Multiphoton microscopic images of the Vybrant DiD-labelled MG-63 cells after 24-hour-long cultivation on the surfaces of ʺtissue cultureʺ plastic plates (a) or PSIDAB (b) or PASPDAB based (c and d) fibrous membranes and PASPDAB membrane without cells as a control (e). The cells show red fluorescence due to the Vybrant DiD staining while the green color indicates the autofluorescence of the PSI or PASP membranes. Red and green channels are both shown on all pictures except the (e) where only the green was active. Viability of MG-63 cells after 1- or 3-day-long cultivation on the surfaces of ʺlow cell bindingʺ plastic plates (control) and PSIDAB or PASPDAB membranes (f). * p < 0.05 compared to the control. + p < 0.05 compared to day 1.</p
<p>(A) Phase-contrast images (20 X) of RPTP-α<sup>+/+</sup> MEFs (left) and HEK 293A cells (right), ...
<p>(A-D) A set of FDA-PI double-staining fluorescent images of cells in Hepatocytes (3D) groups afte...
<p>(A) Transmitted light images of a control MCTS and of a MCTS grown in a PDMS microdevice for 6 da...
<p>Fluorescence microscopic images of GFP-expressing NIH3T3 fibroblasts (<i>N</i> = 4, <i>n</i> = 3)...
<p>(a): Bright-field image of CHO cells in the vicinity of the MFP channel apex in the cell culture ...
<p>Representative fluorescent image of MC 3T3 cells growing on collagen self-assembled at Mg with di...
<p>Representative fluorescent images of MC 3T3 cells growing on collagen self-assembled at AZ31 with...
<p>(A) Representative photomicrographs of MCF-7 cells grown in 2D culture, showing great increasing ...
<p>The morphology of initial MG-63 cells visualized by light microscopy (a), the morphology of MG-63...
<p>Panels A to H were images of <i>442-EGFP</i> cells, among which cells in A to D were in liquid cu...
<p>VICs in these panels were cultured in DMEM and FIB from the point of isolation. B shows dediffere...
<p>2×10<sup>6</sup> cells in 1 ml supernatant were incubated with Rhodamine 123 (5 µg/ml) for 20 min...
<p>Cells stained with PI indicated cells with disrupted membranes (PI<sup>+</sup>, A and D). Cells t...
<p>At 12 h after inoculation, the cells uniformly adhered to the pore walls of the scaffold.</p
<p>(A) Macroscopic images of cell—scaffold constructs cultured for 48-h <i>in vitro</i>. The constru...
<p>(A) Phase-contrast images (20 X) of RPTP-α<sup>+/+</sup> MEFs (left) and HEK 293A cells (right), ...
<p>(A-D) A set of FDA-PI double-staining fluorescent images of cells in Hepatocytes (3D) groups afte...
<p>(A) Transmitted light images of a control MCTS and of a MCTS grown in a PDMS microdevice for 6 da...
<p>Fluorescence microscopic images of GFP-expressing NIH3T3 fibroblasts (<i>N</i> = 4, <i>n</i> = 3)...
<p>(a): Bright-field image of CHO cells in the vicinity of the MFP channel apex in the cell culture ...
<p>Representative fluorescent image of MC 3T3 cells growing on collagen self-assembled at Mg with di...
<p>Representative fluorescent images of MC 3T3 cells growing on collagen self-assembled at AZ31 with...
<p>(A) Representative photomicrographs of MCF-7 cells grown in 2D culture, showing great increasing ...
<p>The morphology of initial MG-63 cells visualized by light microscopy (a), the morphology of MG-63...
<p>Panels A to H were images of <i>442-EGFP</i> cells, among which cells in A to D were in liquid cu...
<p>VICs in these panels were cultured in DMEM and FIB from the point of isolation. B shows dediffere...
<p>2×10<sup>6</sup> cells in 1 ml supernatant were incubated with Rhodamine 123 (5 µg/ml) for 20 min...
<p>Cells stained with PI indicated cells with disrupted membranes (PI<sup>+</sup>, A and D). Cells t...
<p>At 12 h after inoculation, the cells uniformly adhered to the pore walls of the scaffold.</p
<p>(A) Macroscopic images of cell—scaffold constructs cultured for 48-h <i>in vitro</i>. The constru...
<p>(A) Phase-contrast images (20 X) of RPTP-α<sup>+/+</sup> MEFs (left) and HEK 293A cells (right), ...
<p>(A-D) A set of FDA-PI double-staining fluorescent images of cells in Hepatocytes (3D) groups afte...
<p>(A) Transmitted light images of a control MCTS and of a MCTS grown in a PDMS microdevice for 6 da...