2022
DOI: 10.1016/j.bbalip.2022.159140
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Lipid rafts as viral entry routes and immune platforms: A double-edged sword in SARS-CoV-2 infection?

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Cited by 14 publications
(18 citation statements)
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“…In the cases of HIV-1, HSV-1, and Newcastle disease virus, the major role in the fusogenic activity of viral peptides was attributed to cholesterol ( Martín et al, 2012 ; Apellániz et al, 2014 ; Vitiello et al, 2015 ). Recent data also indicate that CHOL-enriched membrane domains are of key importance for SARS-CoV-2 entry into cells ( Li et al, 2021 ; Alketbi et al, 2021 ; Sanders et al, 2021 ; Bakillah et al, 2022 ; Roncato et al, 2022 ). Moreover, viral fusion peptides, particularly that of HIV, preferentially target the L o /L α boundary regions ( Yang et al, 2015 ; Molotkovsky et al, 2018 ).…”
Section: Resultsmentioning
confidence: 99%
“…In the cases of HIV-1, HSV-1, and Newcastle disease virus, the major role in the fusogenic activity of viral peptides was attributed to cholesterol ( Martín et al, 2012 ; Apellániz et al, 2014 ; Vitiello et al, 2015 ). Recent data also indicate that CHOL-enriched membrane domains are of key importance for SARS-CoV-2 entry into cells ( Li et al, 2021 ; Alketbi et al, 2021 ; Sanders et al, 2021 ; Bakillah et al, 2022 ; Roncato et al, 2022 ). Moreover, viral fusion peptides, particularly that of HIV, preferentially target the L o /L α boundary regions ( Yang et al, 2015 ; Molotkovsky et al, 2018 ).…”
Section: Resultsmentioning
confidence: 99%
“…Hypothesized downregulators of ACE2 receptors namely estradiol (3, Figure 3), retinoic acid (4, Figure 3), isotretinoin (5, Figure 3), and spironolactone (6, Figure 3) are also under consideration in line with this strategy (Figure 3). 109 ACE2 modulation by estrogens leading to decreased release of cytokines and inhibiting the activation of host immune response, thrombosis and fibrosis and in a way preventing the deterioration in the COVID-19 outcome has also come to light, making Raloxifene (7, Figure 3) (selective estrogen receptor modulator) an attractive agent for COVID-19 treatment. 110 Another approach necessitates reduced cell surface ACE2 caused by the impairment of ACE2 trafficking which can be brought about by a pharmacological compound, Berbamine (8, Figure 3).…”
Section: Lipid-inspired Therapeutics For Covid-19mentioning
confidence: 99%
“…Treatment of Caco-2 cells with Camostat mesylate ( 9 , Figure ), a TMPRSS2 inhibitor, has been shown to partially prevent SARS-CoV-2 infection, Figure . Apart from inhibiting viral entry into cultured lung cells, Camostat mesylate also prevents the propagation of the virus in human lung tissues as tested in ex vivo experiments. , On account of its role in viral and host membrane fusion, TMPRSS2 inhibitors such as bicalutamide ( 10 , Figure ), bromhexine ( 11 , Figure ), and nafamostat ( 12 , Figure ), are also being hypothesized to be able control SARS-CoV-2 infection …”
Section: Lipid-inspired Therapeutics For Covid-19mentioning
confidence: 99%
“…In both SARS-CoV-2 [ 37 ] and EBOV [ 41 , 42 ], the T cell Ig and mucin domain (TIM) family of proteins is shown to be involved in the above mentioned mechanism. Lipid raft domains rich in cholesterol and sphingolipids, on cellular membranes that play a significant role in viral trafficking and pathogenicity, are also studied in SARS-CoV-2 [ 43 ] and EBOV Virus [ 44 ].…”
Section: A Comparative Look At the Pathogenic Rna Viruses—sars-cov-2 ...mentioning
confidence: 99%