The differentiation of derivatives of the lower germ layers in fundulus following the implantation of shield grafts

1955 ◽  
Vol 128 (3) ◽  
pp. 525-559 ◽  
Author(s):  
Jane M. Oppenheimer
Keyword(s):  
Development ◽  
1974 ◽  
Vol 32 (2) ◽  
pp. 445-459
Author(s):  
B. Levak-Švajger ◽  
A. Švajger

Single germ layers (or combinations of two of them) were isolated from the primitive streak and the head-fold stage rat embryos and grown for 15 days under the kidney capsule of syngeneic adult animals. The resulting teratomas were examined histologically for the presence of mature tissues, with special emphasis on derivatives of the primitive gut. Ectoderm isolated together with the initial mesodermal wings at the primitive streak stage gave rise to tissue derivatives of all three definitive germ layers. Derivatives of the primitive gut were regularly present in these grafts. At the head-fold stage, isolated ectoderm (including the region of the primitive streak) differentiated into ectodermal and mesodermal derivatives only. Endoderm isolated at the primitive streak stage did not develop when grafted and was always completely resorbed. At the head-fold stage, however, definitive endoderm differentiated into derivatives of the primitive gut if grafted together with adjacent mesoderm. These findings indirectly suggest the migration of prospective endodermal cells from the primitive ectoderm, and therefore a general analogy with the course of events during gastrulation in the chick blastoderm.


Development ◽  
1991 ◽  
Vol 111 (4) ◽  
pp. 983-992 ◽  
Author(s):  
A. Alberga ◽  
J.L. Boulay ◽  
E. Kempe ◽  
C. Dennefeld ◽  
M. Haenlin

The zygotic effect gene snail (sna) encodes a zinc-finger protein required for mesoderm formation in Drosophila embryos. By in situ analysis, sna transcripts are first detected at syncytial blastoderm and persist until very late stages of embryogenesis. Expression of sna is transient and is observed in tissues derived from all three germ layers. Prior to germband elongation, sna RNA accumulation is consistent with its genetically determined role in mesoderm formation. Starting at germband elongation, a second phase of sna expression appears to be initiated, characterized by a highly dynamic accumulation of transcripts in the developing central and peripheral nervous systems. Translation of sna RNA is apparently delayed as the sna protein is not detected before the onset of gastrulation. Its regional distribution generally correlates with that of sna transcripts. The complex pattern of sna expression strongly suggests that the function of the gene is not restricted to mesoderm formation.


2018 ◽  
Vol 18 (4) ◽  
pp. 42-46
Author(s):  
Pavel A. Dyban

Spontaneous ovarian teratomas in mice (LT/Sv and LT/SvXBJ) and experimental teratomas (the result of blastocyst transplantation underneath a testicle capsule of CBAXC57 mice) are represented with derivatives of three germ layers. During the process of cytodifferentiation, the epithelium of various origins forms closed cavities (cysts), whereas in more complex morphogenetic processes, the epithelium participates in reduced organogenesis. Intestine analogs have been reported in spontaneous and experimental teratomas, but skin analogs have been shown only in experimental teratomas. The mitotic activity of lining epithelia of organ analogs differs significantly from karyokinetic figures of similar epithelia in cysts. Possible reasons for this phenomenon are discussed in this paper.


2020 ◽  
Author(s):  
Victoria A. Sleight ◽  
J. Andrew Gillis

AbstractPaired fins are a defining feature of the jawed vertebrate body plan, but their evolutionary origin remains unresolved. Gegenbaur proposed that paired fins evolved as gill arch serial homologues, but this hypothesis is now widely discounted, owing largely to the presumed distinct embryonic origins of these structures from mesoderm and neural crest, respectively. Here, we use cell lineage tracing to test the embryonic origin of the pharyngeal and paired fin skeleton in the skate (Leucoraja erinacea). We find that while the jaw and hyoid arch skeleton derive from neural crest, and the pectoral fin skeleton from mesoderm, the gill arches are of dual origin, receiving contributions from both germ layers. We propose that gill arches and paired fins are serially homologous as derivatives of a continuous, dual-origin mesenchyme with common skeletogenic competence, and that this serial homology accounts for their parallel anatomical organization and shared responses to axial patterning signals.


2012 ◽  
Vol 24 (1) ◽  
pp. 285
Author(s):  
Jorge A. Piedrahita ◽  
Sehwon Koh ◽  
Natasha Olby

Pluripotent stem cells such as embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) can give rise to derivatives of all three germ layers and thus have great potential in regenerative medicine. In mice and humans, it has been shown that embryonic and adult fibroblasts can be reprogrammed into pluripotency by introducing four transcription factors, Oct3/4, Klf4, Sox2 and c-Myc (OKSM). In his presentation we will describe the derivation of iPS cells from adult canine fibroblast by retroviral OSKM transduction. The isolated canine iPS cells were expanded in three different iPS culture media (FGF2, LIF and FGF2 plus LIF) and only the cells cultured in FGF2 plus LIF showed strong AP activity expressed pluripotency markers, POU5F1 (OCT4), SOX2, NANOG and LIN28 as well as ES cells-specific genes (PODXL, DPPA5, FGF5, REX1 and LAMP1). In vitro differentiation by formation of embryoid bodies (EBs) and directed differentiation showed cell derivatives of all three germ layers as confirmed by expression for AFP, CXCR4 and SOX17 (endoderm), desmin (DES), vimentin (VIM), MSX1 and BMP2 (mesoderm) and glial fibrillary acidic protein (GFAP), TUJ1, NCAM and bIII-tubulin (TUBB, ectoderm). In vivo, the putative canine iPS cells formed simple teratomas that expressed markers for all three germ layers. In summary, we were able to derive induced pluripotent cells from adult somatic cells by using four transcription factors. The isolated canine iPSCs have similar characteristics to ESCs from other species, but the exact cellular mechanisms behind their unique co-dependency on both FGF and LIF is still unknown. This work was funded by a grant from the America Kennel Club to JAP.


Development ◽  
1979 ◽  
Vol 50 (1) ◽  
pp. 21-30
Author(s):  
H. Fujimoto ◽  
K. O. Yanagisawa

Mouse embryos homozygous for the T-mutation show abnormalities, severer at the posterior embryonic regions, by day 9 of gestation and die before day 11 in utero. To analyse developmental potentiality of the T/T embryos, fragments of their anterior and posterior portions were grafted into the testes of adult T/+ mice, and examined histologically for the tissues formed after 1 month. The grafted tissues of the T/T embryos grew beyond the destined lethal stage and gave rise to benign teratomas composed of mature tissues. Although there were some different features of the tissues formed in the teratomas derived from different portions and stages of the embryos, their types were essentially identical between wild-type and the mutant teratomas. Statistical analysis showed that frequency of the cartilage and/or bone formation was significantly lower in the posterior mutant teratomas. It cannot be concluded, however, that this difference is essentially caused by T-mutation. The main conclusion of present experiments is that grafted portions of T/T embryos have the potentiality to develop intoteratomas containing derivatives of all three germ layers.


Author(s):  
TL Selvakumari
Keyword(s):  

2013 ◽  
Vol 03 (03) ◽  
pp. 188-201 ◽  
Author(s):  
Riccardo Di Fiore ◽  
Rosa Drago-Ferrante ◽  
Antonella D’Anneo ◽  
Anna De Blasio ◽  
Andrea Santulli ◽  
...  

1930 ◽  
Vol 26 (7) ◽  
pp. 78-83
Author(s):  
G. I. Sharafutdinov

Teratomas are tumors that contain different tissues and even different organs at different stages of development. These tumors sometimes consist of more or less cavities - cysts, sometimes they are solid. The tissues that make up the teratoma, taking the same part in its formation, can be derivatives of one, two or all three germ layers. The products of the development of these sheets in teratomas, in contrast to dermoids, are intermixed extremely randomly, and sometimes the excessive growth of one tissue makes the rest hardly noticeable.


Development ◽  
1974 ◽  
Vol 32 (2) ◽  
pp. 461-467
Author(s):  
A. Švajger ◽  
B. Levak-Švajger

Three areas, composed of all three germ layers, were isolated from Fischer strain rat embryonic shields at the head-fold stage, and grafted separately under the kidney capsule of adult male rats of the same strain. The areas were from the neural plate, Hensen's node and the primitive streak. The resulting teratomas were examined histologically for the presence of derivatives of the primitive gut. The grafts differed strikingly in their capacity to develop into different segments of the gut. Endoderm underlying the neural plate developed into derivatives of the foregut, while endoderm underlying the primitive streak developed mainly into derivatives of the mid- and hindgut. It was concluded that, at the head-fold stage, the capacities to develop into different segments of the definitive gut are already roughly limited to particular areas of the endoderm.


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