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Abstract
MATN3 protein expression decreased significantly during intervertebral disc degeneration (IVDD).
- A decrease in MATN3 is closely associated with cellular senescence in nucleus pulposus cells (NPCs).
- Overexpression of MATN3 can effectively inhibit NPC senescence in laboratory conditions.
- In a rat model, MATN3 overexpression delays the pathological progression of IVDD.
- No significant difference in MATN3 levels was found at the mRNA level, suggesting post-transcriptional regulation.
- USP5 was identified as a direct interacting protein of MATN3, stabilizing it through a process that removes ubiquitin tags.
- Functional experiments indicated that USP5 alleviates NPC senescence by increasing MATN3 levels.
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