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c-ABL在登革热病毒2型(DENV-2)感染及Vero细胞肌动蛋白重塑中的作用

Role of c-ABL in DENV-2 Infection and Actin Remodeling in Vero Cells.

作者信息

Carreño-Flórez Grace Paola, Cuartas-López Alexandra Milena, Boudreau Ryan L, Vicente-Manzanares Miguel, Gallego-Gómez Juan Carlos

机构信息

Translational Medicine Group-School of Medicine, Universidad de Antioquia, Medellín 050010, Colombia.

Department of Internal Medicine and Abboud Cardiovascular Research Center, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.

出版信息

Int J Mol Sci. 2025 Apr 29;26(9):4206. doi: 10.3390/ijms26094206.

Abstract

In this study, we address the role of c-ABL (cellular Abelson Tyr kinase) in the cytoskeletal rearrangements induced by DENV (Dengue virus) infection in mammalian cells. Using the specific inhibitor imatinib and targeted RNA interference, we show that c-ABL is necessary for viral entry and subsequent ENV (DENV envelope protein) accumulation in infected cells. In addition, c-ABL targeting attenuates F-actin reorganization induced by DENV infection. Together with the involvement of c-ABL in endothelial dysfunction induced by DENV and host secreted factors, our findings strongly suggest that c-ABL is a potential host-targeted antiviral that could control DENV infection and/or its evolution to more severe forms of the disease.

摘要

在本研究中,我们探讨了c-ABL(细胞Abelson酪氨酸激酶)在登革病毒(DENV)感染哺乳动物细胞诱导的细胞骨架重排中的作用。使用特异性抑制剂伊马替尼和靶向RNA干扰,我们发现c-ABL对于病毒进入以及感染细胞中随后的登革病毒包膜蛋白(ENV)积累是必需的。此外,靶向c-ABL可减弱DENV感染诱导的F-肌动蛋白重组。鉴于c-ABL参与了DENV和宿主分泌因子诱导的内皮功能障碍,我们的研究结果强烈表明,c-ABL是一种潜在的宿主靶向抗病毒药物,可控制DENV感染和/或将其演变为更严重疾病形式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/12071696/d738db50bdae/ijms-26-04206-g001.jpg

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