Figure 2
CXCR7 does not trigger calcium mobilization in response to CXCL12 and modulates that of CXCR4. (A) Representative Ca2+ responses triggered by 1 μM CXCL12 in HEK-293T cells transfected with a Gα16-apoaequorin encoding vector and either CXCR4 or CXCR7. (B) Calcium mobilization assay in CHO-K1-CXCR4 cells expressing or not either CXCR7-GFP or CCR5-GFP (left panel). Cells were loaded with Coelenterazine h, and [Ca2+]i levels were measured after exposure to the indicated CXCL12 concentrations. Values (mean ± SEM, n = 3) are expressed as percentage of the maximal response. CXCR7 and CCR5 cell surface expression levels were determined by fluorescence intensity measurements (right panel). EC50 values for CXCL12 were significantly different in the presence of CXCR7 (CXCR4/CXCR7+ or CXCR4/CXCR7++ cells) compared with cells expressing CXCR4 alone (P < .05).

CXCR7 does not trigger calcium mobilization in response to CXCL12 and modulates that of CXCR4. (A) Representative Ca2+ responses triggered by 1 μM CXCL12 in HEK-293T cells transfected with a Gα16-apoaequorin encoding vector and either CXCR4 or CXCR7. (B) Calcium mobilization assay in CHO-K1-CXCR4 cells expressing or not either CXCR7-GFP or CCR5-GFP (left panel). Cells were loaded with Coelenterazine h, and [Ca2+]i levels were measured after exposure to the indicated CXCL12 concentrations. Values (mean ± SEM, n = 3) are expressed as percentage of the maximal response. CXCR7 and CCR5 cell surface expression levels were determined by fluorescence intensity measurements (right panel). EC50 values for CXCL12 were significantly different in the presence of CXCR7 (CXCR4/CXCR7+ or CXCR4/CXCR7++ cells) compared with cells expressing CXCR4 alone (P < .05).

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