Scientific reports

BMAL1 may reduce intervertebral disc breakdown by activating the SIRT1/PGC-1α pathway: evidence from lab studies

Updated

Abstract

Overexpression of BMAL1 in nucleus pulposus cells led to decreased apoptosis and inflammation while enhancing cell activity.

  • The expression levels of BMAL1, SIRT1, and PINK1 were evaluated in nucleus pulposus cells.
  • Activation of the was associated with improved characteristics of nucleus pulposus cells.
  • Increased BMAL1 expression resulted in reduced levels of apoptosis, inflammation, and reactive oxygen species.
  • Cell activity and density were enhanced following BMAL1 overexpression.
  • Mitophagy levels increased with the overexpression of BMAL1.

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Funding

Competing interests

Declarations. Competing interests: The authors declare no competing interests. Guidelines: All methods were carried out in accordance with relevant guidelines and regulations. Informed consent: This study did not involve human tissue samples or patient data. The research utilized commercially available cell lines obtained from iCell Bioscience Inc., which were ethically sourced and complied with relevant regulatory standards.
PubMed

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