Early development of the gut: new light on an old hypothesis

This review deals with the early development of the gut. It draws largely on information provided from the study of avian embryos. Evidence that concerns the early determination of the regional fate of the endoderm and mesoderm of the gut is reviewed. Gut endoderm can undergo a limited degree of differentiation from a remarkably early age when cultured in the absence of mesoderm and there is evidence that points to the establishment of a pre-pattern in the early mesoderm before the genes responsible for patterning in gut are active. Initially, at least at cranial levels, those parts of the mesoderm and endoderm that are in contact are not those parts that will ultimately be in apposition; the consequence of this for any signalling between these layers is considered. In the light of the above information, the probable role of mesenchyme in gut development is re-examined.     

Cell-autonomous and inductive processes among three embryonic domains control dorsal-ventral and anterior-posterior development of Xenopus laevis

This review aims to propose an integrated model for dorsal-ventral and anterior-posterior development of Xenopus. Fertilized Xenopus eggs contain two determinants, a vegetal half endomesodermal determinant and a vegetal pole dorsal determinant (DD). The organizer forms in the specific intersection of the determinants, in a cell-autonomous manner. At late blastula, different combinations of the determinants form three embryonic domains, the competent animal domain, the organizer domain, and the entire vegetal half domain. These three domains cooperatively form dorsal-ventral and anterior-posterior axes: the organizer domain secrets dorsal inducing signals which induce or 'activate' the competent animal domain to form anterior-most neural tissues. The vegetal non-dorsal-marginal domain secrets posteriorizing signals, which 'transform' the anterior properties of the neural tissue to posterior properties.     

Patterning of mouse embryonic stem cell-derived pan-mesoderm by Activin A/Nodal and Bmp4 signaling requires Fibroblast Growth Factor activity

Abstract Embryonic stem (ES) cells have the potential to differentiate into all cell types of the adult body, and could allow regeneration of damaged tissues. The challenge is to alter differentiation toward functional cell types or tissues by directing ES cells to a specific fate. Efforts have been made to understand the molecular mechanisms that are required for the formation of the different germ layers and tissues from ES cells, and these mechanisms appear to be very similar in the mouse embryo. Differentiation toward mesoderm and mesoderm derivatives such as cardiac tissue or hemangioblasts has been demonstrated; however, the roles of Activin A/Nodal, bone morphogenetic protein (BMP), and fibroblast growth factor (FGF) signaling in the early patterning of ES cell-derived pan-mesoderm and anterior visceral endoderm (aVE) have not been reported yet. We therefore analyzed the roles of Activin A/Nodal, BMP, and FGF signaling in the patterning of ES cell-derived mesoderm as well as specification of the aVE by using a dual ES cell differentiation system combining a loss-of-function with a gain-of-function approach. We found that Activin A or Nodal directed the nascent mesoderm toward axial mesoderm and mesendoderm, while Bmp4 was inducing posterior and extraembryonic mesoderm at the expense of anterior primitive streak cells. FGF signaling appeared to have an important role in mesoderm differentiation by allowing an epithelial-to-mesenchymal transition of the newly formed mesoderm cells that would lead to their further patterning. Moreover, inhibition of FGF signaling resulted in increased expression of axial mesoderm markers. Additionally, we revealed that the formation of aVE cells from ES cells requires FGF-dependent Activin A/Nodal signaling and the attenuation of Bmp4 signaling.     

Nodal signaling establishes a competency window for stochastic cell fate switching

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Cranial cartilages: Players in the evolution of the cranium during evolution of the chordates in general and of the vertebrates in particular

The present contribution is chiefly a review, augmented by some new results on amphioxus and lamprey anatomy, that draws on paleontological and developmental data to suggest a scenario for cranial cartilage evolution in the phylum chordata. Consideration is given to the cartilage-related tissues of invertebrate chordates (amphioxus and some fossil groups like vetulicolians) as well as in the two major divisions of the subphylum Vertebrata (namely, agnathans, and gnathostomes). In the invertebrate chordates, which can be considered plausible proxy ancestors of the vertebrates, only a viscerocranium is present, whereas a neurocranium is absent. For this situation, we examine how cartilage-related tissues of this head region prefigure the cellular cartilage types in the vertebrates. We then focus on the vertebrate neurocranium, where cyclostomes evidently lack neural-crest derived trabecular cartilage (although this point needs to be established more firmly). In the more complex gnathostome, several neural-crest derived cartilage types are present: namely, the trabecular cartilages of the prechordal region and the parachordal cartilage the chordal region. In sum, we present an evolutionary framework for cranial cartilage evolution in chordates and suggest aspects of the subject that should profit from additional study.     

CLEAVAGE PATTERNS AND MESENTOBLAST FORMATION IN THE GASTROPODA: AN EVOLUTIONARY PERSPECTIVE

The larger gastropod taxa are characterized by distinctive cleavage patterns. The cell stage at which the mesentoblast is formed appears to be crucial. In none of the taxa is it formed earlier than the 24- and not later than the 63-cell stage. A heterochronic shift from late to early mesentoblast formation appears to coincide with successive steps in gastropod evolution. Comparison of the early cleavage patterns appears to be a powerful method for investigating the evolutionary relations between major gastropod taxa.     

Substratum attachment of embryonic mesoderm cells in culture

Summary The cell-substratum adhesive characteristics of cultured chick embryo primary mesoderm cells have been examined by inteference reflection microscopy and transmission electron microscoy under various conditions. Correlations were drawn between the type of adhesion and the degree of motility shown by the cells. During the rapid spreading and motility of cells cultured on fibronectin-containing substrate, focal contacts (10 to 15-nm gap) were rare and close contacts (about 30-nm gap) were pedominant. By contrast, when the cells were immobile, after 5 d in cultue, extensive focal contacts were present, together with stress fibers. The results indicate that tight cell-substratum contact is incompatible with rapid cell motility and that fibronectin acts by inducing the formation of close contacts rather than focal contacts. This work was supported by grants from the Medical Research Council of Canada and the Alberta Heritage Foundation for Medical Research.