Alterations in the Growth Rate and Glucose Metabolism of Chinese Hamster Cells in Vitro

1975 ◽  
pp. 265-265
Author(s):  
J. M. Ryan ◽  
D. M. Pace
Keyword(s):  
Growth Rate ◽  
Glucose Metabolism ◽  
Chinese Hamster ◽  
Chinese Hamster Cells

Alterations in the Growth Rate and Metabolism of Chinese Hamster Cells In Vitro

1975 ◽  
Vol 148 (2) ◽  
pp. 320-323
Author(s):  
J. M. Ryan ◽  
D. M. Pace
Keyword(s):  
Growth Rate ◽  
Chinese Hamster ◽  
Chinese Hamster Cells

Polyploidy Induced by X-Rays during the Cell Cycle of Chinese Hamster Cells in Vitro

1972 ◽  
Vol 52 (3) ◽  
pp. 509 ◽  
Author(s):  
C. K. Yu ◽  
W. K. Sinclair
Keyword(s):  
Cell Cycle ◽  
Chinese Hamster ◽  
X Rays ◽  
Chinese Hamster Cells

Killing of Chinese hamster cells in vitro by heating under hypoxic or aerobic conditions

1974 ◽  
Vol 10 (10) ◽  
pp. 691-693 ◽  
Author(s):  
Leo E. Gerweck ◽  
Edward L. Gillette ◽  
William C. Dewey
Keyword(s):  
Chinese Hamster ◽  
Aerobic Conditions ◽  
Chinese Hamster Cells

scholarly journals MAMMALIAN CELL GENETICS I. SELECTION AND CHARACTERIZATION OF MUTATIONS AUXOTROPHIC FOR L-GLUTAMINE OR RESISTANT TO 8-AZAGUANINE IN CHINESE HAMSTER CELLS IN VITRO

Genetics ◽  
1969 ◽  
Vol 62 (2) ◽  
pp. 359-377
Author(s):  
E H Y Chu ◽  
Patricia Brimer ◽  
K B Jacobson ◽  
E Virginia Merriam
Keyword(s):  
Mammalian Cell ◽  
Chinese Hamster ◽  
Chinese Hamster Cells

scholarly journals 8-AZAGUANINE RESISTANCE IN MAMMALIAN CELLS I. HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE

Genetics ◽  
1972 ◽  
Vol 72 (2) ◽  
pp. 239-252 ◽  
Author(s):  
F D Gillin ◽  
D J Roufa ◽  
A L Beaudet ◽  
C T Caskey
Keyword(s):  
Nucleic Acid ◽  
Mammalian Cells ◽  
Chinese Hamster ◽  
Acid Synthesis ◽  
Ethyl Methanesulfonate ◽  
Nucleic Acid Synthesis ◽  
Wild Type ◽  
Chinese Hamster Cells ◽  
Hypoxanthine Guanine Phosphoribosyltransferase

ABSTRACT Chinese hamster cells were treated with ethyl methanesulfonate or N-methyl-N'-nitro-N-nitrosoguanidine, and mutants resistant to 8-azaguanine were selected and characterized. Hypoxanthine-guanine phosphoribosyltransferase activity of sixteen mutants is extremely negative, making them suitable for reversion to HGPRTase+. Ten of the extremely negative mutants revert at a frequency higher than 10-7 suggesting their point mutational character. The remaining mutants have demonstrable HGPRTase activity and are not useful for reversion analysis. Five of these mutants have < 2% HGPRTase and are presumably also HGPRTase point mutants. The remaining 14 mutants utilize exogenous hypoxanthine for nucleic acid synthesis poorly, and possess 20-150% of wild-type HGPRTase activity in in vitro. Their mechanism of 8-azaguanine resistance is not yet defined.

Correction of Genetic Defects in Mammalian Cells by the Input of Small Amounts of Foreign Genetic Material

1973 ◽  
Vol 13 (3) ◽  
pp. 841-861
Author(s):  
YVONNE L. BOYD ◽  
H. HARRIS
Keyword(s):  
Thymidine Kinase ◽  
Mammalian Cells ◽  
Hybrid Cell ◽  
Genetic Material ◽  
Chinese Hamster ◽  
Heat Sensitivity ◽  
Chinese Hamster Cells ◽  
Inosinic Acid ◽  
Mouse Cells

Chinese hamster cells lacking inosinic acid pyrophosphorylase and mouse cells lacking thymidine kinase were fused with chick erythrocytes. The resultant heterokaryons were cultivated in a selective medium in which possession of these enzymes was essential for cell survival and growth. Clones of cells able to grow in this medium were isolated and studied. A detailed karyological analysis of these clones failed to reveal any chick chromosomes; nor could any chick-specific antigens be detected on the surface of the cells. Nonetheless, clones arising from the fusion of chick erythrocytes with Chinese hamster cells were shown to possess an inosinic acid pyrophosphorylase which had the electrophoretic characteristics of chick inosinic acid pyrophosphorylase. However, the clones arising from the fusion of the chick erythrocytes with the mouse cells had a thymidine kinase with the electrophoretic mobility and heat sensitivity of murine, not chick, thymidine kinase. Both types of hybrid cell have now been cultivated in vitro for 18 months without the loss of thymidine kinase or inosinic acid pyrophosphorylase activity.

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