Journal
JOURNAL OF LIPID RESEARCH
Volume 62, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.jlr.2021.100084
Keywords
cholesterol; membrane; inner leaflet; transbilayer asymmetry; cholesterol availability; ratiometric sensors; quantitative fluorescence imaging; perfringolysin O toxin; Osh4; cholesterol pools
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Funding
- National Institutes of Health Training Grant [T32HL007820]
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The study confirms the asymmetric distribution of cholesterol in the mammalian cell membrane, with significantly lower levels in the inner leaflet compared to the outer leaflet. Additionally, primary cells were found to have particularly low levels of cholesterol in the inner leaflet. These findings support the universality of low basal cholesterol concentration in the inner leaflet under physiological conditions.
Cholesterol is an essential component of the mammalian plasma membrane involved in diverse cellular processes. Our recent quantitative imaging analysis using ratiometric cholesterol sensors showed that the available cholesterol concentration in the inner leaflet of the plasma membrane (IPM) is low in unstimulated cells and increased in a stimulus-specific manner to trigger cell signaling events. However, the transbilayer distribution of cholesterol in the plasma membrane of mammalian cells remains controversial. Here we report a systematic and rigorous evaluation of basal IPM cholesterol levels in a wide range of mammalian cells with different properties employing cholesterol sensors derived from the D4 domain of the Perfringolysin O toxin and a sterol-transfer protein, Osh4. Results consistently showed that, although basal IPM cholesterol levels vary significantly among cells, they remain significantly lower than cholesterol levels in the outer leaflets. We found that IPM cholesterol levels were particularly low in all tested primary cells. These results support the universality of the low basal IPM cholesterol concentration under physiological conditions. We also report here the presence of sequestered IPM cholesterol pools, which may become available to cytosolic proteins under certain physiological conditions. We hypothesize that these pools may partly account for the low basal level of available IPM cholesterol. In conclusion, we provide new experimental data that confirm the asymmetric transbilayer distribution of the plasma membrane cholesterol, which may contribute to regulation of various cellular signaling processes at the plasma membrane.
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