IN-VITRO CONTROL OF THE EMBRYONIC FORM OF XENOPUS-LAEVIS BY ACTIVIN-A - TIME-DEPENDENT AND DOSE-DEPENDENT INDUCING PROPERTIES OF ACTIVIN-TREATED ECTODERM

The inducing properties of activin-treated ectoderm of Xenopus laevis were examined by the preculture and sandwich culture methods. Presumptive ectodermal sheets of the late blastula were treated with 10-100 ng/ml of activin A and precultured for 0-7 hr in Steinberg's solution. They were then sandwiched between two sheets of ectoderm from other late blastulae. Ectoderm precultured for a short term induced trunk-tail structures, whereas that precultured for a long term induced head structures in addition to trunk-tail structures. These time-dependent changes in inducing properties occurred more rapidly when the concentration of activin A was higher. These results suggest that the activin-treated ectoderm functioned as a ''head organizer'' or ''trunk-tail organizer'' depending upon the concentration of activin A and the duration of preculture. To trace the cell lineage of the sandwich explants, activin-treated ectoderm labeled with fluorescein-dextran-amine (FDA) was used in this study. The explants sandwiching the long term-precultured ectoderm formed head structures equipped with non-labeled neural tissues (brain and eye) as well as FDA-labeled mesodermal tissues. These results suggest that the activin-treated ectoderm mainly differentiates into mesodermal tissues and induces neural tissues as the organizer does in normal development.