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  • 1
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 28 (1989), S. 1362-1367 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 166 (1983), S. 87-101 
    ISSN: 1432-0568
    Keywords: Avian Embryo ; Myotome ; Dermatome ; Abdominal Muscles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In avian embryos the formation of ventrolateral abdominal muscles was studied by (1) heterospecific grafting experiments between chick and quail embryos and (2) ultrastructural examinations of cells having part in this process. The results demonstrate that the muscle cells are of somitic origin while the connective tissue derives from the somatopleure. Somatopleural cells do not differentiate into myocytes, and somite cells which have entered the ventrolateral abdominal wall, do not contribute to the connective tissue. It is concluded that both dermatome and myotome cells undergo muscular differentiation. The formation of muscles is found to take place in four characteristic steps. During the 4th day of development, epithelially structured ventral somite buds enter the somatopleure. The light cells of the inner myotome layer are elongated in a cranio-caudal direction and contain randomly distributed microfilaments. On the 5th day, the buds lose their epithelial arrangement and change into compact processes in which cells intermingle. The myotome cells show short bundles of thin and thick microfilaments. The third step can be characterized by the appearance of intercellular spaces and the disaggregation of processes becoming invaded by somatopleural cells. Thus, subdivision in single muscle blastemata begins to occur. In 7-day embryos, the muscle anlagen are distinctly separated and the first myotubes containing regularly arranged myofibrils are found. Coincidentally, signs of cell death are observed. Up to the 10th day, the tendons being of somatopleural origin become plainly outlined and the muscle anlagen move to their definitive positions. It is assumed that the formation of muscle pattern is controlled by the somatopleure.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-0568
    Keywords: Fibronectin ; Laminin ; Somitogenesis ; Differentiation and migration of the Wolffian duct ; Synthetic peptides ; Avian embryos
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary It has been suggested that matrix molecules like fibronectin and laminin influence the differentiation and migration of embryonic cells. We investigated the role of these two glycoproteins in somitogenesis as well as in the differentiation and migration of the avian Wolffian (pronephric and mesonephric) duct. At first, we described essential steps in the development of these two organ anlagen by light microscopy, SEM and TEM. To localize fibronectin and laminin more exactly in the actual stages, we used the indirect immunoperoxidase reaction at the light microscopic level and the peroxidase-antiperoxidase technique at the ultrastructural level. Fibronectin was found at the surface of the unsegmented paraxial mesoderm, increasing in the cranial direction, and in the basal laminae of somites and Wolffian duct. The mesenchymal tip of the duct contains a moderate amount of fibronectin. In the two investigated organ anlagen, laminin was found mainly in the basal laminae. The role of fibronectin and laminin was investigated further by using synthetic peptides that mimic the main cell binding domain of either fibronectin or laminin, and that competitively inhibit their cell surface receptors. Thus, the pentapeptides GRGDS, YIGSR, and for control, SHLVE were micro-injected under the ectoderm of 2-day-old embryos. After treatment with GRDS, the Wolffian duct and the segmental plate are more compact. The rounded cells exhibit only short processes and narrow intercellular spaces. At the side of injection the duct shows a delay in migration. After treatment with YIGSR the Wolffian duct migrated laterally over the somatopleure. The basal laminae seem to be incomplete. SHLVE had no effect. Our results suggest that fibronectin is a prerequisite for the migration of the Wolffian duct, and that laminin probably plays a role in guiding the duct. The epithelialization during somitogenesis and differentiation of the duct is a more complex process involving also fibronectin and laminin.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 150 (1977), S. 171-186 
    ISSN: 1432-0568
    Keywords: Avian embryo ; Wing bud myogenesis ; Somitic cells ; Quail ; Chick marker system
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Interspecific grafts of somites, as well as parts of the somatic plate mesoderm, have been made between quail and chick embryos (stages 12–14 H.H.) at the level of the prospective wing bud in order to examine the relationship between somites and wing bud myogenesis. The stability of the natural quail nuclear labelling makes it possible to follow the developmental fate of grafted mesodermal cells in the host embryo. Embryos examined after subsequent incubation periods of 3–7 days show the following distribution of somatic and somitic cells within the wing bud: as soon as the three zones of different cell density within the mesoderm can be distinguished, cells of somitic origin are limited to the prospective myogenic are which is made up of a mixed population of somatic and somitic cells, whereas the prospective chondrogenic area as well as the subectodermal zone only consists of cells originated from the somatic plate mesoderm. After further incubation, single muscle blastema are present which were also seen to be a mixture of somatic and somitic cells. The cells of muscular bundles are of somitic origin, while the muscle connective tissue cells are derived from the somatic plate mesoderm. After grafting into the coelomic cavity or on the chorio-allantoic membrane, fragments of the somatic plate mesoderm previously isolated from quail embryos (stage 14 H.H.) at the level of the prospective wing bud exhibit well developed skeletal elements, but fail to differentiate any musculature. These experimental investigations support previous evidence for a somitic origin of wing bud myogenic cells. Histological and scanning electron microscopic studies of the brachial somites and the adjacent somatic plate mesoderm of chick embryo (stages 13–15 H.H.) reveal that migration of still undifferentiated somitic cells into the brachial somatic plate mesoderm begins to take place in embryos at stage 14.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 138 (1972), S. 82-97 
    ISSN: 1432-0568
    Keywords: Chick ; Embryo ; Somitogenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Nach Voruntersuchungen an Schnittserien normaler Hühnerembryonen werden zur Prüfung der Voraussetzung der Somitogenese folgende Experimente ausgführt: 1. Von Spenderembryonen der Stadien 5–7 (nach Hambruger und Hamilton) wird neben dem Kopffortsatz gelegenes Mesoderm unter das extraembryonale Ektoderm älterer Embryonen verpflanzt. 2. Hinter dem Hensenschen Knoten gelegenes, achsennahes Mesoderm von Spenderembryonen der Stadien 5–7 wird in den extraembryonalen Bereich des Blastoderms oder in das Cölom zwei Tage alter Wirtsembryonen transplantiert. 3. Nach Exstirpation von Neuralrohr bzw. Neuralrohr und Chorda werden die Differenzierungsprozesse des axialen Mesoderms untersucht. Die Auswertung aller Schnittserien ergibt folgende Resultate: Achsennahes Mesoderm vermag sich unter den beschriebenen experimentellen Bedingungen metamer zu gliedern. Als Voraussetzung für die Somitenentstehung hat sich eine enge Lagebeziehung zwischen achsennahem Mesoderm einerseits und angrenzenden Epithelien andererseits erwiesen. Sowohl während der Normalentwicklung als auch unter experimentell veränderten Bedingungen ist das epithelial begrenzte Mesoderm durch eine charakteristische Schichtung, zunehmende Polarisierung der Zellen und nachfolgende metamere Gliederung gekennzeichnet. Da sich im Experiment achsennahes Mesoderm entlang nur des Ektoderms, des Entoderms oder des Aortenendothels segmentiert, kann der Einfluß der Epithelien nicht im Sinne einer „spezifischen Induktionswirkung” gedeutet werden.
    Notes: Summary After preliminary examinations of serial sections of normal chick embryos the following experiments were carried out in order to examine the conditions of somitogenesis: 1. Mesoderm from donors stage 5–7 (Hamburger and Hamilton) located by the side of the head process was transplanted under the ectoderm in the extraembryonic area of older host embryos. 2. Undifferentiated presumptive somite mesoderm of embryos of the stages 5–7 which was located behind Hensen's node, was transplanted into the extraembryonic area of two days old embryos. 3. The development of axial mesoderm after extirpation of the neural tube resp. the neural tube and notochord has been examined. By the examination of the serial histological sections we obtained the following results: Paraxial mesoderm (inclusive undifferentiated presumptive somite mesoderm behind the node) is able to form somites under the experimental conditions described above. The contiguity of paraxial mesoderm with the adjacent epithelial structures has proved essential for somite development. During normal development as well as under experimental conditions the mesoderm surrounded by epithelial structures is distinguished by a characteristic stratification, polarity of the cells and following segmentation. Since under experimental conditions somitogenesis occurs only along the ectoderm, the entoderm or the aortic endothelium, the influence of epithelial structures on the process of segmentation cannot be considered as an effect in the sense of “induction”.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 157 (1979), S. 291-309 
    ISSN: 1432-0568
    Keywords: Chick embryo ; Leg bud ; Cell migration ; Myogenic stem cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The migration of myogenic stem cells into the leg anlagen of chick embryos between stages 16–20 of Hamburger and Hamilton was examined. SEM and TEM studies reveal that cell migration starts at stage 16 from the just-formed somites 26–28. The migrating myogenic cells are elongated and oriented in a medio-lateral direction. The leading ends branch into filopodia which contact a fibrillar network. At first, single cells migrate; later on the cells leaving the ventro-lateral edge of the dermatome migrate in strands and have specialized contacts between them. After reaction with ruthenium red and concanavalin A the migrating cells show a thick surface coat to which ruthenium red-positive particles are attached. The surface coat may be important in the interactions among the migrating cells as well as between the cells and the substrate. The migration of myogenic stem cells was found to take place in a matrix of collagenous fibrils and ruthenium red-positive particles, probably containing glycosaminoglycans. At the onset of migration the fibrillar network exhibits a preferred mediolateral orientation. Therefore, it may be concluded that this alignment of the fibrils influences the direction of cell migration.
    Type of Medium: Electronic Resource
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