Iron metabolism mediates microglia susceptibility in ferroptosis

• Published in: Frontiers in cellular neuroscience Vol. 16; p. 995084
• Main Authors: Jiao, Lingling, Li, Xiaolan, Luo, Yuxiang, Wei, Junfen, Ding, Xulong, Xiong, Huan, Liu, Xuesong, Lei, Peng
• Format: Journal Article
• Language: English
• Published: Lausanne Frontiers Research Foundation 30.08.2022; Frontiers Media S.A
• Subjects: Alzheimer's disease; Antibodies; Apoptosis; Astrocytes; Autophagy; Brain; Cell culture; Cell death; Experiments; Ferroptosis; Flow cytometry; glia; Iron; iron metabolism; Laboratory animals; Lipids; Metabolism; Microglia; Neurological disorders; Neuronal-glial interactions; Neurons; Neuroscience; Parkinson's disease; Plating; Proteins; United States > US; China
• ISSN: 1662-5102; 1662-5102
• DOI: 10.3389/fncel.2022.995084

Ferroptosis is implicated in a range of brain disorders, but it is unknown whether neurons or glia in the brain are particularly effected. Here, we report that primary cortical astrocytes (PA), microglia (PM), and neurons (PN) varied in their sensitivities to ferroptosis. Specifically, PM were the most sensitive to ferroptosis, while PN were relatively insensitive. In contrast, PN and PM were equally susceptible to apoptosis, with PA being less affected, whereas all three cell types were similarly susceptible to autophagic cell death. In the tri-culture system containing PA, PM, and PN, the cells were more resistant to ferroptosis than that in the monoculture. These results demonstrated that brain cells exhibit different sensitivities under ferroptosis stress and the difference may be explained by the differentially regulated iron metabolism and the ability to handle iron. Continued elucidation of the cell death patterns of neurons and glia will provide a theoretical basis for related strategies to inhibit the death of brain cells.