Differentiation capacities of the prospective tail somite region of the neural plate in the embryos of Ambystoma mexicanum

Development ◽  
1969 ◽  
Vol 22 (1) ◽  
pp. 1-14
Author(s):  
I. A. Niazi

The hind part of the neural plate in amphibian embryos has a mesodermal significance although it occupies an ectodermal position till late neurula stage. In anurans it gives rise to the posterior tail somites (Smithberg, 1954) and in urodeles the somites of the posterior trunk region and of the entire tail together with several other mesodermal structures (Bijtel, 1931; Nakamura, 1938; Aufsess, 1941; Spofford, 1945; Chuang, 1947; Ford, 1949). Presence of mesoderm in the neural plate is an interesting developmental problem. During normal gastrulation this region is at first underlaid by the future anterior part of the archenteric roof which exerts a neuralizing inductive influence. It is only later that the posterior part of the notochord with its mesodermalizing influence comes to lie under it. According to Eyal-Giladi (1954), who worked on gastrula stages of the Axolotl, even a short and transient contact of the invaginating archenteric roof with the overlying ectoderm produces archencephalic induction in the latter.

Author(s):  
Len Wen-Yung ◽  
Mei-Jung Lin

Four cone-shaped rectal papillae locate at the anterior part of the rectum in Dacus dorsalis fly. The circular base of the papilla protrudes into the haemolymph (Fig. 1,2) and the rest cone-shaped tip (Fig. 2) inserts in the rectal lumen. The base is surrounded with the cuticle (Fig. 5). The internal structure of the rectal papilla (Fig. 3) comprises of the cortex with the columnar epithelial cells and a rod-shaped medulla. Between them, there is the infundibular space and many trabeculae connect each other. Several tracheae insert into the papilla through the top of the medulla, then run into the cortical epithelium and locate in the intercellular space. The intercellular sinuses distribute in the posterior part of the rectal papilla.The cortex of the base divides into about thirty segments. Between segments there is a radial cell (Fig. 4). Under the cuticle, the apical cell membrane of the cortical epithelium is folded into a regular border of leaflets (Fig. 5).


2017 ◽  
Vol 4 (12) ◽  
pp. 171288 ◽  
Author(s):  
Alexander L. Vereshchaka ◽  
Anastasia A. Lunina ◽  
Jørgen Olesen

Species within Gennadas differ from each other largely only in male (petasma) and female (thelycum) copulatory characters, which were restudied in scanning electron microscopy and used as a basis for phylogenetic analyses. Twenty-six petasma characters and 49 thelycum characters were identified. All 16 recognized species of Gennadas and Aristaeomorpha foliacea (outgroup) were included as terminals. Four robust monophyletic clades were retrieved, described and diagnosed as new species groups. The thelycum characters had greater impact on tree topology and supported deeper nodes than did the petasma characters. We hypothesize that features of the thelycum evolved first followed by aspects of the petasma. Relatively more conservative characters include parts of the sternites of the thelycum and of the petasma, while the scuti and protuberances on the thelycum and the shape and subdivisions of the petasma lobes are evolutionarily plastic. We identified two groups of copulatory characters, which are likely coupled functionally and interlinked evolutionarily: (i) the external part of the petasma and the posterior part of the thelycum and (ii) the internal part of the petasma and anterior part of the thelycum. We reconstruct possible mating position during copulation for each of the new species groups presented here. We also present an updated key to genera of Benthesicymidae and key to species of Gennadas .


Development ◽  
1964 ◽  
Vol 12 (2) ◽  
pp. 317-331
Author(s):  
D. O. E. Gebhardt ◽  
P. D. Nieuwkoop

The influence of lithium on the amphibian egg has been the subject of a number of investigations. From the work of Lehmann (1937), Töndury (1938), and Pasteels (1945) it is known that exposure of amphibian embryos to lithium results in a progressive cranio-caudal reduction of the central nervous system and a simultaneous conversion of the presumptive notochord into somites. Whereas these experiments were made with whole embryos, attempts have been made in recent years to localize the lithium effect by transplanting or explanting specific parts of the embryo. Gallera (1949), for instance, concluded from his experiments with transplants containing lithium treated presumptive chorda mesoderm, that lithium had reduced the ‘morphogenetic potential’ of this inductor. Lombard (1952), on the other hand, claimed that the susceptibility of amphibian eggs towards lithium was the result of the ion's direct influence on the ectoderm rather than on the presumptive archenteron roof.


Development ◽  
1994 ◽  
Vol 120 (5) ◽  
pp. 1137-1150 ◽  
Author(s):  
R. Reuter ◽  
M. Leptin

Two zygotic genes, snail (sna) and twist (twi), are required for mesoderm development, which begins with the formation of the ventral furrow. Both twi and sna are expressed ventrally in the blastoderm, encode transcription factors and promote the invagination of the ventral furrow by activating or repressing appropriate target genes. However, sna and twi alone do not define the position of the ventral furrow, since they are also expressed in ventral cells that do not invaginate. We show that huckebein (hkb) sets the anterior and the posterior borders of the ventral furrow, but acts by different modes of regulation. In the posterior part of the blastoderm, hkb represses the expression of sna in the endodermal primordium (which we suggest to be adjacent to the mesodermal primordium). In the anterior part, hkb antagonizes the activation of target genes by twi and sna. Here, bicoid permits the co-expression of hkb, sna and twi, which are all required for the development of the anterior digestive tract. We suggest that mesodermal fate is determined where sna and twi but not hkb are expressed. Anteriorly hkb together with sna determines endodermal fate, and hkb together with sna and twi are required for foregut development.


Development ◽  
1999 ◽  
Vol 126 (8) ◽  
pp. 1611-1620 ◽  
Author(s):  
C.W. Beck ◽  
J.M. Slack

We have developed a new assay to identify factors promoting formation and outgrowth of the tail bud. A piece of animal cap filled with the test mRNAs is grafted into the posterior region of the neural plate of a host embryo. With this assay we show that expression of a constitutively active Notch (Notch ICD) in the posterior neural plate is sufficient to produce an ectopic tail consisting of neural tube and fin. The ectopic tails express the evenskipped homologue Xhox3, a marker for the distal tail tip. Xhox3 will also induce formation of an ectopic tail in our assay. We show that an antimorphic version of Xhox3, Xhox3VP16, will prevent tail formation by Notch ICD, showing that Xhox3 is downstream of Notch signalling. An inducible version of this reagent, Xhox3VP16GR, specifically blocks tail formation when induced in tailbud stage embryos, comfirming the importance of Xhox3 for tail bud outgrowth in normal development. Grafts containing Notch ICD will only form tails if placed in the posterior part of the neural plate. However, if Xwnt3a is also present in the grafts they can form tails at any anteroposterior level. Since Xwnt3a expression is localised appropriately in the posterior at the time of tail bud formation it is likely to be responsible for restricting tail forming competence to the posterior neural plate in our assay. Combined expression of Xwnt3a and active Notch in animal cap explants is sufficient to induce Xhox3, provoke elongation and form neural tubes. Conservation of gene expression in the tail bud of other vertebrates suggests that this pathway may describe a general mechanism controlling tail outgrowth and secondary neurulation.


ZooKeys ◽  
2019 ◽  
Vol 838 ◽  
pp. 71-84
Author(s):  
Céline Labrune ◽  
Nicolas Lavesque ◽  
Paulo Bonifácio ◽  
Pat Hutchings

A new species of Terebellidae, Pistacolinisp. n., has been identified from the harbour of Banyuls-sur-Mer, north-western Mediterranean Sea. This new species was found in very high densities, exclusively in gravelly sand deposited manually, and was not found in the original source habitat of the gravel. This species is characterized by the colour of the ventral shields with pinkish anterior part and a blood red posterior part in live specimens, a pair of unequal-sized plumose branchiae inserted on segment II and anterior thoracic neuropodia with long-handled uncini. The presence of long-handled uncini even in the smallest specimens constitutes the major difference between Pistacolinisp. n. and other Pista species with a single pair of branchiae such as P.lornensis and P.bansei.


2019 ◽  
Vol S (1) ◽  
pp. 11-14
Author(s):  
Lamiaa A. Hasan ◽  
◽  
Nada M. Al-Sayagh ◽  
Lara R. Al-Banaa ◽  
◽  
...  

Objective: The objective of this study was to evaluate the biomechanical effect of mandibular corpus distraction osteogenesis with different orientations and rates. Materials and Methods: A three-dimensional model of the mandible was created. The vertical surgical cut was made, the force was applied horizontally in a bidirectional manner within two orientations: parallel to the occlusal plane and parallel to the inferior border of the mandible with three rates (0.5mm, 1mm and 1.5mm). Results: The maximum values for von Mises stress when the force was applied parallel to the inferior border of the mandible with all three rates were smaller than those with force direction parallel to the occlusal plane. The displacement in all three directions x, y, and z were not parallel and prominent in the anterior part of the mandible, while the movement at the posterior part is negligible, x and z displacement were bigger when force was applied parallel to the inferior border of the mandible, z displacement was more prominent than x and y displacement, both directions produced upward rotation of the mandible, this rotation was more noticeable when the force was applied parallel to the inferior border of the mandible. Conclusions: A vertical cut can be used in the patient with a long anterior face. This site of distraction achieves more lengthening of mandible than expansion.


2021 ◽  
Vol 43 (2) ◽  
pp. 195-201
Author(s):  
Sergey Moloshnikov ◽  

The terminology and morphology of plates of the posterior part of the antiarch head shield (Placodermi, Antiarchi) are discussed. The terms «zatilochnaya» and «bokovaya (kraevaya) zatilochnaya» was previously accepted in antiarch skulls and are suggested for use in Russian-language literature. These terms are more correct and clearly define a position and development of these plates in the head shield of antiarchs. The titles «zagrivkovaya (nuchalnaya)» and «bokovaya zagrivkovaya (paranuchalnaya)», recently applied to them in Russian-language literature may indicate a connection in development with an anterior part of a trunk. A similar term is used for acipenserid exoskeleton. The acipenserid «nuchalnaya kost’» is located posterior to the «verchnezatilochnaya» (after Gurtovoi), and embryonically developed in an anterior part of the trunk over basidorsals and bones of the shoulder girdle. The name «pervaya spinnaya plastinka» (first dorsal scute: after Hilton and others) is also use for this bone. The term «zagrivkovaya plastinka» is used in other vertebrate skeletons, for example, in turtles; this name denotes the unpaired element of a carapace (postcranial skeleton). Using the terms «zagrivkovaya (nuchalnaya)» and «bokovaya zagrivkovaya (paranuchalnaya)» in the morphology of antiarchs and other placoderms may lead confusion in the terminology of skeletal elements at early vertebrates, incorrect conclusion of their homology, structure and development of the head shield of these unusual fishes.


Development ◽  
1997 ◽  
Vol 124 (11) ◽  
pp. 2143-2154 ◽  
Author(s):  
G. Struhl ◽  
D.A. Barbash ◽  
P.A. Lawrence

The abdomen of adult Drosophila, like that of other insects, is formed by a continuous epithelium spanning several segments. Each segment is subdivided into an anterior (A) and posterior (P) compartment, distinguished by activity of the selector gene engrailed (en) in P but not A compartment cells. Here we provide evidence that Hedgehog (Hh), a protein secreted by P compartment cells, spreads into each A compartment across the anterior and the posterior boundaries to form opposing concentration gradients that organize cell pattern and polarity. We find that anteriorly and posteriorly situated cells within the A compartment respond in distinct ways to Hh: they express different combinations of genes and form different cell types. They also form polarised structures that, in the anterior part, point down the Hh gradient and, in the posterior part, point up the gradient - therefore all structures point posteriorly. Finally, we show that ectopic Hh can induce cells in the middle of each A compartment to activate en. Where this happens, A compartment cells are transformed into an ectopic P compartment and reorganise pattern and polarity both within and around the transformed tissue. Many of these results are unexpected and lead us to reassess the role of gradients and compartments in patterning insect segments.


Development ◽  
1980 ◽  
Vol 59 (1) ◽  
pp. 223-247
Author(s):  
B. Woo Youn ◽  
R. E. Keller ◽  
G. M. Malacinski

A scanning electron microscopic, comparative survey of notochord and somite formation including some details of change in cell morphology and arrangement, was made of selected stages of two species of anuran amphibians (Xenopus laevis and Rana pipiens) and two species of urodeles (Ambystoma mexicanum and Pleurodeles waltlii). The ectoderm or neural plate was removed from fixed embryos and the dorsal aspect of the developing notochord and somite mesoderm was photographed. Micrographs of comparable stages of all species were arranged together to form an atlas of notochord and somite formation. Similar morphogenetic events occur in the same sequence in the four species. Notochordal cells become distinguishable from paraxial mesodermal cells by shape, closeness of packing, and arrangement. Notochordal elongation is accompanied by a decrease in cross-sectional area and by cell rearrangement. Somitic mesoderm becomes distinguished from lateral mesoderm by a change in cell shape and orientation, followed by segmentation of somites. The schedule of somite formation was compared and related to the staging series for each species. The urodeles differ from the anurans in that the notochordal region in the early neurula stages is triangular, with the broadest part in the posterior region of the embryo. In anurans it is uniform in width. This difference may reflect differences in gastrulation and in the mechanism of elongation of the posterior part of the embryo in the neurula.


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