3 research outputs found
Additional file 2: Figure S2. of Caveolin-1 regulates the expression of tight junction proteins during hyperoxia-induced pulmonary epithelial barrier breakdown
Effects of transfection concentration and transfection time of Cav-1 cDNA on mRNA and protein expression of Cav-1 in alveolar cell monolayers. At 48 h after transfection of 1 μg/mL Cav-1 cDNA, significant increases in caveolin-1 mRNA (A, B, E, F) and protein (C, D, G, H) were readily apparent. mRNA and protein expressions were determined by RT-PCR and Western blot analysis, respectively. β-actin was used as an internal control. Values are represented as means ± SD, ## P < 0.01 for comparison between the normoxia and CAV1 cDNA-transfected group, ** P < 0.01 for comparison between different concentration transfected groups or different time ransfected groups. (TIF 1801 kb
Additional file 3: Figure S3. of Caveolin-1 regulates the expression of tight junction proteins during hyperoxia-induced pulmonary epithelial barrier breakdown
Efficacy assessment of Cav-1-siRNA transfection and pCMV6-CAV1 transfection. At 60–70 % confluence, cells exposed to normoxia were transfected with 10 nm of a control siRNA (Fluorescein Conjugate) (Cat.#6201;Cell Signaling Danvers MA) for 72 h to assess transfection efficiency for Cav-1-siRNA, while cells exposed to normoxia or hyperoxia were transfected with 1 μg/mL of pCMV6-AC-GFP (Cat.#PS100010; OriGene Technologies) for 48 h to assess transfection efficiency for pCMV6-CAV1. Images were obtained using a confocal laser scanning microscope at 100× magnification. Green represents transfected cells. The areas of transfected cells and all the cells in the view were measured by image pro plus software, and the ratio represents transfection efficiency. The transfection efficiency of control siRNA was (88.29 ± 8.25)% (A, B). The transfection efficiency of pCMV6-AC-GFP under normoxic conditions was (92.81 ± 4.16)% (C, D). The transfection efficiency of pCMV6-AC-GFP under hyperoxic conditions was (90.42 ± 6.83)% (E, F). (TIF 10078 kb
Additional file 1 of Kupffer cells abrogate homing and repopulation of allogeneic hepatic progenitors in injured liver site
Additional file 1. Fig. S1. KCs ablation supports survival of allo-HPs at the injury site. Fig. S2. Engrafted allo-HPs migrate and navigate to the injury site through portal vein (PV). Fig. S3. Depletion of neutrophils in peripheral blood. Fig. S4. Corresponding full-length immunoblot. Supplementary Table S1: List of primers for qPCR