Suppr超能文献

自噬促进抗体增强的登革病毒在人类前嗜碱性粒细胞/肥大细胞中的感染。

Autophagy facilitates antibody-enhanced dengue virus infection in human pre-basophil/mast cells.

作者信息

Fang Yi-Ting, Wan Shu-Wen, Lu Yi-Tien, Yao Ju-Han, Lin Chiou-Feng, Hsu Li-Jin, Brown Michael G, Marshall Jean S, Anderson Robert, Lin Yee-Shin

机构信息

Department of Microbiology and Immunology, National Cheng Kung University Medical College, Tainan, Taiwan.

Department of Microbiology and Immunology, National Cheng Kung University Medical College, Tainan, Taiwan; Center of Infectious Disease and Signaling Research, National Cheng Kung University, Tainan, Taiwan.

出版信息

PLoS One. 2014 Oct 16;9(10):e110655. doi: 10.1371/journal.pone.0110655. eCollection 2014.

Abstract

BACKGROUND

Dengue virus (DENV) infection can cause severe hemorrhagic disease in humans. Although the pathogenic mechanisms underlying severe DENV disease remain unclear, one of the possible contributing factors is antibody-dependent enhancement (ADE) which occurs when sub-neutralizing antibodies derived from a previous DENV infection enhance viral infection through interaction between virus-antibody complexes and FcR-bearing cells, such as macrophages and basophil/mast cells. Although recent reports showed that DENV induces autophagy, the relationship between antibody-enhanced DENV infection and autophagy is not clear.

METHODOLOGY/PRINCIPAL FINDINGS: We showed that sub-neutralizing antibodies derived from dengue patient sera enhanced DENV infection and autophagy in the KU812 pre-basophil-like cell line as well as the HMC-1 immature mast cell line. Antibody-enhanced DENV infection of KU812 cells increased the number of autophagosome vesicles, LC3 punctation, LC3-II accumulation, and p62 degradation over that seen in cells infected with DENV alone. The percentages of DENV envelope (E) protein-positive cells and LC3 puncta following antibody-enhanced DENV infection of KU812 cells were reduced by the autophagy inhibitor 3-MA. Antibody-enhanced DENV infection of HMC-1 cells showed co-localization of DENV E protein and dsRNA with autophagosomes, which was inhibited by 3-MA treatment. Furthermore, DENV infection and replication were reduced when KU812 cells were transfected with the autophagy-inhibiting Atg4BC74A mutant.

CONCLUSIONS/SIGNIFICANCE: Our results demonstrate a significant induction of autophagy in antibody-enhanced DENV infection of pre-basophil-like KU812 and immature mast cell-like HMC-1 cells. Also, autophagy plays an important role in DENV infection and replication in these cells. Given the importance of ADE and FcR-bearing cells such as monocytes, macrophages and basophil/mast cells in dengue disease, the results provide insights into dengue pathogenesis and therapeutic means of control.

摘要

背景

登革病毒(DENV)感染可导致人类严重出血性疾病。尽管严重登革病毒病的致病机制尚不清楚,但一个可能的促成因素是抗体依赖性增强(ADE),当先前感染登革病毒产生的亚中和抗体通过病毒 - 抗体复合物与携带FcR的细胞(如巨噬细胞和嗜碱性粒细胞/肥大细胞)之间的相互作用增强病毒感染时,就会发生这种情况。尽管最近的报告显示登革病毒可诱导自噬,但抗体增强的登革病毒感染与自噬之间的关系尚不清楚。

方法/主要发现:我们发现,登革热患者血清中的亚中和抗体可增强KU812前嗜碱性粒细胞样细胞系以及HMC-1未成熟肥大细胞系中的登革病毒感染和自噬。与仅感染登革病毒的细胞相比,抗体增强的KU812细胞登革病毒感染增加了自噬体囊泡的数量、LC3斑点、LC3-II积累和p62降解。自噬抑制剂3-MA降低了抗体增强的KU812细胞登革病毒感染后登革病毒包膜(E)蛋白阳性细胞和LC3斑点的百分比。抗体增强的HMC-1细胞登革病毒感染显示登革病毒E蛋白和dsRNA与自噬体共定位,这被3-MA处理所抑制。此外,当KU812细胞用自噬抑制性Atg4BC74A突变体转染时,登革病毒感染和复制减少。

结论/意义:我们的结果表明,在抗体增强的前嗜碱性粒细胞样KU812和未成熟肥大细胞样HMC-1细胞登革病毒感染中,自噬有显著诱导。此外,自噬在这些细胞的登革病毒感染和复制中起重要作用。鉴于ADE和单核细胞、巨噬细胞和嗜碱性粒细胞/肥大细胞等携带FcR的细胞在登革热疾病中的重要性,这些结果为登革热发病机制和控制治疗手段提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d06/4199741/e1520eeb653c/pone.0110655.g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验