Cell sources of inflammatory mediators present in bone marrow areas inside the meniscus
Francisco Airton Castro Rocha1, Virgínia Claudia Carneiro Girão2, Rodolfo de Melo Nunes1
1Departmento de Morfologia, Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, Ceará, Brasil.
Purpose:
To demonstrate the production of inflammatory mediators by cells located in bone marrow spaces inside rodent menisci.
Methods:
Mice subjected to transection of the medial collateral and anterior cruciate ligaments and meniscotomy (osteoarthritis model) or to a sham procedure, as well as non-operated (naive) mice and rats, had knee joints excised. Tissues were stained with hematoxylin-eosin and tartrate-resistant acid phosphatase (TRAP). CD68+ cells, inducible nitric oxide synthase (iNOS), interleukin (IL)-1β, and tumor necrosis factor (TNF) expression were detected using immunohistochemistry.
Results:
Lamellar ossified areas, bone-entrapped osteocytes and bone marrow spaces were found inside menisci of one week up to 6 months-old naïve mice, regardless of gender. Menisci from naive rats also showed the same pattern with bone marrow areas. CD68+ cells were identified in bone marrow areas inside the meniscus of mice. TRAP+ osteoclasts, and hematogenous precursors expressing IL-1β, TNF, and iNOS were identified inside bone marrow areas in meniscal samples from both naïve and sham operated mice. Quantitative immunoexpression of IL-1 β, TNF and iNOS was more intense, P = 0.0194, 0.0293, 0.0124, respectively, in mouse knees from mice sacrificed 49 days after being subjected to an osteoarthritis (OA) model as compared to sham operated animals.
Conclusion:
We provide novel data showing that rodent menisci display bone marrow areas with cells able to produce inflammatory mediators. Immunoexpression of inflammatory mediators in those bone marrow areas is significantly more pronounced in mice subjected to experimental OA.
Insights
Rodent menisci contain bone marrow spaces with cells that produce inflammatory mediators. This production is significantly increased in experimental osteoarthritis, revealing a novel aspect of meniscal biology.
Area of Science:
- Orthopedics
- Immunology
- Histology
Background:
- Menisci are crucial knee joint structures.
- The cellular composition and inflammatory potential of meniscal tissue are not fully understood.
- Bone marrow elements within the meniscus represent an unexplored area.
Purpose of the Study:
- To investigate the presence and function of bone marrow cells within rodent menisci.
- To determine if these cells produce inflammatory mediators.
- To compare mediator expression in healthy and osteoarthritis models.
Main Methods:
- Knee joints from naive, sham-operated, and osteoarthritis-model rodents were analyzed.
- Histological staining (hematoxylin-eosin, TRAP) was performed.
- Immunohistochemistry was used to detect CD68, iNOS, IL-1β, and TNF expression.
Main Results:
- Bone marrow spaces containing CD68+ cells, TRAP+ osteoclasts, and precursor cells were identified within rodent menisci.
- These cells expressed inducible nitric oxide synthase (iNOS), interleukin-1β (IL-1β), and tumor necrosis factor (TNF).
- Inflammatory mediator expression was significantly higher in the osteoarthritis model compared to controls.
Conclusions:
- Rodent menisci harbor bone marrow areas populated by cells capable of producing inflammatory mediators.
- Experimental osteoarthritis exacerbates the production of these inflammatory mediators within the meniscal bone marrow.
- This finding highlights a novel cellular component within the meniscus with implications for joint inflammation and disease.
Related Concept Videos
Mesenchymal Stem Cells
Inflammatory Response
Inflammation can be triggered by various stimuli, such as impact, abrasion, chemical irritation, infections, and extreme hot or cold temperatures. These can damage cells and connective tissue fibers,...
T Cell Types and Functions
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Inflammation
Regulation of Hematopoietic Stem Cells
Inflammatory Response I: Vascular and Cellular


