Is folded by CTF. The parylene film was then etched away with O2 plasma (10 ml/min, 25 W) (RIE-10NR, SAMCO, Japan) at the defined regions with aluminum (Al) mask that was patterned using standard photolithographic technique (Figure S1A i). Before removing the Al, we coated the glass substrate with MPC GW433908G site polymer to inhibit protein adsorption and cell adhesion (Figure S1A ii). Specifically, MPC solution was spun at 2000 rpm for 30 s onto the substrate, and then the substrate was dried in a chamber with an ethanol atmosphere at room temperature for 20 min to form the polymer layer uniformly. The substrate was then baked at 70uC for 4 h to covalently graft the MPC polymer to the surface of the exposed glass area in the substrate by a dehydration reaction. The Al worked as a sacrificial layer for the MPC layer, and the MPC layer was subsequently lifted-off by removing Al with an alkaline solution (NMD developer, Tokyo Ohka, Japan), leaving behindCell OrigamiFigure 5. Sequential images of various 3D cell-laden microstructures folded by CTF. (A)?C) Regular tetragon, regular dodecahedron and cylindrical tube were self-folded. (D) A fluorescent image of regular dodecahedrons. (E) A cross-section (a 9) image of the dodecahedron Galantamine chemical information structure in a hollow shape taken by a confocal scanning laser microscopy. Green and blue colors show actin and nucleus, respectively. NIH/3T3 cells were used. Scale bars, 50 mm. doi:10.1371/journal.pone.0051085.gbare parylene surface (Figure S1A v). Therefore, the cells can only be seeded onto the patterned parylene plates that are coated with FN (Funakoshi, Japan) at 10 mg/ml concentration (Figure S1A i).Figure S2 shows the process flow of producing the microplates with a flexible joint and culturing the cells on the plates. The first step is forming MPC polymer and gelatin layers on a glass substrate, so that the cells cannot adhere the substrate after the 1531364 folding. 3? gelatin solution was spin-coated. We then depositedCell OrigamiCulturing the cellsWe used NIH/3T3 cells (TKG299, RIKEN Cell Bank, Japan) and BAOSMCs (CAB35405, Cell Applications) that are commonly used as adherent cells to study CTFs; they spread on a substrate and generate CTFs 1317923 on its surface [24,31,32]. We also used bovine carotid artery endothelial cells (JCRB cell bank, Japan), HUVECs (CC2519, Lonza Walkersville), and primary rat cardiomyocytes (CMC02, Primary Cell, Japan) to explore further variation of cell types to fold 3D microstructures. The NIH/3T3 cells and bovine carotid artery endothelial cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10 fetal bovine serum (FBS) (JBS-5441, JBS016549, Japan Bioserum) and 1 penicillin-streptomycin solution (AB) (Japan Bioserum) at 37uC under a humidified atmosphere of 5 CO2. In the case of HUVECs and cardiomyocytes, EGMH-2 BulletKitTM (Lonza Walkersville) and CMCM (Primary Cells, Japan) supplemented with 10 FBS, 10 units/ml penicillin, and 10 mg/ml streptomycin were used, respectively. For seeding the cells onto the microplates, the cells were harvested with trypsin (Gibco, Tokyo, Japan) and collected in the culture media containing trypsin inhibitor (Sigma). We prepared cells suspended in culture media at various concentrations (cells/ml). Then, we added 2 ml of the cell suspension into a petri dish containing our substrate with the microplates. The sizes of the dish and the substrate were 35 mm in diameter and 12 mm614 mm, respectively. The percentage of the area to be.Is folded by CTF. The parylene film was then etched away with O2 plasma (10 ml/min, 25 W) (RIE-10NR, SAMCO, Japan) at the defined regions with aluminum (Al) mask that was patterned using standard photolithographic technique (Figure S1A i). Before removing the Al, we coated the glass substrate with MPC polymer to inhibit protein adsorption and cell adhesion (Figure S1A ii). Specifically, MPC solution was spun at 2000 rpm for 30 s onto the substrate, and then the substrate was dried in a chamber with an ethanol atmosphere at room temperature for 20 min to form the polymer layer uniformly. The substrate was then baked at 70uC for 4 h to covalently graft the MPC polymer to the surface of the exposed glass area in the substrate by a dehydration reaction. The Al worked as a sacrificial layer for the MPC layer, and the MPC layer was subsequently lifted-off by removing Al with an alkaline solution (NMD developer, Tokyo Ohka, Japan), leaving behindCell OrigamiFigure 5. Sequential images of various 3D cell-laden microstructures folded by CTF. (A)?C) Regular tetragon, regular dodecahedron and cylindrical tube were self-folded. (D) A fluorescent image of regular dodecahedrons. (E) A cross-section (a 9) image of the dodecahedron structure in a hollow shape taken by a confocal scanning laser microscopy. Green and blue colors show actin and nucleus, respectively. NIH/3T3 cells were used. Scale bars, 50 mm. doi:10.1371/journal.pone.0051085.gbare parylene surface (Figure S1A v). Therefore, the cells can only be seeded onto the patterned parylene plates that are coated with FN (Funakoshi, Japan) at 10 mg/ml concentration (Figure S1A i).Figure S2 shows the process flow of producing the microplates with a flexible joint and culturing the cells on the plates. The first step is forming MPC polymer and gelatin layers on a glass substrate, so that the cells cannot adhere the substrate after the 1531364 folding. 3? gelatin solution was spin-coated. We then depositedCell OrigamiCulturing the cellsWe used NIH/3T3 cells (TKG299, RIKEN Cell Bank, Japan) and BAOSMCs (CAB35405, Cell Applications) that are commonly used as adherent cells to study CTFs; they spread on a substrate and generate CTFs 1317923 on its surface [24,31,32]. We also used bovine carotid artery endothelial cells (JCRB cell bank, Japan), HUVECs (CC2519, Lonza Walkersville), and primary rat cardiomyocytes (CMC02, Primary Cell, Japan) to explore further variation of cell types to fold 3D microstructures. The NIH/3T3 cells and bovine carotid artery endothelial cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10 fetal bovine serum (FBS) (JBS-5441, JBS016549, Japan Bioserum) and 1 penicillin-streptomycin solution (AB) (Japan Bioserum) at 37uC under a humidified atmosphere of 5 CO2. In the case of HUVECs and cardiomyocytes, EGMH-2 BulletKitTM (Lonza Walkersville) and CMCM (Primary Cells, Japan) supplemented with 10 FBS, 10 units/ml penicillin, and 10 mg/ml streptomycin were used, respectively. For seeding the cells onto the microplates, the cells were harvested with trypsin (Gibco, Tokyo, Japan) and collected in the culture media containing trypsin inhibitor (Sigma). We prepared cells suspended in culture media at various concentrations (cells/ml). Then, we added 2 ml of the cell suspension into a petri dish containing our substrate with the microplates. The sizes of the dish and the substrate were 35 mm in diameter and 12 mm614 mm, respectively. The percentage of the area to be.
