Fig. 2.
Fig. 2. [Ca++]i changes in CCR2- and CCR5-transfected cells. / Murine pre-B cells stably expressing human CCR2 or CCR5 were loaded with FURA-2, and [Ca++]i-dependent fluorescence changes were recorded after sequential stimulation with 1 μM eotaxin and 10 nM MCP-1 (for CCR2-expressing cells, A) or with 1 nM MIP-1β (for CCR5-expressing cells, B). Controls were run under the same conditions, using buffer instead of eotaxin. The tracings are representative of 2 independent experiments with each cell line.

[Ca++]i changes in CCR2- and CCR5-transfected cells.

Murine pre-B cells stably expressing human CCR2 or CCR5 were loaded with FURA-2, and [Ca++]i-dependent fluorescence changes were recorded after sequential stimulation with 1 μM eotaxin and 10 nM MCP-1 (for CCR2-expressing cells, A) or with 1 nM MIP-1β (for CCR5-expressing cells, B). Controls were run under the same conditions, using buffer instead of eotaxin. The tracings are representative of 2 independent experiments with each cell line.

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