Journal Article

The Gbetagamma-Src signaling pathway regulates TNF-induced necroptosis via control of necrosome translocation

Ma, Huabin, Ding, Yan, Li, Lisheng, Li, Wenjuan, Ren, Junming, Lin, Juan, Wu, Jianfeng, Han, Felicia, Zhou, Zhenru, Liang, Yaoji, Li, Jie, Han, Jiahuai, Chen, Wanze

2014

Overview

Formation of multi-component signaling complex necrosomes is essential for tumor necrosis factor α (TNF)-induced programmed necrosis (also called necroptosis). However, the mechanisms of necroptosis are still largely unknown. We isolated a TNF-resistant L929 mutant cell line generated by retrovirus insertion and identified that disruption of the guanine nucleotide-binding protein γ 10 (Gγ10) gene is responsible for this phenotype. We further show that Gγ10 is involved in TNF-induced necroptosis and G[beta]2 is the partner of Gγ10. Src is the downstream effector of G[beta]2γ10 in TNF-induced necroptosis because TNF-induced Src activation was impaired upon Gγ10 knockdown. Gγ10 does not affect TNF-induced activation of NF-κB and MAPKs and the formation of necrosomes, but is required for trafficking of necrosomes to their potential functioning site, an unidentified subcellular organelle that can be fractionated into heterotypic membrane fractions. The TNF-induced G[beta]γ-Src signaling pathway is independent of RIP1/RIP3 kinase activity and necrosome formation, but is required for the necrosome to function.

• Publisher: Nature Publishing Group
• Subject: Translocation