| Literature DB >> 24681098 |
Daniel Röth1, Peter H Krammer1, Karsten Gülow2.
Abstract
In T cells mitochondria-derived reactive oxygen species (ROS) are indispensible for activation of the transcription factor NF-κB, expression of cytokines and the CD95 ligand (CD95L/FasL). Here we show that activation-induced ROS generation is dependent on mitochondrial fission. Inhibition of dynamin related protein 1 (Drp1) results in reduced ROS levels and transcriptional activity of NF-κB leading to diminished proliferation and CD95L-dependent activation-induced cell death (AICD). Upon stimulation Drp1 is S-nitrosylated, which is required for oxidative signalling, AICD and cytokine production. In conclusion, we describe a novel signalling pathway that links TCR-induced nitric oxide release to mitochondrial fission and oxidative signalling.Entities:
Keywords: Activation induced T cell death (AICD); Apoptosis; CD95L/FASL; Dynamin related protein 1 (Drp1); Interleukin; Mitochondrial dynamics; Reactive oxygen species (ROS); T cell
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Year: 2014 PMID: 24681098 DOI: 10.1016/j.febslet.2014.03.029
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124