TY - JOUR
T1 - Single-cell imaging of caspase-1 dynamics reveals an all-or-none inflammasome signaling response
AU - Liu, Ting
AU - Yamaguchi, Yoshifumi
AU - Shirasaki, Yoshitaka
AU - Shikada, Koichi
AU - Yamagishi, Mai
AU - Hoshino, Katsuaki
AU - Kaisho, Tsuneyasu
AU - Takemoto, Kiwamu
AU - Suzuki, Toshihiko
AU - Kuranaga, Erina
AU - Ohara, Osamu
AU - Miura, Masayuki
N1 - Funding Information:
We are grateful to K. Kuida (Millennium: The Takeda Oncology Company), R. Uchiyama, and H. Tsutsui (Hyogo College of Medicine, Japan) for providing caspase-1/11-deficient mice, M. Okabe (Osaka University) for providing CAG-Cre mice (Riken BRC), and Y. Sasaki (Kyoto University) for providing the Rosa26-CAG-STOP targeting vector. We thank the University of Tokyo and Leica Microsystems Imaging Center for the imaging analysis. We also thank N. Kambe (Chiba University), T. Chihara, and all the members of the M.M. laboratory for the helpful discussions and comments and M. Sasaki, K. Tomioka, Y. Fujioka, T. Takahashi, and Y. Watanabe for experimental assistance. This work was supported by grants to M.M. and Y.Y. from the Ministry of Education, Culture, Sports, Science and Technology in Japan , the Japan Society for the Promotion of Science , and the Japan Science and Technology Agency .
PY - 2014/8/21
Y1 - 2014/8/21
N2 - 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, weconducted 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 ina digital manner, which identified these macrophages as themain 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.
AB - 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, weconducted 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 ina digital manner, which identified these macrophages as themain 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.
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U2 - 10.1016/j.celrep.2014.07.012
DO - 10.1016/j.celrep.2014.07.012
M3 - Article
C2 - 25127135
AN - SCOPUS:84908356704
SN - 2211-1247
VL - 8
SP - 974
EP - 982
JO - Cell Reports
JF - Cell Reports
IS - 4
ER -