确定小鼠成骨细胞 MC3T3-E1 是对结节性皮肤病病毒做出反应的允许细胞系。

IF 2.2 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Journal of virological methods Pub Date : 2024-03-12 DOI:10.1016/j.jviromet.2024.114916
Ting You , Meng Wang , Hongqiang Zhang , Xiangwei Wang , Xiaolong Gao , Xiangping Yin , Yuefeng Sun , Guirong Wang , Hao-tai Chen , Shanhui Ren
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引用次数: 0

摘要

结节性皮肤病病毒(LSDV)是中国迅速出现的一种病原体。筛选适合 LSDV 复制的细胞对未来的致病机制研究和疫苗开发至关重要。以往的比较研究发现,啮齿类动物来源的 BHK21 是一种极易感染 LSDV 的细胞模型。本研究利用 Western 印迹、间接免疫荧光检测、流式细胞术和透射电子显微镜等方法,首次发现小鼠成骨细胞系 MC3T3-E1 是一种新型的 LSDV 感染易感细胞模型。MC3T3-E1作为一种合适的感染细胞模型的建立,增强了我们对支持LSDV复制的允许细胞和非允许细胞的种类范围和细胞类型的了解。这有助于加速未来对 LSDV 发病机制、临床应用和疫苗开发的研究。
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Identification of the murine osteoblastic cell MC3T3-E1 as a permissive cell line in response to lumpy skin disease virus

Lumpy skin disease virus (LSDV) is a rapidly emerging pathogen in China. Screening suitable cells for LSDV replication is vital for future research on pathogenic mechanisms and vaccine development. Previous comparative studies have identified that the rodent-derived BHK21 is a highly susceptible cell model to LSDV infection. Using western blot, indirect immune-fluorescence assay, flow cytometry, and transmission electron microscopy methods, this study is the first to identify the murine osteoblastic cell line MC3T3-E1 as a novel permissive cell model for LSDV infection. The establishment of MC3T3-E1 as a suitable infectious cell model enhances our understanding of the species range and cell types of the permissive cells and nonpermissive that support LSDV replication. It is helpful to accelerate future research on the pathogenesis, clinical application, and vaccine development of LSDV.

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来源期刊
CiteScore
5.80
自引率
0.00%
发文量
209
审稿时长
41 days
期刊介绍: The Journal of Virological Methods focuses on original, high quality research papers that describe novel and comprehensively tested methods which enhance human, animal, plant, bacterial or environmental virology and prions research and discovery. The methods may include, but not limited to, the study of: Viral components and morphology- Virus isolation, propagation and development of viral vectors- Viral pathogenesis, oncogenesis, vaccines and antivirals- Virus replication, host-pathogen interactions and responses- Virus transmission, prevention, control and treatment- Viral metagenomics and virome- Virus ecology, adaption and evolution- Applied virology such as nanotechnology- Viral diagnosis with novelty and comprehensive evaluation. We seek articles, systematic reviews, meta-analyses and laboratory protocols that include comprehensive technical details with statistical confirmations that provide validations against current best practice, international standards or quality assurance programs and which advance knowledge in virology leading to improved medical, veterinary or agricultural practices and management.
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