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• W2275609101 endingPage "3591" @default.
• W2275609101 startingPage "3585" @default.
• W2275609101 abstract "Abstract Selectin-dependent rolling is the earliest observable event in the recruitment of leukocytes to inflamed tissues. Several glycoproteins decorated with sialic acid, fucose, and/or sulfate have been shown to bind the selectins. The best-characterized selectin ligand is P-selectin glycoprotein-1 (PSGL-1) that supports P-selectin– dependent rolling in vitro and in vivo. In vitro studies have suggested that PSGL-1 may also be a ligand for E- and L-selectins. To study the in vivo function of PSGL-1, without the influence of other leukocyte proteins, the authors observed the interaction of PSGL-1–coated microspheres in mouse venules stimulated to express P- and/or E-selectin. Microspheres coated with functional recombinant PSGL-1 rolled in surgically stimulated and tumor necrosis factor alpha (TNFα)-stimulated mouse venules. P-selectin deficiency or inhibition abolished microsphere rolling in surgically and TNFα-stimulated venules, whereas E-selectin deficiency or inhibition increased microsphere rolling velocity in TNFα-stimulated venules. The results suggest that P-selectin–PSGL-1 interaction alone is sufficient to mediate rolling in vivo and that E-selectin–PSGL-1 interaction supports slow rolling." @default.
• W2275609101 created "2016-06-24" @default.
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• W2275609101 date "2000-11-15" @default.
• W2275609101 modified "2023-09-28" @default.
• W2275609101 title "P-selectin glycoprotein ligand-1 supports rolling on E- and P-selectin in vivo" @default.
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• W2275609101 doi "https://doi.org/10.1182/blood.v96.10.3585" @default.
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