Cell intercalation during notochord development in Xenopus laevis
- 1 August 1989
- journal article
- research article
- Published by Wiley in Journal of Experimental Zoology
- Vol. 251 (2), 134-154
- https://doi.org/10.1002/jez.1402510204
Abstract
Morphometric data from scanning electron micrographs (SEM) of cells in intact embryos and high‐resolution time‐lapse recordings of cell behavior in cultured explants were used to analyze the cellular events underlying the morphogenesis of the notochord during gastrulation and neurulation of Xenopus laevis. The notochord becomes longer, narrower, and thicker as it changes its shape and arrangement and as more cells are added at the posterior end. The events of notochord development fall into three phases. In the first phase, occurring in the late gastrula, the cells of the notochord become distinct from those of the somitic mesoderm on either side. Boundaries form between the two tissues, as motile activity at the boundary is replaced by stabilizing lamel‐liform protrusions in the plane of the boundary. In the second phase, spanning the late gastrula and early neurula, cell intercalation causes the notochord to narrow, thicken, and lengthen. Its cells elongate and align mediolaterally as they rearrange. Both protrusive activity and its effectiveness are biased: the anterioposterior (AP) margins of the cells advance and retract but produce much less translocation than the more active left and right ends. The cell surfaces composing the lateral boundaries of the notochord remain inactive. In the last phase, lasting from the mid‐ to late neurula stage, the increasingly flattened cells spread at all their interior margins, transforming the notochord into a cylindrical structure resembling a stack of pizza slices. The notochord is also lengthened by the addition of cells to its posterior end from the circumblastoporal ring of mesoderm. Our results show that directional cell movements underlie cell intercalation and raise specific questions about the cell polarity, contact behavior, and mechanics underlying these movements. They also demonstrate that the notochord is built by several distinct but carefully coordinated processes, each working within a well‐defined geometric and mechanical environment.This publication has 25 references indexed in Scilit:
- Mediolateral cell intercalation in the dorsal, axial mesoderm of Xenopus laevisDevelopmental Biology, 1989
- Motility of cultured fish epidermal cells in the presence and absence of direct current electric fields.The Journal of cell biology, 1986
- Neural crest cell behavior in white and dark larvae of Ambystoma mexicanum: Time‐lapse cinemicrographic analysis of pigment cell movement in vivo and in cultureJournal of Experimental Zoology, 1983
- The Structure of the Anuran Amphibian Notochord and a Re-evaluation of its Presumed Role in Early EmbryogenesisDifferentiation, 1982
- Response of basal epithelial cell surface and Cytoskeleton to solubilized extracellular matrix molecules.The Journal of cell biology, 1981
- Analysis of the formation of parallel arrays by BHK cells in vitroExperimental Cell Research, 1978
- Locomotory behavior, contact inhibition, and pattern formation of 3T3 and polyoma virus-transformed 3T3 cells in cultureThe Journal of cell biology, 1977
- Vital dye mapping of the gastrula and neurula of Xenopus laevisDevelopmental Biology, 1975
- Cellular Interactions in Mass Cultures of Human Diploid FibroblastsNature, 1972
- The ultrastructure of the developing urodele notochordProceedings of the Royal Society of London. B. Biological Sciences, 1962