Figure 7.
Figure 7. Induction of chemotaxis of CD8+ T cells, but not CD4+ T cells or granulocytes, by poly(I:C)–stimulated BMMCs in vitro. BMMCs were preincubated in the absence (□) or in the presence of 10 μg/mL poly(I:C) (▦) for 48 hours. To analyze migration of CD4+ T cells (A) or CD8+ T cells (B), LN cells from OTII or OTI mice were used, respectively. Percentages of migrated CD4+ or CD8+ T cells were determined by FACS and expressed as “chemotactic index” (**P < .001). One representative experiment of 3 is shown. Bone marrow cells were used to analyze migration of granulocytes. (C) Percentages of migrated granulocytes (Gr1+, CD11b+ double-positive cells) were determined by FACS. The “chemotactic index” was calculated as described in “Materials and methods.” One representative experiment of 3 is shown. BMMCs generated from 3 mice were analyzed in each experiment.

Induction of chemotaxis of CD8+ T cells, but not CD4+ T cells or granulocytes, by poly(I:C)–stimulated BMMCs in vitro. BMMCs were preincubated in the absence (□) or in the presence of 10 μg/mL poly(I:C) (▦) for 48 hours. To analyze migration of CD4+ T cells (A) or CD8+ T cells (B), LN cells from OTII or OTI mice were used, respectively. Percentages of migrated CD4+ or CD8+ T cells were determined by FACS and expressed as “chemotactic index” (**P < .001). One representative experiment of 3 is shown. Bone marrow cells were used to analyze migration of granulocytes. (C) Percentages of migrated granulocytes (Gr1+, CD11b+ double-positive cells) were determined by FACS. The “chemotactic index” was calculated as described in “Materials and methods.” One representative experiment of 3 is shown. BMMCs generated from 3 mice were analyzed in each experiment.

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