Key result
In vitro cyclic strain of human tendon cells significantly upregulated the expression of angiogenic genes including ANGPTL4 (P<0.001) and promoted endothelial cell proliferation and tube formation.
Why the study?
Does repetitive cyclic loading of human tendon cells increase the expression and activity of angiogenic factors?
Does repetitive cyclic loading of human tendon cells increase the expression and activity of angiogenic factors?
p-value: p=<0.001
Cyclic strain induces the expression and release of angiogenic factors, including ANGPTL4, in human tendon cells, suggesting a mechanism for angiogenesis in overuse tendinopathy.
Hypothesis-generating for angiogenesis in overuse tendinopathy; requires human validation before any clinical relevance.
Angiogenesis is associated with the tissue changes underlying chronic overuse tendinopathy. We hypothesized that repetitive, cyclic loading of human tendon cells would lead to increased expression and activity of angiogenic factors. We subjected isolated human tendon cells to overuse tensile loading using an in vitro model (1 Hz, 10% equibiaxial strain). We found that mechanically stimulated human tendon cells released factors that promoted in vitro proliferation and tube formation by human umbilical vein endothelial cells (HUVEC). In response to cyclic strain, there was a transient increase in the expression of several angiogenic genes including ANGPTL4, FGF-2, COX-2, SPHK1, TGF-alpha, VEGF-A and VEGF-C, with no change in anti-angiogenic genes (BAI1, SERPINF1, THBS1 and 2, TIMP1-3). Cyclic strain also resulted in the extracellular release of ANGPTL4 protein by tendon cells. Our study is the first report demonstrating the induction of ANGPTL4 mRNA and release of ANGPTL4 protein in response to cyclic strain. Tenocytes may contribute to the upregulation of angiogenesis during the development of overuse tendinopathy.
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Mousavizadeh et al. (2014) studied Healthy tendon cells (investigating tendinopathy mechanisms) (n=4). Cyclic strain vs. Unstrained tendon cells was evaluated on Expression of angiogenic genes (e.g., ANGPTL4) and induction of endothelial cell proliferation and tube formation (p=<0.001). In vitro cyclic strain of human tendon cells significantly upregulated the expression of angiogenic genes including ANGPTL4 (P<0.001) and promoted endothelial cell proliferation and tube formation.
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