Department of Immunology, Duke University School of Medicine, DUMC 3010, Durham, NC 27710, USA.
Immunology and Microbiology Program, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
J Cell Sci. 2022 Sep 1;135(17). doi: 10.1242/jcs.260091. Epub 2022 Sep 13.
Necroptosis, or programmed necrosis, is an inflammatory form of cell death with important functions in host defense against pathogens and tissue homeostasis. The four cytosolic receptor-interacting protein kinase homotypic interaction motif (RHIM)-containing adaptor proteins RIPK1, RIPK3, TRIF (also known as TICAM1) and ZBP1 mediate necroptosis induction in response to infection and cytokine or innate immune receptor activation. Activation of the RHIM adaptors leads to phosphorylation, oligomerization and membrane targeting of the necroptosis effector protein mixed lineage kinase domain-like (MLKL). Active MLKL induces lesions on the plasma membrane, leading to the release of pro-inflammatory damage-associated molecular patterns (DAMPs). Thus, activities of the RHIM adaptors and MLKL are tightly regulated by posttranslational modifications to prevent inadvertent release of immunogenic contents. In this Cell Science at a Glance article and the accompanying poster, we provide an overview of the regulatory mechanisms of necroptosis and its biological functions in tissue homeostasis, pathogen infection and other inflammatory diseases.
细胞坏死,又称为程序性细胞坏死,是一种具有重要功能的炎症形式的细胞死亡,有助于宿主抵抗病原体和维持组织稳态。四种含有胞质受体相互作用蛋白激酶同源相互作用基序 (RHIM) 的衔接蛋白 RIPK1、RIPK3、TRIF(也称为 TICAM1)和 ZBP1 介导细胞坏死的诱导,以响应感染和细胞因子或先天免疫受体的激活。RHIM 衔接蛋白的激活导致坏死效应蛋白混合谱系激酶结构域样 (MLKL) 的磷酸化、寡聚化和靶向质膜。活性 MLKL 在质膜上诱导损伤,导致促炎损伤相关分子模式 (DAMP) 的释放。因此,RHIM 衔接蛋白和 MLKL 的活性受到严格的翻译后修饰调控,以防止免疫原性内容物的意外释放。在本期《细胞科学一瞥》文章和配套海报中,我们概述了细胞坏死的调控机制及其在组织稳态、病原体感染和其他炎症性疾病中的生物学功能。