Publication | Open Access
E‐selectin and ICAM‐1 are incorporated into detergent‐insoluble membrane domains following clustering in endothelial cells
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Citations
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References
2002
Year
Proteinlipid InteractionEndothelial CellsCell AdhesionImmunologyLeukocyte AdhesionCellular PhysiologyInflammationDetergent‐insoluble Membrane DomainsCell SignalingAtherosclerosisMolecular SignalingLipid RaftsCell TraffickingVascular BiologyMembrane BiologySrc KinasesCell BiologyBiomolecular EngineeringEndothelial DysfunctionCell-matrix InteractionMedicineExtracellular Matrix
Here we present data supporting the role of lipid rafts in endothelial cells during leukocyte adhesion. Following adhesion of THP-1 cells or antibody-mediated clustering, both E-selectin and intercellular adhesion molecule-1 (ICAM-1) partitioned into the detergent-insoluble portion of the endothelial cellular lysate. Sucrose gradient centrifugation revealed the partitioning of clustered E-selectin and ICAM-1 with the low-density fraction where they co-fractionated with src family kinases, markers of lipid rafts. Depleting the plasma membrane of cholesterol inhibited clustering of adhesion molecules following their antibody-induced crosslinking and inhibited their association with src kinases. Thus, our data suggest that E-selectin and ICAM-1 associate with lipid rafts in human endothelial cells following leukocyte adhesion.
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