Transcriptomic analysis of coxsackievirus B3 infection in induced pluripotent stem cell-derived brain-like endothelial cells

Coxsackievirus B3 (CVB3) is a leading cause of viral aseptic meningitis that can produce severe disease in susceptible individuals. To gain access to the central nervous system, CVB3 must cross central nervous system barriers, such as the blood-brain barrier. Previously, we have shown that CVB3 infects a human stem cell-derived brain-like endothelial cell model. Here, we report the global transcriptome of stem cell-derived brain-like endothelial cells to CVB3 infection and provide proof-of-concept validation of the dataset using molecular biology techniques. These data could inform novel mechanisms of CVB3-mediated blood-brain barrier dysfunction.

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Publication Details

Journal
Journal of Virology
Published
2024-12-13
DOI
https://doi.org/10.1128/jvi.01824-24
Citations
2
Primary Topic
Viral Infections and Immunology Research
Type
article
Field-Weighted Citation Impact
0.80

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article

Transcriptomic analysis of coxsackievirus B3 infection in induced pluripotent stem cell-derived brain-like endothelial cells

Sarah F. Hathcock, Mohammad-Reza Shokri, Robert N. Correll, Jon Sin et al.
2 citations
Journal of Virology
Viral Infections and Immunology Research
0.80
article

Transcriptomic analysis of coxsackievirus B3 infection in induced pluripotent stem cell-derived brain-like endothelial cells

Sarah F. Hathcock, Mohammad-Reza Shokri, Robert N. Correll, Jon Sin, Daryl W. Lam, Nadine Vollmuth, Brandon J. Kim, Julia Mamana, Taryn E. Keyzer, H. Mauser
article en
2 citations

Abstract

Coxsackievirus B3 (CVB3) is a leading cause of viral aseptic meningitis that can produce severe disease in susceptible individuals. To gain access to the central nervous system, CVB3 must cross central nervous system barriers, such as the blood-brain barrier. Previously, we have shown that CVB3 infects a human stem cell-derived brain-like endothelial cell model. Here, we report the global transcriptome of stem cell-derived brain-like endothelial cells to CVB3 infection and provide proof-of-concept validation of the dataset using molecular biology techniques. These data could inform novel mechanisms of CVB3-mediated blood-brain barrier dysfunction.

Journal of VirologyVol. 99(1)
University of Alabama (US), University of Alabama at Birmingham (US), Convergent Science (United States) (US)
San Diego State University, National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Neurological Disorders and Stroke
Good health and well-being
Openalex Percentile: Top 22%
Viral Infections and Immunology Research
0.80
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