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芳基功能化α,α'-海藻糖 6,6'-糖苷脂诱导 Mincle 非依赖性细胞焦亡。

Aryl-functionalised α,α'-Trehalose 6,6'-Glycolipid Induces Mincle-independent Pyroptotic Cell Death.

机构信息

School of Chemical and Physical Sciences, Victoria University of Wellington, PO Box 600, Wellington, New Zealand.

Centre for Biodiscovery, Victoria University of Wellington, PO Box 600, Wellington, New Zealand.

出版信息

Inflammation. 2023 Aug;46(4):1365-1380. doi: 10.1007/s10753-023-01814-5. Epub 2023 May 4.

DOI:10.1007/s10753-023-01814-5
PMID:37140682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10359228/
Abstract

α,α'-Trehalose 6,6'-glycolipids have long been known for their immunostimulatory properties. The adjuvanticity of α,α'-trehalose 6,6'-glycolipids is mediated by signalling through the macrophage inducible C-type lectin (Mincle) and the induction of an inflammatory response. Herein, we present an aryl-functionalised trehalose glycolipid, AF-2, that leads to the release of cytokines and chemokines, including IL-6, MIP-2 and TNF-α, in a Mincle-dependent manner. Furthermore, plate-coated AF-2 also leads to the Mincle-independent production of IL-1β, which is unprecedented for this class of glycolipid. Upon investigation into the mode of action of plate-coated AF-2, it was observed that the treatment of WT and Mincle bone marrow derived macrophages (BMDM), murine RAW264.7 cells, and human monocytes with AF-2 led to lytic cell death, as evidenced using Sytox Green and lactate dehydrogenase assays, and confocal and scanning electron microscopy. The requirement for functional Gasdermin D and Caspase-1 for IL-1β production and cell death by AF-2 confirmed pyroptosis as the mode of action of AF-2. The inhibition of NLRP3 and K efflux reduced AF-2 mediated IL-1β production and cell death, and allowed us to conclude that AF-2 leads to Capase-1 dependent NLRP3 inflammasome-mediated cell death. The unique mode of action of plate-coated AF-2 was surprising and highlights how the physical presentation of Mincle ligands can lead to dramatically different immunological outcomes.

摘要

α,α'-海藻糖 6,6'-糖苷已久因其免疫刺激特性而为人所知。α,α'-海藻糖 6,6'-糖苷的佐剂活性是通过巨噬细胞诱导型 C 型凝集素 (Mincle) 的信号转导和炎症反应的诱导来介导的。在此,我们提出了一种芳基功能化的海藻糖糖脂,AF-2,它以 Mincle 依赖性的方式导致细胞因子和趋化因子的释放,包括 IL-6、MIP-2 和 TNF-α。此外,板涂层的 AF-2 也导致 Mincle 非依赖性的 IL-1β 的产生,这在该类糖脂中是前所未有的。在研究板涂层 AF-2 的作用模式时,观察到 AF-2 处理 WT 和 Mincle 骨髓来源的巨噬细胞 (BMDM)、鼠 RAW264.7 细胞和人单核细胞导致裂解细胞死亡,如使用 Sytox Green 和乳酸脱氢酶测定法、共聚焦和扫描电子显微镜所证明的那样。AF-2 诱导 IL-1β 产生和细胞死亡需要功能性 Gasdermin D 和 Caspase-1,这证实了细胞焦亡是 AF-2 的作用模式。NLRP3 和 K 外排的抑制减少了 AF-2 介导的 IL-1β 产生和细胞死亡,使我们能够得出结论,AF-2 导致 Caspase-1 依赖性 NLRP3 炎性体介导的细胞死亡。板涂层 AF-2 的独特作用模式令人惊讶,它突出了 Mincle 配体的物理呈现如何导致截然不同的免疫结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/28a3332205e4/10753_2023_1814_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/8283a996fab6/10753_2023_1814_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/11c487fc64bc/10753_2023_1814_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/3bc3e3babbee/10753_2023_1814_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/a5cae29d0f77/10753_2023_1814_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/a47790125342/10753_2023_1814_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/28a3332205e4/10753_2023_1814_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/8283a996fab6/10753_2023_1814_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/11c487fc64bc/10753_2023_1814_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/3bc3e3babbee/10753_2023_1814_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/a5cae29d0f77/10753_2023_1814_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/a47790125342/10753_2023_1814_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eba/10359228/28a3332205e4/10753_2023_1814_Fig6_HTML.jpg

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