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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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Citations
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Quantitation of yeast ceramides using high-performance liquid chromatography-evaporative light-scattering detection

TL;DR: The HPLC-ELSD method employed a cyanopropyl bonded column that effectively separated the main interfering substance ergosterol without any derivatization process; most other interfering substances were also removed.
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Growth-inhibitory activity of lymphoid cell plasma membranes. II. Partial characterization of the inhibitor.

TL;DR: The results demonstrate that the growth-inhibitory component(s) of the plasma membrane is a minor lipid or lipid-like molecule which retains activity in the absence of other membrane components, and suggest that this novel membrane component may have a role in control of lymphoid cell growth, possibly mediated by cell contacts.
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Effect of nerve growth factor and forskolin on glycosyltransferase activities and expression of a globo-series glycosphingolipid in PC12D pheochromocytoma cells.

TL;DR: The NGF/FRK‐dependent regulation of glycosyltransferase activities and the corresponding GSL expression in PC12D cells may be closely related to the cellular differentiation process in this cell line, which is considered to be more differentiated than the parent PC12 cells.
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Globoside with spin-labelled fatty acid: bilayer lateral distribution and immune recognition.

TL;DR: At least 80% of the globoside was definitely not confined to domains highly enriched in glycolipid, although there was evidence of binary-phase separation in the rigid DPPC/globoside matrix, and temperature profiles derived over the phase-transition region of DPPC using spin-labelled Globoside or an unattached amphiphilic spin label were consistent with these findings.
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Conformational alteration of bradykinin in presence of GM1 micelle

TL;DR: The interaction of bradykinin with ganglioside GM1 is reported by circular dichroism, steady-state fluorescence, and one-dimensional 1H NMR spectroscopy, indicating a shielding of phenylalanine residue of bradaykinin from aqueous environment.
References
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Journal ArticleDOI

Fibronectins—adhesive glycoproteins of cell surface and blood

TL;DR: A recently characterised class of adhesive, high molecular weight glycoproteins is present on the surfaces of cells, in connective tissue matrices, and in extracellular fluids.
Journal ArticleDOI

Monoclonal antibody defining a stage-specific mouse embryonic antigen (SSEA-1).

TL;DR: A monoclonal antibody derived by fusion of mouse myeloma cells with spleen cells from a mouse immunized with F9 teratocarcinoma cells is described, which defines an embryonic stage-specific antigen.
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