Figure 1
Figure 1. Dorsomorphin inhibits leukocyte adhesion to the vascular wall in vivo, whereas BMP2 is up-regulated in vascular inflammation and stimulates leukocyte adhesion. (A) BMP-antagonist dorsomorphin prevents TNFα-mediated leukocyte adhesion in vivo. Four hours after injection of TNFα (10 ng/g bw IP, n = 5) alone or in combination with dorsomorphin (13 μg/g bw IP, n = 6) leukocyte adhesion was quantified by intravital microscopy of mesenterial venules. (B) BMP2 increased TNFα-induced leukocyte adhesion in vivo. C57BL/6 mice were injected with TNFα alone (10 ng/g bw IP, n = 5) or in combination with recombinant BMP2 (0.33 μg/g bw IP, n = 6). Four hours after injection leukocyte adhesion was quantified by intravital microscopy of mesenterial venules (*P < .05 versus control). (C) TNFα enhances BMP2 RNA expression. HUVECs were exposed to TNFα with indicated concentrations. Twenty-four hours after TNFα-stimulation cells were lysed and BMP2 RNA expression was assessed by quantitative real-time PCR. (D) LPS increased BMP2 protein in vivo as demonstrated by Western blotting. C57BL/6 mice were injected with LPS for 3 days (2.5 μg/g/d). Lungs were minced in RIPA buffer to obtain protein. Lysates were used for Western blotting. GAPDH was used as loading control.

Dorsomorphin inhibits leukocyte adhesion to the vascular wall in vivo, whereas BMP2 is up-regulated in vascular inflammation and stimulates leukocyte adhesion. (A) BMP-antagonist dorsomorphin prevents TNFα-mediated leukocyte adhesion in vivo. Four hours after injection of TNFα (10 ng/g bw IP, n = 5) alone or in combination with dorsomorphin (13 μg/g bw IP, n = 6) leukocyte adhesion was quantified by intravital microscopy of mesenterial venules. (B) BMP2 increased TNFα-induced leukocyte adhesion in vivo. C57BL/6 mice were injected with TNFα alone (10 ng/g bw IP, n = 5) or in combination with recombinant BMP2 (0.33 μg/g bw IP, n = 6). Four hours after injection leukocyte adhesion was quantified by intravital microscopy of mesenterial venules (*P < .05 versus control). (C) TNFα enhances BMP2 RNA expression. HUVECs were exposed to TNFα with indicated concentrations. Twenty-four hours after TNFα-stimulation cells were lysed and BMP2 RNA expression was assessed by quantitative real-time PCR. (D) LPS increased BMP2 protein in vivo as demonstrated by Western blotting. C57BL/6 mice were injected with LPS for 3 days (2.5 μg/g/d). Lungs were minced in RIPA buffer to obtain protein. Lysates were used for Western blotting. GAPDH was used as loading control.

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