investigated hypertrophic signaling pathways, less is known about hypertrophy signaling as a whole network and how this network acts in a context-dependent manner. Here, we developed a systematic approach, CLASSED (Context-specific Logic-bASed Signaling nEtwork Development), to revise a large-scale signaling model based on context-specific data and identify main reactions and new crosstalks regulating context-specific response. CLASSED involves four sequential stages with an automated validation module as a core which builds a logic-based ODE model from the interaction graph and outputs the model validation percent. The context-specific model is developed by estimation of default parameters, classified qualitative validation, hybrid Morris-Sobol global sensitivity analysis, and discovery of missing context-dependent crosstalks. Applying this pipeline to our prior-knowledge hypertrophy network with context-specific data revealed key signaling reactions which distinctly regulate cell response to isoproterenol, phenylephrine, angiotensin II and stretch. Furthermore, with CLASSED we developed a context-specific model of [beta]-adrenergic cardiac hypertrophy. The model predicted new crosstalks between calcium/calmodulin-dependent pathways and upstream signaling of Ras in the ISO-specific context. Experiments in cardiomyocytes validated the model's predictions on the role of CaMKII-G[beta][gamma] and CaN-G[beta][gamma] interactions in mediating hypertrophic signals in ISO-specific context and revealed a difference in the phosphorylation magnitude and translocation of ERK1/2 between cardiac myocytes and fibroblasts. CLASSED is a systematic approach for developing context-specific large-scale signaling networks, yielding insights into new-found crosstalks in [beta]-adrenergic cardiac hypertrophy. |
doi_str_mv | 10.1371/journal.pcbi.1008490 |
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M ; Saucerman, Jeffrey J</creator><creatorcontrib>Khalilimeybodi, Ali ; Paap, Alexander M ; Christiansen, Steven L. M ; Saucerman, Jeffrey J</creatorcontrib><description>Cardiac hypertrophy is a context-dependent phenomenon wherein a myriad of biochemical and biomechanical factors regulate myocardial growth through a complex large-scale signaling network. Although numerous studies have investigated hypertrophic signaling pathways, less is known about hypertrophy signaling as a whole network and how this network acts in a context-dependent manner. Here, we developed a systematic approach, CLASSED (Context-specific Logic-bASed Signaling nEtwork Development), to revise a large-scale signaling model based on context-specific data and identify main reactions and new crosstalks regulating context-specific response. CLASSED involves four sequential stages with an automated validation module as a core which builds a logic-based ODE model from the interaction graph and outputs the model validation percent. The context-specific model is developed by estimation of default parameters, classified qualitative validation, hybrid Morris-Sobol global sensitivity analysis, and discovery of missing context-dependent crosstalks. Applying this pipeline to our prior-knowledge hypertrophy network with context-specific data revealed key signaling reactions which distinctly regulate cell response to isoproterenol, phenylephrine, angiotensin II and stretch. Furthermore, with CLASSED we developed a context-specific model of [beta]-adrenergic cardiac hypertrophy. The model predicted new crosstalks between calcium/calmodulin-dependent pathways and upstream signaling of Ras in the ISO-specific context. Experiments in cardiomyocytes validated the model's predictions on the role of CaMKII-G[beta][gamma] and CaN-G[beta][gamma] interactions in mediating hypertrophic signals in ISO-specific context and revealed a difference in the phosphorylation magnitude and translocation of ERK1/2 between cardiac myocytes and fibroblasts. CLASSED is a systematic approach for developing context-specific large-scale signaling networks, yielding insights into new-found crosstalks in [beta]-adrenergic cardiac hypertrophy.</description><identifier>ISSN: 1553-734X</identifier><identifier>EISSN: 1553-7358</identifier><identifier>DOI: 10.1371/journal.pcbi.1008490</identifier><language>eng</language><publisher>Public Library of Science</publisher><subject>Cellular signal transduction ; Computational biology ; Context switching ; Heart enlargement ; Identification and classification ; Methods</subject><ispartof>PLoS computational biology, 2020-12, Vol.16 (12)</ispartof><rights>COPYRIGHT 2020 Public Library of Science</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,865,27929,27930</link.rule.ids></links><search><creatorcontrib>Khalilimeybodi, Ali</creatorcontrib><creatorcontrib>Paap, Alexander M</creatorcontrib><creatorcontrib>Christiansen, Steven L. 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CLASSED involves four sequential stages with an automated validation module as a core which builds a logic-based ODE model from the interaction graph and outputs the model validation percent. The context-specific model is developed by estimation of default parameters, classified qualitative validation, hybrid Morris-Sobol global sensitivity analysis, and discovery of missing context-dependent crosstalks. Applying this pipeline to our prior-knowledge hypertrophy network with context-specific data revealed key signaling reactions which distinctly regulate cell response to isoproterenol, phenylephrine, angiotensin II and stretch. Furthermore, with CLASSED we developed a context-specific model of [beta]-adrenergic cardiac hypertrophy. The model predicted new crosstalks between calcium/calmodulin-dependent pathways and upstream signaling of Ras in the ISO-specific context. Experiments in cardiomyocytes validated the model's predictions on the role of CaMKII-G[beta][gamma] and CaN-G[beta][gamma] interactions in mediating hypertrophic signals in ISO-specific context and revealed a difference in the phosphorylation magnitude and translocation of ERK1/2 between cardiac myocytes and fibroblasts. CLASSED is a systematic approach for developing context-specific large-scale signaling networks, yielding insights into new-found crosstalks in [beta]-adrenergic cardiac hypertrophy.</description><subject>Cellular signal transduction</subject><subject>Computational biology</subject><subject>Context switching</subject><subject>Heart enlargement</subject><subject>Identification and classification</subject><subject>Methods</subject><issn>1553-734X</issn><issn>1553-7358</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqVkEtLw0AQx4MoWKvfwEPAk4fE3e4jyVGKj0JR8AGCSNnHJN023S27W2q_vSkVseBF5jDD_H-_OUySnGOUY1Lgq5lbeSvafKmkyTFCJa3QQdLDjJGsIKw8_Jnp23FyEsIMoW5d8V6ihs5G-IxZWIIytVGphbh2fp4unIbW2CY1GmzsIghdtk6VdyFE0c5TY9N3CVF8ZEJ7sOCbTlfCayNUOt0swUfvltPNaXJUizbA2XfvJ6-3Ny_D-2z8eDcaXo-zBhPGMyK1YnVBJa0opwoPCskrAKJqgsmASap1KTmmDArOBSskQ1tBI0SFGkhO-snF7m4jWpgYW7vohVqYoCbXnKES07LYUvkfVFcaFkY5C7Xp9nvC5Z6gdh9rxCqEyej56R_sw2_2C6xth4s</recordid><startdate>20201218</startdate><enddate>20201218</enddate><creator>Khalilimeybodi, Ali</creator><creator>Paap, Alexander M</creator><creator>Christiansen, Steven L. 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Although numerous studies have investigated hypertrophic signaling pathways, less is known about hypertrophy signaling as a whole network and how this network acts in a context-dependent manner. Here, we developed a systematic approach, CLASSED (Context-specific Logic-bASed Signaling nEtwork Development), to revise a large-scale signaling model based on context-specific data and identify main reactions and new crosstalks regulating context-specific response. CLASSED involves four sequential stages with an automated validation module as a core which builds a logic-based ODE model from the interaction graph and outputs the model validation percent. The context-specific model is developed by estimation of default parameters, classified qualitative validation, hybrid Morris-Sobol global sensitivity analysis, and discovery of missing context-dependent crosstalks. Applying this pipeline to our prior-knowledge hypertrophy network with context-specific data revealed key signaling reactions which distinctly regulate cell response to isoproterenol, phenylephrine, angiotensin II and stretch. Furthermore, with CLASSED we developed a context-specific model of [beta]-adrenergic cardiac hypertrophy. The model predicted new crosstalks between calcium/calmodulin-dependent pathways and upstream signaling of Ras in the ISO-specific context. Experiments in cardiomyocytes validated the model's predictions on the role of CaMKII-G[beta][gamma] and CaN-G[beta][gamma] interactions in mediating hypertrophic signals in ISO-specific context and revealed a difference in the phosphorylation magnitude and translocation of ERK1/2 between cardiac myocytes and fibroblasts. CLASSED is a systematic approach for developing context-specific large-scale signaling networks, yielding insights into new-found crosstalks in [beta]-adrenergic cardiac hypertrophy.</abstract><pub>Public Library of Science</pub><doi>10.1371/journal.pcbi.1008490</doi></addata></record> |
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subjects | Cellular signal transduction Computational biology Context switching Heart enlargement Identification and classification Methods |
title | Context-specific network modeling identifies new crosstalk in [beta]-adrenergic cardiac hypertrophy |
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