Inflammation Research Center, VIB, Technologiepark 927, Zwijnaarde-Ghent 9052, Belgium; Department of Biomedical Molecular Biology, Ghent University, Technologiepark 927, Zwijnaarde-Ghent 9052, Belgium.
Laboratory of Molecular Immunology and Signal Transduction, GIGA-Research, University of Liège, 4000 Liège, Belgium.
Mol Cell. 2015 Oct 1;60(1):63-76. doi: 10.1016/j.molcel.2015.07.032. Epub 2015 Sep 3.
TNF is a master pro-inflammatory cytokine. Activation of TNFR1 by TNF can result in both RIPK1-independent apoptosis and RIPK1 kinase-dependent apoptosis or necroptosis. These cell death outcomes are regulated by two distinct checkpoints during TNFR1 signaling. TNF-mediated NF-κB-dependent induction of pro-survival or anti-apoptotic molecules is a well-known late checkpoint in the pathway, protecting cells from RIPK1-independent death. On the other hand, the molecular mechanism regulating the contribution of RIPK1 to cell death is far less understood. We demonstrate here that the IKK complex phosphorylates RIPK1 at TNFR1 complex I and protects cells from RIPK1 kinase-dependent death, independent of its function in NF-κB activation. We provide in vitro and in vivo evidence that inhibition of IKKα/IKKβ or its upstream activators sensitizes cells to death by inducing RIPK1 kinase-dependent apoptosis or necroptosis. We therefore report on an unexpected, NF-κB-independent role for the IKK complex in protecting cells from RIPK1-dependent death downstream of TNFR1.
肿瘤坏死因子(TNF)是一种主要的促炎细胞因子。TNF 通过肿瘤坏死因子受体 1(TNFR1)的激活可导致 RIPK1 非依赖性凋亡和 RIPK1 激酶依赖性凋亡或坏死性凋亡。这些细胞死亡结果受 TNFR1 信号通路中的两个不同检查点调节。TNF 介导的 NF-κB 依赖性诱导生存或抗凋亡分子是该通路中众所周知的晚期检查点,可保护细胞免受 RIPK1 非依赖性死亡。另一方面,调节 RIPK1 对细胞死亡的贡献的分子机制远未被充分了解。我们在此证明,IKK 复合物在 TNFR1 复合物 I 处磷酸化 RIPK1,并通过其在 NF-κB 激活中的功能来保护细胞免受 RIPK1 激酶依赖性死亡。我们提供了体外和体内证据,表明抑制 IKKα/IKKβ 或其上游激活剂可通过诱导 RIPK1 激酶依赖性凋亡或坏死性凋亡使细胞对死亡敏感。因此,我们报告了 IKK 复合物在保护细胞免受 TNFR1 下游 RIPK1 依赖性死亡中的一个出乎意料的、NF-κB 非依赖性作用。