Elative to HT29 cells. a : Cell morphology on a glass slide

Elative to HT29 cells. a : Cell morphology on a glass slide (glass). c : Cell morphology in a flat silicon region (S). e : Cell morphology in the Photonic Crystal (PhC). Cells are labeled with (a, c, e) green-FITC and red-PI; (b, d, f) only red-PI. doi:10.1371/journal.pone.order 47931-85-1 0048556.gma HT29 cells were grown in complete McCoy supplemented with 10 FBS, glutamine (4 mM), Na/pyruvate (2 mM), penicillin (100 U/ml) and streptomycin (0.1 18325633 mg/ml). All reagents were from Celbio, Lonza and Sigma, Italy.Cell Culture in 58-49-1 Standard Condition (Before Seeding on Silicon Devices)All cells were normally grown at 37uC in a humidified atmosphere containing 5 CO2. Growth conditions were monitored daily by direct observation with an inverted microscopeCell-Selective Three-Dimensional MicroincubatorCell-Selective Three-Dimensional MicroincubatorFigure 3. Comparison between fluorescence images relative to different epithelial cell lines. a : HT29. c : HCT116. e : SW613-B3. g : HeLa. (a, c, e, g) Cell morphology in a flat silicon region (S); (b, d, f, h) Cell morphology in the Photonic Crystals (PhC). Cells are labeled with (a, c, e, g) green-FITC and red-PI; (b, d, f, h) only red-PI. In (b,d,f,h), photos in the right column, the majority of the nuclei have a round shape, typical of cells staying on top of the walls. doi:10.1371/journal.pone.0048556.gand, when confluence was reached, they were trypsinized as previously described in [33]. Some cells were used in subsequent experiments of seeding and growth in contact with silicon whereas the cell line was maintained by re-seeding the remaining cells in plastic plates or flasks.Cell Seeding on SiliconTo define the best culture conditions on silicon and to define the optimal density of cells inside the grooves, we used different concentrations of cells in the medium and increasing culture times. Culture experiments were performed on as-cut or trimmed silicon dice fitting, respectively, in 6- or 12-well plates. Seeding was carried on in two distinct ways: by depositing a drop of medium containing cells over the silicon dice and adding 2 ml of medium only 3 h later, or by directly seeding in the well, hosting the silicon dice, 2 ml of medium containing 36105 cells.tation and emission filters combinations for single color (red-PI) as well as for simultaneous dual color (green-FITC and red-PI) imaging were applied. Blue excitation for dual color green-FITC/ red-PI was performed with a band pass (BP 450?80 nm) excitation filter through a dichroic mirror DM500 combined with a LP 515 nm as barrier filter. Green excitation for single color redPI was performed with a BP 530?60 nm and a dichroic mirror DM590 combined with a LP 620 as barrier filter. Fluorescence microphotographs with different magnifications (Olympus UPlanFl Objectives 206 NA = 0.50, 406 NA = 0.75) were taken using an Olympus Camedia C-4040 digital camera.ResultsExamples of silicon devices, obtained after the technological process described in the Materials and Methods, are illustrated in Figure 1. Figures 1a and 1b show, respectively, a scheme and a photo of HAR PhC with a dimensional reference whereas Figure 1c reports a Scanning Electron Microscope (SEM) picture of HAR PhCs. As a result of the various experiments of cell seeding on silicon, we verified that seeding on silicon dice fitting in a 12-well plates allowed the best density to be reached by minimizing the number of cells that remain attached to the surrounding plastic surface of the well, instead.Elative to HT29 cells. a : Cell morphology on a glass slide (glass). c : Cell morphology in a flat silicon region (S). e : Cell morphology in the Photonic Crystal (PhC). Cells are labeled with (a, c, e) green-FITC and red-PI; (b, d, f) only red-PI. doi:10.1371/journal.pone.0048556.gma HT29 cells were grown in complete McCoy supplemented with 10 FBS, glutamine (4 mM), Na/pyruvate (2 mM), penicillin (100 U/ml) and streptomycin (0.1 18325633 mg/ml). All reagents were from Celbio, Lonza and Sigma, Italy.Cell Culture in Standard Condition (Before Seeding on Silicon Devices)All cells were normally grown at 37uC in a humidified atmosphere containing 5 CO2. Growth conditions were monitored daily by direct observation with an inverted microscopeCell-Selective Three-Dimensional MicroincubatorCell-Selective Three-Dimensional MicroincubatorFigure 3. Comparison between fluorescence images relative to different epithelial cell lines. a : HT29. c : HCT116. e : SW613-B3. g : HeLa. (a, c, e, g) Cell morphology in a flat silicon region (S); (b, d, f, h) Cell morphology in the Photonic Crystals (PhC). Cells are labeled with (a, c, e, g) green-FITC and red-PI; (b, d, f, h) only red-PI. In (b,d,f,h), photos in the right column, the majority of the nuclei have a round shape, typical of cells staying on top of the walls. doi:10.1371/journal.pone.0048556.gand, when confluence was reached, they were trypsinized as previously described in [33]. Some cells were used in subsequent experiments of seeding and growth in contact with silicon whereas the cell line was maintained by re-seeding the remaining cells in plastic plates or flasks.Cell Seeding on SiliconTo define the best culture conditions on silicon and to define the optimal density of cells inside the grooves, we used different concentrations of cells in the medium and increasing culture times. Culture experiments were performed on as-cut or trimmed silicon dice fitting, respectively, in 6- or 12-well plates. Seeding was carried on in two distinct ways: by depositing a drop of medium containing cells over the silicon dice and adding 2 ml of medium only 3 h later, or by directly seeding in the well, hosting the silicon dice, 2 ml of medium containing 36105 cells.tation and emission filters combinations for single color (red-PI) as well as for simultaneous dual color (green-FITC and red-PI) imaging were applied. Blue excitation for dual color green-FITC/ red-PI was performed with a band pass (BP 450?80 nm) excitation filter through a dichroic mirror DM500 combined with a LP 515 nm as barrier filter. Green excitation for single color redPI was performed with a BP 530?60 nm and a dichroic mirror DM590 combined with a LP 620 as barrier filter. Fluorescence microphotographs with different magnifications (Olympus UPlanFl Objectives 206 NA = 0.50, 406 NA = 0.75) were taken using an Olympus Camedia C-4040 digital camera.ResultsExamples of silicon devices, obtained after the technological process described in the Materials and Methods, are illustrated in Figure 1. Figures 1a and 1b show, respectively, a scheme and a photo of HAR PhC with a dimensional reference whereas Figure 1c reports a Scanning Electron Microscope (SEM) picture of HAR PhCs. As a result of the various experiments of cell seeding on silicon, we verified that seeding on silicon dice fitting in a 12-well plates allowed the best density to be reached by minimizing the number of cells that remain attached to the surrounding plastic surface of the well, instead.