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Memory B lymphocytes from secondary lymphoid organs interact with E-selectin through a novel glycoprotein ligand
María C. Montoya, Karin Holtmann, Karen R. Snapp, Eric Borges, Francisco Sánchez-Madrid, Francis W. Luscinskas, Geoffrey Kansas, Dietmar Vestweber, Manuel O. de Landázuri
María C. Montoya, Karin Holtmann, Karen R. Snapp, Eric Borges, Francisco Sánchez-Madrid, Francis W. Luscinskas, Geoffrey Kansas, Dietmar Vestweber, Manuel O. de Landázuri
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Article

Memory B lymphocytes from secondary lymphoid organs interact with E-selectin through a novel glycoprotein ligand

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Abstract

Recirculation of B lymphocytes through the secondary lymphoid organs is key for recognition and response to foreign antigen. B lymphocytes within secondary lymphoid organs comprise a heterogeneous population of cells at distinct differentiation stages. To ascribe a particular adhesive behavior to discrete B-cell subsets within secondary lymphoid organs, we investigated their functional interaction with endothelial selectins under flow. We describe herein the characterization of a subset of human tonsillar B cells that interact with E-selectin but not P-selectin. E-selectin–interacting B cells had a phenotype of non–germinal center (CD10–, CD38–, CD44+), memory (IgD–) cells. Furthermore, FucT-VII was expressed selectively in CD44+ E-selectin–adherent B lymphocytes. B-cell rolling on E-selectin required sialic acid but was independent of previously described selectin ligands. A novel glycoprotein ligand of 240 kDa carrying N-linked glycans was isolated from B-cell membranes by an E-selectin immunoadhesin. Binding of this protein was strictly Ca2+ dependent, was inhibited by a cell adhesion–blocking mAb against E-selectin, and required the presence of sialic acid but not N-linked carbohydrates. Our results enable us to assign to resident memory B lymphocytes a novel adhesion function, the rolling on E-selectin, that provides insights on the adhesion pathways involved in homing of memory B cells to tertiary sites.

Authors

María C. Montoya, Karin Holtmann, Karen R. Snapp, Eric Borges, Francisco Sánchez-Madrid, Francis W. Luscinskas, Geoffrey Kansas, Dietmar Vestweber, Manuel O. de Landázuri

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Figure 4

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The E-selectin–binding subpopulation consists of CD19+, CD5–, CD44++, CD...
The E-selectin–binding subpopulation consists of CD19+, CD5–, CD44++, CD23–, CD38–, CD10–, and IgD– memory B lymphocytes. B cells purified from human tonsils were allowed to attach to CHO-E monolayers in C6 wells under rotation conditions (72 rpm) at 37°C; then wells were washed, and adherent cells were collected and analyzed by FACS as described in Methods. (a) Histograms showing expression of CD19, CD5, CD44, CD23, CD38, and CD10 on the total and adherent B-cell populations. The percentage of positive cells (highly positive for CD44, ++) is shown in the upper right corner of each histogram box. (b) Double staining of total and adherent subpopulations was carried out. Staining with mAb directed to CD38, CD44 in FL-2, and IgD in FL-1 is shown.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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