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The Journal of Immunology, 2001, 166: 966-972.
Copyright © 2001 by The American Association of Immunologists

The Serine/Threonine Phosphatase, PP2A: Endogenous Regulator of Inflammatory Cell Signaling1

Thomas P. Shanley2, Niti Vasi, Alvin Denenberg and Hector R. Wong

Division of Critical Care Medicine, Children’s Hospital Medical Center, Cincinnati, OH 45229

We have investigated the regulation of kinases and phosphatases in early gene activation in monocytes because these cells are implicated in the pathogenesis of acute inflammatory states, such as sepsis and acute lung injury. One early gene up-regulated by endotoxin is c-Jun, a member of the activating protein (AP) family. C-Jun is phosphorylated by c-Jun N-terminal kinase (JNK) and associates with c-Fos to form the AP-1 transcriptional activation complex that can drive cytokine expression. Inhibition of the serine/threonine phosphatase, PP2-A, with okadaic acid resulted in a significant increase in JNK activity. This finding was associated with increased phosphorylation of c-Jun, AP-1 transcriptional activity, and IL-1{beta} expression. Activation of PP2A inhibited JNK activity and JNK coprecipitated with the regulatory subunit, PP2A-A{alpha}, supporting the conclusion that PP2A is a key regulator of JNK in the context of an inflammatory stimulus.




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