Phenytoin inhibits necroptosis.
Anne von MässenhausenWulf TonnusNina HimmerkusSimon ParmentierDanish SalehDiego RodriguezJiraporn OusingsawatRosalind L AngJoel M WeinbergAna B SanzAlberto Ortiz ArduanAdrian ZierleynJan Ulrich BeckerBlandine BaratteNathalie DesbanStéphane BachIna Maria SchiesslShoko NogusaSiddharth BalachandranHans Joachim AndersAdrian T TingMarkus BleichAlexei DegterevKarl KunzelmannStefan R BornsteinDouglas R GreenChristian HugoAndreas LinkermannPublished in: Cell death & disease (2018)
Receptor-interacting protein kinases 1 and 3 (RIPK1/3) have best been described for their role in mediating a regulated form of necrosis, referred to as necroptosis. During this process, RIPK3 phosphorylates mixed lineage kinase domain-like (MLKL) to cause plasma membrane rupture. RIPK3-deficient mice have recently been demonstrated to be protected in a series of disease models, but direct evidence for activation of necroptosis in vivo is still limited. Here, we sought to further examine the activation of necroptosis in kidney ischemia-reperfusion injury (IRI) and from TNFα-induced severe inflammatory response syndrome (SIRS), two models of RIPK3-dependent injury. In both models, MLKL-ko mice were significantly protected from injury to a degree that was slightly, but statistically significantly exceeding that of RIPK3-deficient mice. We also demonstrated, for the first time, accumulation of pMLKL in the necrotic tubules of human patients with acute kidney injury. However, our data also uncovered unexpected elevation of blood flow in MLKL-ko animals, which may be relevant to IRI and should be considered in the future. To further understand the mode of regulation of cell death by MLKL, we screened a panel of clinical plasma membrane channel blockers and we found phenytoin to inhibit necroptosis. However, we further found that phenytoin attenuated RIPK1 kinase activity in vitro, likely due to the hydantoin scaffold also present in necrostatin-1, and blocked upstream necrosome formation steps in the cells undergoing necroptosis. We further report that this clinically used anti-convulsant drug displayed protection from kidney IRI and TNFα-induces SIRS in vivo. Overall, our data reveal the relevance of RIPK3-pMLKL regulation for acute kidney injury and identifies an FDA-approved drug that may be useful for immediate clinical evaluation of inhibition of pro-death RIPK1/RIPK3 activities in human diseases.
Keyphrases
- acute kidney injury
- cell death
- inflammatory response
- blood flow
- endothelial cells
- ischemia reperfusion injury
- rheumatoid arthritis
- cardiac surgery
- drug induced
- protein kinase
- oxidative stress
- metabolic syndrome
- big data
- transcription factor
- cell cycle arrest
- lipopolysaccharide induced
- small molecule
- adverse drug
- induced pluripotent stem cells
- tyrosine kinase
- skeletal muscle
- cell proliferation
- anti inflammatory
- pluripotent stem cells
- high fat diet induced
- toll like receptor
- signaling pathway
- angiotensin ii
- diabetic rats
- pi k akt
- adipose tissue
- tissue engineering