Measurement of Chemically Induced Mitotic Nondisjunction using a Monochromosomal Human/Mouse Hybrid Cell Line

Author(s):  
Raghbir S. Athwal ◽  
Shahbeg S. Sandhu
2001 ◽  
Vol 41 (supplement) ◽  
pp. S139
Author(s):  
T Tojima ◽  
M Takahashi ◽  
T Obinata ◽  
E Ito

Blood ◽  
1988 ◽  
Vol 71 (6) ◽  
pp. 1669-1675 ◽  
Author(s):  
JJ Emeis ◽  
CJ Edgell

Abstract The fibrinolytic characteristics of the endothelial hybrid cell line EA.hy 926, established by fusing a human umbilical vein endothelial cell with a human carcinoma cell line, were studied. The hybrid cell line produced large amounts of tissue-type plasminogen activator (t- PA), plasminogen activator inhibitor type 1, and a small amount of urokinase. All plasminogen activator present in conditioned medium was complexed with inhibitor because the cells secreted plasminogen activator inhibitor in excess over plasminogen activator and no activator activity was detectable in conditioned media by direct activity assays. t-PA activator activity was, however, demonstrable in conditioned media after treatment with sodium dodecyl sulfate, in agreement with t-PA antigen determinations. Increased plasminogen activator inhibitor activity could be induced by incubating the cells in the presence of endotoxin or microtubule inhibitors, whereas increased t-PA activity could be induced by microtubule inhibitors. Interleukin-1 had no effect. The fibrinolytic characteristics of the hybrid cell line were stable for at least 30 passages. The perpetual human hybrid cell line EA.hy 926 therefore may be a useful tool for the study of fibrinolysis in cultured endothelial cells.


Nature ◽  
1975 ◽  
Vol 256 (5512) ◽  
pp. 57-59 ◽  
Author(s):  
ROBERT GULLIS ◽  
JÖRG TRABER ◽  
BERND HAMPRECHT

1991 ◽  
Vol 545 (1-2) ◽  
pp. 80-86 ◽  
Author(s):  
Philip M. Dunn ◽  
Paul R. Coote ◽  
John N. Wood ◽  
Gillian M. Burgess ◽  
Humphrey P. Rang

1984 ◽  
Vol 4 (3) ◽  
pp. 475-483 ◽  
Author(s):  
C D Lobaton ◽  
A Moreno ◽  
D L Oxender

We have studied leucine transport in several Chinese hamster-human hybrid cell lines obtained by fusion of a temperature-sensitive line of Chinese hamster ovary cells, ts025C1, and normal human leukocytes. A hybrid cell line exhibiting a twofold increase in L-leucine uptake over that in the parental cell line was found. This hybrid cell line, 158CnpT-1, was temperature resistant, whereas the parental Chinese hamster ovary mutant, ts025C1, contained a temperature-sensitive leucyl-tRNA synthetase mutation. An examination of the different amino acid transport systems in this hybrid cell line revealed a specific increase of system L activity with no significant changes in systems A and ASC. The Vmax for L-leucine uptake exhibited by the hybrid 158CnpT-1 was twice that in the CHO parental mutant, ts025C1. Cytogenetic analysis showed that the hybrid 158CnpT-1 contains four complete human chromosomes (numbers 4, 5, 10, and 21) and three interspecific chromosomal translocations in a total complement of 34 chromosomes. Biochemical and cytogenetic analysis of segregant clones obtained from hybrid 158CnpT-1 showed that the primary temperature resistance and high system L transport phenotypes can be segregated from this hybrid independently. The loss of the primary temperature resistance was associated with the loss of the human chromosome 5, as previously reported by other laboratories, whereas the loss of the high leucine transport phenotype, which is associated with a lesser degree of temperature resistance, was correlated with the loss of human chromosome 20.


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