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Sh sy5y cells

Manufactured by BNCC
Sourced in China

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.

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4 protocols using sh sy5y cells

1

Neuroprotective Potential of Astragaloside IV in SH-SY5Y Cells

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SH-SY5Y cells purchased from BeNa Culture Collection (Suzhou, Jiangsu, China) were seeded in culture flasks containing complete medium [90% basic Dulbecco’s modified Eagle’s medium (DMEM, Invitrogen, Carlsbad, CA, United States), 10% heat inactivated fetal bovine serum, 100 μg/mL streptomycin and 100 U/mL penicillin (Sangon Biotech Co., Ltd, Shanghai, China)] at 37°C and 5% CO2. The medium was refreshed every other day and cells were passaged every 2–3 days. The cells at passage 3 were used for the subsequent experiments.
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)).
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2

SH-SY5Y Cell Culture Protocol

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SH-SY5Y cells (BNCC338056, BeNa Culture Collection, Beijing, China) were grown in high-glucose Dulbecco’s-modified eagle medium (DMEM-H) with 10% fetal bovine serum (FBS) containing glutamine and sodium pyruvate, in a 5% CO2 humidified incubator at 37°C.
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3

Cell Lines and Molecular Reagents

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Aβ1-42 was bought from the Peptide Institute (Osaka, Japan). VBIT-4 was bought from ChemPartner (Chengdu, China). Ferrostatin-1, Emricasan, and Necrostatin-1 were purchased from Selleckchem (Selleck Chemicals; USA). Antibodies were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). PC12 cells and SH-SY5Y cells were obtained from the Bena Culture Collection (Beijing, China).
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4

Curcumin Protects Against MPP+ Induced Toxicity

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2.9714 mg of MPP + was dissolved with 1 mL of double distilled water to obtain 10 mmol/L MPP + solution. The solution was filtrated and stored in dark at -20 °C. Digested SH-SY5Y cells (BNCC338056, BeNa Culture Collection, Beijing, China) were grown in high-glucose Dulbecco's modified eagle medium (DMEM-H) with 10% Fetal Bovine Serum (FBS) containing glutamine and sodium pyruvate, in a 5% CO 2 humidified incubator at 37 °C.
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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