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TNF-α Regulated Bidirectional Interaction Between Bone Marrow Mesenchymal Stem Cells and Articular Chondrocytes
Yu Huang1, Fengqiong Zuo2, Jue Wu1
1Department of Science and Education, Sichuan Taikang Hospital, Chengdu, China.
Tumor necrosis factor-alpha (TNF-α) triggers bidirectional communication between bone marrow mesenchymal stem cells (BMSCs) and articular chondrocytes (ACs). This interaction influences cell viability and cytokine expression, impacting osteoarthritis pathogenesis.
Area of Science:
- Cell Biology
- Stem Cell Biology
- Osteoarthritis Research
Background:
- Articular chondrocytes (ACs) maintain cartilage function; their degeneration leads to osteoarthritis.
- Bone marrow mesenchymal stem cells (BMSCs) protect ACs, making them a potential osteoarthritis treatment.
Purpose of the Study:
- To investigate the bidirectional effects of BMSC and AC secretions on each other in osteoarthritis.
- To understand the role of tumor necrosis factor-alpha (TNF-α) in mediating these interactions.
Main Methods:
- Isolated rabbit BMSCs and ACs were characterized.
- Cells were treated with conditioned media from TNF-α-stimulated BMSCs and ACs.
- Cell viability was assessed using CCK-8 assays.
- Gene and protein expression (Runx2, Alp, TNF, IL6, IL17A, IL10) and cytokine levels were measured via RT-qPCR, immunoblotting, and ELISA.
Main Results:
- Conditioned media affected cell viability after 12 hours, increasing BMSC viability and decreasing AC viability.
- TNF-α treatment dose-dependently elevated gene and protein expression of Runx2, Alp, and inflammatory/anti-inflammatory cytokines (TNF-α, IL-6, IL-17A, IL-10) in both cell types.
- Concentrations of these cytokines in the supernatant increased dose-dependently with TNF-α stimulation.
Conclusions:
- Results indicate a TNF-α-regulated bidirectional interaction between BMSCs and ACs.
- This interaction provides insights into osteoarthritis pathogenesis.
- Findings may aid in osteoarthritis prevention and treatment strategies.
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