Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
Experimental Systems Immunology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
Cell Rep. 2020 Jan 28;30(4):1260-1270.e5. doi: 10.1016/j.celrep.2019.12.079.
The inflammatory functions of the cytokine tumor necrosis factor (TNF) rely on its ability to induce cytokine production and to induce cell death. Caspase-dependent and caspase-independent pathways-apoptosis and necroptosis, respectively-regulate immunogenicity by the release of distinct sets of cellular proteins. To obtain an unbiased, systems-level understanding of this important process, we here applied mass spectrometry-based proteomics to dissect protein release during apoptosis and necroptosis. We report hundreds of proteins released from human myeloid cells in time course experiments. Both cell death types induce receptor shedding, but only apoptotic cells released nucleosome components. Conversely, necroptotic cells release lysosomal components by activating lysosomal exocytosis at early stages of necroptosis-induced membrane permeabilization and show reduced release of conventionally secreted cytokines.
细胞因子肿瘤坏死因子 (TNF) 的炎症功能依赖于其诱导细胞因子产生和诱导细胞死亡的能力。半胱天冬酶依赖性和半胱天冬酶非依赖性途径——分别为细胞凋亡和坏死性凋亡——通过释放不同的细胞蛋白来调节免疫原性。为了获得对这一重要过程的无偏、系统水平的理解,我们在这里应用基于质谱的蛋白质组学来剖析细胞凋亡和坏死性凋亡过程中的蛋白质释放。我们报告了数百种在时间过程实验中从人髓样细胞中释放的蛋白质。两种细胞死亡类型都诱导受体脱落,但只有凋亡细胞释放核小体成分。相反,坏死性凋亡诱导的膜通透性早期,坏死性凋亡细胞通过激活溶酶体胞吐作用释放溶酶体成分,并减少传统分泌细胞因子的释放。