Home LiteratureArticle Details
PMID: 6430353 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Isolation of a storage and secretory organelle containing Von Willebrand protein from cultured human endothelial cells.

Biochimica et biophysica acta ·Vol. 804 ·No. 3 ·1984-07-20 ·Pages 361-9

Reinders JH, De Groot PG, Gonsalves MD, Zandbergen J, Loesberg C, Van Mourik JA

Abstract

Von Willebrand protein was synthesized and secreted by human endothelial cells in culture. Ca2+ ionophore A23187 and phorbol myristate acetate stimulated the release of Von Willebrand protein from the cultured cells. Stimulated release was accompanied by the disappearance of rod-like structures from the cultured endothelial cells immunostained for Von Willebrand protein, suggesting the existence of a storage organelle for Von Willebrand protein in these cells (Loesberg, C., Gonsalves, M.D., Zandbergen, J., Willems, C., Van Aken, W.G., Stel, H.V., Van Mourik, J.A. and De Groot, P.G. (1983) Biochim. Biophys. Acta 763, 160-168). Cultured human endothelial cells were fractionated on a density gradient of colloidal silica. Von Willebrand protein was found in two organelle populations: a buoyant one sedimenting with a variety of cell organelle marker enzymes, including those of the Golgi apparatus, mitochondria, lysosomes, peroxisomes, endoplasmic reticulum and plasma membrane fragments (peak density of this fraction: 1.08 g X ml-1), and a dense one with a peak density of 1.12 g X ml-1. The dense organelles containing Von Willebrand protein were apparently free of other organelles. Stimulating Von Willebrand protein release with phorbol myristate acetate or Ca2+ ionophore A23187 resulted in a decrease or even complete disappearance of Von Willebrand protein from the high-density organelle fraction, implying a role of this organelle in the stimulus-induced release of Von Willebrand protein. The Von Willebrand protein content of the buoyant fraction was lowered to some extent or did not change upon incubation of the cells with ionophore A23187 and phorbol myristate acetate. Restoration of Von Willebrand protein content of the dense organelle fraction after stimulation occurred within 2 days; this was accompanied by recurrence of immunostaining of rod-shaped structures in cells and an increase in cellular Von Willebrand protein. The excretion of restored Von Willebrand protein could be stimulated again.

MeSH Terms
Blood Coagulation Factors/metabolism Calcimycin/pharmacology Cell Fractionation Cells, Cultured Centrifugation, Density Gradient Endothelium/ultrastructure Humans Organoids/drug effects,metabolism,ultrastructure Tetradecanoylphorbol Acetate/pharmacology Umbilical Veins/metabolism von Willebrand Factor/metabolism
Chemicals
Blood Coagulation Factors von Willebrand Factor Calcimycin Tetradecanoylphorbol Acetate
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Reinders J H
De Groot P G
Gonsalves M D
Zandbergen J
Loesberg C
Van Mourik J A
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
1984-07-20
Pages
361-9
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com