TY - JOUR
T1 - Involvement of ferroptosis in human motor neuron cell death
AU - Matsuo, Tsuyoshi
AU - Adachi-Tominari, Keiko
AU - Sano, Osamu
AU - Kamei, Takayuki
AU - Nogami, Masahiro
AU - Ogi, Kazuhiro
AU - Okano, Hideyuki
AU - Yano, Masato
N1 - Funding Information:
This work was supported by grants from the SIL Research Fund from Takeda Pharmaceutical Company, Ltd , Japan, the MEXT Grant-in- Aid, Japan, grant no. JP20H00485 and JP19H03543 to M. Y. and H. O., the Takeda Science Foundation , Japan and the Serika Fund , Japan to M.Y.
Publisher Copyright:
© 2021 Elsevier Inc.
PY - 2021/8/20
Y1 - 2021/8/20
N2 - Ferroptosis was recently defined as a novel type of programmed cell death depending on iron and lipid peroxidation. It is biologically different from other types of cell death such as apoptosis. While the involvement of ferroptosis in cancer, patient and animal model have been intensely studied, ferroptosis in human motor neuron model is still clearly unknown. Here we carefully assessed ferroptosis using human iPS cell-derived motor neuron (hiMNs). We found that almost all hiMNs died by the treatment of glutathione peroxidase 4 (GPX4) inhibitors. Importantly, the cell death was rescued by one antioxidant, vitamin E acetate, iron chelators and lipid peroxidase inhibitors with high dynamic ranges. Finally, these data clearly indicated that ferroptosis constitutively occurs in hiMNs, suggesting the possibility that it might play a biologically and pathologically important roles in motor neuron death such as motor neuron disease (MND)/Amyotrophic lateral sclerosis (ALS).
AB - Ferroptosis was recently defined as a novel type of programmed cell death depending on iron and lipid peroxidation. It is biologically different from other types of cell death such as apoptosis. While the involvement of ferroptosis in cancer, patient and animal model have been intensely studied, ferroptosis in human motor neuron model is still clearly unknown. Here we carefully assessed ferroptosis using human iPS cell-derived motor neuron (hiMNs). We found that almost all hiMNs died by the treatment of glutathione peroxidase 4 (GPX4) inhibitors. Importantly, the cell death was rescued by one antioxidant, vitamin E acetate, iron chelators and lipid peroxidase inhibitors with high dynamic ranges. Finally, these data clearly indicated that ferroptosis constitutively occurs in hiMNs, suggesting the possibility that it might play a biologically and pathologically important roles in motor neuron death such as motor neuron disease (MND)/Amyotrophic lateral sclerosis (ALS).
KW - Amyotrophic lateral sclerosis
KW - Cell death
KW - Ferroptosis
KW - Glutathione peroxidase 4
KW - Human motor neuron
KW - iPS cell
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U2 - 10.1016/j.bbrc.2021.05.095
DO - 10.1016/j.bbrc.2021.05.095
M3 - Article
C2 - 34111668
AN - SCOPUS:85107443402
SN - 0006-291X
VL - 566
SP - 24
EP - 29
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
ER -