Grunz Horst
Institut für Physiologische Chemie der Freien Universität Berlin, Deutschland.
Wilhelm Roux Arch Entwickl Mech Org. 1970 Jun;165(2):91-102. doi: 10.1007/BF00650138.
Isolated Amphibian gastrula ectoderm was pretreated in different ways and induced with a mesodermal/neural (Series I) or a mesodermal/endodermal (Series II) fraction ("sandwich" method).In the controls (K) the inducer was implanted directly into early gastrula ectoderm. The explants of series K were cultured in vitro for 20 (Series I) or 24 hours, respectively (Series II), and then combinated with the inducer. In series Ak the explants were treated with an inhibitor of protein synthesis (2μg/ml Actidion = Cycloheximid) for 20 or 24 hours and then cultured with inducer for 12 days.Ectoderm, cultured for 24 hours in vitro (Series K) lost its ability to respond to inducing factor. There is no loss of competence when ectoderm is treated with actidion for the same time and then treated with inducer.
将分离出的两栖类原肠胚外胚层进行不同方式的预处理,然后用中胚层/神经(系列I)或中胚层/内胚层(系列II)组分进行诱导(“三明治”法)。在对照组(K)中,将诱导物直接植入早期原肠胚外胚层。K系列的外植体分别在体外培养20小时(系列I)或24小时(系列II),然后与诱导物结合。在Ak系列中,外植体用蛋白质合成抑制剂(2μg/ml放线菌酮=环己酰亚胺)处理20或24小时,然后与诱导物一起培养12天。在体外培养24小时的外胚层(K系列)失去了对诱导因子作出反应的能力。当外胚层用放线菌酮处理相同时间然后再用诱导物处理时,其感受态并未丧失。