VEGF-induced tubulogenesis of endothelial cells from human brain malignant glioma in the three dimentional model.
- Author:
Xue-feng JIANG
1
;
Jin-si BAI
;
Xiu-wu BIAN
;
Jia-you LU
;
Wen ZHAO
;
Jing-quan SHI
Author Information
- Publication Type:Journal Article
- MeSH: Brain Neoplasms; blood supply; Cells, Cultured; Dose-Response Relationship, Drug; Endothelial Cells; drug effects; Endothelium, Vascular; cytology; Glioma; blood supply; Humans; Immunomagnetic Separation; Microcirculation; pathology; Neovascularization, Pathologic; Vascular Endothelial Growth Factors; administration & dosage; pharmacology
- From: Chinese Journal of Pathology 2005;34(9):579-582
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo compare the tubulogenesis capability of malignant glioma-derived microvessel endothelial cells (GDMEC) from human brain with that of ECV304 cells in a three dimentional model and to explore the significance of GDMEC in the study on angiogenesis.
METHODSThe GDMEC were isolated from malignant gliomas of human brain and purified by selective binding to the monoclonal antibody against CD105 bound to the magnetic MACS MicroBeads. GDMEC and endothelial-like cell line ECV304 were compared with their capabilities of formatting tubule-like structure (TLS) in the three dimentional collagen matrix, with or without inducement by various concentration of vascular endothelial growth factor (VEGF).
RESULTSThe obtained GDMEC had a high purification (98%) and could be successfully cultured in vitro. GDMECs formed more TLS than ECV304 cells of the same number and at the same time points. VEGF could induce rapid formation of TLS in a dose-dependent manner, however, ECV304 cells were less response to VEGF stimulation.
CONCLUSIONSGDMEC could maintain their endothelial characteristics and potential capability of angiogenesis. They were more response to VEGF than ECV304, therefore, more suitable for in vitro studies on tumor angiogenesis.
