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. 2020 Feb 4;34(3):4653–4669. doi: 10.1096/fj.201902455R

Figure 3.

Figure 3

Live cell imaging of the TGEV internalization via caveolae‐mediated endocytosis. A, Representative immunofluorescence images of TGEVs in control and nystatin treated cells. The ST cells were treated or untreated with 10 μM nystatin for 30 min and subsequently inoculated with TGEVs for 2 h, and then the ST cells were fixed and the infected TGEVs were stained with the anti‐TGEV primary antibody and the fluorescent secondary antibody. Scale bar, 20 μm. B, Effects of nystatin with different concentrations on TGEV infection. The ST cells were treated or untreated with the indicated concentrations of nystatin for 30 min and inoculated with TGEVs for 2 h, subsequently, the relative TGEV levels were measured by qPCR. Data present as mean ± SD from three independent experiments. **P < .01 by t test. C, Time‐lapse images of the internalization of three TGEVs via caveolae‐mediated endocytosis shown in Video S4‐S6. Circles indicate the positions of the TGEVs in each panel. Scale bar, 2 μm. D, Fluorescence intensity curves of Cav1 at the site of virus and velocity curves of viral diffusion corresponding to (C). E, Trajectories of viral diffusion corresponding to (C). F and G, MSD vs time plots of viral movement. The colors are in accordance with those in (E)