TNF-alpha-induced sphingosine 1-phosphate inhibits apoptosis through a phosphatidylinositol 3-kinase/Akt pathway in human hepatocytes

Human hepatocytes usually are resistant to TNF-alpha cytotoxicity. In mouse or rat hepatocytes, repression of NF-kappaB activation is sufficient to in duce TNF-alpha -mediated apoptosis. However, in both Huh-7 human hepatoma c ells and He human normal hepatocytes, when infected with an adenovirus expr essing a mutated form of I kappaB alpha (Ad5I kappaB), which almost complet ely blocks NF-kappaB activation, > 80% of the cells survived 24 h after TNF -alpha stimulation. Here, we report that TNF-alpha activates other antiapop totic factors, such as sphingosine kinase (SphK), phosphatidylinositol 3-ki nase (PI3K), and Akt kinase. Pretreatment of cells with N,N-dimethylsphingo sine (PI3K), an inhibitor of SphK, or LY 294002, an inhibitor of PI3K that acts upstream of Akt, increased the number of apoptotic cells induced by TN F-alpha in Ad5I kappaB-infected Huh-7 and He cells. TNF-alpha -induced acti vations of PI3K and Akt were inhibited by DMS. In contrast, exogenous sphin gosine I-phosphate, a product of SphK, was found to activate Akt and partia lly rescued the cells from TNF-alpha -induced apoptosis. Although Akt has b een reported to activate NF-kappaB, DMS and LY 294002 failed to prevent TNF -alpha -induced NF-kappaB activation, suggesting that the antiapoptotic eff ects of SphK and Akt are independent of NF-kappaB. Furthermore, apoptosis m ediated by Fas ligand (FasL) involving Akt activation also was potentiated by DMS pretreatment in He cells. Sphingosine 1-phosphate administration par tially protected cells from FasL-mediated apoptosis. These results indicate that not only NF-kappaB but also SphK and PI3K/Akt are involved in the sig naling pathway(s) for protection of human hepatocytes from the apoptotic ac tion of TNF-alpha and probably FasL.