Tenocyte response to cyclical strain and transforming growth factor beta is dependent upon age and site of origin.
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
The study investigates the influence of cyclic strain and transforming growth factor beta on tendon cells from horses of various ages and anatomical sites. It reveals tissue-specific and age-dependent responses that suggest early differentiation of tendon cells.
Methodology
The researchers conducted an in-vitro study with tendon fibroblasts (tenocytes) from horses of age ranging from the fetus to 10 years old. They extracted these cells from two kinds of tendons – flexor and extensor.
- For the experiment, cells were grown on collagen-coated silicone dishes until a cell collective covered the dish surface, a state termed “confluence.”
- The researchers then applied a regular cyclic biaxial strain of around 9% at a frequency of 0.5 Hz for 24 hours, with or without the addition of Transforming Growth Factor Beta 1 or 3 (also known as TGF-beta).
Findings
The study found distinct reaction patterns depending on the cells’ tendon origin.
- No significant proliferation was observed when flexor tenocytes were subjected to strain or TGF-beta. However, extensor tenocytes showed significant proliferation when subjected to strain alone.
- Both strain and TGF-beta enhanced the protein production in both types of cells, primarily increasing the incorporation of a radioactive protein ([3H]-proline) and the production of collagen types I and III, and Cartilage Oligomeric Matrix Protein (COMP).
- Flexor tenocytes enhanced COMP production even more, possibly reflecting the higher COMP levels present in flexor tendons in the actual anatomy of the horse.
- The study also found variable responses in cells based on the age of the cell’s original host. Younger flexor tenocytes produced more collagen and COMP than those from older hosts, while cell age had a negligible effect in extensor tenocytes.
Conclusion
These findings indicate that tendon cells adapt to different mechanical conditions and biological factors, showing that these cells undergo differentiation at an early stage. Such insights can help understand tendon tissue engineering and related clinical applications better.
Cite This Article
Publication
Researcher Affiliations
- Department of Veterinary Clinical Sciences, Royal Veterinary College, Hawkshead Lane, North Mymms, Hatfield, Hertfordshire, UK AL9 7TA.
MeSH Terms
- Aging / physiology
- Animals
- Cell Differentiation
- Cell Proliferation
- Cells, Cultured
- Collagen Type I / biosynthesis
- Collagen Type III / biosynthesis
- Extracellular Matrix Proteins / biosynthesis
- Fibroblasts
- Glycoproteins / biosynthesis
- Horses
- Matrilin Proteins
- Stress, Mechanical
- Tendons / cytology
- Tendons / metabolism
- Transforming Growth Factor beta / pharmacology
Citations
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