PRDM1 promotes nucleus pulposus cell pyroptosis leading to intervertebral disc degeneration via activating CASP1 transcription.

Autor: Yu C; Department of Spinal Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, 510260, China., Li J; Department of Spinal Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, 510260, China., Kuang W; Department of Spinal Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, 510260, China., Ni S; Department of Trauma Orthopaedics, Zhujiang Hospital, Southern Medical University, Guangzhou, 510260, China., Cao Y; Department of Spinal Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, 510260, China., Duan Y; Department of Spinal Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, 510260, China. duanxy@smu.edu.cn.
Jazyk: angličtina
Zdroj: Cell biology and toxicology [Cell Biol Toxicol] 2024 Oct 21; Vol. 40 (1), pp. 89. Date of Electronic Publication: 2024 Oct 21.
DOI: 10.1007/s10565-024-09932-y
Abstrakt: Intervertebral disc degeneration (IVDD) is a primary contributor to low back pain and poses a considerable burden to society. However, the molecular mechanisms underlying IVDD remain to be elucidated. PR/SET domain 1 (PRDM1) regulates cell proliferation, apoptosis, and inflammatory responses in various diseases. Despite these regulatory functions, the mechanism of action of PRDM1 in IVDD remains unexplored. In this study, we investigated the role and underlying mechanisms of action of PRDM1 in IVDD progression. The expression of PRDM1 in nucleus pulposus (NP) tissues and NP cells (NPCs) was assessed using western blotting, immunohistochemistry, and immunofluorescence. The effects of PRDM1 on IVDD progression were investigated in vitro and in vivo. Mechanistically, mRNA sequencing, chromatin immunoprecipitation, and dual-luciferase reporter assays were performed to confirm that PRDM1 triggered CASP1 transcription. Our study demonstrated for the first time that PRDM1 expression was substantially upregulated in degenerated NP tissues and NPCs. PRDM1 overexpression promoted NPCs pyroptosis by inhibiting mitophagy and exacerbating IVDD progression, whereas PRDM1 silencing exerted the opposite effect. Furthermore, PRDM1 activated CASP1 transcription, thereby promoting NPCs pyroptosis in vitro. Notably, CASP1 silencing reversed the effects of PRDM1 on the NPCs. To the best of our knowledge, this study is the first to demonstrate that PRDM1 silencing inhibits NPCs pyroptosis by repressing CASP1 transcription, which may be a promising new therapeutic target for IVDD.
(© 2024. The Author(s).)
Databáze: MEDLINE
Externí odkaz: