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Journal ArticleDOI

Glycosphingolipids in Cellular Interaction, Differentiation, and Oncogenesis

Sen-itiroh Hakomori
- 01 Jan 1981 - 
- Vol. 50, Iss: 1, pp 733-764
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TLDR
The majority of neutral glycolipids present in plasma membranes are cryptic, and further extensive studies of the organization of glycolIPid in other eukaryotic cell membranes are necessary.
Abstract
The idea that glycosphingolipids (or, briefly, glycolipids) are ubiquitous components of plasma membrane and display cell type-specific patterns perhaps stemmed from the classical studies on glycolipids of erythrocyte membranes.(1,2) Subsequently, plasma membranes of various animal cells were successfully isolated and analyzed; all were characterized by their much higher content of glycolipid than was found in intracellular membranes.(3–8) It is generally assumed that glycolipids are present at the outer leaflet of the plasma membrane bilayer, although this assumption is based only on experiments with surface-labeling by galactose oxidase-NaB[3H]4 of intact and lysed erythrocyte membranes and inside-out vesicles.(9,10) Obviously, further extensive studies of the organization of glycolipid in other eukaryotic cell membranes are necessary. Interestingly, the majority of neutral glycolipids present in plasma membranes are cryptic (see Section 4.2.1).

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Two distinct classes of carbohydrate-recognition domains in animal lectins.

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New Methods for the Synthesis of Glycosides and Oligosaccharides—Are There Alternatives to the Koenigs‐Knorr Method? [New Synthetic Methods (56)]

TL;DR: Emphasis is placed on glycoside and saccharide formation by 1-O-alkylation, on the trichloroacetimidate method, and on activation through the formation of glycosylsulfonium salts and Glycosyl fluorides.
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Inhibition of sphingolipid biosynthesis by fumonisins. Implications for diseases associated with Fusarium moniliforme.

TL;DR: Findings suggest that disruption of the de novo pathway of sphingolipid biosynthesis may be a critical event in the diseases that have been associated with consumption of fumonisins.
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A monoclonal antibody-defined antigen associated with gastrointestinal cancer is a ganglioside containing sialylated lacto-N-fucopentaose II.

TL;DR: Two monoclonal antibodies produced by hybridomas obtained from a mouse immunized with a colorectal carcinoma cell line bind specifically to human gastrointestinal cancer cells.
References
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Journal Article

Cancer antigens: how specific should they be?

TL;DR: The title assigned to me ("Cancer-specific Antigens") is modified in order to focus attention on several aspects of this subject of which you may all be implicitly aware, but which are sometimes difficult ~ to = keep explicitly in mind.
Journal ArticleDOI

Biosynthesis of globoside and Forssman-related glycosphingolipid in mouse adrenal Y-1 tumor cells*

TL;DR: The ratio between long chain oligoglycosylceramides and short chain glycosphingolipids was higher in the case of Y-l-K cells treated with dibutyryl cAMP than in concanavalin A, colchicine treated, or untreated control cells in culture.
Journal ArticleDOI

Immunochemical characterization of surface antigens of TerC, a teratocarcinoma-derived cell line.

TL;DR: Rabbit and mouse antisera prepared against teratocarcinoma cells precipitate both glycoproteins and glycolipids from detergent extracts of radiolabeled cells to form coated cells that absorb at least 80% of the activity of antisersa against ter atocarc inoma targets.
Journal ArticleDOI

Ganglioside patterns and phenotypic characteristics in a normal variant and a transformed back variant of a simian virus 40-induced hamster tumor cell line

TL;DR: Ganglioside patterns of a cloned Simian virus 40- (SV40) induced hamster tumor cell, its normal variant, and its back variant, which are Cl2TSV5-R cells grown in the absence of actinomycin D for more than 60 passages and which exhibit greater phenotypic similarity to Cl2 TSV 5-S cells, have been analyzed.
Book ChapterDOI

Lymphokines: Physiologic Control and Pharmacological Modulation of Their Production and Action

TL;DR: The methods used for the detection and quantitation of LKs are biological, and are based on the ability of a culture supernatant to inhibit the migration of macrophages or polymorphonuclear leukocytes in vitro, to act as a chemotactic attractant for a variety of cells, and to be cytotoxic for certain target cells.
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