Alteration of glycolipids in ras-transfected NIH 3T3 cells

Journal Article · Tue Sep 01 00:00:00 EDT 1987 · Proc. Natl. Acad. Sci. U.S.A.; (United States)

DOI:https://doi.org/10.1073/pnas.84.17.6065· OSTI ID:5294148

Matyas, G R; Aaronson, S A; Brady, R O; Fishman, P H

Glycosphingolipid alterations upon viral transformation are well documented. Transformation of mouse 3T3 cells with murine sarcoma viruses results in marked decreases in the levels of gangliosides GM1 and GD1a and an increase in gangliotriaosylceramide. The transforming oncogenes of these viruses have been identified as members of the ras gene family. The authors analyzed NIH 3T3 cells transfected with human H-, K- and N-ras oncogenes for their glycolipid composition and expression of cell surface gangliosides. Using conventional thin-layer chromatographic analysis, they found that the level of GM3 was increased and that of GD1a was slightly decreased or unchanged, and GM1 was present but not in quantifiable levels. Cell surface levels of GM1 were determined by /sup 125/I-labeled cholera toxin binding to intact cells. GD1a was determined by cholera toxin binding to cells treated with sialidase prior to toxin binding. All ras-transfected cells had decreased levels of surface GM1 and GD1 as compared to logarithmically growing normal NIH 3T3 cells. Levels of GM1 and, to a lesser extent, GD1a increased as the latter cells became confluent. Using a monoclonal antibody assay, they found that gangliotriaosylceramide was present in all ras-transfected cells studied but not in logarithmically growing untransfected cells. These results indicated that ras oncogenes derived form human tumors are capable of inducing alterations in glycolipid composition.

• Research Organization: National Institutes of Health, Bethesda, MD (USA)
• OSTI ID: 5294148
• Journal Information: Proc. Natl. Acad. Sci. U.S.A.; (United States), Vol. 84:17
• Country of Publication: United States
• Language: English

Related Subjects

62 RADIOLOGY AND NUCLEAR MEDICINE
59 BASIC BIOLOGICAL SCIENCES
GLYCOLIPIDS
RADIORECEPTOR ASSAY
ONCOGENES
GENE REGULATION
FIBROBLASTS
IODINE 125
MICE
MONOCLONAL ANTIBODIES
ONCOGENIC VIRUSES
SARCOMAS
THIN-LAYER CHROMATOGRAPHY
TOXINS
ANIMAL CELLS
ANIMALS
ANTIBODIES
ANTIGENS
BETA DECAY RADIOISOTOPES
CARBOHYDRATES
CHROMATOGRAPHY
CONNECTIVE TISSUE CELLS
DAYS LIVING RADIOISOTOPES
DISEASES
ELECTRON CAPTURE RADIOISOTOPES
GENES
INTERMEDIATE MASS NUCLEI
IODINE ISOTOPES
ISOTOPE APPLICATIONS
ISOTOPES
LIPIDS
MAMMALS
MATERIALS
MICROORGANISMS
NEOPLASMS
NUCLEI
ODD-EVEN NUCLEI
ORGANIC COMPOUNDS
PARASITES
RADIOISOTOPES
RODENTS
SACCHARIDES
SEPARATION PROCESSES
SOMATIC CELLS
TOXIC MATERIALS
TRACER TECHNIQUES
VERTEBRATES
VIRUSES
550601* - Medicine- Unsealed Radionuclides in Diagnostics
550401 - Genetics- Tracer Techniques