Gangliosides in cell recognition and membrane protein regulation

被引:253
作者
Lopez, Pablo H. H. [1 ]
Schnaar, Ronald L. [1 ]
机构
[1] Johns Hopkins Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
MYELIN-ASSOCIATED GLYCOPROTEIN; GROWTH-FACTOR RECEPTOR; NEURITE OUTGROWTH INHIBITION; TYROSINE KINASE-ACTIVITY; INSULIN SENSITIVITY; NERVE REGENERATION; HUMAN-LEUKOCYTES; ADIPOSE-TISSUE; LECTIN-BINDING; E-SELECTIN;
D O I
10.1016/j.sbi.2009.06.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Gangliosides, sialic acid-bearing glycosphingolipids, are expressed on all vertebrate cells, and are the major glycans on nerve cells. They are anchored to the plasma membrane through their ceramide lipids with their varied glycans extending into the extracellular space. Through sugar-specific interactions with glycan-binding proteins on apposing cells, gangliosides function as receptors in cell-cell recognition, regulating natural killer cell cytotoxicity via Siglec-7, myelinaxon interactions via Siglec-4 (myelin-associated glycoprotein), and inflammation via E-selectin. Gangliosides also interact laterally in their own membranes, regulating the responsiveness of signaling proteins including the insulin, epidermal growth factor, and vascular endothelial growth factor receptors. In these ways, gangliosides act as regulatory elements in the immune system, in the nervous system, in metabolic regulation, and in cancer progression.
引用
收藏
页码:549 / 557
页数:9
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