Title : NOX4 mediates BMP4-induced upregulation of TRPC1 and 6 protein expressions in distal pulmonary arterial smooth muscle cells.

Pub. Date : 2014

PMID : 25203114






4 Functional Relationships(s)
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1 Moreover, external ROS (H2O2 100 microM, 24 h) rescued the effects of NOX4 knockdown, which included the declining of TRPC1 and 6 expression, basal intracellular calcium concentration ([Ca2+]i) and store-operated calcium entry (SOCE), suggesting that NOX4 plays as an important mediator in BMP4-induced proliferation and intracellular calcium homeostasis. Reactive Oxygen Species bone morphogenetic protein 4 Rattus norvegicus
2 Moreover, external ROS (H2O2 100 microM, 24 h) rescued the effects of NOX4 knockdown, which included the declining of TRPC1 and 6 expression, basal intracellular calcium concentration ([Ca2+]i) and store-operated calcium entry (SOCE), suggesting that NOX4 plays as an important mediator in BMP4-induced proliferation and intracellular calcium homeostasis. Hydrogen Peroxide bone morphogenetic protein 4 Rattus norvegicus
3 CONCLUSION: These results suggest that BMP4 may increase ROS level, enhance TRPC1 and 6 expression and proliferation by up-regulating NOX4 expression in PASMCs. Reactive Oxygen Species bone morphogenetic protein 4 Rattus norvegicus
4 CONCLUSION: These results suggest that BMP4 may increase ROS level, enhance TRPC1 and 6 expression and proliferation by up-regulating NOX4 expression in PASMCs. pasmcs bone morphogenetic protein 4 Rattus norvegicus