2022
DOI: 10.3389/fphar.2022.971017
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Single-cell sequencing of brain tissues reveal the central nervous system’s susceptibility to SARS-CoV-2 and the drug

Abstract: Background: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) caused the current COVID-19 pandemic, resulting in a public health crisis that required immediate action. The SARS-CoV-2 virus enters human cells via three receptors, namely cathepsin, angiotensin-converting enzyme 2 (ACE2) and SARS-CoV receptors. Cathepsin destroys the spike protein (S protein), thereby allowing the entry of viral nucleic acid into human host cells.Methods: Utilizing single-cell transcriptome analysis of brain tissue… Show more

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Cited by 4 publications
(4 citation statements)
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“…Automatic annotation of the cells was done with the SingleR program. We conducted pseudotime trajectory analysis using the default configuration parameters of the Monocle 2 program [ 22 ].…”
Section: Methodsmentioning
confidence: 99%
“…Automatic annotation of the cells was done with the SingleR program. We conducted pseudotime trajectory analysis using the default configuration parameters of the Monocle 2 program [ 22 ].…”
Section: Methodsmentioning
confidence: 99%
“…Ultimately, all cells in the dataset met quality control standards. Principal component analysis (PCA) ( 13 )was performed using the Seurat package ( 14 ) (version 3.2.2) in R software (version 4.0.2), along with JackStraw and PCEIbowPlot ( 15 ) functions, to select important principal components (PCs). Seurat’s FindAllMarkers function was used to identify specific genes for each cell subgroup.…”
Section: Methodsmentioning
confidence: 99%
“…However, many of those did so by immunostaining or in situ hybridization and without co-staining for endothelial markers [ 40 42 ]. And while the question of whether endothelial cell express ACE2 should easily be resolved by single cell RNA-Seq experiments, even those results are contradicting, with some results indicating little or no expression [ 43 46 ] and other stating that there is high expression in endothelial cells [ 47 ]. In papers that specifically looked at the heart, only cardiomyocytes and pericytes were found to have any significant expression of ACE2 [ 46 , 48 , 49 ].…”
Section: Endothelial Cell Damage and Microthrombi Formationmentioning
confidence: 99%