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Binding Assay for Selectins

Jianing Zhang, Michiko N. Fukuda

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Abstract

Selectins form a group of C-type lectins, which bind to carbohydrates in a calcium dependent manner. Three selectins, E-, L-, and P-selectins are known. All selectins bind to sialyl Lewis X (sLe x ). E-selectin (endothelial cell adhesion molecule-1 or ELAM-1; CD62E) is expressed in the endothelial cells in response to inflammatory cytokines such as IL-1β or TNFα. E-selectin binds to the carbohydrate structure terminated by sialyl Lewis x (sLe x ) and sialyl Lewis a (sLe a ) ( 1 ). Counter receptors recognized by E-selectin are expressed by neutrophils, monocytes, eosinophils, memory T-lymphocytes, and natural killer cells. E-selectin recruits these leukocytes to the inflammatory site. Characterization of E-selectin-deficient mice confirmed a critical role of E-selectin in acute inflammatory models ( 2 ). These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Selectins form a group of C-type lectins, which bind to carbohydrates in a calcium dependent manner. Three selectins, E-, L-, and P-selectins are known. All selectins bind to sialyl Lewis X (sLe x ). E-selectin (endothelial cell adhesion molecule-1 or ELAM-1; CD62E) is expressed in the endothelial cells in response to inflammatory cytokines such as IL-1β or TNFα. E-selectin binds to the carbohydrate structure terminated by sialyl Lewis x (sLe x ) and sialyl Lewis a (sLe a ) ( 1 ). Counter receptors recognized by E-selectin are expressed by neutrophils, monocytes, eosinophils, memory T-lymphocytes, and natural killer cells. E-selectin recruits these leukocytes to the inflammatory site. Characterization of E-selectin-deficient mice confirmed a critical role of E-selectin in acute inflammatory models ( 2 ). These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Available abstract

Selectins form a group of C-type lectins, which bind to carbohydrates in a calcium dependent manner. Three selectins, E-, L-, and P-selectins are known. All selectins bind to sialyl Lewis X (sLe x ). E-selectin (endothelial cell adhesion molecule-1 or ELAM-1; CD62E) is expressed in the endothelial cells in response to inflammatory cytokines such as IL-1β or TNFα. E-selectin binds to the carbohydrate structure terminated by sialyl Lewis x (sLe x ) and sialyl Lewis a (sLe a ) ( 1 ). Counter receptors recognized by E-selectin are expressed by neutrophils, monocytes, eosinophils, memory T-lymphocytes, and natural killer cells. E-selectin recruits these leukocytes to the inflammatory site. Characterization of E-selectin-deficient mice confirmed a critical role of E-selectin in acute inflammatory models ( 2 ). These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Key concepts: Selectin, Sialyl-Lewis X, E-selectin, Cell adhesion molecule, Chemistry, Cell adhesion, L-selectin, Cell biology

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