Developmental stage-specific shift in responsiveness to chemokines during human B-cell development

Tools

Item Type:	Article
Title:	Developmental stage-specific shift in responsiveness to chemokines during human B-cell development
Creators Name:	Honczarenko, M., Glodek, A.M., Swierkowski, M., Na, I.K. and Silberstein, L.E.
Abstract:	Objectives: To better understand the role of chemokines during human B-cell development in bone marrow. Methods: Differentiation stage-specific B cells (pro-B, pre-B, immature, and mature) were analyzed for chemokine receptor expression and for migration to corresponding ligands. We also hypothesized that inflammatory conditions may cause the upregulation of certain chemokine receptors on early B cells, rendering them sensitive to extramedullary chemotactic cues. To test this hypothesis, we used human pre-B 697 cells to investigate whether various inflammatory agents could modify chemokine receptor expression and function. Results: Chemotaxis to CXCL12 was observed for all B cell subsets. However, chemotactic responses to CCL19, CCL21, CXCL13, and CCL20 were limited to late-stage, IgM+ bone marrow B cells (immature B and mature B). Chemotactic responses to corresponding ligands correlated with the pattern of chemokine receptor expression. The expression of CCR7, however, was low on early (pro-B and pre-B) B cells and did not induce chemotaxis. Interestingly, both CCL19 and CCL21 could trigger ERK1/2 phosphorylation in early B cells. Exposure of pre-B 697 cells to TNF-alpha upregulated CCR7 and CXCR5 expression, whereas it had no effect on CCR6 surface expression. Correspondingly, TNF-alpha-stimulated pre-B cells chemotaxed towards CCL19 and CXCL13, in contrast to non-TNF-alpha-stimulated controls. Conclusion: We postulate that CXCR5, CCR7, and CCR6 participate in bone marrow trafficking and/or bone marrow egress of late-stage B cells under steady-state conditions, whereas inflammation-induced expression of CCR7 and CXCR5 may facilitate early B-cell emigration out of the bone marrow and their positioning in secondary lymphoid organs.
Keywords:	B-Lymphocytes, CC Chemokines, CCR6 Receptors, CCR7 Receptors, Chemokine CCL19, Chemokine CCL21, Chemokine Receptors, Chemotaxis, CXCR5 Receptors, Cytokine Receptors, Extracellular Signal-Regulated MAP Kinases, Gene Expression Regulation, Hematopoiesis, Immunoglobulin M, Phosphorylation, Tumor Necrosis Factor-alpha
Source:	Experimental Hematology
ISSN:	0301-472X
Publisher:	Elsevier
Volume:	34
Number:	8
Page Range:	1093-1100
Date:	August 2006
Official Publication:	https://doi.org/10.1016/j.exphem.2006.05.013
PubMed:	View item in PubMed

Repository Staff Only: item control page