70 research outputs found

    Detektion der Side Population zur Identifizierung von Stammzellen

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    Inclusions under remnant pressure in diamond: a multi-technique approach

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    Measurement of the remnant pressure sustained by a mineral inclusion within a diamond can allow calculation of the source pressure and temperature conditions of the diamond formation. While Raman spectroscopy (point analyses and 2D mapping) has been the most commonly used non-destructive method for measuring this remnant pressure, two new techniques (quantitative birefringence analysis and in situ X-ray diffraction) have recently been developed. In this paper we apply all of these techniques to the study of two diamonds. The first is a diamond twin (made) from Shandong (China), containing two olivine inclusions. Analysis of the largest inclusion by the birefringence and X-ray techniques returned compatible values for the remnant pressure of 0.1-0.2 GPa. However, while 2D Raman mapping of the diamond host qualitatively confirmed the presence of a radial stress field, the low remnant pressures values were too small to be detected by pressure shifts in the olivine's Raman spectrum. The second sample studied was a rounded dodecahedral diamond (unknown origin) containing several coesite inclusions. Its morphology prevented quantitative birefringence analysis or Raman mapping being performed but Raman analyses on three inclusions (2.2-2.5 GPa) provided similar results to those obtained by X-ray diffraction from a single inclusion (2.7 GPa); all of these values lie within the range of previous published remnant pressures for coesite in diamond. Calculation of the source pressure and temperature conditions for both diamond samples returned anomalously low values, both below the diamond stability field for a range of mantle temperatures (950-1350 degrees C). The reasons for this are due to violations of the fundamental assumptions upon which such studies of these elastic effects in diamond are based. Although previous studies showed that olivine inclusions have the potential to record reasonable formation pressures under favourable conditions, the present study re-iterates the serious concerns of using the coesite-in-diamond geobarometer. It is inferred that, as the remnant pressures in the coesite-diamond pair are so high, there is a high probability that the diamond will undergo some plastic deformation, thus reducing the elastic behaviour and leading to severe underestimation of entrapment pressure

    Erratum to : Quantifying strain birefringence halos around inclusions in diamond

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    This erratum is for an article that appeared in Contributions to mineral petrol, Vol. 160, No. 5, p.705-717, and may be found at http://dx.doi.org/10.1007/s00410-010-0503-5.1 page(s

    Junctional adhesion molecule A participates in the formation of apico-basal polarity through different domains

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    Junctional adhesion molecule (JAM)-A is an integral membrane protein at tight junctions of epithelial cells which associates with the cell polarity protein PAR-3. Here, we demonstrate that downregulation of JAM-A impairs the ability of MDCK II cells to form cysts in a threedimensional matrix indicating the requirement of JAM-A for the development of apico-basal polarity. To define the regions of JAM-A important for this function, we have generated MDCK II cell lines stably expressing inducible JAM-A mutants. Mutants of JAM-A which were designed to mislocalize strongly impaired the development of cysts and the formation of functional tight junctions. Surprisingly, similar mutants that lacked the PDZ domainbinding motif at the C-terminus were still impaired in apico-basal polarity formation suggesting that additional regions within the cytoplasmic tail of JAM-A are important for the function of JAM-A. A JAM-A mutant lacking the first Ig-like domain necessary for homophilic binding localized to cell–cell contacts similar to wild-type JAM-A. However, despite this same localization, this mutant interfered with cell polarity and tight junction formation. Together our findings suggest an important role for JAM-A in the development of apicobasal polarity in epithelial cells and identify regions in JAM-A which are critical for this role
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