bioimagesUnknownYapeng GuThe Journal of Cell Biologyhttps://www.ebi.ac.uk/biostudies/studies/S-JCBD-201010075JCB

An HBE monolayer was treated with UV to induce apoptosis and stained with DRAQ5 (blue), phalloidin (red), anti-S1P mAb (green). Confocal micrographs were obtained using a TCS SP5 microscope (Leica).

An HBE monolayer was treated with UV to induce apoptosis and stained with DRAQ5 (blue), phalloidin (red), and anti-S1P mAb (green). Cinfocal micrographs were obtained using a TCS SP5 microscope (Leica).

An HBE monolayer was treated with UV in the presence of SKI and stained with DAPI (blue), phalloidin (red), and anti-S1P mAb (green). Confocal micrographs were obtained using a Nikon Eclipse TE300 inverted microscope converted for spinning disc confocal microscopy (Andor Technologies).

An HBE monolayer was treated with UV to induce apoptosis and stained with DRAQ5 (blue), phalloidin (red), and anti-S1P mAb (green). Confocal micrographs were obtained using a TCS SP5 microscope (Leica).

An HBE monolayer was treated with UV to induce apoptosis in the presence of the S1P2 antagonist JTE-013 and stained with DRAQ5 (blue), phalloidin (red), and anti-S1P mAb (green). Confocal micrographs were obtained using a TCS SP5 microscope (Leica).

bioimagesFigure 4 - AImage 32477 (Figure 4 - D)Figure 4Figure 4 - BImage 32475 (Figure 4 - B)Image 32474 (Figure 4 - A)Image 32476 (Figure 4 - C)Figure 4 - EImage 32478 (Figure 4 - E)Figure 4 - CFigure 4 - DJody RosenblattRoger SabbadiniTetyana ForostyanYapeng GufalseEpithelial cell extrusion requires the sphingosine-1-phosphate receptor 2 pathway2011-05-09T11:21:24Z2018-11-29T11:21:24Z2018-11-29T11:21:24ZS-JCBD-20101007510.1083/jcb.201010075