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刺胞毒素是一种来自海洋海葵的成孔蛋白,可通过 TLR4 依赖途径诱导树突状细胞成熟。

Sticholysins, pore-forming proteins from a marine anemone can induce maturation of dendritic cells through a TLR4 dependent-pathway.

机构信息

Laboratory of Toxins and Liposomes, Center for Protein Studies, Faculty of Biology, University of Havana (UH), Lab UH-CIM, Havana, 10400, Cuba.

Discipline of Immunology, Department of Microbiology, Immunology and Parasitology, Federal University of São Paulo (UNIFESP), 04023-062, São Paulo, Brazil.

出版信息

Mol Immunol. 2021 Mar;131:144-154. doi: 10.1016/j.molimm.2020.12.032. Epub 2021 Jan 6.

Abstract

Sticholysins (Sts) I and II (StI and StII) are pore-forming proteins (PFPs), purified from the Caribbean Sea anemone Stichodactyla helianthus. StII encapsulated into liposomes induces a robust antigen-specific cytotoxic CD8 T lymphocytes (CTL) response and in its free form the maturation of bone marrow-derived dendritic cells (BM-DCs). It is probable that the latter is partially supporting in part the immunomodulatory effect on the CTL response induced by StII-containing liposomes. In the present work, we demonstrate that the StII's ability of inducing maturation of BM-DCs is also shared by StI, an isoform of StII. Using heat-denatured Sts we observed a significant reduction in the up-regulation of maturation markers indicating that both PFP's ability to promote maturation of BM-DCs is dependent on their conformational characteristics. StII-mediated DC maturation was abrogated in BM-DCs from toll-like receptor (TLR) 4 and myeloid differentiation primary response gene 88 (MyD88)-knockout mice but not in cells from TLR2-knockout mice. Furthermore, the antigen-specific CTL response induced by StII-containing liposomes was reduced in TLR4-knockout mice. These results indicate that StII, and probably by extension StI, has the ability to induce maturation of DCs through a TLR4/MyD88-dependent pathway, and that this activation contributes to the CTL response generated by StII-containing liposomes.

摘要

海葵毒素 I 和 II(StI 和 StII)是从加勒比海海葵 Stichodactyla helianthus 中纯化出来的孔形成蛋白(PFPs)。包封在脂质体中的 StII 诱导强烈的抗原特异性细胞毒性 CD8 T 淋巴细胞(CTL)反应,而其游离形式则诱导骨髓来源的树突状细胞(BM-DCs)成熟。可能部分原因是后者部分支持 StII 脂质体诱导的 CTL 反应的免疫调节作用。在本工作中,我们证明了 StI,即 StII 的一种同工型,也具有诱导 BM-DCs 成熟的能力。使用热变性的 Sts,我们观察到成熟标志物的上调显著减少,表明这两种 PFPs 促进 BM-DCs 成熟的能力依赖于它们的构象特征。StII 介导的 DC 成熟在 TLR4 和髓样分化初级反应基因 88(MyD88)敲除小鼠的 BM-DCs 中被阻断,但在 TLR2 敲除小鼠的细胞中没有被阻断。此外,StII 脂质体诱导的抗原特异性 CTL 反应在 TLR4 敲除小鼠中减少。这些结果表明,StII(可能通过扩展)具有通过 TLR4/MyD88 依赖性途径诱导 DC 成熟的能力,并且这种激活有助于 StII 脂质体诱导的 CTL 反应的产生。

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