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    Post-translational control of RIPK3 and MLKL mediated necroptotic cell death.

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    24
    Author
    Murphy, JM; Vince, JE
    Date
    2015
    Source Title
    F1000Research
    Publisher
    F1000 Research Ltd
    University of Melbourne Author/s
    Vince, James; Murphy, James
    Affiliation
    Medical Biology (W.E.H.I.)
    Metadata
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    Document Type
    Journal Article
    Citations
    Murphy, J. M. & Vince, J. E. (2015). Post-translational control of RIPK3 and MLKL mediated necroptotic cell death.. F1000Res, 4, pp.1297-1297. https://doi.org/10.12688/f1000research.7046.1.
    Access Status
    Open Access
    URI
    http://hdl.handle.net/11343/259291
    DOI
    10.12688/f1000research.7046.1
    Open Access at PMC
    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4851234
    Abstract
    Several programmed lytic and necrotic-like cell death mechanisms have now been uncovered, including the recently described receptor interacting protein kinase-3 (RIPK3)-mixed lineage kinase domain-like (MLKL)-dependent necroptosis pathway. Genetic experiments have shown that programmed necrosis, including necroptosis, can play a pivotal role in regulating host-resistance against microbial infections. Alternatively, excess or unwarranted necroptosis may be pathological in autoimmune and autoinflammatory diseases. This review highlights the recent advances in our understanding of the post-translational control of RIPK3-MLKL necroptotic signaling. We discuss the critical function of phosphorylation in the execution of necroptosis, and highlight the emerging regulatory roles for several ubiquitin ligases and deubiquitinating enzymes. Finally, based on current evidence, we discuss the potential mechanisms by which the essential, and possibly terminal, necroptotic effector, MLKL, triggers the disruption of cellular membranes to cause cell lysis.

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