Fig. 3.
Fig. 3. CCL21 and CCL19 chemotaxis of total T cells is reduced in homozygous lck/lck-mCCL21 transgenic versus normal mice. / Chemotaxis assays were performed comparing normal (WT/WT) and homozygous transgenic (lck/lck-mCCL21) mouse splenocytes (A-C) and thymocytes (D,E). Dose responses to 0, 200, 400, and 800 ng/mL chemokine were obtained. Flow cytometric analysis was performed to characterize starting and migrating cell populations. Severe deficiencies in transgenic CD3+ splenocyte and thymocyte chemotaxis in response to CCL21 (A,D) and CCL19 (B,E) are observed. Splenocyte chemotactic response to CXCL12 was unchanged (C).

CCL21 and CCL19 chemotaxis of total T cells is reduced in homozygous lck/lck-mCCL21 transgenic versus normal mice.

Chemotaxis assays were performed comparing normal (WT/WT) and homozygous transgenic (lck/lck-mCCL21) mouse splenocytes (A-C) and thymocytes (D,E). Dose responses to 0, 200, 400, and 800 ng/mL chemokine were obtained. Flow cytometric analysis was performed to characterize starting and migrating cell populations. Severe deficiencies in transgenic CD3+ splenocyte and thymocyte chemotaxis in response to CCL21 (A,D) and CCL19 (B,E) are observed. Splenocyte chemotactic response to CXCL12 was unchanged (C).

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