Journal Article

HIF‐1α‐induced expression of the m6A reader YTHDF1 inhibits the ferroptosis of nucleus pulposus cells by promoting SLC7A11 translation

Ma, Xiaosheng, Jiang, Jianyuan, Lu, Xiao, Lin, Zhidi, Gao, Tian, Lu, Feizhou, Song, Jian, Li, Dachuan, Wang, Hongli, Xu, Guangyu, Zou, Fei, Gong, Zhaoyang, Zhang, Yuxuan, Xia, Xinlei

2024

Overview

The nucleus pulposus is in a hypoxic environment in the human body, and when intervertebral disc degeneration (IVDD) occurs, the hypoxic environment is disrupted. Nucleus pulposus cell (NPC) ferroptosis is one of the causes of IVDD. N6‐methyladenosine (m6A) and its reader protein YTHDF1 regulate cellular activities by affecting RNA metabolism. However, the regulation of ferroptosis in NPCs by m6A‐modified RNAs under hypoxic conditions has not been as well studied. In this study, through in vitro and in vivo experiments, we explored the underlying mechanism of HIF‐1α and YTHDF1 in regulating ferroptosis in NPCs. The results indicated that the overexpression of HIF‐1α or YTHDF1 suppressed NPC ferroptosis; conversely, the knockdown of HIF‐1α or YTHDF1 increased ferroptosis levels in NPCs. Luciferase reporter assays and chromatin immunoprecipitation demonstrated that HIF‐1α regulated YTHDF1 transcription by directly binding to its promoter region. Polysome profiling results showed that YTHDF1 promoted the translation of SLC7A11 and consequently the expression of the anti‐ferroptosis protein GPX4 by binding to m6A‐modified SLC7A11 mRNA. In conclusion, HIF‐1α‐induced YTHDF1 expression reduces NPC ferroptosis and delays IVDD by promoting SLC7A11 translation in a m6A‐dependent manner. HIF‐1α regulated YTHDF1 transcription by directly binding to its promoter region. YTHDF1 promoted the translation of SLC7A11 and consequently the expression of the anti‐ferroptosis protein GPX4 by binding to m6A‐modified SLC7A11 mRNA. HIF‐1α‐induced YTHDF1 expression reduces NPC ferroptosis and delays IVDD by promoting SLC7A11 translation in a m6A‐dependent manner.

• Publisher: John Wiley & Sons, Inc,John Wiley and Sons Inc
• Subject: Adenosine - analogs & derivatives / Adenosine - metabolism / Amino Acid Transport System y+ - genetics / Amino Acid Transport System y+ - metabolism / Animals / Antibodies / Cell death / Chromatin / Degenerative disc disease / Extracellular matrix / Fatty acids / Ferroptosis / Ferroptosis - genetics / HIF‐1α / Humans / Hypoxia / Hypoxia-Inducible Factor 1, alpha Subunit - genetics / Hypoxia-Inducible Factor 1, alpha Subunit - metabolism / Immunoprecipitation / intervertebral disc degeneration / Intervertebral Disc Degeneration - genetics / Intervertebral Disc Degeneration - metabolism / Intervertebral Disc Degeneration - pathology / Intervertebral discs / m6A / Male / Metabolism / Mice / N6-methyladenosine / Nucleus pulposus / Nucleus Pulposus - metabolism / Nucleus Pulposus - pathology / Plasmids / Protein Biosynthesis / Protein turnover / Proteins / RNA-Binding Proteins - genetics / RNA-Binding Proteins - metabolism / SLC7A11 / Transcription factors / Translation / Wang, Chen / YTHDF1