Kosher R A, Savage M P, Chan S C
J Embryol Exp Morphol. 1979 Apr;50:75-97.
It has been suggested that one of the major functions of the apical ectodermal ridge (AER) of the embryonic chick limb-bud is to maintain mesenchymal cells directly subjacent to it (i.e. cells extending 0.4-- 0.5 mm from the AER) in a labile, undifferentiated condition. We have attempted to directly test this hypothesis by subjecting the undiffertiated subridge mesoderm of stage-25 embryonic chick wing-buds to organ culture in the presence and absence of the AER and the ectoderm that normally surrounds the mesoderm dorsally and ventrally. During the period of culture, control explants comprised of the subridge mesoderm capped by the AER and surrounded by the dorsal/ventral ectoderm undergo progressive morphogenesis characterized by polarized proximal to distal outgrowth and changes in the contour of the developing explant, and ultimately form a structure grossly resembling a normal distal wing-bud tip. In contrast, explants from which the AER and dorsal/ventral ectoderm have been removed (minus ectoderm explants) or from which just the AER has been removed (minus AER explants) form compact, rounded masses exhibiting no signs of morphogenesis. During the polarized proximal to distal outgrowth control explants undergo during the first 3 days of culture, as cells of the explant become located greater than 0.4--0.5 mm from the AER, they concomitantly undergo a sequence of changes indicative of their differentiation into cartilage. However, those cells which remain 0.4--0.5 mm from the AER during this period retain the characteristics of non-specialized mesenchymal cells. In marked contrast to control explants, virtually all of the cells of minus ectoderm explants initiate chondrogenic differentiation during the first day of culture. Cells comprising the central core of minus AER explants also initiate chondrogenic differentiation during the first day of culture, but in contrast to minus ecotderm explants, non-chondrogenic tissue types form along the periphery of the explants subjacent to the dorsal/ventral ectoderm. These results indicate that the AER maintains cells directly subjacent to it in a labile, undifferentiated condition, and that when mesenchymal cells are freed from the AER's influence either artificially or as a result of normal polarized outgrowth, they are freed to commence cytodifferentiation. The results further suggest that the dorsal/ventral ectoderm may have an influence on the differentiation of the mesenchymal cells directly subjacent to it, once the cells have been removed from the influence of the AER.
有人提出,胚胎期鸡胚肢芽的顶端外胚层嵴(AER)的主要功能之一,是使紧邻其下方的间充质细胞(即从AER延伸0.4 - 0.5毫米的细胞)维持在不稳定的未分化状态。我们试图通过将第25期胚胎鸡胚翼芽的未分化嵴下中胚层,在有和没有AER以及正常情况下背腹面包围中胚层的外胚层存在的条件下进行器官培养,来直接验证这一假说。在培养期间,由AER覆盖并被背/腹外胚层包围的嵴下中胚层组成的对照外植体经历渐进的形态发生,其特征为从近端到远端的极化生长以及发育中外植体轮廓的变化,并最终形成一个外观上大致类似于正常远端翼芽尖端的结构。相比之下,去除了AER和背/腹外胚层的外植体(无外胚层外植体)或仅去除了AER的外植体(无AER外植体)形成紧密的圆形团块,没有形态发生的迹象。在培养的头3天,对照外植体经历从近端到远端的极化生长过程中,随着外植体细胞距离AER超过0.4 - 0.5毫米,它们会同时经历一系列表明其分化为软骨的变化。然而,在此期间距离AER保持在0.4 - 0.5毫米的那些细胞,保留了未特化间充质细胞的特征。与对照外植体形成显著对比的是,几乎所有无外胚层外植体的细胞在培养的第一天就开始软骨形成分化。组成无AER外植体中央核心的细胞在培养的第一天也开始软骨形成分化,但与无外胚层外植体不同的是,在紧邻背/腹外胚层的外植体周边形成了非软骨形成的组织类型。这些结果表明,AER使紧邻其下方的细胞维持在不稳定的未分化状态,并且当间充质细胞通过人为方式或由于正常的极化生长而摆脱AER的影响时,它们就会开始细胞分化。结果还进一步表明,一旦细胞摆脱了AER的影响,背/腹外胚层可能会对紧邻其下方的间充质细胞的分化产生影响。