The Selective 3-MST Inhibitor I3MT-3 Works as a Potent Caspase-1 Inhibitor

I3MT-3 (HMPSNE) has been identified as a selective inhibitor of the supersulfide-producing enzyme 3-MST. In this study, we found that I3MT-3 inhibits inflammatory responses, including the secretion of the pro-inflammatory cytokine interleukin-1β (IL-1β) and inflammatory cell death pyroptosis, induced by the activation of the inflammasomes composed of NLRP1, NLRP3, or AIM2. However, interestingly, the knockdown of 3-MST did not affect the activation of the inflammasomes, suggesting that the inhibitory effect of I3MT-3 on inflammasome activation is mediated by alternative ways rather than the inhibition of 3-MST. Interestingly, an in vitro caspase assay revealed that I3MT-3 directly inhibits caspase-1 activation, and molecular docking simulations raised the possibility that the pyrimidone ring in I3MT-3 stabilizes direct interaction of I3MT-3 with caspase-1. Taken together, our data suggest that I3MT-3 inhibits inflammasome activation by targeting caspase-1, and show I3MT-3 as a potent inhibitor of caspase-1.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-03-02
DOI
https://doi.org/10.3390/ijms26052237
Citations
4
Primary Topic
Inflammasome and immune disorders
Type
article
Field-Weighted Citation Impact
3.22

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article

The Selective 3-MST Inhibitor I3MT-3 Works as a Potent Caspase-1 Inhibitor

Atsushi Matsuzawa, Ryuto Komatsu, Yusuke Hirata, Takuya Noguchi et al.
4 citations
International Journal of Molecular Sciences
Inflammasome and immune disorders
3.22
article

The Selective 3-MST Inhibitor I3MT-3 Works as a Potent Caspase-1 Inhibitor

Atsushi Matsuzawa, Ryuto Komatsu, Yusuke Hirata, Takuya Noguchi, Wakana Suzuki, Kohei Otani
article en
4 citations

Abstract

I3MT-3 (HMPSNE) has been identified as a selective inhibitor of the supersulfide-producing enzyme 3-MST. In this study, we found that I3MT-3 inhibits inflammatory responses, including the secretion of the pro-inflammatory cytokine interleukin-1β (IL-1β) and inflammatory cell death pyroptosis, induced by the activation of the inflammasomes composed of NLRP1, NLRP3, or AIM2. However, interestingly, the knockdown of 3-MST did not affect the activation of the inflammasomes, suggesting that the inhibitory effect of I3MT-3 on inflammasome activation is mediated by alternative ways rather than the inhibition of 3-MST. Interestingly, an in vitro caspase assay revealed that I3MT-3 directly inhibits caspase-1 activation, and molecular docking simulations raised the possibility that the pyrimidone ring in I3MT-3 stabilizes direct interaction of I3MT-3 with caspase-1. Taken together, our data suggest that I3MT-3 inhibits inflammasome activation by targeting caspase-1, and show I3MT-3 as a potent inhibitor of caspase-1.

International Journal of Molecular SciencesVol. 26(5)
Tohoku University (JP)
Japan Agency for Medical Research and Development
Good health and well-being
Openalex Percentile: Top 9%
Inflammasome and immune disorders
3.22
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The Selective 3-MST Inhibitor I3MT-3 Works as a Potent Caspase-1 Inhibitor — Atsushi Matsuzawa, Ryuto Komatsu, et al. · International Journal of Molecular Sciences (2025) | TGRS Research Map | TGRS