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从蛋白质组学角度看 TNF 介导的信号转导和细胞死亡。

A proteomic perspective on TNF-mediated signalling and cell death.

机构信息

Department of Proteomics and Signal Transduction, Max-Planck Institute of Biochemistry, Martinsried 82152, Germany.

出版信息

Biochem Soc Trans. 2022 Feb 28;50(1):13-20. doi: 10.1042/BST20211114.

Abstract

The tumour necrosis factor (TNF) is the most potent inducer of cell death amongst cytokines. It is crucial for processes including homeostasis, the development of the immune system and fighting infections. However, high levels of TNF due to genetic disorders or persistent infections can contribute to autoinflammatory and autoimmune diseases or life-threatening conditions like sepsis. These diseases generally display increased levels of cell death, which, downstream of the TNF receptor, can either be caspase-dependent (apoptosis) or caspase-independent (necroptosis). Significant efforts have been invested in unravelling and manipulating signalling mechanisms regulating these two different types of cell death. Here I discuss how modern proteomic approaches like phosphoproteomics and secretomics provide a novel perspective on this central cytokine and its effect on inflammation and cell survival.

摘要

肿瘤坏死因子(TNF)是细胞因子中最能诱导细胞死亡的物质。它对于包括体内平衡、免疫系统发育和抗感染在内的过程至关重要。然而,由于遗传疾病或持续感染导致的 TNF 水平升高,可能会导致自身炎症性和自身免疫性疾病,或危及生命的败血症等情况。这些疾病通常表现出细胞死亡水平的增加,而在 TNF 受体下游,这种增加可以是 caspase 依赖性的(细胞凋亡)或 caspase 非依赖性的(坏死性凋亡)。人们已经投入了大量的努力来揭示和操纵调节这两种不同类型细胞死亡的信号转导机制。在这里,我将讨论现代蛋白质组学方法(如磷酸化蛋白质组学和分泌组学)如何为这种核心细胞因子及其对炎症和细胞存活的影响提供新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c51d/9022982/58068347274e/BST-50-13-g0001.jpg

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