Search results for "Embryonic Stem Cell"

showing 10 items of 223 documents

Early asymmetric cues triggering the dorsal/ventral gene regulatory network of the sea urchin embryo

2014

Dorsal/ventral (DV) patterning of the sea urchin embryo relies on a ventrally-localized organizer expressing Nodal, a pivotal regulator of the DV gene regulatory network. However, the inceptive mechanisms imposing the symmetry-breaking are incompletely understood. In Paracentrotus lividus, the Hbox12 homeodomain-containing repressor is expressed by prospective dorsal cells, spatially facing and preceding the onset of nodal transcription. We report that Hbox12 misexpression provokes DV abnormalities, attenuating nodal and nodal-dependent transcription. Reciprocally, impairing hbox12 function disrupts DV polarity by allowing ectopic expression of nodal. Clonal loss-of-function, inflicted by b…

Embryo NonmammalianTranscription GeneticEctodermp38 Mitogen-Activated Protein Kinasessymmetry breakingdorsal ventral axis sea urchin embryo nodal homeodomain repressor p38 MAPKAnimals Genetically ModifiedCell polarityMorphogenesisGene Regulatory NetworksBiology (General)ZebrafishSea urchinsea urchin embryoGeneticsbiologyGeneral NeuroscienceQRdorsal/ventral polarityCell PolarityGene Expression Regulation DevelopmentalEmbryoGeneral MedicineCell biologymedicine.anatomical_structureGene Knockdown Techniquesembryonic structuresParacentrotusMedicineCuesResearch Articleanimal structuresQH301-705.5Nodal ProteinScienceEmbryonic DevelopmentSettore BIO/11 - Biologia Molecolarep38 MAPKModels BiologicalGeneral Biochemistry Genetics and Molecular Biologybiology.animalEctodermmedicineAnimalsBody PatterningHomeodomain ProteinsGeneral Immunology and MicrobiologyotherCell Biologybiology.organism_classificationEmbryonic stem cellhomeodomain repressorRepressor ProteinsDevelopmental Biology and Stem CellsnodalNODALDevelopmental biologyeLife
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Sea urchin embryos as a model system for studying autophagy induced by cadmium stress

2011

It is well known that sea urchin embryos are able to activate different defense strategies against stress. We previously demonstrated that cadmium treatment triggers the accumulation of metal in embryonic cells and the activation of defense systems depending on concentration and exposure time, through the synthesis of heat shock proteins and/or the initiation of apoptosis. Here we show that Paracentrotus lividus embryos exposed to Cd adopt autophagy as an additional stratagem to safeguard the developmental program. At present, there are no data focusing on the role of this process in embryo development of marine organisms. In this paper we utilized different techniques to detect autophagy i…

Embryo Nonmammaliananimal structuresImmunoblottingFluorescent Antibody Techniquechemistry.chemical_elementBiologyModels BiologicalParacentrotus lividusStress PhysiologicalHeat shock proteinBotanyAutophagyAnimalsSettore BIO/06 - Anatomia Comparata E Citologiaautophagy cadmium stress acidic vesicular organelles bafilomycin A1 LC3 Paracentrotus lividus embryosMolecular BiologyOrganellesCadmiumStaining and LabelingAutophagyEmbryogenesisEmbryoCell Biologybiology.organism_classificationEmbryonic stem cellAcridine OrangeCell biologychemistryNeutral RedApoptosisembryonic structuresParacentrotusMicrotubule-Associated ProteinsCadmiumDensitometryAutophagy
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An Incremental Analysis of the Embryonic Development of the Tobacco Hornworm,Manduca sexta

1987

Summary A timetable of the embryonic development of Manduca sexta has been compiled to serve as a basis for physiological studies. Embryogenesis is complete within 117 hr at 24° C and was analyzed by examining specimens representing 20 stages, i.e. intervals of 5% of the total developmental time. Stage 0 denotes the newly deposited egg. Germ band formation, gastrulation, differentiation of tissues and organs, and blastokinesis are described in detail. By stage 1 (6 hr post-oviposition) the cellular blastoderm is evident and the presumptive serosal and embryonic cells are distinguishable. At stage 2 the germ band has separated from the blastoderm, and by stage 3 it has elongated enormously, …

EmbryogenesisOrganogenesisCell BiologyAnatomyBiologyProthoracic glandbiology.organism_classificationEmbryonic stem cellDorsal closureGastrulationManduca sextaAnimal Science and ZoologyBlastodermDevelopmental BiologyInternational Journal of Invertebrate Reproduction and Development
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Disruption of apical-basal polarity of human embryonic stem cells enhances hematoendothelial differentiation

2007

Abstract During murine development, the formation of tight junctions and acquisition of polarity are associated with allocation of the blastomeres on the outer surface of the embryo to the trophoblast lineage, whereas the absence of polarization directs cells to the inner cell mass. Here, we report the results of ultrastructural analyses that suggest a similar link between polarization and cell fate in human embryos. In contrast, the five human embryonic stem cell (hESC) lines displayed apical-basal, epithelial-type polarity with electron-dense tight junctions, apical microvilli, and asymmetric distribution of organelles. Consistent with these findings, molecules that are components of tigh…

Embryoid bodyBiologyCell fate determinationMiceCell polarityAnimalsHumansInner cell massCells CulturedEmbryonic Stem Cellsreproductive and urinary physiologyembryoid body formationTight junctionMesenchymal stem cellapical-basal polarityCell PolarityCell DifferentiationEpithelial CellsCell Biologyinner cell masshuman embryonic stem cellsEmbryonic stem cellHematopoiesisCell biologyDrug CombinationsIntercellular JunctionsPhenotypeembryonic structuresMolecular Medicinehernatoendothelial differentiationProteoglycansCollagenEndothelium VascularLamininStem cellDevelopmental Biology
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Defining the genomic signature of totipotency and pluripotency during early human development.

2013

The genetic mechanisms governing human pre-implantation embryo development and the in vitro counterparts, human embryonic stem cells (hESCs), still remain incomplete. Previous global genome studies demonstrated that totipotent blastomeres from day-3 human embryos and pluripotent inner cell masses (ICMs) from blastocysts, display unique and differing transcriptomes. Nevertheless, comparative gene expression analysis has revealed that no significant differences exist between hESCs derived from blastomeres versus those obtained from ICMs, suggesting that pluripotent hESCs involve a new developmental progression. To understand early human stages evolution, we developed an undifferentiation netw…

EmbryologyBlastomeresMicroarraysCellular differentiationGene ExpressionCell Fate DeterminationMolecular Cell BiologyGene Regulatory NetworksInduced pluripotent stem cellreproductive and urinary physiologyGeneticsMultidisciplinarySystems BiologyStem CellsQTotipotentRGenomic signatureCell DifferentiationGenomicsCell biologyFunctional GenomicsBlastocyst Inner Cell MassBlastocyst Inner Cell Massembryonic structuresMedicineResearch ArticlePluripotent Stem CellsSystems biologyCell PotencyScienceEmbryonic DevelopmentBiologyMolecular GeneticsGeneticsHumansGene NetworksBiologyEmbryonic Stem CellsGenome HumanGene Expression ProfilingBio-OntologiesComputational BiologyMolecular Sequence AnnotationComparative GenomicsMolecular DevelopmentEmbryonic stem cellSignalingSignaling NetworksGene expression profilingGenome Expression AnalysisTotipotent Stem CellsDevelopmental BiologyPLoS ONE
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Hormonal and embryonic regulation of chemokines IL-8, MCP-1 and RANTES in the human endometrium during the window of implantation.

2002

Chemokines are a family of small polypeptides which specialize in the attraction of leukocytes. The presence of specific leukocyte subsets at the implantation site is an important element of the complex, and not completely understood, process of embryonic implantation. This report includes the investigation of the in-vivo immunolocalization and hormonal regulation of interleukin (IL)-8, monocyte chemotactic protein (MCP)-1 and RANTES (regulated upon activation normal T-cell expressed and secreted) in the human endometrium during hormone replacement therapy cycles for oocyte recipients in an IVF programme. In addition, we have analysed the embryonic regulation of these endometrial epithelial…

Embryologymedicine.medical_specialtyChemokineStromal cellmedicine.medical_treatmentFertilization in VitroEndometriumAndrologyEndometriumPregnancyInternal medicineGeneticsmedicineHumansBlastocystInterleukin 8Embryo ImplantationMolecular BiologyChemokine CCL5Chemokine CCL2biologyMonocyteInterleukin-8Obstetrics and GynecologyCell BiologyEmbryonic stem cellCoculture TechniquesEndocrinologymedicine.anatomical_structureCytokineBlastocystReproductive MedicineCulture Media Conditionedbiology.proteinFemaleDevelopmental BiologyMolecular human reproduction
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Hsa-miR-30d, secreted by the human endometrium, is taken up by the pre-implantation embryo and might modify its transcriptome.

2015

During embryo implantation, the blastocyst interacts with and regulates the endometrium, and endometrial fluid secreted by the endometrial epithelium nurtures the embryo. Here, we propose that maternal microRNAs (miRNAs) might act as transcriptomic modifier of the pre-implantation embryo. Microarray profiling revealed that six of 27 specific, maternal miRNAs were differentially expressed in the human endometrial epithelium during the window of implantation – a brief phase of endometrial receptivity to the blastocyst – and were released into the endometrial fluid. Further investigation revealed that hsa-miR-30d, the expression levels of which were most significantly upregulated, was secreted…

Endometrial fluidanimal structuresBlotting WesternEmbryonic DevelopmentBiologyEndometriumPolymerase Chain ReactionTranscriptomeEndometriumMiceMicroscopy Electron TransmissionmicroRNAmedicineAnimalsHumansBlastocystMolecular BiologyEmbryo adhesionPre-implantation embryoMicroarray analysis techniquesEmbryogenesisGene Expression Regulation DevelopmentalEmbryoMicroarray AnalysisMolecular biologyEmbryonic stem cellImmunohistochemistryCell biologyHas-miR-30dMicroRNAsmedicine.anatomical_structureBlastocystMicroscopy Fluorescenceembryonic structuresFemaleTranscriptomeDevelopmental BiologyDevelopment (Cambridge, England)
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In Vitro Differentiation of Mouse Embryonic Stem Cells: Hematopoietic and Vascular Cell Types

2003

Publisher Summary Embryonic stem cells have been posited as sources of differentiated cell types for regenerative medicine. One of the most enticing cell types is the recently described endothelial progenitor cell (EPC) which can contribute to blood vessels and is a candidate for therapy against vascular diseases. This chapter describes an in vitro differentiation system, which results in the generation of endothelial, smooth muscle, and hematopoietic cells from ES cells. An ES-derived equivalent of the lateral plate mesoderm (LPM) has been generated, a critical source of vascular and hematopoietic cells during embryonic development. This in vitro differentiation system is useful for the an…

Endothelial stem cellCell typeCellular differentiationImmunologyEmbryoid bodyStem cellBiologyEndothelial progenitor cellEmbryonic stem cellCell biologyAdult stem cell
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Lymphatic endothelial progenitors bud from the cardinal vein and intersomitic vessels in mammalian embryos.

2012

Abstract The lymphatic vasculature preserves tissue fluid balance by absorbing fluid and macromolecules and transporting them to the blood vessels for circulation. The stepwise process leading to the formation of the mammalian lymphatic vasculature starts by the expression of the gene Prox1 in a subpopulation of blood endothelial cells (BECs) on the cardinal vein (CV) at approximately E9.5. These Prox1-expressing lymphatic endothelial cells (LECs) will exit the CV to form lymph sacs, primitive structures from which the entire lymphatic network is derived. Until now, no conclusive information was available regarding the cellular processes by which these LEC progenitors exit the CV without co…

EndotheliumMesenchymegovernment.form_of_governmentRecombinant Fusion ProteinsImmunologyEmbryonic DevelopmentMice TransgenicBiologyBiochemistryMiceMicroscopy Electron TransmissionCell MovementVascular BiologymedicineAnimalsLymph sacsProgenitor cellEmbryonic Stem CellsHomeodomain ProteinsMice KnockoutBuddingMembrane GlycoproteinsCommon cardinal veinsTumor Suppressor ProteinsfungiCell BiologyHematologyAnatomyAdherens JunctionsCadherinsEmbryo MammalianCoronary VesselsCell biologyPlatelet Endothelial Cell Adhesion Molecule-1Lymphatic Endotheliummedicine.anatomical_structureLymphatic systemgovernmentsense organsEndothelium LymphaticBlood
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Mechanosensory Genes Pkd1 and Pkd2 Contribute to the Planar Polarization of Brain Ventricular Epithelium

2015

Directional beating of ependymal (E) cells9 cilia in the walls of the ventricles in the brain is essential for proper CSF flow. E cells display two forms of planar cell polarity (PCP): rotational polarity of individual cilium and translational polarity (asymmetric positioning of cilia in the apical area). The orientation of individual E cells varies according to their location in the ventricular wall (location-specific PCP). It has been hypothesized that hydrodynamic forces on the apical surface of radial glia cells (RGCs), the embryonic precursors of E cells, could guide location-specific PCP in the ventricular epithelium. However, the detection mechanisms for these hydrodynamic forces hav…

Ependymal Cellurogenital systemGeneral NeuroscienceCiliumciliaplanar cell polarityBiologyurologic and male genital diseasesEmbryonic stem cellNeural stem cellEpitheliumfemale genital diseases and pregnancy complicationsCell biologyneural stem cellmedicine.anatomical_structureCell polaritymedicinepolycystinEpendymaepitheliumEpendymoglial Cellsependymal cell
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