Itoh K, Sakurai Y, Asou H, Umeda M
Department of Molecular Biodynamics, The Tokyo Metropolitan Institute of Medical Science, Tokyo Metropolitan Organization for Medical Research, Bunkyo-ku, Tokyo, Japan.
J Neurosci Res. 2000 Jun 1;60(5):579-86. doi: 10.1002/(SICI)1097-4547(20000601)60:5<579::AID-JNR2>3.0.CO;2-#.
The expression of neural cell adhesion molecules and myelin-specific molecules is precisely regulated according to cell type and developmental age. We investigated whether different isoforms of these molecules change during development of oligodendrocytes. Immature oligodendrocytes cultured from embryonic day 18 rat cerebrum were distinguished into early stage and late stage by morphological and immunocytochemical criteria. mRNA levels of the neural cell adhesion molecule L1 in late-stage immature oligodendrocytes were approximately fivefold higher than in early-stage cells, but early-stage immature oligodendrocytes predominantly expressed an L1 spliced isoform lacking two region (exon 2 and 27). Late-stage cells expressed full-length L1 identical to the neuronal form. mRNA for the neural cell adhesion molecules NCAM and MAG did not show any difference in expression pattern. These results suggest that alternatively spliced isoforms of L1 might be regulated by temporal and spatial factors during oligodendrocyte development.
神经细胞黏附分子和髓鞘特异性分子的表达根据细胞类型和发育年龄受到精确调控。我们研究了这些分子的不同亚型在少突胶质细胞发育过程中是否发生变化。从胚胎第18天大鼠大脑培养的未成熟少突胶质细胞,通过形态学和免疫细胞化学标准分为早期和晚期。晚期未成熟少突胶质细胞中神经细胞黏附分子L1的mRNA水平比早期细胞高约五倍,但早期未成熟少突胶质细胞主要表达一种缺少两个区域(外显子2和27)的L1剪接亚型。晚期细胞表达与神经元形式相同的全长L1。神经细胞黏附分子NCAM和MAG的mRNA在表达模式上没有任何差异。这些结果表明,L1的可变剪接亚型可能在少突胶质细胞发育过程中受到时间和空间因素的调控。