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Susceptibility to erastin‐induced ferroptosis decreases during maturation in a human oligodendrocyte cell line

机译:在人少突胶细胞细胞系中成熟期间,对欧虫诱导的恶性裂菌剂的易感性降低

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Ferroptosis, a form of iron‐dependent cell death caused by lipid peroxidation, has been implicated in neurological and other disorders. However, the mechanism of ferroptosis in oligodendrocytes is unclear. We tested the susceptibility of MO3.13 cells, an oligodendrocyte line, to ferroptosis after erastin treatment. Immature MO3.13 cells were more susceptible to erastin‐induced ferroptosis than chemically differentiated mature MO3.13 cells. Increased expression of solute carrier family 7 member 11 (SLC7A11), which encodes a cystine/glutamate transporter, and greater glutathione concentrations were observed in mature compared with immature MO3.13 cells, linking glutathione to the resistance of mature MO3.13 cells to erastin‐induced ferroptosis. These findings highlight the usefulness of immature MO3.13 cells in studies of ferroptosis and investigations into neuropathologies that involve oligodendrocytes.
机译:糖凋亡,一种由脂质过氧化引起的铁依赖性细胞死亡的形式,涉及神经系统和其他疾病。然而,脱霉素中的硬质裂解剂的机制尚不清楚。我们测试了Mo3.13细胞,少突胶质细胞系,脱硫治疗后的脱霉菌。未成熟的MO 3.13细胞比化学分化的成熟MO3.13细胞更容易易受杂种诱导的脱裂剂。与未成熟的MO 3.13细胞相比,在成熟中,观察到编码胱氨酸/谷氨酸转运蛋白11(SLC7A11)的溶质载体家族7构件11(SLC7A11)的表达,以及更大的谷胱甘肽浓度,与未成熟的MO 3.13细胞相比,将谷胱甘肽连接到成熟MO 3.13细胞的抗性 - 诱导的裂解盘。这些发现突出了未成熟的MO3.13细胞在涉及寡突胶质细胞的神经病理学研究中的未成熟MO3.13细胞的有用性。

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