<p>ASCs were grown on biomaterial PEUU (A-D), PEU (E-H) and PLLA (I-L) for 48 hours. Viability was detected by fluorescein diacetate (living cells; A, E, I) and ethidium-homodimer-1 (nuclei of dead cells; B, F, J) staining. C, G and K are merged pictures. Morphology was detected by TRITC-phalloidin (cytoskeleton, red) and DAPI (nuclei, blue) staining (D, H, L). Bars represent 100 µm (A-C, E-G, I-K) or 50 µm (D, H, L).</p
<p>(a) Colorimetric viability test showed that cells flowed through the device remain highly viable ...
<p>Light microscopic overview shows no visual differences between coated and uncoated parts, whereas...
<p>Relative cell viability after 72 h growth on unmodified polymer surfaces, n = 6 (for each cell ty...
<p>(A) ASC were adherent to culture flaks and exhibited a fibroblast-like spindle-shaped morphology....
<p>One representative experiment out of four independent experiments is shown.</p
(A) Cell morphology of CTRL and TENO hPL-ASCs and SF-ASCs at 3 days of differentiation is shown (opt...
<p>Living cells (white arrows) were in green and dead cells (white arrowheads) were in red. (D) The ...
<p>Distribution and morphology of the differentiated BMSCs cultured on the oriented (A, B) and the r...
<p>A and B: live/dead staining; green: vital cells, red: dead cells; scale bars 500 µm (A), 100 µm (...
<p>ASCs vitality on glass (A) and SLM-NiTi (B and C); green: vital cells, red: dead cells; scale bar...
<p>The morphology of HUCs and ASCs at passage number 3 and ASCs after induction by conditioned mediu...
<p>ASCs cultivated on biomaterials PEUU (A), PEU (B) and PLLA (C) and differentiated for 21 days int...
<p>(a) Alginate, (b) Alginate+PLL and alginate layers, (c) Alginate mixed with collagen, (d) Alginat...
<p>(A-D) A set of FDA-PI double-staining fluorescent images of cells in Hepatocytes (3D) groups afte...
<p>Staining also suggested directed growth of the cells on the 3D-printed scaffold in parallel with ...
<p>(a) Colorimetric viability test showed that cells flowed through the device remain highly viable ...
<p>Light microscopic overview shows no visual differences between coated and uncoated parts, whereas...
<p>Relative cell viability after 72 h growth on unmodified polymer surfaces, n = 6 (for each cell ty...
<p>(A) ASC were adherent to culture flaks and exhibited a fibroblast-like spindle-shaped morphology....
<p>One representative experiment out of four independent experiments is shown.</p
(A) Cell morphology of CTRL and TENO hPL-ASCs and SF-ASCs at 3 days of differentiation is shown (opt...
<p>Living cells (white arrows) were in green and dead cells (white arrowheads) were in red. (D) The ...
<p>Distribution and morphology of the differentiated BMSCs cultured on the oriented (A, B) and the r...
<p>A and B: live/dead staining; green: vital cells, red: dead cells; scale bars 500 µm (A), 100 µm (...
<p>ASCs vitality on glass (A) and SLM-NiTi (B and C); green: vital cells, red: dead cells; scale bar...
<p>The morphology of HUCs and ASCs at passage number 3 and ASCs after induction by conditioned mediu...
<p>ASCs cultivated on biomaterials PEUU (A), PEU (B) and PLLA (C) and differentiated for 21 days int...
<p>(a) Alginate, (b) Alginate+PLL and alginate layers, (c) Alginate mixed with collagen, (d) Alginat...
<p>(A-D) A set of FDA-PI double-staining fluorescent images of cells in Hepatocytes (3D) groups afte...
<p>Staining also suggested directed growth of the cells on the 3D-printed scaffold in parallel with ...
<p>(a) Colorimetric viability test showed that cells flowed through the device remain highly viable ...
<p>Light microscopic overview shows no visual differences between coated and uncoated parts, whereas...
<p>Relative cell viability after 72 h growth on unmodified polymer surfaces, n = 6 (for each cell ty...