Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1984 Sep;81(18):5767-71.
doi: 10.1073/pnas.81.18.5767.

Localization of the gangliosides GD2 and GD3 in adhesion plaques and on the surface of human melanoma cells

Localization of the gangliosides GD2 and GD3 in adhesion plaques and on the surface of human melanoma cells

D A Cheresh et al. Proc Natl Acad Sci U S A. 1984 Sep.

Abstract

The predominant gangliosides produced by two cultured human melanoma cell lines are GD3 and/or GD2. These gangliosides were found to be cell associated and present in substratum-attached material after cell removal by EDTA. Monoclonal antibodies directed to GD2 and GD3 specified the cell-surface distribution of these gangliosides and localized them in focal adhesion plaques at the interface of cells and their substratum. These attachment sites did not represent indiscriminant membrane fragments remaining after removal of cells with EDTA, because neither melanoma-associated proteoglycan nor class I histocompatibility antigens were detected by their respective antibodies. Our data suggest that the disialogangliosides GD2 and GD3 may be involved in the interaction between human melanoma cells and solid substrata.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Biol Chem. 1971 Jan 25;246(2):430-5 - PubMed
    1. Biochemistry. 1972 May 23;11(11):2161-72 - PubMed
    1. Infect Immun. 1976 Jan;13(1):289-91 - PubMed
    1. Proc Natl Acad Sci U S A. 1979 Oct;76(10):4913-7 - PubMed
    1. Somatic Cell Genet. 1979 Nov;5(6):957-71 - PubMed

Publication types