Embryonic Lethality and Host Immunity of RelA-Deficient Mice Are Mediated by Both Apoptosis and Necroptosis

• Published in: The Journal of immunology (1950) 2018-01, Vol.200 (1), p.271-285
• Main Authors: Xu, Chengxian, Wu, Xiaoxia, Zhang, Xixi, Xie, Qun, Fan, Cunxian, Zhang, Haibing
• Format: Article
• Language: English
• Subjects: Activation; Animals; Antibiotics; Apoptosis; Apoptosis - genetics; Cell activation; Cell death; Cells, Cultured; Clonal deletion; Embryo Loss - genetics; Embryogenesis; Embryonic growth stage; FADD protein; Fas-Associated Death Domain Protein - genetics; Fas-Associated Death Domain Protein - metabolism; Female; Homeostasis; Immunity; Inflammation; Lethality; Life span; Mammalian cells; Mice; Mice, Knockout; Necroptosis; Necrosis - genetics; NF-kappa B - metabolism; NF-κB protein; Pneumonia; Pneumonia - genetics; Pneumonia - immunology; Pregnancy; Protein Kinases - genetics; Protein Kinases - metabolism; Signal Transduction; Skin diseases; Transcription Factor RelA - genetics; Transcription Factor RelA - metabolism; Transcriptional Activation; Tumor necrosis factor
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.1700859

In mammalian cells, signaling pathways triggered by TNF can be switched from NF-κB activation to apoptosis and/or necroptosis. The in vivo mechanisms underlying the mutual regulation of these three signaling pathways are poorly understood. In this article, we report that the embryonic lethality of -deficient mice is partially prevented by the deletion of or but it is fully rescued by the combined ablation of and or or by blocking RIP1 kinase activity (RIP1 ). triple-knockout (TKO) and mice displayed bacterial pneumonia leading to death ∼2 wk after birth. Moreover, mice, but not TKO mice, developed severe inflammation associated with inflammatory skin lesion. Antibiotic treatment improved bacterial pneumonia, extended the lifespan of TKO and mice, and alleviated skin inflammation in mice. These results show the mechanisms underlying the in vivo mutual regulation between NF-κB activation and the cell death pathway and provide new insights into this interplay in embryonic development and host immune homeostasis.