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Before gastrulation, the embryo is a continuous epithelial sheet of cells; by the end of gastrulation, the embryo has begun differentiation to establish distinct cell lineages, set up the basic axes of the body (e.g. dorsal–ventral, anterior–posterior), and internalized one or more cell types including the prospective gut. [2]
The endoderm is one of the germ layers formed during animal embryogenesis. Cells migrating inward along the archenteron form the inner layer of the gastrula , which develops into the endoderm . Initially, the endoderm consists of flattened cells, which subsequently become columnar...
The cells continue to be rearranged until the shallow dip formed by invagination transforms into a deeper, narrower pouch formed by the gastrula's endoderm. This pouch narrows and lengthens to become the archenteron, a process driven by convergent extension. The open end of the archenteron is called the blastopore.
One of the early gastrulation movements in sea urchins is the invagination of a region of cells at the vegetal side of the embryo (vegetal plate) to become the archenteron, or future gut tube. There are multiple stages of archenteron invagination: a first stage where the initial folding in of tissue occurs, a second stage where the archenteron ...
The endoderm consists at first of flattened cells, which subsequently become columnar. It forms the epithelial lining of multiple systems. In plant biology, endoderm corresponds to the innermost part of the cortex in young shoots and young roots often consisting of a single cell layer. As the plant becomes older, more endoderm will lignify.
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Epiboly in zebrafish is the first coordinated cell movement, beginning at the dome stage late in the blastula period and continuing throughout gastrulation. [3] At this point the zebrafish embryo contains three portions: an epithelial monolayer known as the enveloping layer (EVL), a yolk syncytial layer (YSL) which is a membrane-enclosed group of nuclei that lie on top of the yolk cell, and ...
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