Organ culture of kidneys from mouse embryos exposed to the transplacental action of 7, 12-dimethylbenz[a]anthracene (DMBA)

1970 ◽  
Vol 69 (1) ◽  
pp. 73-75
Author(s):  
Yu. D. Sorokina
Keyword(s):  
Organ Culture ◽  
Mouse Embryos ◽  
Transplacental Action

scholarly journals The role of the Wolffian ducts in the formation of the sinus vagina: an organ culture study

Development ◽  
1983 ◽  
Vol 73 (1) ◽  
pp. 275-295
Author(s):  
Gabriele Bok ◽  
Ulrich Drews
Keyword(s):  
Organ Culture ◽  
Mouse Embryos ◽  
The Other ◽  
Urogenital Sinus ◽  
Female Development ◽  
Culture Study ◽  
Male Development ◽  
Stage Of Development ◽  
Sinus Formation

In mammals formation of a sinus vagina is inhibited in the male by endogenous testosterone from the embryonic testes. To answer the question which morphogenetic events during formation of thevagina are influenced by testosterone, we explanted genital tracts of mouse embryos in the indifferent stage of development in organ culture. Half of the explants were treated with testosterone and therefore developed in male direction. The other half was kept without testosterone and developed constitutively in female direction. Since the antiMüller factor was not present, in both types of cultures the Müllerian ducts were preserved. During female development the Müllerian ducts fused with the dorsolaterally apposed caudal segments of the Wolffian ducts. Thus the caudal segments of the Wolffian ducts were incorporated in the vaginal plate, while cranially the Wolffian ducts degenerated as expected. During male development fusion between Müllerian and Wolffian ducts did not occur. Under the influence of testosterone the respective caudal segments of the Wolffian ducts were surrounded by dense mesenchyme and further male differentiation took place. We conclude that the ‘sinus protrusions’ or ‘sinovaginal bulbs’ observed during development of the vagina, are in fact the caudal segments of the Wolffian ducts. They serve as a link between Müllerian ducts and urogenital sinus. Formation of a sinus vagina is prevented by testosterone simply by induction of male development in this area.

Biotin Influences Palatal Development of Mouse Embryos in Organ Culture

1995 ◽  
Vol 125 (8) ◽  
pp. 2114-2121 ◽  
Author(s):  
Toshiaki Watanabe ◽  
Krishnamurti Dakshinamurti ◽  
Trivedi V. N. Persaud
Keyword(s):  
Organ Culture ◽  
Mouse Embryos ◽  
Palatal Development

Development of embryonic rat eyes in organ culture

Development ◽  
1968 ◽  
Vol 19 (3) ◽  
pp. 397-405
Author(s):  
R. Christy Armstrong ◽  
Joel J. Elias
Keyword(s):  
Organ Culture ◽  
Defined Medium ◽  
Mouse Embryos ◽  
Biological Media ◽  
Chemically Defined Media ◽  
Culture Systems ◽  
Defined Media ◽  
The Media ◽  
Rats And Mice ◽  
Work Done

Previous studies on the differentiation of whole embryonic eyes in culture have been carried out mainly in the chick (Strangeways & Fell, 1926; Dorris, 1938; Harrison & Berry, 1959) and in one case in the rat (Tansley, 1933). Early postnatal intact eyes of rats and mice were cultured by Lucas & Trowell (1958), while more recently intact and trypsinized early eye rudiments (9 and 10 days) of mouse embryos have been grown in various modified organ culture systems (Muthukkaruppan, 1965). In all these experiments the media employed were either entirely biological or chemically defined media supplemented with biological media. Also, with the exception of the work done by Muthukkaruppan (1965), eye differentiation was well advanced at the start of the culture period. The present study was designed to test the feasibility of observing early embryonic rat eye development in organ culture with a totally defined medium.

Effect of culture in vitro and organ culture on the dry mass of preimplantation mouse embryos

1994 ◽  
Vol 6 (2) ◽  
pp. 229 ◽  
Author(s):  
K Turner ◽  
AW Rogers ◽  
EA Lenton
Keyword(s):  
Organ Culture ◽  
Culture System ◽  
Dry Mass ◽  
Mouse Embryos ◽  
Preimplantation Embryos ◽  
Cell Stage ◽  
Organ Culture System ◽  
Preimplantation Mouse

The dry mass of mouse embryos cultured in vitro in medium alone or in an organ culture system were measured by means of the Vickers M86 scanning microinterferometer. The data were compared with previous data on the dry mass of preimplantation embryos in vivo. The metabolism of embryos cultured in vitro differs from that of fresh embryos. In cultured embryos, dry mass decreases throughout the 2-cell stage whereas the dry mass is increasing at this stage in vivo. Embryos in an organ culture system regain a dry mass profile, similar to that observed in vivo at the late cleavage stage. These results support the view that conditions for embryo metabolism are suboptimal in vitro and that, although the oviduct may confer some advantage on developing embryos in vitro, it is unable fully to support the pattern of metabolism, as assessed by dry mass, observed in vivo.

Freeze-etch observations on the tight junctions of sertoli cells grown in organ culture with FSH

1978 ◽  
Vol 36 (2) ◽  
pp. 340-341
Author(s):  
Rita Meyer ◽  
Zoltan Posalaky ◽  
Dennis Mcginley
Keyword(s):  
Organ Culture ◽  
Tight Junctions ◽  
Sertoli Cell ◽  
Germ Cells ◽  
Sertoli Cells ◽  
Barrier Function ◽  
Cell Junction ◽  
Intramembranous Particles ◽  
Junctional Complexes ◽  
Oriented Parallel

The Sertoli cell tight junctional complexes have been shown to be the most important structural counterpart of the physiological blood-testis barrier. In freeze etch replicas they consist of extensive rows of intramembranous particles which are not only oriented parallel to one another, but to the myoid layer as well. Thus the occluding complex has both an internal and an overall orientation. However, this overall orientation to the myoid layer does not seem to be necessary to its barrier function. The 20 day old rat has extensive parallel tight junctions which are not oriented with respect to the myoid layer, and yet they are inpenetrable by lanthanum. The mechanism(s) for the control of Sertoli cell junction development and orientation has not been established, although such factors as the presence or absence of germ cells, and/or hormones, especially FSH have been implicated.

Human Adenovirus Uptake by Preirnplantation Mouse Embryos

1972 ◽  
Vol 30 ◽  
pp. 268-269
Author(s):  
D. G. Chase ◽  
W. Winters ◽  
L. Piko
Keyword(s):  
Hela Cells ◽  
Human Adenovirus ◽  
Mouse Embryos ◽  
Equilibrium Density ◽  
Cell Stage ◽  
Virus Attachment ◽  
Preimplantation Mouse Embryos ◽  
Embryo Culture Medium ◽  
Preimplantation Mouse ◽  
Mouse Cells

Although the outlines of human adenovirus entry and uncoating in HeLa cells has been clarified in recent electron microscope studies, several details remain unclear or controversial. Furthermore, morphological features of early interactions of human adenovirus with non-permissive mouse cells have not been extensively documented. In the course of studies on the effects of human adenoviruses type 5 (AD-5) and type 12 on cultured preimplantation mouse embryos we have examined virus attachment, entry and uncoating. Here we present the ultrastructural findings for AD-5.AD-5 was grown in HeLa cells and purified by successive velocity gradient and equilibrium density gradient centrifugations in CsCl. After dialysis against PBS, virus was sedimented and resuspended in embryo culture medium. Embryos were placed in culture at the 2-cell stage in Brinster's medium.

Preplate neurons in embryonic mouse cortex: Ultrastructural observations using photoconversion of the fluorescent lipophilic dye dil

1992 ◽  
Vol 50 (1) ◽  
pp. 906-907
Author(s):  
Linda C. Hassinger ◽  
James E. Crandall
Keyword(s):  
Mouse Embryos ◽  
Embryonic Mouse ◽  
Cortical Afferents ◽  
Mouse Cortex ◽  
Carbocyanine Dye ◽  
Increased Sensitivity

We have begun to look directly at small numbers of afferent axons to early generated neurons that form the preplate in the developing mouse cortex. The carbocyanine dye Dil (1’1, dioctadecyl-3,3,3’3’-tetramethyl-indocarbocyanine) has proved especially useful for this goal. DiI labels axons and their terminals with greater sensitivity and without some of the disadvantages of axon filling with HRP. The increased sensitivity provided by labeling embryonic axons with DiI has given us new insights into the development of cortical afferents. For instance, we reported originally that afferents from the thalamus were present below the cortex as early as embryonic day 15 (E15) based on HRP injections into mouse embryos. By using DiI placements into the thalamus in aldehyde-fixed brains, we now know that thalamic fibers reach the cortex 24 hrs earlier.

Localization of Intracisternal a Particle Antigens in Neoplastic Cells and Preimplantation Mouse Embryos

1980 ◽  
Vol 38 ◽  
pp. 696-697
Author(s):  
Thomas T.F. Huang ◽  
Patricia G. Calarco
Keyword(s):  
Endoplasmic Reticulum ◽  
Normal Development ◽  
Mouse Embryos ◽  
Neoplastic Cells ◽  
Large Numbers ◽  
Preimplantation Mouse Embryos ◽  
Preimplantation Mouse ◽  
Intracisternal A Particle ◽  
Normal Feature

The stage specific appearance of a retravirus, termed the Intracisternal A particle (IAP) is a normal feature of early preimplantation development. To date, all feral and laboratory strains of Mus musculus and even Asian species such as Mus cervicolor and Mus pahari express the particles during the 2-8 cell stages. IAP form by budding into the endoplasmic reticulum and appear singly or as groups of donut-shaped particles within the cisternae (fig. 1). IAP are also produced in large numbers in several neoplastic cells such as certain plasmacytomas and rhabdomyosarcomas. The role of IAP, either in normal development or in neoplastic behavior, is unknown.

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