Figure 4.
Figure 4. Cognate recognition of ECs enhances antigen-specific T-cell diapedesis in vivo. Cognate recognition of endothelial cells enhances antigen-specific T-cell diapedesis in vivo. Male C57BL/6 (H2b; ▪), congenic male B10.BR (H2k, ▦), or BALB/C and CBA/Ca (H2d, H2k; □) mice were treated with intrascrotal administration of IFN-γ (600 U in 400 μL saline). After 72 hours, fluorescently labeled HY-specific T cells (“Materials and methods”) were injected intravenously after surgical exteriorization of the cremaster muscle and T-cell interactions with venular walls were visualized and quantified by intravital microscopy for up to 40 minutes after injection of the cells (“Materials and methods”). Results are from 3 to 5 mice per group, and significant differences between the H2b in comparison with the H2k and H2d or the H2-congenic H2k strains of mice are shown by asterisk (*P < .05). (A) T-cell firm adhesion. (B) Extravasation.

Cognate recognition of ECs enhances antigen-specific T-cell diapedesis in vivo. Cognate recognition of endothelial cells enhances antigen-specific T-cell diapedesis in vivo. Male C57BL/6 (H2b; ▪), congenic male B10.BR (H2k, ▦), or BALB/C and CBA/Ca (H2d, H2k; □) mice were treated with intrascrotal administration of IFN-γ (600 U in 400 μL saline). After 72 hours, fluorescently labeled HY-specific T cells (“Materials and methods”) were injected intravenously after surgical exteriorization of the cremaster muscle and T-cell interactions with venular walls were visualized and quantified by intravital microscopy for up to 40 minutes after injection of the cells (“Materials and methods”). Results are from 3 to 5 mice per group, and significant differences between the H2b in comparison with the H2k and H2d or the H2-congenic H2k strains of mice are shown by asterisk (*P < .05). (A) T-cell firm adhesion. (B) Extravasation.

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