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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 132 (1970), S. 325-338 
    ISSN: 1432-0568
    Keywords: Rat embryo ; Lung ; In vitro differentiation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Lungengewebe von Rattenembryonen des Tages 15 wurde in einer modifizierten Trowell-Kultur für 3, 7 und 10 Tage kultiviert und licht- sowie elektronenmikroskopisch untersucht. Nach einer Kultivationsdauer von 3 Tagen entspricht das Bild der Epithelzellen bis auf die vermehrte Zahl von Cyto- und Phagolysosomen den in vivo-Kontrollen. Nach 7 Tagen zeigen die in die Gasphase hineinreichenden Abschnitte eine deutliche Erweiterung der epithelialen Hohlräume, wobei sich die auskleidenden Zellen abflachen und ein Septen-ähnliches Bindegewebsgerüst entsteht. Die Zone nahe der Auflagefläche ist oft unverändert. Nach 10 Tagen Aufenthalt in der Kultur sind die umgewandelten Gewebsbezirke stark geschädigt oder schon nekrotisch. Die Epithelschläuche sind jedoch teilweise noch gut erhalten. Die Zellen haben sich hier zu Flimmerzellen und sezernierenden Zellen mit stark entwickeltem rauhen endoplasmatischen Reticulum differenziert. An der Prägung der typischen Morphologie und Funktion der Lunge sind also neben mechanischen Faktoren (Lungenblähung) auch genuine Differenzierungsvorgänge wesentlich beteiligt.
    Notes: Summary Electron microscopic studies on embryonic lungs of rats (day 15) in a tissue culture. Lung tissue taken from rat embryos on day 15 were cultivated in a modified Trowellculture for 3, 7 and 10 days and studied under the light and electron microscope. After 3 days culture the picture of the epithelial cells is the same as the in vivo controls apart from an increase in cyto- and phagolysosomes. After 7 days a widening of the epithelial vesicles is distinguishable in those parts which have been in the gas phase. The cells in the outer parts are flattened and a septum-like connective tissue layer has developed. The area near the contact surface is often unchanged. After having been cultured for 10 days, the transformed tissue areas in the outer zone are severely damaged or even necrotic. On the whole the epithelial tubes are well maintained. The cells have differentiated into ciliated and secretory cells with a very well developed rough endoplasmic reticulum. True differentiation processes are clearly involved in the development of the typical morphology and function of the lungs as well as mechanical factors (pulmonary expansion).
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 187 (1993), S. 67-73 
    ISSN: 1432-0568
    Keywords: Glucocorticoids ; Chondrogenesis ; Organoid culture ; Differentiation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of dexamethasone on morphogenesis and differentiation of cells obtained from mouse embryos grown at high density in vitro was investigated. Cells from decapitated mouse embryos of day 10 to day 13 were isolated by enzymatic treatment and grown at high density at the medium/air interface in organoid culture. After 28 days in culture, organoid-like structures such as vesicles, gland-like structures and cell aggregates had developed, dependent on the stage of the embryos. After the addition of 10−7 M dexamethasone, cartilage had formed in cultures of cells from day-10, -11 and-12 embryos. It was maximal in cultures of day-11 cells and rare in day-10 cells. No cartilage was found in cultures of day-13 cells. Cartilage induction was similar in cultures treated with 10−6 and 10−7 M dexamethasone, but clearly less in cultures treated with 10−8 M. Only minute amounts of cartilage were detectable after dexamethasone treatment of cells obtained from decapitated embryos (day-11 and -12) whose limb buds had been cut off. In organoid cultures of pure limb bud cells, 10−7 M dexamethasone had no influence on chondrogenesis. The results indicate that the cells inducible to form cartilage by dexamethasone originate from the limb buds. Glucocorticoid induction of chondrogenesis has not been described in vivo. The dependency of both chondrogenesis and expression of glucocorticoid receptor on cell density in vitro may be the cause for this effect.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 197 (1998), S. 155-165 
    ISSN: 1432-0568
    Keywords: Key words Calvaria ; Suture closure ; Osteogenesis ; Mouse
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Syndesmotic sutures of the skull are formed by dense connective tissue and called ”open”; they are ”closed” by formation of a synostosis between adjacent bones. Open sutures are considered as areas of growth and as hinges. The importance of open sutures during the period of skull growth is reflected by pathological situations in which premature closure of the sutures occurs. As alterations of the FGF receptor have been reported in genetical disorders accompanied by premature suture closure (Bellus et al. 1996), the role of fibroblasts and connective tissue in the development of the sagittal suture of mice has been investigated by light and electron microscopy. Morphological changes of the sagittal suture at the following stages are reported: at embryonic day 18, days 1, 5, 9, 14, 20, 26, 28 after birth and in adult mice. Two skulls per stage were investigated. Early osteogenesis appeared in a thin plate, followed by a second plate underneath the first one. Both were separated by blood vessels. In general, vascularization preceded desmoid mineralization; the space around blood vessels was occupied by non-bone-forming cells leaving cavities for the presumptive bone marrow. Mineralization of the collagen-rich osteoid at the mineralizing rim of the bone plates was accompanied by apoptoses and cell disintegration. Newly formed bone was immediately covered by osteoblasts forming a sheet of bone-lining cells. At day 9, the double-layered bone plates of both sides reached the median area of the skull but were separated by non-mineralizing, collagen-rich connective tissue. From day 14 onwards, the bone plates thickened. Bone apposition, recognizable by the formation of collagen-rich osteoid and proceeding from day 14 pp onwards, occurred mainly at the outer and inner surfaces of the calvariae, but neither at bone marrow surfaces nor at the medial edges of the parietal bones. These opposite bone faces showed fewer osteoblasts and bone-lining cells, but an increased number of fibroblasts. Tendon-like collagen bundles connected both bone plates of the open suture of day 26 pp as well as in the adult mice, whereby synostotically closed areas alternated. Formation of an open, syndesmotic suture can, therefore, be described as a transition of bone-forming tissue into a bone-tendon junction. The results indicate the importance of the replacement of osteoblasts by fibroblasts at the sutural front of the bone plates in order to prevent a premature suture closure.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1750
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Epithelzellen aus den Lungen 9tägiger Hühnerembryonen wurden in Deckglas-, Monolayer- und Stückkulturen unter verschiedenen Bedingungen gezüchtet und licht- oder elektronenmikroskopisch untersucht. Mit den beiden ersten Kulturmethoden gelingt es, ein Epithelwachstum in zusammenhängenden Platten zu erreichen. Die Monolayer-Kulturen scheinen besonders brauchbar zu sein, da Epithel isoliert zu gewinnen ist und beim Wachstum auf organischen Filmen (Fibrin, Agar) auch eine Weiterverarbeitung in toto möglich ist. Elektronenmikroskopisch gelingt es, das Substrat der epithelialen Adhäsion genau darzustellen. Die in vitro-Epithelien werden morphologisch mit den Alveolardeckzellen in vivo verglichen und ihre Differenzierungsstufe diskutiert. — Die Epithelzellen in der Stückkultur sind noch nach 4 Tagen gut erhalten und damit als vital anzusehen.
    Notes: Summary Epithelial cells from the lungs of chicken embryos after 9 days incubation had been grown in culture and observed with the light- and electron microscope. We used cover-glass-, monolayer- and organoid-cultures in several culture-mediums. The epithelium grows in coherent plaques in cover-glass- and in monolayer-cultures. From the monolayer culture growing on fibrin or agar the epithelium is separated easily for subsequent experiments. With the electron-microscope we visualized the morphology of epithelial adhesions. The in vitro epitheliums are compared with in vivo alveolar lining cells morphologically and their stage of development in vitro is discussed. The epithelial cells in the organoid-cultures are preserved well even after four days of culture.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1858
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Technology
    Notes: Abstract  The present study is focused on the development of a gas sensor for application in a high temperature environment. The sensor has been realised using thin films prepared on silicon substrates including a high temperature stable heating and wiring system. TiO2 acts as sensitive layer. Measurements have been carried out in synthetic gas mixtures as well as in gases in a given application. Neural networks and multivariate data analysis have been used for determining the gas concentrations. The capability to detect CO, NO x , and toluene is shown.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 277 (1985), S. 98-104 
    ISSN: 1432-069X
    Keywords: Chondrogenesis ; Retinoids ; Differentiation ; Limb-bud mesenchyme ; In vitro
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The influence of all-trans retinoic acid, 13-cis retinoid acic and two aromatic retinoids (Ro 10-1670, Ro 11-1430) on the chondrogenic differentiation of mesenchymal cells in vitro was studied electronmicroscopically. Organ cultures of limb buds from mouse embryos (Day 11) and high-density cultures of embryonic-mouse mesenchymal cells (Day 12) were used as experimental models. After a 6-day culture in the control medium, the development of hyaline cartilage was observed in both systems. In cultures which were treated with retinoids from Day 1 through Day 3 and then incubated in the control medium for 3 more days, the mesenchymal cells still maintained the morphological features of the blastema stage; cartilage synthesis was reduced (low retinoid concentrations) or completely absent (high retinoid concentrations). These findings indicate that the treatment of embryonic-mouse mesenchymal cells with retinoids induces a persistent and dose-dependent inhibition of chondrogenic differentiation, which in quantitative terms, is variably expressed during treatment with different retinoids. These inhibitory effects of retinoids on chondrogenesis are probably implicated in the pathogenetic mechanisms of their teratogenic action in vivo.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-0827
    Keywords: Endochondral mineralization ; Cartilage ; Alkaline phosphatase ; In vitro ; Levamisole
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Isolated mesenchymal limb bud cells from day-12 mouse embryos grown at high density in organoid culture at the medium/air interphase differentiate into chondrocytes and form cartilage nodules. Upon addition of β-glycerophosphate (β-GP), cartilage undergoes endochondral mineralization. This β-GP-induced mineralization was investigated by measuring the calcium content in the cultures and the activity of alkaline phosphatase (AP) in the cell mass and the medium. Calcium incorporation depended on the amount of β-GP added. After continuous treatment, mineralization began on day 8 of the culture period and increased linearly until day 15. In long-term cultures, periodical treatment for 6 days caused an increase in mineralization the older the cultures were, but the slope of increase was proportionately less steep. Treatment at the latest period on days 19–24 resulted in a markedly reduced mineralization. After short-term treatment (48 hours), mineralization increased also the older the cultures were and proceeded during further cultivation in β-GP-free medium. This kinetic behavior indicates a dependency of mineralization on cartilage maturation in this in vitro system. AP activity increased enormously and nearly logarithmically in the cell mass in β-GP-free medium, whereas β-GP treatment inhibited this drastic increase. In the medium, considerable activities of AP were also measurable from day 10 onward. It increased in β-GP-free medium up to day 14, but was diminished after mineralization had been induced. Levamisole inhibited AP activity dose dependently when added directly to the enzyme-containing medium (100% inhibition at 10-3 M). Added to the cultures from day 7 to 14, it partially inhibited AP activity and mineralization at 5×10-5 M; mineralization was totally inhibited at 10-3 M, but AP activity was still present. This high concentration was cytotoxic, as revealed ultrastructurally and by GAG estimation. This in vitro system comprises cartilage development and maturation, β-GP-inducible endochondral mineralization, and final degenerative changes; it may be an appropriate model for investigations on endochondral mineralization.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Cell Differentiation and Development 31 (1990), S. 11-22 
    ISSN: 0922-3371
    Keywords: Cartilage ; Endochondral mineralization ; In vitro ; Organoid culture
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical Medicine and Metabolic Biology 52 (1994), S. 120-127 
    ISSN: 0885-4505
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Cell Differentiation and Development 25 (1988), S. 145-154 
    ISSN: 0922-3371
    Keywords: Calvarial cell ; Mineralization in vitro ; Organoid culture
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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