Akt Regulates TNFα Synthesis Downstream of RIP1 Kinase Activation during Necroptosis

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Akt Regulates TNFα Synthesis Downstream of RIP1 Kinase Activation during Necroptosis

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Title: Akt Regulates TNFα Synthesis Downstream of RIP1 Kinase Activation during Necroptosis
Author: McNamara, Colleen R.; Ahuja, Ruchita; Osafo-Addo, Awo D.; Barrows, Douglas; Kettenbach, Arminja; Skidan, Igor; Teng, Xin; Cuny, Gregory Douglas; Gerber, Scott; Degterev, Alexei

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Citation: McNamara, Colleen R., Ruchita Ahuja, Awo D. Osafo-Addo, Douglas Barrows, Arminja Kettenbach, Igor Skidan, Xin Teng, Gregory D. Cuny, Scott Gerber, and Alexei Degterev. 2013. Akt regulates TNFα synthesis downstream of RIP1 kinase activation during necroptosis. PLoS ONE 8(3): e56576.
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Abstract: Necroptosis is a regulated form of necrotic cell death that has been implicated in the pathogenesis of various diseases including intestinal inflammation and systemic inflammatory response syndrome (SIRS). In this work, we investigated the signaling mechanisms controlled by the necroptosis mediator receptor interacting protein-1 (RIP1) kinase. We show that Akt kinase activity is critical for necroptosis in L929 cells and plays a key role in TNFα production. During necroptosis, Akt is activated in a RIP1 dependent fashion through its phosphorylation on Thr308. In L929 cells, this activation requires independent signaling inputs from both growth factors and RIP1. Akt controls necroptosis through downstream targeting of mammalian Target of Rapamycin complex 1 (mTORC1). Akt activity, mediated in part through mTORC1, links RIP1 to JNK activation and autocrine production of TNFα. In other cell types, such as mouse lung fibroblasts and macrophages, Akt exhibited control over necroptosis-associated TNFα production without contributing to cell death. Overall, our results provide new insights into the mechanism of necroptosis and the role of Akt kinase in both cell death and inflammatory regulation.
Published Version: doi:10.1371/journal.pone.0056576
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585731/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10611829
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