Key result
Heparin at doses between 0.25 and 2 U/ml increased the content of high molecular weight von Willebrand factor in endothelial cells in a growth factor-dependent manner.
Why the study?
Does heparin enhance von Willebrand factor content in endothelial cells?
Does heparin enhance von Willebrand factor content in endothelial cells?
Heparin enhances the synthesis and storage of high molecular weight von Willebrand factor in endothelial cells via growth factor-dependent mechanisms.
Answers are grounded in this paper and cite their sources.
May modulate endothelial vWF in animal models; leaves open clinical effects on thrombosis or bleeding risk.
Von Willebrand factor (vWf), a multimeric adhesive glycoprotein synthesized, stored, and secreted in megakaryocytes and endothelial cells, is normally found in plasma, platelets and subendothelium. While many substances mediate the release of vWf from endothelial cells, factors that enhance vWf synthesis and partitioning to its regulated pathway are currently unknown. We studied the effect of pharmacologic doses of heparin on the vWf content of endothelial cells. After a lag of 8 h and in the presence of crude or purified growth factor, heparin at doses between 0.25 and 2 U (1.4-11 micrograms)/ml, increased the content of high molecular weight vWf. The increased amounts of vWf were localized to Weibel-Palade bodies and extracellular matrix. Lower molecular weight highly sulfated heparin or heparin-like compounds were most active in growth factor dependent endothelial cell vWf expression. There was no clear importance of polysaccharide sequence or protein core.
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Tannenbaum et al. (1994) studied this question. Heparin was evaluated on vWf content of endothelial cells. Heparin at doses between 0.25 and 2 U/ml increased the content of high molecular weight von Willebrand factor in endothelial cells in a growth factor-dependent manner.
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