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• W2080663602 startingPage "67" @default.
• W2080663602 abstract "Cell adhesion plays an important role in cell–cell contact formation and cell migration. Thus, the assessment of cellular adhesiveness is one important feature when studying cell-mediated immune responses. The interaction of lymphocytes with other cell types such as antigen-presenting cells or vascular–endothelial cells occurs via adhesion molecules including L-selectin, VCAM-1 or ICAM-1. There are principally two mechanisms by which cell adhesion can be enhanced: namely changes in the affinity or avidity of receptor interactions. Conventional plate-based adhesion assays detect both forms. However, they do not permit discrimination between affinity- and avidity-mediated changes in the adhesiveness. Moreover, analysis of cell subpopulations requires cell separation prior to performance of the adhesion assay. Conventional flow-cytometry-based tests make it possible to determine changes in the affinity of integrins at the single cell level. However, they fail to quantify avidity-mediated adhesiveness. Here we describe a novel flow-cytometry-based assay, which allows the detection of both integrin-mediated affinity as well as avidity changes at the single cell level. This opens up the possibility of precisely characterizing the adhesive capacity of subpopulations in heterogeneous cell populations." @default.
• W2080663602 created "2016-06-24" @default.
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• W2080663602 date "2006-03-01" @default.
• W2080663602 modified "2023-10-13" @default.
• W2080663602 title "A novel flow-cytometry-based assay for quantification of affinity and avidity changes of integrins" @default.
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• W2080663602 doi "https://doi.org/10.1016/j.jim.2005.12.005" @default.
• W2080663602 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16458321" @default.
• W2080663602 hasPublicationYear "2006" @default.
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