Functional characterization of the spontaneously transformed human umbilical vein endothelial cell line ECV304: Use in an in vitro model of angiogenesis

被引:109
作者
Hughes, SE
机构
[1] Division of Histopathology, U. Medical and Dental Schools (UMDS), St. Thomas's Campus, London
关键词
D O I
10.1006/excr.1996.0168
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To gain insight into the role of the endothelial cell during the pathophysiology of the angiogenic response, investigators have isolated micro- and macrovascular endothelial cells from a wide range of both animal and human vessels, including the umbilical vein. Human umbilical vein endothelial cells (HUVECs) isolated from umbilical cords remain a readily available and popular source of endothelial cell. However, the isolation and culture of these cells have several disadvantages, including the risk of infection, exogenous growth factor requirement, and low proliferative capacity. The heterogeneity of endothelial cells from different vascular beds as well as the heterogeneity between HUVEC isolates from different cords can make the critical interpretation of results difficult. ECV304 is a unique spontaneously transformed human umbilical vein endothelial cell line. In this report, the novel use of ECV304 cells as an alternative to HUVECs in an in vitro model of angiogenesis using the reconstituted basement membrane extract (Matrigel) was investigated. ECV304 cells were characterized immunohistochemically and their angiogenic behavior on Matrigel was analyzed functionally by phase-contrast, electron, and time-lapse video microscopy. ECV304 cells had several practical advantages over HUVEC culture and in contrast to HUVECs, ECV304 cells exhibited an enhanced and highly reproducible capacity for in vitro angiogenesis. However, several differentiated functions were lost or reduced in the ECV304 cell line which also exhibited anomalous cytokeratin expression, ECV304 cells may provide novel insights into the mechanisms governing angiogenesis under both normal physiological and pathological conditions. (C) 1996 Academic Press, Inc.
引用
收藏
页码:171 / 185
页数:15
相关论文
共 49 条
[41]   HUMAN-ENDOTHELIAL CELLS - USE OF HEPARIN IN CLONING AND LONG-TERM SERIAL CULTIVATION [J].
THORNTON, SC ;
MUELLER, SN ;
LEVINE, EM .
SCIENCE, 1983, 222 (4624) :623-625
[42]   PHENOTYPIC ANALYSIS OF CULTURED MELANOMA-CELLS - EXPRESSION OF CYTOKERATIN-TYPE INTERMEDIATE FILAMENTS BY THE M5-HUMAN MELANOMA CELL-LINE [J].
TREJDOSIEWICZ, LK ;
SOUTHGATE, J ;
KEMSHEAD, JT ;
HODGES, GM .
EXPERIMENTAL CELL RESEARCH, 1986, 164 (02) :388-398
[43]   CORRELATION OF CELL-MIGRATION, CELL INVASION, RECEPTOR NUMBER, PROTEINASE PRODUCTION, AND BASIC FIBROBLAST GROWTH-FACTOR LEVELS IN ENDOTHELIAL-CELLS [J].
TSUBOI, R ;
SATO, Y ;
RIFKIN, DB .
JOURNAL OF CELL BIOLOGY, 1990, 110 (02) :511-517
[44]  
VERNON RB, 1992, LAB INVEST, V66, P536
[45]   IDENTIFICATION AND ISOLATION OF ENDOTHELIAL-CELLS BASED ON THEIR INCREASED UPTAKE OF ACETYLATED-LOW DENSITY LIPOPROTEIN [J].
VOYTA, JC ;
VIA, DP ;
BUTTERFIELD, CE ;
ZETTER, BR .
JOURNAL OF CELL BIOLOGY, 1984, 99 (06) :2034-2040
[46]   IDENTIFICATION OF MULTIPLE ACTIVE GROWTH-FACTORS IN BASEMENT-MEMBRANE MATRIGEL SUGGESTS CAUTION IN INTERPRETATION OF CELLULAR-ACTIVITY RELATED TO EXTRACELLULAR-MATRIX COMPONENTS [J].
VUKICEVIC, S ;
KLEINMAN, HK ;
LUYTEN, FP ;
ROBERTS, AB ;
ROCHE, NS ;
REDDI, AH .
EXPERIMENTAL CELL RESEARCH, 1992, 202 (01) :1-8
[47]   IMMUNOLOCALIZATION OF VON-WILLEBRAND PROTEIN IN WEIBEL-PALADE BODIES OF HUMAN-ENDOTHELIAL CELLS [J].
WAGNER, DD ;
OLMSTED, JB ;
MARDER, VJ .
JOURNAL OF CELL BIOLOGY, 1982, 95 (01) :355-360
[48]   ENDOTHELIOMA CELLS EXPRESSING THE POLYOMA MIDDLE-T ONCOGENE INDUCE HEMANGIOMAS BY HOST-CELL RECRUITMENT [J].
WILLIAMS, RL ;
RISAU, W ;
ZERWES, HG ;
DREXLER, H ;
AGUZZI, A ;
WAGNER, EF .
CELL, 1989, 57 (06) :1053-1063
[49]  
WILLIAMS S K, 1987, P204