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NU6300 与 gasdermin D 的半胱氨酸 191 发生共价反应,阻止其裂解和棕榈酰化。

NU6300 covalently reacts with cysteine-191 of gasdermin D to block its cleavage and palmitoylation.

机构信息

Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China.

School of Pharmacy, Chengdu Medical College, Chengdu 610500, China.

出版信息

Sci Adv. 2024 Feb 9;10(6):eadi9284. doi: 10.1126/sciadv.adi9284. Epub 2024 Feb 7.

DOI:10.1126/sciadv.adi9284
PMID:38324683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10849585/
Abstract

Gasdermin D (GSDMD) serves as a vital mediator of inflammasome-driven pyroptosis. In our study, we have identified NU6300 as a specific GSDMD inhibitor that covalently interacts with cysteine-191 of GSDMD, effectively blocking its cleavage while not affecting earlier steps such as ASC oligomerization and caspase-1 processing in AIM2- and NLRC4-mediated inflammation. On the contrary, NU6300 robustly inhibits these earlier steps in NLRP3 inflammasome, confirming a unique feedback inhibition effect in the NLRP3-GSDMD pathway upon GSDMD targeting. Our study reveals a previously undefined mechanism of GSDMD inhibitors: NU6300 impairs the palmitoylation of both full-length and N-terminal GSDMD, impeding the membrane localization and oligomerization of N-terminal GSDMD. In vivo studies further demonstrate the efficacy of NU6300 in ameliorating dextran sodium sulfate-induced colitis and improving survival in lipopolysaccharide-induced sepsis. Overall, these findings highlight the potential of NU6300 as a promising lead compound for the treatment of inflammatory diseases.

摘要

Gasdermin D (GSDMD) 作为炎性体驱动的细胞焦亡的重要介质。在我们的研究中,我们鉴定出 NU6300 是一种特异性的 GSDMD 抑制剂,它与 GSDMD 的半胱氨酸 191 发生共价相互作用,有效阻断其裂解,而不影响 ASC 寡聚化和 caspase-1 在 AIM2 和 NLRC4 介导的炎症中的加工。相反,NU6300 强烈抑制 NLRP3 炎性体中的这些早期步骤,证实了 NLRP3-GSDMD 途径中针对 GSDMD 的靶向作用具有独特的反馈抑制效应。我们的研究揭示了 GSDMD 抑制剂的一个以前未定义的机制:NU6300 损害全长和 N 端 GSDMD 的棕榈酰化,阻碍 N 端 GSDMD 的膜定位和寡聚化。体内研究进一步证明了 NU6300 在改善葡聚糖硫酸钠诱导的结肠炎和提高脂多糖诱导的脓毒症中的生存率方面的疗效。总的来说,这些发现突出了 NU6300 作为治疗炎症性疾病的有前途的先导化合物的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3233/10849585/7b0e13582434/sciadv.adi9284-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3233/10849585/c7e989c47fbc/sciadv.adi9284-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3233/10849585/89f6d8f22937/sciadv.adi9284-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3233/10849585/7db53951a4ec/sciadv.adi9284-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3233/10849585/b1349df2bd37/sciadv.adi9284-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3233/10849585/64e4d10279fd/sciadv.adi9284-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3233/10849585/7b0e13582434/sciadv.adi9284-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3233/10849585/c7e989c47fbc/sciadv.adi9284-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3233/10849585/769b4cc9c3f6/sciadv.adi9284-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3233/10849585/c17831ed63e1/sciadv.adi9284-f3.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3233/10849585/7db53951a4ec/sciadv.adi9284-f5.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3233/10849585/7b0e13582434/sciadv.adi9284-f8.jpg

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