Maden M, Ong D E, Summerbell D, Chytil F
National Institute for Medical Research, Ridgeway, Mill Hill, London, UK.
Development. 1989;107 Suppl:109-19. doi: 10.1242/dev.107.Supplement.109.
We summarize existing data and describe new information on the levels and distribution of cellular retinoic acid-binding protein (CRABP) and cellular retinol-binding protein (CRBP) in the regenerating axolotl limb, the developing chick limb bud and the nervous system of the chick embryo in the light of the known morphogenetic effects of retinoids on these systems. In the regenerating limb, levels of CRABP rise 3- to 4-fold during regeneration, peaking at the time when retinoic acid (RA) is most effective at causing pattern duplications. The levels of CRBP are low. The potency of various retinoids in causing pattern respecification correlates well with the ability of these compounds to bind to CRABP. In the chick limb bud, the levels of CRABP are high and the levels of CRBP are low. Again the binding of various retinoids to CRABP correlates well with their ability to cause pattern duplications. By immunocytochemistry, we show that CRABP is present at high levels in the progress zone of the limb bud and is distributed across the anteroposterior axis in a gradient with the high point at the anterior margin. In the chick embryo, CRABP levels are high and CRBP levels are low. By immunocytochemistry, CRABP is localised primarily to the developing nervous system, labelling cells and axons in the mantle layer of the neural tube. These become the neurons of the commissural system. Also sensory axons label intensely with CRABP whereas motor axons do not and in the mixed nerves at the brachial plexus sensory and motor components can be distinguished on this basis. In the neural tube, CRBP only stains the ventral floor plate. Since the ventral floor plate may be a source of chemoattractant for commissural axons, we suggest on the basis of these staining patterns that RA may fulfill this role and thus be involved morphogenetically in the developing nervous system.
我们总结现有数据,并根据视黄酸对这些系统已知的形态发生作用,描述有关再生蝾螈肢体、发育中的鸡胚肢芽和鸡胚神经系统中细胞视黄酸结合蛋白(CRABP)和细胞视黄醇结合蛋白(CRBP)水平及分布的新信息。在再生肢体中,CRABP水平在再生过程中升高3至4倍,在视黄酸(RA)最有效地导致模式重复时达到峰值。CRBP水平较低。各种视黄酸导致模式重新指定的效力与这些化合物结合CRABP的能力密切相关。在鸡胚肢芽中,CRABP水平较高而CRBP水平较低。同样,各种视黄酸与CRABP的结合与其导致模式重复的能力密切相关。通过免疫细胞化学,我们表明CRABP在肢芽的进展区高水平存在,并以前后轴梯度分布,在前缘处最高点。在鸡胚中,CRABP水平较高而CRBP水平较低。通过免疫细胞化学,CRABP主要定位于发育中的神经系统,标记神经管套层中的细胞和轴突。这些细胞将成为连合系统的神经元。此外,感觉轴突与CRABP强烈结合,而运动轴突则不结合,在臂丛神经的混合神经中,可以据此区分感觉和运动成分。在神经管中,CRBP仅染色腹侧底板。由于腹侧底板可能是连合轴突化学引诱剂的来源,基于这些染色模式我们推测RA可能发挥这一作用,从而在发育中的神经系统形态发生中发挥作用。