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Updated: May 13, 2026

Static Adhesion Assay for the Study of Integrin Activation in T Lymphocytes
Published on: June 13, 2014
[Selectins as adhesion molecules and potential therapeutic target].
J Jebali1, C Jeanneau, A Bazaa
1Laboratoire des Venins et Toxines, Institut Pasteur de Tunis 13, Place Pasteur 1002 Tunis Belvédère, Tunisie.
Selectins are adhesion molecules crucial for immune responses, mediating cell interactions via sugar recognition. This review details their structures, functions, and roles in inflammation and cancer.
Area of Science:
- Molecular Biology
- Immunology
- Glycobiology
Context:
- Selectins are key adhesion molecules mediating leukocyte trafficking and immune cell interactions.
- They recognize specific carbohydrate structures (sialyl-Lewis antigens) on their ligands.
- These interactions are vital at the blood-vessel wall interface during inflammation.
Purpose:
- To review the current understanding of selectin and selectin-ligand structures and functions.
- To update knowledge on the involvement of selectins in pathophysiological processes.
- To highlight their roles in inflammation and tumor development.
Summary:
- Selectins (L-, P-, and E-selectin) are structurally homologous adhesion molecules utilizing their Carbohydrate Recognition Domain (CRD) to bind specific glycans.
- Selectin-ligand interactions are fundamental to regulating inflammatory and immunological responses.
- This review consolidates knowledge on selectin biology and their implications in disease.
Impact:
- Provides a comprehensive overview of selectin-mediated cell adhesion.
- Enhances understanding of selectin roles in inflammatory diseases and cancer progression.
- Serves as a resource for researchers in immunology, glycobiology, and molecular medicine.
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