PHLDA2 overexpression facilitates senescence and apoptosis via the mitochondrial route in human nucleus pulposus cells by regulating Wnt/β‐catenin signalling pathway

• Published in: IUBMB life 2024-10, Vol.76 (10), p.788-802
• Main Authors: Chang, Xian, Cao, Ya, Hu, Zhi‐Lei, Zhai, Yu, Zhang, Yu‐Yao, Lv, Yang‐Fan, Li, Chang‐Qing
• Format: Article
• Language: English
• Subjects: Adult; Animals; Apoptosis; beta Catenin - genetics; beta Catenin - metabolism; Catenin; Cells, Cultured; Cellular Senescence; Degeneration; Female; Flow cytometry; Humans; intervertebral disc degeneration; Intervertebral Disc Degeneration - genetics; Intervertebral Disc Degeneration - metabolism; Intervertebral Disc Degeneration - pathology; Intervertebral discs; Low back pain; Magnetic resonance imaging; Male; Membrane potential; Middle Aged; Mitochondria; Mitochondria - metabolism; Mitochondria - pathology; Nuclear Proteins; Nucleus pulposus; Nucleus Pulposus - metabolism; Nucleus Pulposus - pathology; nucleus pulposus cells; Phenotypes; PHLDA2; Quality of life; Rats; Rats, Sprague-Dawley; Senescence; Signal transduction; Transmission electron microscopy; Wnt protein; Wnt Signaling Pathway
• ISSN: 1521-6543; 1521-6551; 1521-6551
• DOI: 10.1002/iub.2829

Low back pain is a common clinical symptom of intervertebral disc degeneration (IVDD), which seriously affects the quality of life of the patients. The abnormal apoptosis and senescence of nucleus pulposus cells (NPCs) play important roles in the pathogenesis of IVDD. PHLDA2 is an imprinted gene related to cell apoptosis and tumour progression. However, its role in NPC degeneration is not yet clear. Therefore, this study was set to explore the effects of PHLDA2 on NPC senescence and apoptosis and the underlying mechanisms. The expression of PHLDA2 was examined in human nucleus pulposus (NP) tissues and NPCs. Immunohistochemical staining, magnetic resonance imaging imaging and western blot were performed to evaluate the phenotypes of intervertebral discs. Senescence and apoptosis of NPCs were assessed by SA‐β‐galactosidase, flow cytometry and western blot. Mitochondrial function was investigated by JC‐1 staining and transmission electron microscopy. It was found that the expression level of PHLDA2 was abnormally elevated in degenerated human NP tissues and NPCs. Furthermore, knockdown of PHLDA2 can significantly inhibit senescence and apoptosis of NPCs, whereas overexpression of PHLDA2 can reverse senescence and apoptosis of NPCs in vitro. In vivo experiment further confirmed that PHLDA2 knockdown could alleviate IVDD in rats. Knockdown of PHLDA2 could also reverse senescence and apoptosis in IL‐1β‐treated NPCs. JC‐1 staining indicated PHLDA2's knockdown impaired disruption of the mitochondrial membrane potential and also ameliorated superstructural destruction of NPCs as showed by transmission electron microscopy. Finally, we found the PHLDA2 knockdown promoted Collagen‐II expression and suppressed MMP3 expression in NPCs by repressing wnt/β‐catenin pathway. In conclusion, the results of the present study showed that PHLDA2 promotes IL‐1β‐induced apoptosis and senescence of NP cells via mitochondrial route by activating the Wnt/β‐catenin pathway, and suggested that therapy targeting PHLDA2 may provide valuable insights into possible IVDD therapies.