Schachner M
Department of Neurobiology, University of Heidelberg, Federal Republic of Germany.
Ciba Found Symp. 1989;145:156-69, discussion 169-72. doi: 10.1002/9780470513828.ch10.
The neural cell adhesion molecules L1 and N-CAM share a common carbohydrate epitope that is recognized by the monoclonal antibodies L2 and HNK-1. The L2/HNK-1 epitope is also present on the myelin-associated glycoprotein (MAG) and secreted J1 glycoprotein, both of which have been identified as cell adhesion molecules. Each of the four adhesion molecules is differentially expressed during development on distinct cell types. Expression of the L2/HNK-1 epitope is regulated independently of the protein backbone, is phylogenetically conserved, and plays a role in cell-cell and, particularly, cell-substrate interactions. Another set of glycoproteins shares a common carbohydrate epitope designated L3. This epitope is present on the novel adhesion molecule on glia (AMOG), L1 and MAG, but not on J1 and N-CAM. As in the L2/HNK-1 family, the number of glycoproteins expressing this epitope is not yet known. It is therefore possible that heterogeneities in carbohydrate structures are associated with different sets of adhesion molecules and may have functional implications.
神经细胞黏附分子L1和N-CAM具有一个共同的碳水化合物表位,该表位可被单克隆抗体L2和HNK-1识别。L2/HNK-1表位也存在于髓鞘相关糖蛋白(MAG)和分泌型J1糖蛋白上,这两种蛋白均已被鉴定为细胞黏附分子。这四种黏附分子中的每一种在发育过程中在不同的细胞类型上都有差异表达。L2/HNK-1表位的表达独立于蛋白质主干进行调控,在系统发育上是保守的,并且在细胞-细胞相互作用,特别是细胞-底物相互作用中发挥作用。另一组糖蛋白具有一个共同的碳水化合物表位,称为L3。该表位存在于神经胶质细胞上的新型黏附分子(AMOG)、L1和MAG上,但不存在于J1和N-CAM上。与L2/HNK-1家族一样,表达该表位的糖蛋白数量尚不清楚。因此,碳水化合物结构的异质性可能与不同的黏附分子组相关,并且可能具有功能意义。