Figure 2.
Figure 2. Stimulation of lymphangiogenesis. At day 14 after pellet implantation, corneal tissues were used for whole mount double staining with antibodies against Lyve-1 (A, E, I, M, and Q) and CD31 (B, F, J, N, and R). Lyve-1–positive signals are in blue color and CD31+ signals are in red color. Lyve-1–positive and CD31+ signals in the same areas did not show overlapping staining (C, D, G, H, K, L, O, P, S, and T). Panels D, H, L, P, and T represent enlargement of the boxed areas of panels C, G, K, O, and S, respectively. Bar = 100 μm. White arrows point to Lyve-1–positive structures and yellow arrows point to CD31+ structures. Images were captured with a Zeiss LSM 510 confocal laser-scanning microscope (Carl Zeiss, Jena, Germany) that includes an Axiovert 100M confocal microscope and a camera, and with Image Browser 5 LSM ver3.2 (Carl Zeiss). Images were taken with Plan Neofluar 10 ×/0.3 NA objective lenses. Figure panels were prepared with Adobe Photoshop 7.0 (Adobe Systems, San Jose, CA).

Stimulation of lymphangiogenesis. At day 14 after pellet implantation, corneal tissues were used for whole mount double staining with antibodies against Lyve-1 (A, E, I, M, and Q) and CD31 (B, F, J, N, and R). Lyve-1–positive signals are in blue color and CD31+ signals are in red color. Lyve-1–positive and CD31+ signals in the same areas did not show overlapping staining (C, D, G, H, K, L, O, P, S, and T). Panels D, H, L, P, and T represent enlargement of the boxed areas of panels C, G, K, O, and S, respectively. Bar = 100 μm. White arrows point to Lyve-1–positive structures and yellow arrows point to CD31+ structures. Images were captured with a Zeiss LSM 510 confocal laser-scanning microscope (Carl Zeiss, Jena, Germany) that includes an Axiovert 100M confocal microscope and a camera, and with Image Browser 5 LSM ver3.2 (Carl Zeiss). Images were taken with Plan Neofluar 10 ×/0.3 NA objective lenses. Figure panels were prepared with Adobe Photoshop 7.0 (Adobe Systems, San Jose, CA).

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