Timsit S, Martinez S, Allinquant B, Peyron F, Puelles L, Zalc B
Laboratoire de Neurobiologie Cellulaire, Moléculaire et Clinique, INSERM U-134, Hôpital de la Salpêtrière, Université Pierre et Marie Curie, Paris, France.
J Neurosci. 1995 Feb;15(2):1012-24. doi: 10.1523/JNEUROSCI.15-02-01012.1995.
Products of the PLP gene, proteolipid protein and its isoform DM-20, are the most abundant proteins in CNS myelin, and are markers of the oligodendrocyte, the myelin-forming cell in the CNS. The DM-20 transcript has previously been reported to be expressed in newborn oligodendrocyte progenitor cells and during embryonic development. We have therefore used a DM-20 cRNA probe to follow, by in situ hybridization, the oligodendrocyte lineage during embryonic development. DM-20-expressing cells were first detected at E9.5 in the ventricular germinal layer of the laterobasal plate of the diencephalon. At E14.5, DM-20+ cells had largely disappeared from the diencephalic ventricular germinal layer and had colonized the ventral mantle layer at the posterior part of the basal diencephalon. Between E17.5 and P1, the number of DM-20+ cells increased and progressively invaded the major white matter tracts. In the hindbrain, DM-20+ cells appeared at E12.5 in the caudal part of the rhombencephalon, and at E14.5 all along the ventral spinal cord. Between E14.5 and P1, DM-20+ cells progressively colonized, first ventrally then dorsally, all the spinal cord and more extensively the white matter tracts. At E14.5, a large gap separated, rostrally, the medullary columns from the mantle layer cells in the prosencephalon, suggesting that oligodendrocytes in the mid- and forebrain originate from a different pool of precursors than in the rhombencephalon and the spinal cord. Together, these observations suggest that expression of the DM-20 transcript is an early marker of commitment to the oligodendrocyte lineage, and that oligodendrocyte precursors originate in a ventrally restricted region.
PLP基因的产物,即蛋白脂蛋白及其异构体DM-20,是中枢神经系统髓鞘中含量最丰富的蛋白质,也是少突胶质细胞(中枢神经系统中形成髓鞘的细胞)的标志物。先前有报道称,DM-20转录本在新生少突胶质细胞祖细胞和胚胎发育过程中表达。因此,我们使用DM-20 cRNA探针,通过原位杂交追踪胚胎发育过程中的少突胶质细胞谱系。在胚胎第9.5天,首先在间脑外侧基板的脑室生发层中检测到表达DM-20的细胞。在胚胎第14.5天,DM-20+细胞已基本从间脑脑室生发层消失,并定位于间脑基部后部的腹侧套层。在胚胎第17.5天至出生后第1天之间,DM-20+细胞数量增加,并逐渐侵入主要的白质束。在后脑,DM-20+细胞在胚胎第12.5天出现在菱脑尾部,在胚胎第14.5天沿腹侧脊髓全长出现。在胚胎第14.5天至出生后第1天之间,DM-20+细胞逐渐定位于整个脊髓,首先是腹侧,然后是背侧,并且更广泛地定位于白质束。在胚胎第14.5天,在前脑,髓质柱与套层细胞在头侧有很大的间隙,这表明中脑和前脑的少突胶质细胞起源于与菱脑和脊髓不同的前体细胞池。总之,这些观察结果表明,DM-20转录本的表达是少突胶质细胞谱系定向分化的早期标志物,并且少突胶质细胞前体起源于腹侧受限区域。