Objective using a light direct microscope and endothelial photographs were acquired. In order to examine the cytoskeleton structure, phalloidin was used to investigate the distribution of actin filament in cells. In control corneas, actin filaments were assembled into large radial and circumferential bundles, with a main localization along the membrane of the endothelial cells. After treatment with ten mMY- 27632, the distribution of F-actin was dramatically altered, with only a residual staining associated with the cell periphery. The formation of circular membrane ruffles of variable size and actin content could also be observed in the endothelium of treated corneas. Inhibition of Rho-ROCK pathway in corneal endothelium induces rearrangement of cytoskeleton. Proliferation kinetic was evaluated by cell density and EdU incorporation every day until cells order 1239358-86-1 reached confluency with or without Y-27632 addition in Low and High Medium. A difference in cell proliferation could be observed between the different groups. As shown in Figure 7A, cells reached confluency more quickly in High Medium than in Low Medium demonstrating, as expected, that High Medium is better to expand HCEC. Furthermore, cell shape in the two mediums were different, with bigger cells and a more regular endothelial mosaic in Low Medium, comparable to the in vivo structure, than in the High Medium where a pleomorphism was detected. The addition of Y- 27632 induced also some modifications in cell proliferative potential and morphology. In both mediums, cells adopted a fibroblastic-like appearance suggesting a higher 66547-09-9 capacity to migrate than to proliferate. Indeed additional time was necessary for cells to reach the confluency in the presence of Y-27632 whatever the medium, demonstrating a reduction of the HCEC proliferative capacity. These results were also evaluated by Ki67 immunostaining and EdU incorporation assay on HCEC at confluency. Only few Ki67 positive cells were detected in all conditions, which showed a low cell proliferative capacity of HCEC at confluency. Representative micrographs of the cell-viability assay are presented in Figure 6A. For this assay, methanol-fixed cultures acted as positive controls for cell death. Fluorescence microscopy of methanol-fixed cultures revealed red-s
