GROWTH AND PHYSIOLOGICAL FUNCTIONS OF VASCULAR ENDOTHELIAL-CELLS IN A NEW SERUM-FREE MEDIUM (SFM)

被引:37
作者
GORFIEN, S
SPECTOR, A
DELUCA, D
WEISS, S
机构
[1] UNIV IOWA,DEPT BIOCHEM,IOWA CITY,IA 52242
[2] BIOSYS,PALO ALTO,CA 94303
[3] CASE WESTERN RESERVE UNIV,SCH MED,CLEVELAND,OH 44106
关键词
D O I
10.1006/excr.1993.1149
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Endothelial cells grown in vitro are widely used for the study of vascular physiology and pathology. The high levels of serum supplementation normally used in endothelial cell culture may create problems in experimental design or in interpretation of results. A serum-free medium (SFM) has been designed specifically for culture of nonhuman vascular endothelial cells. Growth as well as retention of various physiological markers in this medium was demonstrated in large-vessel endothelial cells from bovine, porcine, ovine, and canine species. Cells from all species tested took up DiI-acetylated LDL. Factor VIII-related antigen was demonstrated in cultures of bovine and canine cells. Bovine and porcine cells were shown to have retained the ability to produce prostacyclin. Further supplementation of the SFM with various lipid-containing additives failed to stimulate either growth or prostacyclin production. PDGF produced by bovine, porcine, and canine endothelial cells was measured and found to be present at lower concentration than in serum supplemented cultures. All cells grown in SFM exhibited the histiotypic “cobblestone” morphology normally associated with cultured endothelial cells. While not optimized for culture of human endothelial cells, short-term growth ≤ 4 passages) of human umbilical vein endothelial cells was achieved by supplementing the SFM with hydrocortisone, bovine pituitary extract, and epidermal growth factor. © 1993 Academic Press, Inc.
引用
收藏
页码:291 / 301
页数:11
相关论文
共 46 条
[1]  
BARNES D, 1987, BIOTECHNIQUES, V5, P534
[2]   EXPRESSION OF THE SIS GENE BY ENDOTHELIAL-CELLS IN CULTURE AND INVIVO [J].
BARRETT, TB ;
GAJDUSEK, CM ;
SCHWARTZ, SM ;
MCDOUGALL, JK ;
BENDITT, EP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (21) :6772-6774
[3]  
BERLINER JA, 1978, J CELL BIOL, V79, pA79
[4]  
BOWENPOPE DF, 1985, METHOD ENZYMOL, V109, P69
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   THE VASCULAR ENDOTHELIAL-CELL AS A VEHICLE FOR GENE-THERAPY [J].
CALLOW, AD .
JOURNAL OF VASCULAR SURGERY, 1990, 11 (06) :793-798
[7]   LIPID REQUIREMENT FOR CELL CYCLING - EFFECT OF SELECTIVE-INHIBITION OF LIPID-SYNTHESIS [J].
CORNELL, R ;
GROVE, GL ;
ROTHBLAT, GH ;
HORWITZ, AF .
EXPERIMENTAL CELL RESEARCH, 1977, 109 (02) :299-307
[8]  
DARFLER FJ, 1990, IN VITRO CELL DEV B, V26, P779
[9]  
DEGROOT PG, 1983, THROMB HAEMOSTASIS, V50, P242
[10]   LOW-LEVEL INVIVO GENE-TRANSFER INTO THE ARTERIAL-WALL THROUGH A PERFORATED BALLOON CATHETER [J].
FLUGELMAN, MY ;
JAKLITSCH, MT ;
NEWMAN, KD ;
CASSCELLS, W ;
BRATTHAUER, GL ;
DICHEK, DA .
CIRCULATION, 1992, 85 (03) :1110-1117