Artículos de revistas
Filamin a expression negatively regulates Sphingosine-1-phosphate-induced NF-κB activation in melanoma cells by inhibition o Akt signaling
Fecha
2015-11Registro en:
Campos, Ludmila Estefanía; Rodriguez, Yamila Isabel; Machado Leopoldino, Andreia; Hait, Nitai C.; Lopez Bergami, Pablo Roberto; et al.; Filamin a expression negatively regulates Sphingosine-1-phosphate-induced NF-κB activation in melanoma cells by inhibition o Akt signaling; American Society for Microbiology; Molecular and Cellular Biology; 36; 2; 11-2015; 320-329
0270-7306
Autor
Campos, Ludmila Estefanía
Rodriguez, Yamila Isabel
Machado Leopoldino, Andreia
Hait, Nitai C.
Lopez Bergami, Pablo Roberto
Castro, Melina Gabriela
Sanchez, Emilse Silvina
Maceyka, Michael
Spiegel, Sarah
Alvarez, Sergio Eduardo
Resumen
Sphingosine-1-phosphate (S1P) is a bioactive lipid mediator that regulates many processes in inflammation and cancer. S1P is a ligand for five G-protein-coupled receptors, S1PR1 to -5, and also has important intracellular actions. Previously, we showed that intracellular S1P is involved in tumor necrosis factor alpha (TNF)-induced NF-κB activation in melanoma cell lines that express filamin A (FLNA). Here, we show that extracellular S1P activates NF-κB only in melanoma cells that lack FLNA. In these cells, S1P, but not TNF, promotes IκB kinase (IKK) and p65 phosphorylation, IκBα degradation, p65 nuclear translocation, and NF-κB reporter activity. NF-κB activation induced by S1P was mediated via S1PR1 and S1PR2. Exogenous S1P enhanced the phosphorylation of protein kinase Cδ (PKCδ), and its downregulation reduced S1P-induced the phosphorylation of IKK and p65. In addition, silencing of Bcl10 also inhibited S1P-induced IKK phosphorylation. Surprisingly, S1P reduced Akt activation in melanoma cells that express FLNA, whereas in the absence of FLNA, high phosphorylation levels of Akt were maintained, enabling S1P-mediated NF-κB signaling. In accord, inhibition of Akt suppressed S1P-mediated IKK and p65 phosphorylation and degradation of IκBα. Hence, these results support a negative role of FLNA in S1P-mediated NF-κB activation in melanoma cells through modulation of Akt.