Edelman G M, Gallin W J, Delouvée A, Cunningham B A, Thiery J P
Proc Natl Acad Sci U S A. 1983 Jul;80(14):4384-8. doi: 10.1073/pnas.80.14.4384.
N-CAM, the neural cell-adhesion molecule, has previously been found to be expressed during several epochs of development and function, first as an early marker in embryo-genesis, later during organogenesis, and finally in adult life. L-CAM, the liver cell-adhesion molecule, has now been localized in embryonic and adult tissues of the chicken by fluorescent antibody techniques. In the early embryonic epoch, L-CAM and N-CAM appeared in epiblastic and hypoblastic tissues. L-CAM was distributed thereafter across all three germ layers. By the onset of neurulation, however, L-CAM disappeared in the region of the neural plate and N-CAM increased in amount in that region. L-CAM appeared strongly on all budding endodermal structures (liver, pancreas, lung, thyroid, parathyroid, thymus, and bursa of Fabricius) whereas N-CAM appeared most strongly in the neural plate, neural tube, and in cardiac mesoderm but was not found in endodermal derivatives. In placodes, both L-CAM and N-CAM were present until the formation of definitive neural structures, at which time L-CAM disappeared. In kidney precursors, the two CAMs followed a complex reciprocal pattern of appearance and disappearance. For the most part, however, the distributions of the two molecules did not overlap during organogenesis. Like N-CAM, L-CAM persisted in a distinctive pattern of expression in adult tissues. During embryonic development, the two different CAMs were distributed on tissues derived from more than two-thirds of the early embryonic surface. Interpretation of maps summarizing CAM distributions over a defined developmental epoch suggested a key role for both L-CAM and N-CAM in embryonic induction. Consistent with this interpretation and with the fact that the continuity of germ layers is lost when organ rudiments are formed, neither of the CAMs was limited in distribution to a single germ layer. The regions of the early epochal maps that lacked both L-CAM and N-CAM comprised some portions of the splanchnopleure and somatopleure. Certain adult tissues that derive from this lateral plate mesoderm such as smooth muscle also lacked L-CAM and N-CAM. Such observations suggest that at least one more CAM may exist in these and similarly derived tissues.
神经细胞黏附分子N-CAM先前已被发现会在发育和功能的多个时期表达,最初是胚胎发育早期的一个标志物,随后在器官发生期表达,最终在成年期表达。肝细胞黏附分子L-CAM现已通过荧光抗体技术定位在鸡的胚胎和成年组织中。在胚胎发育早期,L-CAM和N-CAM出现在外胚层和内胚层组织中。此后,L-CAM分布于所有三个胚层。然而,到神经胚形成开始时,L-CAM在神经板区域消失,而该区域的N-CAM数量增加。L-CAM在所有正在出芽的内胚层结构(肝脏、胰腺、肺、甲状腺、甲状旁腺、胸腺和法氏囊)上强烈表达,而N-CAM在神经板、神经管和心脏中胚层中表达最强,但在内胚层衍生物中未发现。在基板中,L-CAM和N-CAM一直存在,直到确定的神经结构形成,此时L-CAM消失。在肾前体中,这两种细胞黏附分子呈现出复杂的相互交替的出现和消失模式。然而,在器官发生过程中,这两种分子的分布在很大程度上并不重叠。与N-CAM一样,L-CAM在成年组织中以独特的表达模式持续存在。在胚胎发育过程中,这两种不同的细胞黏附分子分布在超过三分之二的早期胚胎表面衍生的组织上。对总结特定发育时期细胞黏附分子分布的图谱的解读表明,L-CAM和N-CAM在胚胎诱导中都起着关键作用。与这一解读一致,也与器官原基形成时胚层连续性丧失这一事实一致,这两种细胞黏附分子的分布都不限于单一胚层。早期图谱中既缺乏L-CAM也缺乏N-CAM的区域包括脏壁中胚层和体壁中胚层的一些部分。某些源自该侧板中胚层的成年组织,如平滑肌,也缺乏L-CAM和N-CAM。这些观察结果表明,在这些组织以及类似来源的组织中可能至少还存在一种细胞黏附分子。