Expression and localisation of vascular ribonucleases in endothelial cells

The functions of extracellular RNA in the vascular system as new procoagulatory and permeability-increasing factor in vivo and in vitro were shown to be counteracted by pancreatic type RNase1. Based on the identification of RNase1 in plasma and serum, it is proposed that the enzyme is expressed by v...

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Bibliographic Details
Published in:	Thrombosis and haemostasis Vol. 105; no. 2; p. 345
Main Authors:	Fischer, Silvia, Nishio, Miwako, Dadkhahi, Sara, Gansler, Julia, Saffarzadeh, Mona, Shibamiyama, Aya, Kral, Nicolé, Baal, Nelli, Koyama, Takatoshi, Deindl, Elisabeth, Preissner, Klaus T
Format:	Journal Article
Language:	English
Published:	Germany 01-02-2011
Subjects:	Animals Cells, Cultured Endothelial Cells - enzymology Exocytosis Humans Mice P-Selectin - metabolism Ribonuclease, Pancreatic - metabolism Time Factors von Willebrand Factor - metabolism Weibel-Palade Bodies - enzymology
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Summary:	The functions of extracellular RNA in the vascular system as new procoagulatory and permeability-increasing factor in vivo and in vitro were shown to be counteracted by pancreatic type RNase1. Based on the identification of RNase1 in plasma and serum, it is proposed that the enzyme is expressed by vascular cells to contribute in the regulation of extracellular RNA. It is demonstrated that RNase1 and RNase5 (also termed angiogenin) were differentially expressed in various types of endothelial cells, whereby human umbilical vein endothelial cells (HUVEC) expressed and released the highest concentration of active RNase1. Expression and release of RNase5 were similar in all types of endothelial cells tested. Both RNases were constitutively produced and secreted, whereby a portion of RNase1, but not RNase5, was stored in Weibel-Palade bodies, co-localising with von Willlebrand factor and P-selectin. Accordingly, immediate release of RNase1 from these granules was demonstrated in vitro and in vivo using Weibel-Palade body exocytosis-inducing agents. Additionally, extracellular RNA or poly:IC (but not DNA) induced this short-term release of RNase1. Our results indicate that vascular RNase1 and RNase5 are mainly produced by vascular endothelial cells and can serve, depending on the vascular bed, different functions in vascular homeostasis and endothelial cell responses.
ISSN:	0340-6245
DOI:	10.1160/TH10-06-0345