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. 1998 Jul 1;188(1):181–191. doi: 10.1084/jem.188.1.181

Figure 5.

Figure 5

Chemotactic activity of ELC on resting and acutely activated mouse lymphocytes. Results are expressed as the percentage of input cells of each subtype migrating to the lower chamber of a transwell filter. Panels show migration of spleen lymphocyte subsets: (A) CD4 T cells, CD8 T cells, and B cells; (B) L-selectinhi and L-selectinlo CD4 T cells; (C) B cells preincubated with anti-IgM (17 μg/ml) or media alone (control) for 4 h; (D) duplicate experiment to C with cells preincubated with media alone (−) or anti-IgM (aμ) for 4 h; (E) purified B cells preincubated with media alone (−), anti-IgM at 17 μg/ml (aμ), or LPS at 20 μg/ml (L) for 6 h; (F) total spleen cells in the absence of a gradient (no gradient, equal concentration of ELC in upper and lower chamber) or preincubated with pertussis toxin at 200 ng/ml (PTX) for 2 h. In A–E, SDF1α was included at 300 ng/ml as a positive control. In D, ELC was at 200 ng/ml, and in E and F at 300 ng/ml. The results in A–C are representative of three independent experiments, and results in D–F of two experiments.