Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA.
Methods Mol Biol. 2022;2543:179-189. doi: 10.1007/978-1-0716-2553-8_15.
Pyroptosis is a highly regulated inflammatory form of cell death that plays a role in many different diseases, including cancer. Pyroptosis was initially described to be mediated by caspase-1, which is activated by innate immune signaling complexes called inflammasomes. Inflammasomes trigger caspase-dependent activation of the pore-forming protein, gasdermin D, and plasma membrane disruption. In this protocol, we describe a method to simultaneously detect two hallmarks of inflammasome-mediated pyroptosis. Using a fluorescently tagged inflammasome adaptor protein (ASC-Citrine) and membrane-impermeable nuclear dyes, we can track inflammasome formation and plasma membrane disruption over time in the same cell population.
细胞焦亡是一种高度调控的炎症性细胞死亡形式,在许多不同的疾病中发挥作用,包括癌症。细胞焦亡最初被描述为由称为炎性体的先天免疫信号复合物激活的半胱天冬酶-1(caspase-1)介导。炎性体触发依赖半胱天冬酶的孔形成蛋白,gasdermin D 的激活和质膜破裂。在本方案中,我们描述了一种同时检测炎性体介导的细胞焦亡的两种特征的方法。使用荧光标记的炎性体衔接蛋白(ASC-Citrine)和膜不可渗透的核染料,我们可以在同一细胞群中随时间跟踪炎性体的形成和质膜的破坏。