BASAL TISSUE FACTOR EXPRESSION IN ENDOTHELIAL-CELL CULTURES IS CAUSED BY CONTAMINATING SMOOTH-MUSCLE CELLS - REDUCTION BY USING CHYMOTRYPSIN INSTEAD OF COLLAGENASE

被引:43
作者
MULDER, AB
BLOM, NR
SMIT, JW
RUITERS, MHJ
VANDERMEER, J
HALIE, MR
BOM, VJJ
机构
[1] UNIV GRONINGEN HOSP, CENT LAB CLIN HAEMATOL, 9700 RB GRONINGEN, NETHERLANDS
[2] UNIV GRONINGEN HOSP, CTR BIOMED TECHNOL, 9700 RB GRONINGEN, NETHERLANDS
关键词
ENDOTHELIAL CELLS; TISSUE FACTOR; SMOOTH MUSCLE CELLS; COLLAGENASE; CHYMOTRYPSIN;
D O I
10.1016/0049-3848(95)00192-T
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A discrepancy exists between basal tissue factor (TF) expression found in endothelial cell cultures and the failure to detect TF in unpertubated endothelial cells in vivo. We demonstrated that basal TF expression in endothelial cell cultures originated from contaminating cells. These cells were ultrastructurally and flowcytometrically identified as smooth muscle cells. The cell cultures had been obtained from collagenase-treated human umbilical cord vessels. Histologic studies revealed that after collagenase treatment the basement membrane was digested and underlying structures were disrupted at some areas of the vein. We selected chymotrypsin as an alternative for the isolation of endothelial cells. Using chymotrypsin, the endothelial lining was selectively lost leaving the basement membrane undisturbed. Furthermore, use of chymotrypsin instead of collagenase minimized the level of basal TF activity. Taken together, we demonstrated that basal TF expression in endothelial cell cultures is caused by contaminating smooth muscle cells. This contamination can strongly be reduced using chymotrypsin instead of collagenase for isolation of endothelial cells.
引用
收藏
页码:399 / 411
页数:13
相关论文
共 31 条
[1]  
ALMUS FE, 1990, BLOOD, V76, P354
[2]   SERUM STIMULATION OF QUIESCENT HUMAN-FIBROBLASTS INDUCES THE SYNTHESIS OF TISSUE FACTOR MESSENGER-RNA FOLLOWED BY THE APPEARANCE OF TISSUE FACTOR ANTIGEN AND PROCOAGULANT ACTIVITY [J].
BLOEM, LJ ;
CHEN, L ;
KONIGSBERG, WH ;
BACH, R .
JOURNAL OF CELLULAR PHYSIOLOGY, 1989, 139 (02) :418-423
[3]  
BOM VJJ, 1991, THROMB HAEMOSTASIS, V66, P283
[4]   THE CONTRIBUTIONS OF CA-2+, PHOSPHOLIPIDS AND TISSUE-FACTOR APOPROTEIN TO THE ACTIVATION OF HUMAN BLOOD-COAGULATION FACTOR-X BY ACTIVATED FACTOR-VII [J].
BOM, VJJ ;
BERTINA, RM .
BIOCHEMICAL JOURNAL, 1990, 265 (02) :327-336
[5]   OXIDIZED LDL ENHANCES LIPOPOLYSACCHARIDE-INDUCED TISSUE FACTOR EXPRESSION IN HUMAN ADHERENT MONOCYTES [J].
BRAND, K ;
BANKA, CL ;
MACKMAN, N ;
TERKELTAUB, RA ;
FAN, ST ;
CURTISS, LK .
ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (05) :790-797
[6]   CULTURED HUMAN-ENDOTHELIAL CELLS GENERATE TISSUE FACTOR IN RESPONSE TO ENDOTOXIN [J].
COLUCCI, M ;
BALCONI, G ;
LORENZET, R ;
PIETRA, A ;
LOCATI, D ;
DONATI, MB ;
SEMERARO, N .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 71 (06) :1893-1896
[7]  
CROSSMAN DC, 1990, J BIOL CHEM, V265, P9782
[8]   REGULATION OF TISSUE FACTOR GENE-EXPRESSION IN EPITHELIAL-CELLS - INDUCTION BY SERUM AND PHORBOL 12-MYRISTATE 13-ACETATE [J].
CUI, MZ ;
PARRY, GCN ;
EDGINGTON, TS ;
MACKMAN, N .
ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (05) :807-814
[9]   G(ANH)MTETRA, A NATURALLY-OCCURRING 1,6-ANHYDRO MURAMYL DIPEPTIDE, INDUCES GRANULOCYTE-COLONY-STIMULATING FACTOR EXPRESSION IN HUMAN MONOCYTES - A MOLECULAR ANALYSIS [J].
DOKTER, WHA ;
DIJKSTRA, AJ ;
KOOPMANS, SB ;
MULDER, AB ;
STULP, BK ;
HALIE, MR ;
KECK, W ;
VELLENGA, E .
INFECTION AND IMMUNITY, 1994, 62 (07) :2953-2957
[10]  
DRAKE TA, 1993, AM J PATHOL, V142, P1458