Glycosphingolipid Modification: Structural Diversity, Functional and Mechanistic Integration of Diabetes.
10.4093/dmj.2011.35.4.309
- Author:
Tadashi YAMASHITA
1
Author Information
1. Graduate School of Advanced Life Science, Hokkaido University, Sapporo, Japan. ty11106@sci.hokudai.ac.jp
- Publication Type:Review
- Keywords:
Cell membrane;
Diabetes mellitus;
Glycosphingolipids;
Mouse model
- MeSH:
Animals;
Caveolae;
Cell Death;
Cell Membrane;
Cell Survival;
Cholesterol;
Diabetes Mellitus;
Gangliosides;
Glycosphingolipids;
Guillain-Barre Syndrome;
Intracellular Membranes;
Leg;
Mice;
Models, Animal;
Muscles;
Receptor, Epidermal Growth Factor;
Receptor, Insulin;
Second Messenger Systems;
Signal Transduction;
Sphingolipids
- From:Diabetes & Metabolism Journal
2011;35(4):309-316
- CountryRepublic of Korea
- Language:English
-
Abstract:
Glycosphingolipids (GSLs) are present in all mammalian cell plasma membranes and intracellular membrane structures. They are especially concentrated in plasma membrane lipid domains that are specialized for cell signaling. Plasma membranes have typical structures called rafts and caveola domain structures, with large amounts of sphingolipids, cholesterol, and sphingomyelin. GSLs are usually observed in many organs ubiquitously. However, GSLs, including over 400 derivatives, participate in diverse cellular functions. Several studies indicate that GSLs might have an effect on signal transduction related to insulin receptors and epidermal growth factor receptors. GSLs may modulate immune responses by transmitting signals from the exterior to the interior of the cell. Guillain-Barre syndrome is one of the autoimmune disorders characterized by symmetrical weakness in the muscles of the legs. The targets of the immune response are thought to be gangliosides, which are one group of GSLs. Other GSLs may serve as second messengers in several signaling pathways that are important to cell survival or programmed cell death. In the search for clear evidence that GSLs may play critical roles in various biological functions, many researchers have made genetically engineered mice. Before the era of gene manipulation, spontaneous animal models or chemical-induced disease models were used.
