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At least 955 records · Page 53Linked to original sources
PubMed1979

Development of the diencephalon in the rat. VI. Re-evaluation of the embryonic development of the thalamus on the basis of thymidine-radiographic datings.

The development of the thalamus was examined in normal and X-irradiated embryos from day 13 (E13) to the day before birth (E22). The differentiating, radioresistant neurons of the lateral habenular nucleus, derived from a portion of the superior neuroepithelial lobule (SL1), were settling by day E15 and by this time the habenulopeduncular tract was forming. The neurons of the reticular nucleus, derived from the middle neuroepithelial lobe, began to settle on day E15 but a massive migration was still evident on day E16. Adjacent to the reticular nucleus the internal capsule appeared on day E16; this fiber bundle seemed to be continuous with fibers embedded in the first transitory zone of cells issuing from the dorsal neuroepithelial lobe. Because of the immaturity of the neocortex at this time, it was postulated that thalamocortical fibers of the dorsal thalamus are the earliest components of the internal capsule. By day E17 all the sensory relay nuclei of the thalamus were recognizable and it was assumed that the second transitory zone issuing from the receding dorsal neuroepithelial lobe contained the neurons of the later forming intralaminar nuclei. Suggestive evidence was obtained that the late arising neurons of the medial thalamus (the anterior nuclei, the mediodorsal nucleus, and some or all of the midline nuclei) originate in a portion of the superior neuroepithelial lobule designated as SL2. Our present and previous studies showed that the major divisions of the hypothalamus and thalamus are derived embryonically from distinguishable parts of the third ventricle neuroepithelium. This implies the te third ventricle neuroepithelium has a "mosaic" organization and suggests that the fate of hypothalamic and thalamic neurons may be determined to some extent while their precursors are still proliferating.

Animals↗
PubMed1989

[Experimental studies on the stimulation of prenatal development in swine by PMSG treatment in early pregnancy. 1. Clinical results of embryonic development in young slaughtered sows and litter results in young and old sows after PMSG treatment on the 11th day of pregnancy].

Thirty-eight gilts were slaughtered on the 25th and 39th days of pregnancy, after they had received 400 I.U. PMSG treatment on the eleventh day of pregnancy. Treated and untreated animals in a group of 140 gilts and 195 adult sows were compared with each other for post-farrowing fertility performance. Weight development of embryos obtained from the slaughtered sows depended on the number of embryos alive. The survival rate of embryos from treated sows was about 5% higher than that recorded from untreated animals. Clearly increased litter sizes which, however, were associated with lower piglet birth weights were recorded from farrowing gilts and adult sows, following PMSG treatment. The conclusion is drawn that PMSG treatment, via luteotrophic action of luteinising hormone, is capable of stabilising pregnancy-related corpora lutei, resulting in higher litter sizes. Further studies will be necessary, and emphasis will have to be laid on the problem of weight development of newborn piglets, following litter-size boosting treatment.

Animals↗
PubMed1984

Embryonic development of monoaminergic neurons in the chick retina.

By means of a histofluorescence technique, embryonic and postnatal development of monoaminergic neurons was followed in the chicken retina with or without intravitreal injection of monoamines 30-60 minutes before eye removal. Fluorescent cells were tentatively classified into five subsets with respect to the soma shape, localization, migration of somata during retinal development, uptake capacity (color and intensity in fluorescence), and sensitivity to neurotoxins. The five subsets of cells were endogenous dopaminergic (DA), catecholamine-accumulating (CA), indoleamine-accumulating (IA), CA-bipolarlike, and IA-bipolarlike cells. Greenish endogenous DA-cells first appeared at the 14-15th embryonic day. The cell body of DA-cells was initially fusiform and located slightly distal to the innermost level of the inner nuclear layer (INL). They became round or oval and migrated to the innermost level of the INL by day 20. Both large and small bottle-shaped CA-cells were visualized at an intermediate portion of INL by intravitreal injection of exogenously applied dopamine or noradrenaline (1-2 micrograms/eye) at day 10. Large bottle-shaped cells, like the DA cells, changed to round or oval and migrated to the innermost level of the INL by day 20. On the other hand, small bottle-shaped CA-cells retained their cell shape and location in the INL as retinal development progressed. Therefore, the large bottle-shaped CA-cells seen in an early developmental stage correspond to the DA-cells. IA-cells were visualized one or two cell rows outward in the INL first at day 13-14 by intravitreal injection of 5,6-dihydroxytryptamine or 5-hydroxytryptamine (1-5 micrograms).(ABSTRACT TRUNCATED AT 250 WORDS)

5,7-Dihydroxytryptamine↗
PubMed2002

Docking protein SNT1 is a critical mediator of fibroblast growth factor signaling during Xenopus embryonic development.

The docking protein SNT1/FRS2 (fibroblast growth factor receptor substrate 2) is implicated in the transmission of extracellular signals from several growth factor receptors to the mitogen-activated protein (MAP) kinase signaling cascade, but its biological function during development is not well characterized. Here, we show that the Xenopus homolog of mammalian SNT1/FRS-2 (XSNT1) plays a critical role in the appropriate formation of mesoderm-derived tissue during embryogenesis. XSNT1 has an expression pattern that is quite similar to the fibroblast growth factor receptor-1 (FGFR1) during Xenopus development. Ectopic expression of XSNT1 markedly enhanced the embryonic defects induced by an activated FGF receptor, and increased the MAP kinase activity as well as the expression of a mesodermal marker in response to FGF receptor signaling. A loss-of-function study using antisense XSNT1 morpholino oligonucleotides (XSNT-AS) shows severe malformation of trunk and posterior structures. Moreover, XSNT-AS disrupts muscle and notochord formation, and inhibits FGFR-induced MAP kinase activation. In ectodermal explants, XSNT-AS blocks FGFR-mediated induction of mesoderm and the accompanying elongation movements. Our results indicate that XSNT1 is a critical mediator of FGF signaling and is required for early Xenopus development.

Adaptor Proteins, Signal Transducing↗
PubMed2006

An unexpected role for IL-3 in the embryonic development of hematopoietic stem cells.

Cytokines are important in adult hematopoiesis, yet their function in embryonic hematopoiesis has been largely unexplored. During development, hematopoietic stem cells (HSCs) are found in the aorta-gonad-mesonephros (AGM) region, yolk sac (YS), and placenta and require the Runx1 transcription factor for their normal generation. Since IL-3 is a Runx1 target and this cytokine acts on adult hematopoietic cells, we examined whether IL-3 affects HSCs in the mouse embryo. Using Runx1 haploinsufficient mice, we show that IL-3 amplifies HSCs from E11 AGM, YS, and placenta. Moreover, we show that IL-3 mutant embryos are deficient in HSCs and that IL-3 reveals the presence of HSCs in the AGM and YS prior to the stage at which HSCs are normally detected. Thus, our studies support an unexpected role for IL-3 during development and strongly suggest that IL-3 functions as a proliferation and/or survival factor for the earliest HSCs in the embryo.

Animals↗