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HACE1 alleviates intervertebral disc degeneration by inhibiting ferroptosis in nucleus pulposus cells
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  • Published: 13 February 2026

HACE1 alleviates intervertebral disc degeneration by inhibiting ferroptosis in nucleus pulposus cells

  • Jiyue Xia1,
  • Wei Zhang1,
  • Youhong Jiang1,
  • Ting Li2,
  • Huaize Dong1,
  • Lu Zhu1,
  • Qiuqiu Xia1,
  • Yan Zhao1,
  • Jiangbi Yi1,
  • Zijing Weng1,
  • Shuai Feng1 &
  • …
  • Zhijun Xin1,3 

Scientific Reports , Article number:  (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Medical research
  • Molecular medicine

Abstract

HACE1 (HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1) is an antioxidant gene that plays a key role in activating antioxidant pathways to maintain cellular homeostasis. Recent studies suggest that the antioxidant gene HACE1 may be a potential therapeutic target for age-related degenerative diseases. However, its role in intervertebral disc degeneration (IDD) has not been reported in any study. To clarify the role of HACE1 in IDD, we performed in vivo and in vitro basal experiments. The MRI results indicated that the degeneration grade of intervertebral discs in old rats was significantly higher compared to that in juvenile rats. Additionally, the expression of HACE1 in the degenerated intervertebral discs of aged rats was reduced. In cellular experiments, HACE1 overexpression could restore IL-1β-induced apoptosis, mitochondrial damage and iron overload. In animal experiments, HACE1 activated antioxidant signaling pathways, attenuated oxidative stress, and increased the expression of ECM and anti-ferroptosis proteins. In summary, HACE1 alleviates the progression of IDD by inhibiting oxidative stress and ferroptosis in nucleus pulposus cells. Its protective effect may be related to the activation of the Nrf2/ARE signaling pathway. In conclusion, our results support that the antioxidant gene HACE1 could serve as a novel potential target for treating IDD.

Data availability

All other data in this study are included in the published manuscript and supplementary information files.

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Acknowledgements

We thank the Graduate Education Innovation Project of Guizhou Province and the Graduate Research Fund of Zunyi Medical University for providing fund support.

Funding

This work was supported by the Graduate Education Innovation Project of Guizhou Province [No. 2024YJSKYJJ342] and the Graduate Research Fund of Zunyi Medical University [No. ZYK242].

Author information

Authors and Affiliations

  1. Department of Spine Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou, China

    Jiyue Xia, Wei Zhang, Youhong Jiang, Huaize Dong, Lu Zhu, Qiuqiu Xia, Yan Zhao, Jiangbi Yi, Zijing Weng, Shuai Feng & Zhijun Xin

  2. Department of Respiratory and Critical Care Medicine, Qixingguan District People’s Hospital of Bijie, Bijie, 551700, Guizhou, China

    Ting Li

  3. Department of Orthopedic Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou, China

    Zhijun Xin

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Contributions

The author contributions were as follows: Z.X. and J.X. designed the experiments, Y.J., S.F., J.Y. and Z.W. conducted the in vitro experiments, and W.Z., Q.X., Y.Z., H.D. and J.X. conducted in vivo experiments. J.X., L.Z. and T.L. analyzed the data and wrote the manuscript, and Z.X. revised the manuscript.

Corresponding author

Correspondence to Zhijun Xin.

Ethics declarations

Ethical approval and consent to participate

This study was approved by the Experimental Animal Welfare and Ethics Committee of the Affiliated Hospital of Zunyi Medical University (No. zyfy-an-2023-0217). And the study followed the ARRIVE guidelines (https://arriveguidelines.org).

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All authors gave their consent for publication.

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The authors declare no competing interests.

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Cite this article

Xia, J., Zhang, W., Jiang, Y. et al. HACE1 alleviates intervertebral disc degeneration by inhibiting ferroptosis in nucleus pulposus cells. Sci Rep (2026). https://doi.org/10.1038/s41598-026-39017-1

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  • Received: 14 February 2025

  • Accepted: 02 February 2026

  • Published: 13 February 2026

  • DOI: https://doi.org/10.1038/s41598-026-39017-1

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Keywords

  • Ferroptosis
  • HACE1
  • Intervertebral disc degeneration
  • Nrf2
  • Oxidative stress
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