期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 280, 期 28, 页码 26415-26424出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M501492200
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资金
- NINDS NIH HHS [R01NS046835] Funding Source: Medline
We have reported that ceramide mediates binding of atypical protein kinase C (PKC) zeta to its inhibitor protein, PAR-4 ( prostate apoptosis response-4), thereby inducing apoptosis in differentiating embryonic stem cells. Using a novel method of lipid vesicle-mediated affinity chromatography, we showed here that endogenous ceramide binds directly to the PKC zeta(.)PAR-4 complex. Ceramide and its analogs activated PKC zeta prior to binding to PAR-4, as determined by increased levels of phosphorylated PKC zeta and glycogen synthase kinase-3 beta and emergence of a PAR-4-to-phosphorylated PKC zeta fluorescence resonance energy transfer signal that co- localizes with ceramide. Elevated expression and activation of PKC zeta increased cell survival, whereas expression of PAR-4 promoted apoptosis. This suggests that PKC zeta counteracts apoptosis, unless its ceramide-induced activation is compromised by binding to PAR-4. A luciferase reporter assay showed that ceramide analogs activate nuclear factor (NF)-kappa B unless PAR-4-dependent inhibition of PKC zeta suppresses NF-kappa B activation. Taken together, our results show that direct physical association with ceramide and PAR-4 regulates the activity of PKC zeta. They also indicate that this interaction regulates the activity of glycogen synthase kinase-3 beta and NF-kappa B.
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