上睑下垂
炎症体
细胞生物学
程序性细胞死亡
光遗传学
多蛋白复合物
半胱氨酸蛋白酶1
化学
半胱氨酸蛋白酶
细胞凋亡
生物
神经科学
生物化学
受体
基因
作者
Julien Nadjar,Sylvain Monnier,Estelle Bastien,Anne-Laure Huber,Christiane Oddou,Léa Bardoulet,Hubert B. Leloup,Gabriel Ichim,Christophe Vanbelle,Bénédicte F. Py,Olivier Destaing,Virginie Pétrilli
出处
期刊:Science Signaling
[American Association for the Advancement of Science (AAAS)]
日期:2024-04-23
卷期号:17 (833)
标识
DOI:10.1126/scisignal.abn8003
摘要
Inflammasomes are multiprotein platforms that control caspase-1 activation, which process the inactive precursor forms of the inflammatory cytokines IL-1β and IL-18, leading to an inflammatory type of programmed cell death called pyroptosis. Studying inflammasome-driven processes, such as pyroptosis-induced cell swelling, under controlled conditions remains challenging because the signals that activate pyroptosis also stimulate other signaling pathways. We designed an optogenetic approach using a photo-oligomerizable inflammasome core adapter protein, apoptosis-associated speck–like containing a caspase recruitment domain (ASC), to temporally and quantitatively manipulate inflammasome activation. We demonstrated that inducing the light-sensitive oligomerization of ASC was sufficient to recapitulate the classical features of inflammasomes within minutes. This system showed that there were two phases of cell swelling during pyroptosis. This approach offers avenues for biophysical investigations into the intricate nature of cellular volume control and plasma membrane rupture during cell death.
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