The aim of this study performed in the embryonic chick wing is to test the ability of the tendons to form and develop in the absence of the muscle bellies. The experiments were performed on 2-day chick embryos by destroying a portion of the somitic mesoderm by local X-irradiation. The irradiated part included the wing somite level 15-20 and extended three somites (or presumptive somites) in fro...

The segmental heritage of all vertebrates is evident in the character of the vertebral column. And yet, the extent to which direct translation of pattern from the somitic mesoderm and de novo cell and tissue interactions pattern the vertebral column remains a fundamental, unresolved issue. The elements of vertebral column pattern under debate include both segmental pattern and anteroposterior r...

The contribution of active cell movement to somite formation (segmentation) and the later dispersal of the somite sclerotome was examined using cytochalasin D (CD). Stage 14-16 chick embryos were grown over liquid medium. After 8 hr in culture, control embryos had an average of six additional pairs of somites while CD (l-2 *g/ml dissolved in DMSO)-treated embryos had no new somites. DMSO alone ...

In the prospective lumbo-sacral region of the chick embryo, neurulation is achieved by cavitation of the medullary cord, a process called secondary neurulation. Neural crest cells (NCC) are generated in this region and they give rise to the same types of derivatives as in more rostral parts of the trunk where neurulation occurs by dorsal fusion of the neural plate borders (primary neurulation)....

We have shown previously by means of quail/chick transplantations that external and visceral organs, i.e., somatopleural and splanchnopleural derivatives, acquire their endothelial network through different mechanisms, namely immigration (termed angiogenesis) versus in situ emergence of precursors (or vasculogenesis). We have traced the distribution of QH1-positive cells in chick hosts after re...

The absence of ectoderm impairs somite formation in cultured presomitic mesoderm (PSM) explants, suggesting that an ectoderm-derived signal is essential for somitogenesis. Here we show in chick that the standard enzymatic treatments used for explant isolation destroy the fibronectin matrix surrounding the anterior PSM, which fails to form somites when cultured for 6 hours. By contrast, explants...

The body and tissues of the developing embryo are repeatedly divided into sub-regions specified by characteristic gene expression and morphology. The process that gives rise to these sub-regions, according to a defined pattern, is called “pattern formation” or “patterning.” The most popular model to explain the patterning process is the “morphogen gradient and threshold” theory. Many genetic re...

In the vertebrate embryo, segmentation is built on repetitive structures, named somites, which are formed progressively from the most rostral part of presomitic mesoderm, every 90 minutes in the avian embryo. The discovery of the cyclic expression of several genes, occurring every 90 minutes in each presomitic cell, has shown that there is a molecular clock linked to somitogenesis. We demonstra...

CS (chondroitin sulfate) has been implicated in a variety of biological processes during development. Its biological functions are closely associated with characteristic sulfated structures. Here, we report the characterization of a zebrafish counterpart of C4ST-1 (chondroitin 4-O-sulfotransferase-1) and its functional importance in embryogenesis. Recombinant C4ST-1 showed a substrate preferenc...

In zebrafish embryos, each myotome is typically innervated by three primary motoneurons (PMNs): the caudal primary (CaP), middle primary (MiP) and rostral primary (RoP). PMN axons first exit the spinal cord through a single exit point located at the midpoint of the overlying somite, which is formed beneath the CaP cell body and is pioneered by the CaP axon. However, the placement of CaP cell bo...