Targeting nucleus pulposus cell death in the treatment of intervertebral disc degeneration DOI Creative Commons

Hong Sun,

Jiajie Guo,

Zhilin Xiong

et al.

JOR Spine, Journal Year: 2024, Volume and Issue: 7(4)

Published: Dec. 1, 2024

Abstract Background Intervertebral disc degeneration (IDD) is a progressive age‐related disorder characterized by the reduction in number of nucleus pulposus cells (NPCs) and degradation extracellular matrix (ECM), thereby leading to chronic pain disability. The pathogenesis IDD multifaceted, current therapeutic strategies remain limited. (NP), primarily composed NPCs, proteoglycans, type II collagen, constitutes essential components for maintaining intervertebral (IVD) function spinal motion. disturbed homeostasis NPCs closely associated with IDD. Accumulating evidence increasingly suggests crucial role programmed cell death (PCD) regulating NPCs. Aims This review aimed elucidate various forms PCD their respective roles IDD, investigate diverse targeting treatment. Materials & Methods We collected relevant literature regarding development Subsequently, we comprehensively summarized intricate association between also explored potential application therapy traditional Chinese medicine (TCM) prevention treatment Results Current indicated that was Additionally, targeted pharmaceuticals based on mechanisms could effectively impede loss Conclusion demonstrated may be promising strategy

Language: Английский

A new target for treating intervertebral disk degeneration: gut microbes DOI Creative Commons
Kaizhong Wang, Xiangyan Liu,

Huagui Huang

et al.

Frontiers in Microbiology, Journal Year: 2024, Volume and Issue: 15

Published: Nov. 29, 2024

Intervertebral disk degeneration (IDD) is a common clinical spinal disease and one of the main causes low back pain (LBP). Generally speaking, IDD considered natural degenerative process with age. However, deepening research, people have discovered that not only related to age, but also has many factors can induce accelerate its progression. In addition, pathogenesis remains unclear, resulting in limited traditional treatment methods cannot effectively prevent treat IDD. Conservative may lead patients’ dependence on drugs, relief effect obvious. Similarly, surgical highly invasive, longer recovery time higher recurrence rate. With exploration, intestinal microorganisms are an important symbiotic microbial community human body closely occurrence development various diseases. Changes their metabolites affect body’s inflammatory response, immune regulation, metabolic processes, thereby affecting health intervertebral disk. this context, gut microbiota received considerable attention as potential target for delaying or treating This article first introduces impact microbes distal organs, then focuses three mechanisms by which influence Finally, we summarized interfering metabolites. Further understanding between will help formulate reasonable strategies achieve ideal therapeutic effects.

Language: Английский

Citations

0

Integrating bioinformatics and experimental validation to Investigate IRF1 as a novel biomarker for nucleus pulposus cells necroptosis in intervertebral disc degeneration DOI Creative Commons

Kai‐Sheng Zhou,

Shaobo Wu, Zuolong Wu

et al.

Scientific Reports, Journal Year: 2024, Volume and Issue: 14(1)

Published: Dec. 3, 2024

Intervertebral disc degeneration (IDD) is a prevalent spinal disorder and the principal cause of lower back pain (LBP). Diverse forms programmed cell death (PCD) have been identified as key phenotypes disease potential to serve new indicators for diagnosis prognosis IDD. However, mechanism underlying necroptosis in IDD remains unclear. This study aimed identify novel biomarkers that promote nucleus pulposus using bioinformatic analysis experimental validation. We analyzed multiple datasets from Gene Expression Omnibus (GEO) database necroptosis-related differential genes (NRDEGs). Ontology (GO) Kyoto Encyclopedia Genes Genomes (KEGG) analyses were performed, followed by logistic least absolute shrinkage selection operator (LASSO) support vector machine-recursive (SVM) algorithms genes. set enrichment (GSEA) regression used ascertain functions these genes, respectively. then constructed mRNA-miRNA, mRNA-TF, mRNA-drug, functional similarity gene interaction networks seven identified. clinical samples necroptotic model validate our findings. Immunohistochemical staining, RT-qPCR, western blotting results indicated IRF1 may be hub gene. To further elucidate function IRF1, we knockdown overexpression models, which revealed promotes rat cells, increases mitochondrial ROS levels, decreases ATP levels. These findings provide insights into development and, first time, role biomarker treatment

Language: Английский

Citations

0

Machine learning-based analysis of programmed cell death types and key genes in intervertebral disc degeneration DOI

Yigang Lv,

Jiawei Du,

Haoning Xiong

et al.

APOPTOSIS, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 4, 2024

Language: Английский

Citations

0

Targeting oxidative stress, iron overload and ferroptosis in bone-degenerative conditions DOI Creative Commons
Junxiao Ren, Chen Meng, Li Rui

et al.

Turkish Journal of Biochemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 4, 2024

Abstract Introduction Bone-degenerative conditions, including osteoporosis, rheumatoid arthritis, and osteoarthritis, are major public health concerns worldwide, associated with oxidative stress iron overload that disrupts bone homeostasis. Ferroptosis, an iron-mediated form of cell death, has emerged as a critical factor in degeneration, necessitating comprehensive review its role these conditions. Content This comprehensively examined the latest research on stress, metabolism, ferroptosis related to biology focusing their interconnections potential therapeutic implications. The revealed affects various types, osteoclasts, osteoblasts, chondrocytes, contributing loss cartilage degradation. Iron homeostasis was found be crucial for function, both deficiency potentially leading pathological Ferroptosis regulation involves complex interplay between lipid peroxidation, antioxidant systems, SLC7A11-GSH-GPX4 network FSP1-CoQ10H2 pathway. Different lineages, mesenchymal stem cells, exhibit varied responses induction regulation. Summary Understanding molecular mechanisms underlying cells offers promising avenues developing targeted therapies bone-degenerative Outlook Future should focus elucidating specific roles different disorders exploring interventions targeting overload, pathways improve management debilitating

Language: Английский

Citations

0

Targeting nucleus pulposus cell death in the treatment of intervertebral disc degeneration DOI Creative Commons

Hong Sun,

Jiajie Guo,

Zhilin Xiong

et al.

JOR Spine, Journal Year: 2024, Volume and Issue: 7(4)

Published: Dec. 1, 2024

Abstract Background Intervertebral disc degeneration (IDD) is a progressive age‐related disorder characterized by the reduction in number of nucleus pulposus cells (NPCs) and degradation extracellular matrix (ECM), thereby leading to chronic pain disability. The pathogenesis IDD multifaceted, current therapeutic strategies remain limited. (NP), primarily composed NPCs, proteoglycans, type II collagen, constitutes essential components for maintaining intervertebral (IVD) function spinal motion. disturbed homeostasis NPCs closely associated with IDD. Accumulating evidence increasingly suggests crucial role programmed cell death (PCD) regulating NPCs. Aims This review aimed elucidate various forms PCD their respective roles IDD, investigate diverse targeting treatment. Materials & Methods We collected relevant literature regarding development Subsequently, we comprehensively summarized intricate association between also explored potential application therapy traditional Chinese medicine (TCM) prevention treatment Results Current indicated that was Additionally, targeted pharmaceuticals based on mechanisms could effectively impede loss Conclusion demonstrated may be promising strategy

Language: Английский

Citations

0