The Lck inhibitor, AMG-47a, blocks necroptosis and implicates RIPK1 in signalling downstream of MLKL

• Published in: Cell death & disease Vol. 13; no. 4; p. 291
• Main Authors: Jacobsen, Annette V., Pierotti, Catia L., Lowes, Kym N., Au, Amanda E., Zhang, Ying, Etemadi, Nima, Fitzgibbon, Cheree, Kersten, Wilhelmus J. A., Samson, André L., van Delft, Mark F., Huang, David C. S., Sabroux, Hélène Jousset, Lessene, Guillaume, Silke, John, Murphy, James M.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.04.2022; Springer Nature B.V; Nature Publishing Group
• Subjects: 13/95; 38/47; 631/45/275; 631/80/82/2344; 82/16; 82/80; 96/106; 96/31; Animals; Antibodies; Apoptosis; Biochemistry; Biomedical and Life Sciences; Caspase; Cell Biology; Cell Culture; Cell Death; Cell lines; Cell membranes; Enzyme inhibitors; Immunology; Inflammation; Kinases; Lck protein; Life Sciences; Lymphocyte Specific Protein Tyrosine Kinase p56(lck); Lymphocytes; MAP kinase; Mice; Mutants; Necroptosis; Protein Kinases - genetics; Protein Kinases - metabolism; Protein-tyrosine kinase; Receptor-Interacting Protein Serine-Threonine Kinases - genetics; Receptor-Interacting Protein Serine-Threonine Kinases - metabolism; Signal Transduction
• ISSN: 2041-4889; 2041-4889
• DOI: 10.1038/s41419-022-04740-w

Necroptosis is a form of caspase-independent programmed cell death that arises from disruption of cell membranes by the mixed lineage kinase domain-like (MLKL) pseudokinase after its activation by the upstream kinases, receptor interacting protein kinase (RIPK)-1 and RIPK3, within a complex known as the necrosome. Dysregulated necroptosis has been implicated in numerous inflammatory pathologies. As such, new small molecule necroptosis inhibitors are of great interest, particularly ones that operate downstream of MLKL activation, where the pathway is less well defined. To better understand the mechanisms involved in necroptosis downstream of MLKL activation, and potentially uncover new targets for inhibition, we screened known kinase inhibitors against an activated mouse MLKL mutant, leading us to identify the lymphocyte-specific protein tyrosine kinase (Lck) inhibitor AMG-47a as an inhibitor of necroptosis. We show that AMG-47a interacts with both RIPK1 and RIPK3, that its ability to protect from cell death is dependent on the strength of the necroptotic stimulus, and that it blocks necroptosis most effectively in human cells. Moreover, in human cell lines, we demonstrate that AMG-47a can protect against cell death caused by forced dimerisation of MLKL truncation mutants in the absence of any upstream signalling, validating that it targets a process downstream of MLKL activation. Surprisingly, however, we also found that the cell death driven by activated MLKL in this model was completely dependent on the presence of RIPK1, and to a lesser extent RIPK3, although it was not affected by known inhibitors of these kinases. Together, these results suggest an additional role for RIPK1, or the necrosome, in mediating human necroptosis after MLKL is phosphorylated by RIPK3 and provide further insight into reported differences in the progression of necroptosis between mouse and human cells.