Stress-Activated Protein Kinases in Intervertebral Disc Degeneration: Unraveling the Impact of JNK and p38 MAPK.
Lei LiGuang-Zhi ZhangZhili YangXuewen KangPublished in: Biomolecules (2024)
Intervertebral disc degeneration (IDD) is a major cause of lower back pain. The pathophysiological development of IDD is closely related to the stimulation of various stressors, including proinflammatory cytokines, abnormal mechanical stress, oxidative stress, metabolic abnormalities, and DNA damage, among others. These factors prevent normal intervertebral disc (IVD) development, reduce the number of IVD cells, and induce senescence and apoptosis. Stress-activated protein kinases (SAPKs), particularly, c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein kinase (p38 MAPK), control cell signaling in response to cellular stress. Previous studies have shown that these proteins are highly expressed in degenerated IVD tissues and are involved in complex biological signal-regulated processes. Therefore, we summarize the research reports on IDD related to JNK and p38 MAPK. Their structure, function, and signal regulation mechanisms are comprehensively and systematically described and potential therapeutic targets are proposed. This work could provide a reference for future research and help improve molecular therapeutic strategies for IDD.
Keyphrases
- induced apoptosis
- oxidative stress
- dna damage
- cell death
- endoplasmic reticulum stress
- cell cycle arrest
- signaling pathway
- stress induced
- dna repair
- protein kinase
- endothelial cells
- gene expression
- single cell
- tyrosine kinase
- protein protein
- heat stress
- transcription factor
- amino acid
- emergency department
- cell therapy
- stem cells
- small molecule
- ischemia reperfusion injury
- climate change
- single molecule
- electronic health record
- human health