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• W1994533075 abstract "A novel fluorescence microscope/laser optical system was developed to measure fast transients of membrane-proximal versus bulk cytoplasmic intracellular calcium levels in cells labeled with a fluorescent calcium indicator. The method is based on the rapid chopping of illumination of the cells between optical configurations for epifluorescence, which excites predominantly the bulk intracellular region, and total internal reflection fluorescence, which excites only the region within approximately 100 nm of the cell-substrate contact. This method was applied to Fluo-3-loaded neutrophils that were activated by the chemoattractant N-formyl-met-leu-phe. Chemoattractant-activated cells showed 1) transient increases in both membrane-proximal and bulk cytosolic Ca2+ that peaked simultaneously; 2) a larger fractional change (20-60%) in membrane-proximal Ca2+ relative to bulk cytosolic Ca2+ that peaked at a time when the main Ca2+ transient was decreasing in both regions and that persisted well after the main transient was over. This method should be applicable to a wide variety of cell types and fluorescent ion indicators in which membrane-proximal ionic transients may be different from those deeper within the cytosol." @default.
• W1994533075 created "2016-06-24" @default.
• W1994533075 creator A5070769503 @default.
• W1994533075 creator A5087088078 @default.
• W1994533075 date "1996-11-01" @default.
• W1994533075 modified "2023-10-15" @default.
• W1994533075 title "Membrane-proximal calcium transients in stimulated neutrophils detected by total internal reflection fluorescence" @default.
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• W1994533075 doi "https://doi.org/10.1016/s0006-3495(96)79485-7" @default.
• W1994533075 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1233774" @default.
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