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- W2131799581 abstract "The ability of chemokines, particularly MCP-1, to induce integrin-dependent binding of T lymphocytes to endothelial adhesion molecules or extracellular matrix (ECM) components was examined. MCP-1 induced significant adhesion to fibronectin (FN) and to endothelial-secreted ECM but not to purified ICAM-1 or VCAM-1, or to activated endothelium. The MCP-1- induced binding of T lymphocytes to FN was rapid, dose dependent, and resulted from activation of both VLA-4 and VLA-5. Like MCP-1, the chemokines RANTES and MIP-1β induced T lymphocyte binding to FN, but not to ICAM-1. We suggest, therefore, that these T lymphocyte chemokines may be most important, not in initiating integrin-dependent firm adhesion of T lymphocytes to the vascular wall, but rather, in subsequent adhesive interactions during migration into tissue." @default.
- W2131799581 created "2016-06-24" @default.
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- W2131799581 date "1996-02-01" @default.
- W2131799581 modified "2023-10-12" @default.
- W2131799581 title "The C–C Chemokine MCP-1 Differentially Modulates the Avidity of β1 and β2 Integrins on T Lymphocytes" @default.
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- W2131799581 doi "https://doi.org/10.1016/s1074-7613(00)80682-2" @default.
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