| Literature DB >> 25127135 |
Ting Liu1, Yoshifumi Yamaguchi2, Yoshitaka Shirasaki3, Koichi Shikada1, Mai Yamagishi3, Katsuaki Hoshino4, Tsuneyasu Kaisho5, Kiwamu Takemoto6, Toshihiko Suzuki7, Erina Kuranaga8, Osamu Ohara9, Masayuki Miura10.
Abstract
Inflammasome-mediated caspase-1 activation is involved in cell death and the secretion of the proinflammatory cytokine interleukin-1β (IL-1β). Although the dynamics of caspase-1 activation, IL-1β secretion, and cell death have been examined with bulk assays in population-level studies, they remain poorly understood at the single-cell level. In this study, we conducted single-cell imaging using a genetic fluorescence resonance energy transfer sensor that detects caspase-1 activation. We determined that caspase-1 exhibits all-or-none (digital) activation at the single-cell level, with similar activation kinetics irrespective of the type of inflammasome or the intensity of the stimulus. Real-time concurrent detection of caspase-1 activation and IL-1β release demonstrated that dead macrophages containing activated caspase-1 release a local burst of IL-1β in a digital manner, which identified these macrophages as the main source of IL-1β within cell populations. Our results highlight the value of single-cell analysis in enhancing understanding of the inflammasome system and chronic inflammatory diseases.Entities:
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Year: 2014 PMID: 25127135 DOI: 10.1016/j.celrep.2014.07.012
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423