Suppr超能文献

CD82 控制 CpG 依赖的 TLR9 信号转导。

CD82 controls CpG-dependent TLR9 signaling.

机构信息

Division of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.

Biomedical Engineering and Biotechnology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.

出版信息

FASEB J. 2019 Nov;33(11):12500-12514. doi: 10.1096/fj.201901547R. Epub 2019 Aug 13.

Abstract

The tetraspanin CD82 is a potent suppressor of tumor metastasis and regulates several processes including signal transduction, cell adhesion, motility, and aggregation. However, the mechanisms by which CD82 participates in innate immunity are unknown. We report that CD82 is a key regulator of TLR9 trafficking and signaling. TLR9 recognizes unmethylated cytosine-phosphate-guanine (CpG) motifs present in viral, bacterial, and fungal DNA. We demonstrate that TLR9 and CD82 associate in macrophages, which occurs in the endoplasmic reticulum (ER) and post-ER. Moreover, CD82 is essential for TLR9-dependent myddosome formation in response to CpG stimulation. Finally, CD82 modulates TLR9-dependent NF-κB nuclear translocation, which is critical for inflammatory cytokine production. To our knowledge, this is the first time a tetraspanin has been implicated as a key regulator of TLR signaling. Collectively, our study demonstrates that CD82 is a specific regulator of TLR9 signaling, which may be critical in cancer immunotherapy approaches and coordinating the innate immune response to pathogens.-Khan, N. S., Lukason, D. P., Feliu, M., Ward, R. A., Lord, A. K., Reedy, J. L., Ramirez-Ortiz, Z. G., Tam, J. M., Kasperkovitz, P. V., Negoro, P. E., Vyas, T. D., Xu, S., Brinkmann, M. M., Acharaya, M., Artavanis-Tsakonas, K., Frickel, E.-M., Becker, C. E., Dagher, Z., Kim, Y.-M., Latz, E., Ploegh, H. L., Mansour, M. K., Miranti, C. K., Levitz, S. M., Vyas, J. M. CD82 controls CpG-dependent TLR9 signaling.

摘要

四跨膜蛋白 CD82 是肿瘤转移的有效抑制剂,调节包括信号转导、细胞黏附、运动和聚集在内的几个过程。然而,CD82 参与先天免疫的机制尚不清楚。我们报告 CD82 是 TLR9 运输和信号转导的关键调节因子。TLR9 识别病毒、细菌和真菌 DNA 中未甲基化的胞嘧啶-磷酸-鸟嘌呤(CpG)基序。我们证明 TLR9 和 CD82 在巨噬细胞中相互作用,这种相互作用发生在内质网(ER)和 ER 后。此外,CD82 是 TLR9 依赖的 CpG 刺激后 MyD88 形成所必需的。最后,CD82 调节 TLR9 依赖的 NF-κB 核易位,这对于炎症细胞因子的产生至关重要。据我们所知,这是第一次有四跨膜蛋白被牵连为 TLR 信号的关键调节因子。总的来说,我们的研究表明 CD82 是 TLR9 信号的特异性调节因子,这在癌症免疫治疗方法中以及协调先天免疫反应以对抗病原体方面可能是至关重要的。

相似文献

1
CD82 controls CpG-dependent TLR9 signaling.CD82 控制 CpG 依赖的 TLR9 信号转导。
FASEB J. 2019 Nov;33(11):12500-12514. doi: 10.1096/fj.201901547R. Epub 2019 Aug 13.

引用本文的文献

4
Toll-like receptors in cardiac hypertrophy.心脏肥大中的Toll样受体
Front Cardiovasc Med. 2023 Apr 11;10:1143583. doi: 10.3389/fcvm.2023.1143583. eCollection 2023.
9
Role of Metastasis Suppressor KAI1/CD82 in Different Cancers.转移抑制因子KAI1/CD82在不同癌症中的作用
J Oncol. 2021 Jul 9;2021:9924473. doi: 10.1155/2021/9924473. eCollection 2021.
10
Regulation of the nucleic acid-sensing Toll-like receptors.核酸感应 Toll 样受体的调控。
Nat Rev Immunol. 2022 Apr;22(4):224-235. doi: 10.1038/s41577-021-00577-0. Epub 2021 Jul 16.

本文引用的文献

5
IRAP endosomes restrict TLR9 activation and signaling.IRAP 内涵体限制 TLR9 的激活和信号转导。
Nat Immunol. 2017 May;18(5):509-518. doi: 10.1038/ni.3711. Epub 2017 Mar 20.
7
TLR9 and its signaling pathway in multiple sclerosis.Toll样受体9(TLR9)及其在多发性硬化症中的信号通路
J Neurol Sci. 2017 Feb 15;373:95-99. doi: 10.1016/j.jns.2016.12.027. Epub 2016 Dec 19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验