Interrogating endothelial barrier regulation by temporally resolved kinase network generation

• Published in: Life science alliance 2024-05, Vol.7 (5), p.e202302522
• Main Authors: Wei, Ling, Dankwa, Selasi, Vijayan, Kamalakannan, Smith, Joseph D, Kaushansky, Alexis
• Format: Article
• Language: English
• Subjects: Endothelial Cells - metabolism; Mitogen-Activated Protein Kinase 14; p38 Mitogen-Activated Protein Kinases - metabolism; Protein Kinase Inhibitors; Thrombin - pharmacology
• ISSN: 2575-1077; 2575-1077
• DOI: 10.26508/lsa.202302522

Kinases are key players in endothelial barrier regulation, yet their temporal function and regulatory phosphosignaling networks are incompletely understood. We developed a novel methodology, Temporally REsolved KInase Network Generation (TREKING), which combines a 28-kinase inhibitor screen with machine learning and network reconstruction to build time-resolved, functional phosphosignaling networks. We demonstrated the utility of TREKING for identifying pathways mediating barrier integrity after activation by thrombin with or without TNF preconditioning in brain endothelial cells. TREKING predicted over 100 kinases involved in barrier regulation and discerned complex condition-specific pathways. For instance, the MAPK-activated protein kinase 2 (MAPKAPK2/MK2) had early barrier-weakening activity in both inflammatory conditions but late barrier-strengthening activity exclusively with thrombin alone. Using temporal Western blotting, we confirmed that MAPKAPK2/MK2 was differentially phosphorylated under the two inflammatory conditions. We further showed with lentivirus-mediated knockdown of MAPK14/p38α and drug targeting the MAPK14/p38α-MAPKAPK2/MK2 complex that a MAP3K20/ZAK-MAPK14/p38α axis controlled the late activation of MAPKAPK2/MK2 in the thrombin-alone condition. Beyond the MAPKAPK2/MK2 switch, TREKING predicts extensive interconnected networks that control endothelial barrier dynamics.