The Importance of Physiologically Relevant Cell Lines for Studying Virus-Host Interactions

被引:28
作者
Hare, David [1 ]
Collins, Susan [1 ]
Cuddington, Breanne [1 ]
Mossman, Karen [1 ,2 ]
机构
[1] McMaster Univ, Pathol & Mol Med, 1280 Main Str West, Hamilton, ON L8S 4L8, Canada
[2] McMaster Univ, Biochem & Biomed Sci, 1280 Main Str West, Hamilton, ON L8S 4L8, Canada
来源
VIRUSES-BASEL | 2016年 / 8卷 / 11期
关键词
primary cell; immortalized cell; interferon; interferon regulatory factor 3; interferon-stimulated genes; signal transduction; antiviral defense; INTERFERON REGULATORY FACTOR-3; TRANSCRIPTION FACTOR IRF-1; ALPHA/BETA GENE INDUCTION; CYTOSOLIC DNA SENSOR; HUMAN-DIPLOID CELLS; INNATE IMMUNITY; T-ANTIGEN; ANTIVIRAL IMMUNITY; HUMAN FIBROBLASTS; VIRAL-INFECTIONS;
D O I
10.3390/v8110297
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Viruses interact intimately with the host cell at nearly every stage of replication, and the cell model that is chosen to study virus infection is critically important. Although primary cells reflect the phenotype of healthy cells in vivo better than cell lines, their limited lifespan makes experimental manipulation challenging. However, many tumor-derived and artificially immortalized cell lines have defects in induction of interferon-stimulated genes and other antiviral defenses. These defects can affect virus replication, especially when cells are infected at lower, more physiologically relevant, multiplicities of infection. Understanding the selective pressures and mechanisms underlying the loss of innate signaling pathways is helpful to choose immortalized cell lines without impaired antiviral defense. We describe the trials and tribulations we encountered while searching for an immortalized cell line with intact innate signaling, and how directed immortalization of primary cells avoids many of the pitfalls of spontaneous immortalization.
引用
收藏
页数:10
相关论文
共 38 条
  • [21] Visualizing Infection Spread: Dual-Color Fluorescent Reporting of Virus-Host Interactions
    Swick, Adam
    Baltes, Ashley
    Yin, John
    BIOTECHNOLOGY AND BIOENGINEERING, 2014, 111 (06) : 1200 - 1209
  • [22] Virus-host mucosal interactions during early SIV rectal transmission
    Lu, Wuxun
    Ma, Fangrui
    Churbanov, Alexander
    Wan, Yanmin
    Li, Yue
    Kang, Guobin
    Yuan, Zhe
    Wang, Dong
    Zhang, Chi
    Xu, Jianqing
    Lewis, Mark
    Li, Qingsheng
    VIROLOGY, 2014, 464 : 406 - 414
  • [23] Virus-host interactions during tick-borne bunyavirus infection
    Fares, Mazigh
    Brennan, Benjamin
    CURRENT OPINION IN VIROLOGY, 2022, 57
  • [24] Dengue virus-host interactions: Structural and mechanistic insights for future therapeutic strategies
    Khanra, Moumita
    Ghosh, Indrani
    Khatun, Samima
    Ghosh, Nilanjan
    Gayen, Shovanlal
    JOURNAL OF STRUCTURAL BIOLOGY, 2025, 217 (02)
  • [25] Recent Updates on Research Models and Tools to Study Virus-Host Interactions at the Placenta
    Lee, Jae Kyung
    Oh, Soo-Jin
    Park, Hosun
    Shin, Ok Sarah
    VIRUSES-BASEL, 2020, 12 (01):
  • [26] Organoids to Dissect Gastrointestinal Virus-Host Interactions: What Have We Learned?
    Crawford, Sue E.
    Ramani, Sasirekha
    Blutt, Sarah E.
    Estes, Mary K.
    VIRUSES-BASEL, 2021, 13 (06):
  • [27] UL24 herpesvirus determinants of pathogenesis: Roles in virus-host interactions
    Pearson, Angela
    Bouhamar, Amel
    VIROLOGY, 2025, 603
  • [28] The use of single-cell RNA-seq to study heterogeneity at varying levels of virus-host interactions
    Swaminath, Sharmada
    Russell, Alistair B.
    PLOS PATHOGENS, 2024, 20 (01)
  • [29] Granulocyte macrophage colony stimulating factor in virus-host interactions and its implication for immunotherapy
    Bouzeineddine, Nasry Zane
    Philippi, Alecco
    Gee, Katrina
    Basta, Sam
    CYTOKINE & GROWTH FACTOR REVIEWS, 2025, 81 : 54 - 63
  • [30] Epitranscriptomic(N6-methyladenosine) Modification of Viral RNA and Virus-Host Interactions
    Imam, Hasan
    Kim, Geon-Woo
    Siddiqui, Aleem
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2020, 10