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. 1997 Nov 17;186(10):1725–1735. doi: 10.1084/jem.186.10.1725

Figure 5.

Figure 5

The effect of anti-α6 and anti-α4 integrin antibodies on TNF-α–induced epidermal LC migration in vivo. Groups of four mice received 40 μg of (A) anti-α6 integrin (GoH3) or (B) anti-α4 integrin (PS/2) antibody intraperitoneally. Controls either received isotype-matched control antibody or were left untreated. 2 h after administration of antibody, two mice per group received 30 μl injection intradermally into both ear pinnae of 50 ng murine TNF-α in 0.1% BSA. The remaining two mice received 30 μl intradermal injection of 0.1% BSA. Ears were removed 30 min later, epidermal sheets were prepared, and the number of LCs/mm2 was determined by immunofluorescence analysis. Results are means ± SD (n = 40). Treatment of mice with TNF-α (in both A and B) caused a significant decrease in the frequency of LCs compared with either untreated controls or mice exposed to BSA alone (P <0.005). Treatment with anti-α6 resulted in a significantly higher frequency of LC compared with mice exposed to TNF-α together with an isotype-matched control antibody (P <0.005; A). In contrast, anti-α4 failed to affect significantly LC frequency compared with isotype controls.