Abstract
Receptor-interacting protein 1 (RIP1) is the founding member of the RIP family proteins that consist of seven members. Although it was initially found that RIP1 plays an important role in TNF receptor 1 (TNFR1)-mediated NF-κB activation that protects cells from apoptosis, later research found that RIP1 is also required for TNF-induced apoptosis and necrosis under certain conditions. In addition, RIP1 is also involved in signaling by other death receptors for FASL and TRAIL, and TLR and intracellular sensors/adaptors such as PIDD. When cells are responding to different stimulations or intracellular stresses such as DNA damage, RIP1 can transduce either pro-survival or pro-death signals. Thus, RIP1 plays a pivotal role in the decision of cells’ fate. In this chapter, recent reports on RIP1-mediated cell signaling with a focus on cell survival and death control will be summarized.
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Acknowledgements
We apologize to researchers whose work was unable to be cited due to the space limit. The studies in my laboratory are supported by grants from NIEHS/NIH (R01ES017328) and the Department of Energy Low Dose Radiation Research Program (DE-SC0001173).
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Lin, Y. (2014). RIP1-Mediated Signaling Pathways in Cell Survival and Death Control. In: Shen, HM., Vandenabeele, P. (eds) Necrotic Cell Death. Cell Death in Biology and Diseases. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4614-8220-8_2
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