The behaviour of embryonic chick and quail tissues in culture

Development ◽  
1981 ◽  
Vol 61 (1) ◽  
pp. 15-33
Author(s):  
Ruth Bellairs ◽  
G. W. Ireland ◽  
E. J. Sanders ◽  
C. D. Stern

Pieces of tissue were dissected from early chick and quail embryos (Stages XTII and XIV of Eyal-Giladi & Kochav, 1976; and stages 3–5 of Hamburger & Hamilton, 1951). These tissues were taken from three different regions of the early embryos, and from eight different regions of the older ones, and were derived mainly from the lower layer. Epiblast tissues were also used. The experiments were designed to test the ability of one tissue to penetrate another. A single tissue was grown in culture in a Falcon dish for 18–24 h until it had formed a coherent sheet of cells (Explant I). A second tissue was then combined with it in one of two ways: (a) A small piece of tissue (Explant II) was explanted on top of Explant I. In most cases Explant II penetrated through Explant I and spread on the Falcon dish. (b) Another small piece of tissue (Explant III) was explanted beside (in confrontation with) Explant I. Usually, Explant III penetrated into Explant 1 rather than vice versa. The results were analysed to see if there were any variations in behaviour of the different tissues. The main result was that important differences were found to exist between certain types of chick and quail cells when grown in culture; the implications of this finding for the widely used technique of xenoplastic grafting are mentioned. Another result was that Explant I was more likely to be penetrated when the second tissue was placed on top of it (Explant II) than when it was confronted with it (Explant III). The significance of these results is discussed.

Development ◽  
1960 ◽  
Vol 8 (1) ◽  
pp. 54-59
Author(s):  
T. S. Okada ◽  
J. L. Sirlin

During embryonic development the differentiation of different tissues depends largely on the synthesis of specific substances characteristic of each tissue. From this viewpoint it is of interest to study the uptake of sulphur by the early embryo, especially since the incorporation and retention of this isotope in sulpho-muco-polysaccharides has now been well established by various authors working on fully differentiated tissues (see review by Dziewiatkowski, 1958). So far some work has been done on the distribution of radiosulphate in early embryos (Amprino, 1955 a, b; Friberg & Ringertz, 1956; Johnston & Comar, 1957), but for amphibians in particular no information is yet available. The present paper deals with the incorporation of radiosulphate in various embryonic tissues of Xenopus, in particular in the visceral cartilage of ectomesodermal (neural crest) origin. Embryos of X. laevis in stages 29–47 (Nieuwkoop & Faber, 1956) were used.


1979 ◽  
Vol 82 (2) ◽  
pp. 565-571 ◽  
Author(s):  
E C Beyer ◽  
K T Tokuyasu ◽  
S H Barondes

Extracts of adult chicken liver, pancreas, and intestine contain high levels of a lectin which appears to be identical to one previously purified from embryonic chick muscle. This lectin is virtually absent from adult muscle, but is highly concentrated in cells lining liver sinusoids, intestinal goblet cells, and the extracellular spaces surrounding pancreatic acini. These findings suggest that the lectin may play different roles in different tissues and at different times in the life of a chicken.


Author(s):  
M.R. Richter ◽  
R.V. Blystone

Dexamethasone and other synthetic analogs of corticosteroids have been employed clinically as enhancers of lung development. The mechanism(s) by which this steroid induction of later lung maturation operates is not clear. This study reports the effect on lung epithelia of dexamethasone administered at different intervals during development. White Leghorn chick embryos were used so as to remove possible maternal and placental influences on the exogenously applied steroid. Avian lung architecture does vary from mammals; however, respiratory surfactant produced by the lung epithelia serves an equally critical role in avian lung physiology.


1981 ◽  
Vol 45 (02) ◽  
pp. 110-115 ◽  
Author(s):  
György Csákó ◽  
Eva A Suba

SummaryPlatelet aggregations were studied by a turbidimetric method in citrated human platelet-rich plasmas (PRP) in vitro. Human Clq inhibited the aggregations caused by collagens derived from different tissues and species. Clq was needed by weight in comparable quantities to collagen for neutralizing the aggregating effect. The dependence of the inhibitory reaction on the preincubation of platelets with Clq and the differences in the occurrence of aggregating substances in supernatants of PRP triggered with collagen in the presence or absence of Clq, confirmed that Clq exerts its effect by preventing fixation of collagen to platelets. In addition, the high specificity of the inhibitory action of Clq for collagen-induced platelet aggregation was demonstrated by results obtained for testing a variety of aggregating agents in combination with Clq and/or collagen.Since normal concentrations of Clq in the blood are in the range of inhibitory doses of Clq for collagen-induced platelet aggregations in vitro and upon activation of complement Clq is known to dissociate from Cl, it is proposed that Clq may participate in a highly specific manner in regulating platelet reactivity to collagen in vivo.


Sign in / Sign up

Export Citation Format

Share Document