Figure 3
Figure 3. Increased lymphangiogenesis in LTβ−/− mouse skin after induction of inflammation. (A) Fluorescence microscopy of the site of immunization with ovalbumin and CFA after injection of FITC-conjugated nanoparticles reveals more prominent and extensive lymphatic vessel networks near immunization sites in LTβ−/− mice compared with LTα−/− and WT mice. Pale green at day 0 represents autofluorescence. Black blood vessels are apparent and even more obvious after immunization. Lymphatic vessels are bright green (6.5× objective). (B) More peri-immunization depot sites showed uptake of the nanoparticles by lymphatics in LTβ−/− than WT and LTα−/− mice (n = 3 per group with total of 6 depot regions per group).

Increased lymphangiogenesis in LTβ−/− mouse skin after induction of inflammation. (A) Fluorescence microscopy of the site of immunization with ovalbumin and CFA after injection of FITC-conjugated nanoparticles reveals more prominent and extensive lymphatic vessel networks near immunization sites in LTβ−/− mice compared with LTα−/− and WT mice. Pale green at day 0 represents autofluorescence. Black blood vessels are apparent and even more obvious after immunization. Lymphatic vessels are bright green (6.5× objective). (B) More peri-immunization depot sites showed uptake of the nanoparticles by lymphatics in LTβ−/− than WT and LTα−/− mice (n = 3 per group with total of 6 depot regions per group).

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