Figure 4.
Figure 4. Neutrophil recruitment is reduced in Tln13mut mice. (A-D) In vivo leukocyte rolling velocity, adhesion efficiency, and extravasation were analyzed in mouse cremaster muscle venules of WT and Tln13mut mice 2 hours after intrascrotal injection of TNF-α. Rolling velocity (A) and adhesion efficiency (B) (adherent cells per mm2 normalized to the total neutrophil count) were analyzed using intravital microscopy. (C) Leukocyte extravasation was assessed in the perivascular region upon Giemsa staining of cremaster muscle whole mounts (n = 17 vessels in 4 WT and 4 Tln3mut mice). Values are given as means ± standard errors of the mean. (D) Representative images of Giemsa-stained whole mounts of WT and Tln13mut mice. Arrows point to extravasated neutrophils. Scale bar, 30 µm. *P < .05, ***P < .001.

Neutrophil recruitment is reduced in Tln13mutmice. (A-D) In vivo leukocyte rolling velocity, adhesion efficiency, and extravasation were analyzed in mouse cremaster muscle venules of WT and Tln13mut mice 2 hours after intrascrotal injection of TNF-α. Rolling velocity (A) and adhesion efficiency (B) (adherent cells per mm2 normalized to the total neutrophil count) were analyzed using intravital microscopy. (C) Leukocyte extravasation was assessed in the perivascular region upon Giemsa staining of cremaster muscle whole mounts (n = 17 vessels in 4 WT and 4 Tln3mut mice). Values are given as means ± standard errors of the mean. (D) Representative images of Giemsa-stained whole mounts of WT and Tln13mut mice. Arrows point to extravasated neutrophils. Scale bar, 30 µm. *P < .05, ***P < .001.

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