Abstract
Background/Aims: The complex process of fracture healing relies on the reciprocal action of microvascular
endothelial cells and osteoblasts. We hypothesized that, in addition to revascularization,
stimulated microendothelial cells secrete growth factors known to influence osteoblasts
in vitro and in animal trials. Methods: The study describes the effect of L-glycine, L-arginine, and L-lysine on human microvascular
endothelial cells (HDMEC) with respect to the in-vitro expression of basic fibroblast
growth factor (b-FGF), vascular endothelial growth factor (VEGF), and endothelial
and inducible nitric oxide synthases (e-NOS, i-NOS). The amino acids were added on
day 0, and b-FGF, VEGF, e-NOS, and i-NOS were measured by ELISA on days 0, 1, 3, and
6. Results: The number of HDMEC was not significantly influenced by the addition of amino acids,
suggesting that the observed effects were not related to proliferation. HDMEC immediately
released b-FGF into the cellular supernatant when L-glycine was added. In addition,
HDMEC were stimulated to produce i-NOS and e-NOS after a single addition of L-arginine.
Conclusion: These findings suggest that L-arginine and L-glycine stimulate HDMEC to express NOS
and b-FGF, compounds well-known for their osteoblast modulating activities. If confirmed
in animal studies, supplementation with L-arginine or L-glycine may be an attractive
therapeutic approach to enhance fracture repair.
Key words
L-arginine - L-glycine - human microvascular endothelial cells - fracture healing
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Ass. Prof. Dr. R. Kdolsky
Department of Traumatology · University of Vienna Medical School · AKH
Währinger Gürtel 18-20
1090 Vienna
Austria
Phone: +43/1/4 04 00 56 19
Fax: +43/1/4 04 00 59 49
Email: richard.kdolsky@meduniwien.ac.at