SH-SY5Y cells in good conditions were treated with different concentrations (10, 50, 100, 150, and 200 μM) of 6-OHDA (Sigma-Aldrich, Merck KGaA, Darmstadt, Germany) for different time (0, 3, 6, 12, 24, and 48 h) (Chen et al., 2020 (link)). The concentration and time of 6-OHDA intervention at 50% cell activity were selected as the experimental conditions. Different concentrations (25, 50, 100, 150, and 200 μM) of AS-IV (National Institute for the Control of Pharmaceutical and Biological Products, Beijing, China) was added to the medium 2 h before 6-OHDA treatment, or 15 μL JAK2/STAT3 pathway inhibitor SC99 [2-(2-(3-chloro-4-fluorophenyl)hydrazono)-3-(4-chlorophenyl)-3-oxo-propanenitrile, 2-(2-(2-(3-4-fluorophenyl)hydrazine)-3-(4-chlorophenyl)-3-oxo-acrylonitrile)] (15 mM, Sigma-Aldrich) was added to interfere with the pathway (Zhang et al., 2016 (link)).
Sh sy5y cells
SH-SY5Y cells are a human-derived neuroblastoma cell line commonly used in research. They exhibit characteristics of human neuron-like cells and are a widely accepted in vitro model for studying neurodegenerative diseases and other neurological processes.
Lab products found in correlation
4 protocols using sh sy5y cells
Neuroprotective Potential of Astragaloside IV in SH-SY5Y Cells
SH-SY5Y cells in good conditions were treated with different concentrations (10, 50, 100, 150, and 200 μM) of 6-OHDA (Sigma-Aldrich, Merck KGaA, Darmstadt, Germany) for different time (0, 3, 6, 12, 24, and 48 h) (Chen et al., 2020 (link)). The concentration and time of 6-OHDA intervention at 50% cell activity were selected as the experimental conditions. Different concentrations (25, 50, 100, 150, and 200 μM) of AS-IV (National Institute for the Control of Pharmaceutical and Biological Products, Beijing, China) was added to the medium 2 h before 6-OHDA treatment, or 15 μL JAK2/STAT3 pathway inhibitor SC99 [2-(2-(3-chloro-4-fluorophenyl)hydrazono)-3-(4-chlorophenyl)-3-oxo-propanenitrile, 2-(2-(2-(3-4-fluorophenyl)hydrazine)-3-(4-chlorophenyl)-3-oxo-acrylonitrile)] (15 mM, Sigma-Aldrich) was added to interfere with the pathway (Zhang et al., 2016 (link)).
SH-SY5Y Cell Culture Protocol
Cell Lines and Molecular Reagents
Curcumin Protects Against MPP+ Induced Toxicity
Then cells were incubated for 12 h in 96-well plates at a density of 1×10 5 / mL and 100 μL per well.
Well-cultivated SH-SY5Y PD cells were divided into several groups according to treatments of different concentrations of MPP + and Cur. A normal group was left with treatment of neither MPP + nor Cur. A group of 400 μmol/L MPP + treatment went in contrast with groups of 400 μmol/L MPP + + 10, 20 or 40 μmol/L Cur treatment. Cells morphology was observed under an electron microscope (Olympus, Tokyo, Japan) after 24 h cultivation.
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