The influence of the lower beak on the interorbital septum-prenasal process complex in the chick embryo

Development ◽  
1979 ◽  
Vol 49 (1) ◽  
pp. 61-72
Author(s):  
F. G. Wouterlood ◽  
W. van Pelt

The effect of removal of the lower beak on the development of the interorbital septumprenasal process (ISPP) complex was studied in chick embryos. In normal development the angle between the ventral contour of the interorbital septum and the long axis of the prenasal process increases. At the same time the angle between the ventral contour of the interorbital septum and the basal plate increases. After surgical removal of the prospective lower beak at stage 29, the position of the entire ISPP complex was altered in stage-38 embryos and the prenasal process showed elongation. In stage-38 embryos in which the prospective upper beak had been removed at stage 29, Meckel's cartilage was elongated. It is concluded that straightening of the angle between the ventral contour of the interorbital septum and the long axis of the prenasal process is not influenced by the lower beak, whereas the position of the entire ISPP complex and the size of the prenasal process are under the epigenetic influence of the lower beak. The position and size of Meckel's cartilage are under the epigenetic influence of the upper beak.

1937 ◽  
Vol 14 (2) ◽  
pp. 229-231 ◽  
Author(s):  
C. H. WADDINGTON

1. The heart was removed from chick embryos of seven to twelve somites, and the embryos cultivated in vitro. The operation abolished the normal twisting of the anterior part of the embryo on to its left side and the general bending of the brain region into an arc. These two processes therefore seem to be dependent on the normal development of the heart. 2. The embryos showed a bending of the forebrain relative to the midbrain, which is therefore independent of the development of the heart. 3. The embryonic blood system, including the aortic arches, developed normally in many cases, but the blood vessels became enormously dilated. 4. The lateral evaginations of the foregut and the visceral arch mesenchyme underwent the first stages of differentiation in atypical positions, seemingly independently of each other or of any other structures.


1965 ◽  
Vol 13 (3) ◽  
pp. 351 ◽  
Author(s):  
PDF Murray ◽  
M Smiles

The effects of two very different experimental procedures, (1) chorio-allantoic grafting and (2) dosing with decamethonium, a "curarizing" drug, on the development of adventitious (secondary) cartilage at several articulations, was studied in the chick embryo. Both procedures paralyse the muscles, the first by their physical destruction, the second by the paralysing action of the drug. The quadratojugal-quadrate articulation and that between the surangular bone and Meckel's cartilage, when grafted from 9-day embryos, formed no adventitious cartilage as grafts. Adventitious cartilage is in normal development formed on the bony component of both articulations. In grafts from many 10-day, and from 11-day embryos, adventitious cartilage was formed in the grafts, was resorbed after its differentiation (as happens also in normal embryos), but was not renewed by continued chondrification of derivatives of the germinal cells (as does happen in normal embryos). Decamethonium, as the commercial preparation Eulissin A, injected via the chorio-allantois into 9-day embryos, totally or almost totally paralysed the skeletal muscles of the embryos which, however, survived several days (their respiratory system and their cardiac and smooth muscles not being involved in the paralysis). Treatment with the drug from 9 to 14 days, followed by fixation, almost totally prevented the development of adventitious cartilage in the four articulations studied (three mobile joints: quadratojugal-quadrate, pterygoid-"roller" of quadrate, quadrate-squamosal, and one non-mobile: surangular-Meckel's cartilage). In other experiments with Eulissin it was found that after cessation of dosing only very limited recovery of movement occurred and there was limited formation of adventitious cartilage; it was, however, shown that as late as 16 days cells exist which can form adventitious cartilage. When dosing began at 12 days the adventitious cartilage already then present was found, after fixation at 16 days, buried under a new bony articular surface and in process of resorption. In some articulations in some embryos there had been a development of young articular cartilage in the late stages of the experiment. Earlier work had shown that adventitious cartilage develops from germinal cells appearing to be identical with those which earlier differentiate as osteoblasts, and in the present work the histology left little doubt that germinal cells, which normally would have formed cartilage, in grafted and paralysed embryos formed bone. In the present paper it is concluded that these cells are ambivalent, differentiating as osteoblasts if they are not subjected to the mechanical conditions existing at articulations, and as chondroblasts if they are so subjected, but that cells which have attained to some early stage in chondrogenesis continue and complete their differentiation as cartilage in grafts and paralysed joints in which the mechanical conditions normal at articulations do not exist. The evocation of cartilage in this instance and in general, the nature of the mechanical factor involved, a possible common factor underlying the variety of circumstances which may in different cases induce chondrogenesis, the present instance as an example of modulation or change of differentiation, and the failure of adventitious chondrification in this instance to have become genetically assimilated, are discussed. It is suggested that given bivalent germinal cells with the ability to form cartilage or bone under appropriate conditions, and the invariable existence of such conditions, there is no opportunity for the action of selection and therefore none for genetic assimilation.


1963 ◽  
Vol 11 (3) ◽  
pp. 368 ◽  
Author(s):  
PDF Murray

The development of a number of articulations in the chick embryo skull, and of adventitious (secondary) cartilages associated with them, is described. The cells of the adventitious cartilages differed from the hyaline cartilage of the chondrocranium in being encapsulated and rapidly becoming hypertrophic. In every case but one the adventitious cartilage was formed in direct association with an articulation. The articulations may have articular cavities (quadrate-quadratojugal; quadratepterygoid; pterygoid-cranium; squamosal-quadrate) or be without these (squamosalotic capsule; pterygoid-palatine; surangular- and angular-Meckel's cartilage). The adventitious cartilage developed in "germinal cells" which, immediately before the onset of chondrification, had been engaged in ossification. Later, the same group of cells often reverted to bone formation, and the adventitious cartilage became partly covered by bone. Where there were articular cavities, fibrous membranes lining the articulations appeared on each side of the cavity and these usually became fibrocartilaginous. These membranes continued into the fibrous layers of the periostea of the elements concerned, while the germinal cells from which the adventitious cartilages were formed became cambial layers continuous with the cambial layers of the periostea. Movement, and mechanical strains resulting from the action of muscles, is obvious at articulations having articular cavities. In those lacking articular cavities, the anatomy of the muscles makes it extremely probable that the site on the membrane bone is pulled upon, or moved against, the cartilage with which the articulation is made. The facts of the development of adventitious cartilage, and of the anatomy of the musculature, are in harmony with the hypothesis that the change in morphogenetic direction of the germinal cells, from osteogenesis to chondrogenesis, is mechanically induced.


Development ◽  
1987 ◽  
Vol 99 (3) ◽  
pp. 341-351 ◽  
Author(s):  
S.E. Wedden

The development of the chick face involves outgrowth of buds of tissue, accompanied by the differentiation of cartilage and bone in spatially defined patterns. To investigate the role of epithelial-mesenchymal interactions in facial morphogenesis, small fragments of facial tissue have been grafted to host chick wing buds to continue their development in isolation. Fragments of the frontonasal mass give rise to typical upper-beak-like structures: a long central rod of cartilage, the prenasal cartilage and an egg tooth. Meckel's cartilage, characteristic of the lower beak, develops from fragments of the mandible. Removal of the ectoderm prior to grafting leads to truncated development. In fragments of frontonasal mass mesenchyme only a small spur of cartilage differentiates and there is no outgrowth. The mandible is less affected; a rod of cartilage still forms but the amount of outgrowth is reduced. Retinoid treatment of chick embryos specifically affects the development of the upper beak and outgrowth and cartilage differentiation in the frontonasal mass are inhibited. The mandibles, however, are unaffected and develop normally. In order to investigate whether the epithelium or the mesenchyme of the frontonasal mass is the target of retinoid action, recombinations of retinoid-treated and untreated facial tissue have been grafted to host wing buds. Recombinations of retinoid-treated frontonasal mass ectoderm with untreated mesenchyme develop normally whereas recombinations of untreated ectoderm with retinoid-treated mesenchyme lead to truncations. The amount of outgrowth in fragments of mandibular tissue is slightly reduced when either the ectoderm or the mesenchyme has been treated with retinoids. These recombination experiments demonstrate that the mesenchyme of the frontonasal mass is the target of retinoid action. This suggests that retinoids interfere with the reciprocal epithelial-mesenchymal interactions necessary for outgrowth and normal upper beak development.


Development ◽  
1969 ◽  
Vol 22 (3) ◽  
pp. 349-371
Author(s):  
P. D. F. Murray ◽  
Daniel B. Drachman

Skeletal muscle contractions are necessary during embryonic life for the normal development of joints. The general features of joint development in immobile limbs were first studied with the techniques of grafting and organ culture. (Murray, 1926; Murray & Selby, 1930; Fell, 1925; Fell & Canti, 1934; Hamburger & Waugh, 1940; Lelkes, 1958). However, these methods of necessity entail a drastic alteration in the environment of the developing articulations, which may result in gross distortions of the skeletal structures themselves. More recently, neuromuscular blocking agents have been used to produce paralysis of chick embryos in ovo. When administered intravenously, these pharmacological substances produce profound paralysis, which may be continued for prolonged periods during embryonic development (Drachman & Coulombre, 1962a, b). Drachman & Sokoloff (1966) have analyzed the primary development of the knee, ankle and toe joints of the chick embryo by the use of these methods.


1995 ◽  
Vol 170 (2) ◽  
pp. 387-396 ◽  
Author(s):  
Kun Sung Chung ◽  
Howard H. Park ◽  
Kang Ting ◽  
Hiroko Takita ◽  
Suneel S. Apte ◽  
...  

Development ◽  
1992 ◽  
Vol 114 (3) ◽  
pp. 729-741 ◽  
Author(s):  
K.G. Storey ◽  
J.M. Crossley ◽  
E.M. De Robertis ◽  
W.E. Norris ◽  
C.D. Stern

Induction and regionalisation of the chick nervous system were investigated by transplanting Hensen's node into the extra-embryonic region (area opaca margin) of a host embryo. Chick/quail chimaeras were used to determine the contributions of host and donor tissue to the supernumerary axis, and three molecular markers, Engrailed, neurofilaments (antibody 3A10) and XlHbox1/Hox3.3 were used to aid the identification of particular regions of the ectopic axis. We find that the age of the node determines the regions of the nervous system that form: young nodes (stages 2–4) induced both anterior and posterior nervous system, while older nodes (stages 5–6) have reduced inducing ability and generate only posterior nervous system. By varying the age of the host embryo, we show that the competence of the epiblast to respond to neural induction declines after stage 4. We conclude that during normal development, the initial steps of neural induction take place before stage 4 and that anteroposterior regionalisation of the nervous system may be a later process, perhaps associated with the differentiating notochord. We also speculate that the mechanisms responsible for induction of head CNS differ from those that generate the spinal cord: the trunk CNS could arise by homeogenetic induction by anterior CNS or by elongation of neural primordia that are induced very early.


2011 ◽  
Vol 218 (5) ◽  
pp. 517-533 ◽  
Author(s):  
Tamaki Yokohama-Tamaki ◽  
Takashi Maeda ◽  
Tetsuya S. Tanaka ◽  
Shunichi Shibata

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