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Human soluble dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin inhibits phagocytosis of Staphylococcus aureus by immature dendritic cells / 南方医科大学学报
Article de Zh | WPRIM | ID: wpr-355331
Bibliothèque responsable: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To study the effect and mechanism of soluble dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin (sDC-SIGN) on the phagocytosis of Staphylococcus aureus (S. aureus) by immature dendritic cells (imDCs).</p><p><b>METHODS</b>Flow cytometry was employed to examine the effect of sDC-SIGN on the phagocytosis of S. aureus by imDCs. Enzyme-linked immunosorbent assay (ELISA) was used to analyze the binging of sDC-SIGN to S. aureus, lipoteichoic acid (LTA) and lipopolysaccharides (LPS) and investigate the effect of the ligands mannan and LTA and anti-DC-SIGN antibodies 1C6 and 4H3 on the binging of sDC-SIGN to S. aureus.</p><p><b>RESULTS</b>sDC-SIGN inhibited the phagocytosis of S. aureus by imDCs. sDC-SIGN bound to S. aureus in a Ca(2+)-dependent manner. sDC-SIGN concentration-dependently bound to LTA, but not to LTA, and the binging of sDC-SIGN to S. aureus was blocked by mannan, LTA, 1C6 and 4H3.</p><p><b>CONCLUSION</b>sDC-SIGN preferentially binds to the carbohydrate constituents on S. aureus to affect the binding between membrane-bound DC-SIGN and S. aureus, thus suppressing the phagocytosis of S. aureus by imDCs.</p>
Sujet(s)
Texte intégral: 1 Indice: WPRIM Sujet Principal: Phagocytose / Staphylococcus aureus / Acides teichoïques / Cellules dendritiques / Molécules d&apos;adhérence cellulaire / Lipopolysaccharides / Récepteurs de surface cellulaire / Biologie cellulaire / Lectines de type C / Métabolisme Limites du sujet: Humans langue: Zh Texte intégral: Journal of Southern Medical University Année: 2015 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Phagocytose / Staphylococcus aureus / Acides teichoïques / Cellules dendritiques / Molécules d&apos;adhérence cellulaire / Lipopolysaccharides / Récepteurs de surface cellulaire / Biologie cellulaire / Lectines de type C / Métabolisme Limites du sujet: Humans langue: Zh Texte intégral: Journal of Southern Medical University Année: 2015 Type: Article