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Cell surface changes accompanying viral transformation: N-acetylneuraminic acid ectotransferase system activity.
- Source :
-
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.) [Proc Soc Exp Biol Med] 1975 Jun; Vol. 149 (2), pp. 486-90. - Publication Year :
- 1975
-
Abstract
- The activity of the sialyl ectotransferase system of normal chick embryo fibroblasts (CEF) and chick embryo fibroblasts transformed with the Schmidt-Ruppin strain of Rous sarcoma virus (SR-RSV) have been compared. Neuraminidase treatment of the intact cells increased the sialyl ectotransferase system activity of control and transformed cells two to three times. The ectotransferase system activity increased as the pH was decreased from 7.8 to 6.0. The temperature optimum for both systems was 40 degrees C. Approximately 60% of the 14C-sialic acid incorporated at pH 6.5 or above could be removed with neuraminidase. The activity of the transformed cell system with or without neuraminidase treatment was more stimulated by addition of Mn2+ ions, particularly above pH 7.0. This difference in ion sensitivity indicates that a different cell surface phenomenon is being studied after transformation.
- Subjects :
- Animals
Calcium pharmacology
Carbon Radioisotopes
Chick Embryo
Cytopathogenic Effect, Viral
Fibroblasts enzymology
Hydrogen-Ion Concentration
Manganese pharmacology
Neuraminidase metabolism
Proteins analysis
Sialic Acids metabolism
Temperature
Time Factors
Acetyltransferases metabolism
Avian Sarcoma Viruses pathogenicity
Cell Membrane enzymology
Sialyltransferases metabolism
Transferases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0037-9727
- Volume :
- 149
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)
- Publication Type :
- Academic Journal
- Accession number :
- 239405
- Full Text :
- https://doi.org/10.3181/00379727-149-38833