315 research outputs found

    Transient pluripotent cell populations during primitive ectoderm formation: correlation of in vivo and in vitro pluripotent cell development.

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    Formation and differentiation of a pluripotent cell population is central to mammalian development, and the isolation, identification and manipulation of human pluripotent cells is predicted to be of therapeutic use. Within the early mammalian embryo, two distinct populations of pluripotent cells have been described: the inner cell mass (ICM), which differentiates to form a second pluripotent cell populations, the primitive ectoderm. Indirect evidence suggests the existence of temporally distinct intermediate pluripotent cell populations as primitive ectoderm is formed. We coupled an in vitro model of primitive ectoderm formation (the transition of embryonic stem cells to early primitive ectoderm-like (EPL) cells) with ddPCR-based techniques to identify three novel genes, Psc1, CRTR-1 and PRCE, that were expressed differently during pluripotent cell progression. Detailed mapping of these genes with Oct4, Rex1 and Fgf5 on pregastrulation embryos provided the first molecular evidence for the existence of successive, temporally distinct pluripotent cell populations in the embryo between the ICM and primitive ectoderm. No evidence was found for spatial heterogeneity within the Oct4+ pool. The transition between populations correlated with morphological or developmental alterations in pluripotent cells in vivo. Genes that are temporally expressed during pluripotent cell progression may provide an opportunity for molecular discrimination of pluripotent cells at different stages of maturation in vivo and an understanding of the cellular origins and properties of pluripotent cell lines isolated from diverse sources. Furthermore, the strong correlation of gene expression demonstrated between EPL cell formation in vitro and primitive ectoderm formation in vivo validates EPL cells as a model for primitive ectoderm, thereby providing a model system for the investigation of pluripotent differentiation and an opportunity for directed differentiation of pluripotent cells to therapeutically useful cell populations.T. A. Pelton, S. Sharma, T. C. Schulz, J. Rathjen and P. D. Rathje

    Characterization of functional domains of the tenascin-R (restrictin) polypeptide: cell attachment site, binding with F11 and enhancement of F11 mediated neurite outgrowth by tenascin-R

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    The extracellular matrix glycoprotein tenascin-R (TN-R) is a multidomain protein implicated in neural cell adhesion. To analyze the structure-function relationship of the different domains of TN-R, several recombinant TN-R fragments were expressed in bacterial cells. Two distinct binding regions were localized on the TN-R polypeptide: a region binding the axon-associated immunoglobulin (Ig)-like F11 protein and a cell attachment site. The binding region of the glycosylphosphatidylinositol (GPI)-anchored F11 was allocated to the second and third fibronectin type III (FNIII)-like domain within TN-R. By using a mutant polypeptide of F11 containing only Ig-like domains, a direct interaction between the Ig-like domains of F11 and FNIII-like domains 2-3 of TN-R was demonstrated. The interaction of TN-R with F11 in in vitro cultures enhanced F11-mediated neurite outgrowth, suggesting that the combined action of F11 and TN-R might be of regulatory influence on axon extension. A cell attachment region was identified in the FNIII-like domain eight of TN-R by domain-specific antibodies and fusion constructs. This site is distinct from the F11 binding site within TN-R

    Micro-managing the pancreatic β cell

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    A new foundational crisis in mathematics, is it really happening?

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    The article reconsiders the position of the foundations of mathematics after the discovery of HoTT. Discussion that this discovery has generated in the community of mathematicians, philosophers and computer scientists might indicate a new crisis in the foundation of mathematics. By examining the mathematical facts behind HoTT and their relation with the existing foundations, we conclude that the present crisis is not one. We reiterate a pluralist vision of the foundations of mathematics. The article contains a short survey of the mathematical and historical background needed to understand the main tenets of the foundational issues.Comment: Final versio

    44 Resistenzzüchtung / Widerstandsfähigkeit gegen Schadorganismen I

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    44-1 - Bewertung der Feldresistenz verschiedener Winterrapssorten gegenüber Verticillium longisporum mittels quantitativer PCRClassification of winter oilseed rape resistance towards the soilborne pathogen Verticillium longisporum by quantitative PCRJessica Knüfer, Daniel Teshome Lopisso, Birger Koopmann, Andreas von Tiedemann44-2 - Identification and characterization of three putative compatibility factor genes involved in the plant – Verticillium interactionIdentifikation und Charakterisierung drei putativer Kompatibilitätsfaktoren in der Pflanze – Verticillium InteraktionRoxana Hossain, Lisa Krapoth, Dirk Schenke, Daguang Cai44-3 - Impact of cultivar resistance to Verticillium longisporum on drought stress tolerance of winter oilseed rape (Brassica napus)Einfluss der Sortenresistenz gegen Verticillium longisporum auf die Trockenstresstoleranz von Winterraps (Brassica napus)Daniel Lopisso, Jessica Knüfer, Birger Koopmann, Andreas von Tiedemann44-4 - Wirksamkeit von Majorgenen in Raps gegenüber Phoma lingam unter Berücksichtigung steigender Temperaturen und des PathotypenspektrumsEfficacy of major genes in oilseed rape against Phoma lingam with regard to rising temperatures and the population structureMark Winter, Coretta Klöppel , Fadeke Fajemisin, Birger Koopmann44-5 - Anfälligkeit von Raps -Resynthesen und -Sorten auf den Rapsstängelrüssler (Ceutorhynchus napi Gyll.) Befall – potentielle ResistenzfaktorenSusceptibility of resynthesized lines and cultivars of oilseed rape on rape stem weevil (Ceutorhynchus napi Gyll.) infestation – potential plant traits responsible for resistanceHeike Schäfer-Kösterke, Bernd Ulber44-6 - Zweijähriges Rassen-Monitoring von Exserohilum turcicum in europäischen MaisanbaugebietenTwo-year race monitoring for Exserohilum turcicum in European maize growing regionsHendrik Hanekamp, Andreas von Tiedemann, Birger Koopmann44-7 - Smart breeding und Nutzung des Genpools von Wildarten zur Verbesserung der Krankheitsresistenz von KartoffelnSmart breeding and exploitation of the genepool from wild species for the improvement of disease resistance in potatoJanine König, Marion Nachtigall, Ramona Thieme, Jörg Schubert44-8 - Neue Ansätze für eine effizientere Resistenzzüchtung bei RebenNew approaches for increasing efficieny of grapevine resistance breedingRudolf Eibach, Reinhard Töpfe

    The tomato Prf complex is a molecular trap for bacterial effectors based on Pto transphosphorylation

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    The bacteria Pseudomonas syringae is a pathogen of many crop species and one of the model pathogens for studying plant and bacterial arms race coevolution. In the current model, plants perceive bacteria pathogens via plasma membrane receptors, and recognition leads to the activation of general defenses. In turn, bacteria inject proteins called effectors into the plant cell to prevent the activation of immune responses. AvrPto and AvrPtoB are two such proteins that inhibit multiple plant kinases. The tomato plant has reacted to these effectors by the evolution of a cytoplasmic resistance complex. This complex is compromised of two proteins, Prf and Pto kinase, and is capable of recognizing the effector proteins. How the Pto kinase is able to avoid inhibition by the effector proteins is currently unknown. Our data shows how the tomato plant utilizes dimerization of resistance proteins to gain advantage over the faster evolving bacterial pathogen. Here we illustrate that oligomerisation of Prf brings into proximity two Pto kinases allowing them to avoid inhibition by the effectors by transphosphorylation and to activate immune responses

    A Computation of the Maximal Order Type of the Term Ordering on Finite Multisets

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    We give a sharpening of a recent result of Aschenbrenner and Pong about the maximal order type of the term ordering on the finite multisets over a wpo. Moreover we discuss an approach to compute maximal order types of well-partial orders which are related to tree embeddings

    Mechanical Behaviour of the Short Models of LHC Main Dipole Magnets

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    A series of single and twin aperture 1 metre magnet models has been built and tested in the framework of the R&D program of main superconducting dipole magnets for the Large Hadron Collider project. The se models, designed for a nominal field of 8.3 T at 1.8 K, have been constructed to test the performance of SC coils and to optimise various design options for the full length 15 metre long dipoles. T he models have been extensively equipped with a specially developed mechanical instrumentation, enabling both the control of main assembly parameters - like coil azimuthal and axial pre-load, stress i n the outer shrinking cylinder - and also the monitoring of magnet behaviour during cooling and energising, under the action of electromagnetic forces. The instrumentation used, mainly based on strain gauge transducers, is described and the results of mechanical measurements obtained during power tests of the models are discussed and compared with the design predictions based on Finite Element calc ulations

    SORCS1 and SORCS3 control energy balance and orexigenic peptide production

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    SORCS1 and SORCS3 are two related sorting receptors expressed in neurons of the arcuate nucleus of the hypothalamus. Using mouse models with individual or dual receptor deficiencies, we document a previously unknown function of these receptors in central control of metabolism. Specifically, SORCS1 and SORCS3 act as intracellular trafficking receptors for tropomyosin-related kinase B to attenuate signaling by brain-derived neurotrophic factor, a potent regulator of energy homeostasis. Loss of the joint action of SORCS1 and SORCS3 in mutant mice results in excessive production of the orexigenic neuropeptide agouti-related peptide and in a state of chronic energy excess characterized by enhanced food intake, decreased locomotor activity, diminished usage of lipids as metabolic fuel, and increased adiposity, albeit at overall reduced body weight. Our findings highlight a novel concept in regulation of the melanocortin system and the role played by trafficking receptors SORCS1 and SORCS3 in this process

    Argonaute2 regulates the pancreatic β-cell secretome

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    Argonaute2 (Ago2) is an established component of the microRNA-induced silencing complex. Similar to miR-375 loss-of-function studies, inhibition of Ago2 in the pancreatic beta-cell resulted in enhanced insulin release underlining the relationship between these two genes. Moreover, as the most abundant microRNA in pancreatic endocrine cells, miR-375 was also observed to be enriched in Ago2-associated complexes. Both Ago2 and miR-375 regulate the pancreatic beta-cell secretome and we identified using quantitative mass spectrometry the enhanced release of a set of proteins or secretion signature in response to a glucose stimulus using the murine beta-cell line, MIN6. In addition, loss of Ago2 resulted in the increased expression of miR-375 target genes, including gephyrin and ywhaz. These targets positively contribute to exocytosis indicating they may mediate the functional role of both miR-375 and Ago proteins in the pancreatic beta-cell by influencing the secretory pathway. This study specifically addresses the role of Ago2 in the systemic release of proteins from beta-cells and highlights the contribution of the microRNA pathway to the function of this cell type
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