Home LiteratureArticle Details
PMID: 2834372 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A novel ganglioside, de-N-acetyl-GM3 (II3NeuNH2LacCer), acting as a strong promoter for epidermal growth factor receptor kinase and as a stimulator for cell growth.

The Journal of biological chemistry ·Vol. 263 ·No. 13 ·1988-05-05 ·Pages 6296-301

Hanai N, Dohi T, Nores GA, Hakomori S

Abstract

A novel ganglioside, de-N-acetyl-GM3 (neuraminyllactosylceramide, II3NeuNH2LacCer), was found in the monosialoganglioside fraction of A431 cells and B16 melanoma cells by high-performance liquid chromatography, thin-layer chromatography, and immunoblotting with its specific monoclonal antibody DH5. This novel type of membrane ganglioside strongly enhanced the kinase activity associated with the epidermal growth factor (EGF) receptor, and it showed 32, 35, and 12% growth stimulation as compared with control cultures of A431, Swiss 3T3, and B16 melanoma cells, respectively. Exogenously added de-N-acetyl-GM3 did not alter the affinity of EGF binding to its receptor. These properties of de-N-acetyl-GM3 are in striking contrast to those of GM3 and its lyso derivative (lyso-GM3) which were previously shown to inhibit EGF receptor kinase activity and to inhibit growth in the same cells. These data indicate that de-N-acetylation at the sialic acid moiety of GM3 ganglioside is an important mechanism for modulation of EGF-dependent cell growth. The mechanism is antagonistic to that of GM3-dependent modulation of receptor function.

MeSH Terms
Animals Antibodies, Monoclonal Cell Division/drug effects Cell Line Chromatography, High Pressure Liquid Chromatography, Thin Layer ErbB Receptors G(M3) Ganglioside/analogs & derivatives,metabolism,pharmacology Gangliosides/pharmacology Immunosorbent Techniques Melanoma/enzymology Mice Promoter Regions, Genetic Protein-Tyrosine Kinases/metabolism
Chemicals
Antibodies, Monoclonal G(M3) Ganglioside Gangliosides de-N-acetylneuraminyllactosylceramide ErbB Receptors Protein-Tyrosine Kinases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hanai N
Department of Biochemical Oncology, Fred Hutchinson Cancer Center, Seattle, Washington.
Dohi T
Nores G A
Hakomori S
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1988-05-05
Pages
6296-301
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · CA 42505 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]