Division of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA.
FEBS J. 2019 Jul;286(14):2628-2644. doi: 10.1111/febs.14926. Epub 2019 May 27.
Members of the mammalian inflammatory caspase family, including caspase-1, caspase-4, caspase-5, caspase-11, and caspase-12, are key regulators of the innate immune response. Most studies to date have focused on the role of caspase-1 in the maturation of the proinflammatory cytokine interleukin-1β and its upstream regulation by the inflammasome signaling complexes. However, an emerging body of research has supported a role for caspase-4, caspase-5, and caspase-11 in both regulating caspase-1 activation and inducing the inflammatory form of cell death called pyroptosis. This inflammatory caspase pathway appears essential for the regulation of cytokine processing. Consequently, insight into this noncanonical pathway may reveal important and, to date, understudied targets for the treatment of autoinflammatory disorders where the inflammasome pathway is dysregulated. Here, we will discuss the mechanisms of inflammasome and inflammatory caspase activation and how these pathways intersect to promote pathogen clearance.
哺乳动物炎症半胱天冬酶家族的成员,包括 caspase-1、caspase-4、caspase-5、caspase-11 和 caspase-12,是先天免疫反应的关键调节剂。迄今为止,大多数研究都集中在 caspase-1 在促炎细胞因子白细胞介素-1β 的成熟及其炎症小体信号复合物的上游调节中的作用。然而,越来越多的研究支持 caspase-4、caspase-5 和 caspase-11 在调节 caspase-1 激活和诱导称为细胞焦亡的炎症形式细胞死亡中的作用。这种炎症半胱天冬酶途径似乎对于细胞因子加工的调节至关重要。因此,对这条非经典途径的深入了解可能会揭示自身炎症性疾病治疗中的重要且迄今为止研究不足的靶点,其中炎症小体途径失调。在这里,我们将讨论炎症小体和炎症性半胱天冬酶激活的机制,以及这些途径如何相互作用以促进病原体清除。