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Image Search Results
Journal: Journal of Nanobiotechnology
Article Title: Mesenchymal stem cells-derived extracellular vesicles protect against oxidative stress-induced xenogeneic biological root injury via adaptive regulation of the PI3K/Akt/NRF2 pathway
doi: 10.1186/s12951-023-02214-5
Figure Lengend Snippet: Human adipose-derived mesenchymal stem cell extracellular vesicles (hASC-EVs) inhibited oxidative damage, promoted antioxidant activity, and alleviated H 2 O 2 -stimulated oxidative reactivity in dental follicle cells (DFCs). The oxidative stress and antioxidant activity of the experimental group in response to H 2 O 2 stimulation were examined after hASC-EV administration. a Representative images showing DCF (green) and reactive oxygen species (ROS) production in each group. Scale bar = 200 μm. b Representative images showing 8-OHdG (green nuclei) immunostaining results and the cytoskeleton (red) in each group. Scale bar = 50 μm. c Representative images showing the MMP of DFCs, detected using JC-1 staining, which was identified by green fluorescence for the monomeric form of JC-1 and red fluorescence for potential-dependent aggregation. Scale bar = 100 μm. d Histograms showing lipid peroxidation (MDA) concentrations in the different groups. e – g Histograms showing quantification of the mean fluorescence intensity (MFI) of DCFH ( e ), 8-OHdG ( f ), and JC-1 ratio ( g ) in DFCs. h – k Histograms showing the FRAP ( h ), GSH-PX ( i ), SOD ( j ), and CAT ( k ) concentrations in different groups (n = 5 for each group). ** P < 0.01, *** P < 0.001, and **** P < 0.001, compared to the control
Article Snippet: The samples and reaction reagents included those from the
Techniques: Derivative Assay, Antioxidant Activity Assay, Immunostaining, Staining, Fluorescence, Control
Journal: Oncology Letters
Article Title: Increased soluble E‑cadherin of spheroid formation supplemented with fetal bovine serum in colorectal cancer cells
doi: 10.3892/ol.2023.13793
Figure Lengend Snippet: Cell viability changes after spheroid formation of colorectal cancer cells in different environments. (A) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for 3 days. The extent of cell viability was determined by MTT assay. Data are presented as the mean ± SD (n=3). *P<0.05, **P<0.01 and ***P<0.001 vs. DMSO; # P<0.05 and ## P<0.01 vs. sphere/GF. (B) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for indicated days. The extent of cell viability was determined by MTT assay using the aforementioned procedures. Data are presented as the mean ± SD (n=3). (C) Expression levels of cell cycle-related proteins in monolayer and spheroid formation cultures in SNU-C5 and SNU-C5/5-FUR cells were detected by immunoblotting. Immunoblotting analysis was performed for p21, β-catenin and GSK3β, while GAPDH was used for a loading control. Band density was analyzed by AzureSpot analysis software, and results are expressed as the mean ± SD (n=3). **P<0.01 and ***P<0.001 vs. monolayer; ## P<0.01 vs. sphere/FBS. 5-FU, 5-fluorouracil; FBS, fetal bovine serum; GF, growth factor.
Article Snippet: CREB (1:1,000; cat. no. CSB-PA005947HA01HU; Cusabio Technology, LLC), fibronectin (1:2,000; cat. no. CL54951AP; Cedarlane Laboratories),
Techniques: MTT Assay, Expressing, Western Blot, Control, Software
Journal: Oncology Letters
Article Title: Increased soluble E‑cadherin of spheroid formation supplemented with fetal bovine serum in colorectal cancer cells
doi: 10.3892/ol.2023.13793
Figure Lengend Snippet: Densitometric results of western blotting on SNU-C5 and SNU-C5/5-FUR cells.
Article Snippet: CREB (1:1,000; cat. no. CSB-PA005947HA01HU; Cusabio Technology, LLC), fibronectin (1:2,000; cat. no. CL54951AP; Cedarlane Laboratories),
Techniques: Western Blot, Marker