31 research outputs found

    Microstructured blood vessel surrogates reveal structural tropism of motile malaria parasites

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    Plasmodium sporozoites, the highly motile forms of the malaria parasite, are transmitted naturally by mosquitoes and traverse the skin to find, associate with, and enter blood capillaries. Research aimed at understanding how sporozoites select blood vessels is hampered by the lack of a suitable experimental system. Arrays of uniform cylindrical pillars can be used to study small cells moving in controlled environments. Here, an array system displaying a variety of pillars with different diameters and shapes is developed in order to investigate how Plasmodium sporozoites associate to the pillars as blood vessel surrogates. Investigating the association of sporozoites to pillars in arrays displaying pillars of different diameters reveals that the crescent-shaped parasites prefer to associate with and migrate around pillars with a similar curvature. This suggests that after transmission by a mosquito, malaria parasites may use a structural tropism to recognize blood capillaries in the dermis in order to gain access to the blood stream

    Crystallographic analysis of temperate ice on Rhonegletscher, Swiss Alps

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    Crystal orientation fabric (COF) analysis provides information about the c-axis orientation of ice grains and the associated anisotropy and microstructural information about deformation and recrystallisation processes within the glacier. This information can be used to introduce modules that fully describe the microstructural anisotropy or at least direction-dependent enhancement factors for glacier modelling. The COF was studied at an ice core that was obtained from the temperate Rhonegletscher, located in the central Swiss Alps. Seven samples, extracted at depths between 2 and 79 m, were analysed with an automatic fabric analyser. The COF analysis revealed conspicuous four-maxima patterns of the c-axis orientations at all depths. Additional data, such as microstructural images, produced during the ice sample preparation process, were considered to interpret these patterns. Furthermore, repeated high-precision global navigation satellite system (GNSS) surveying allowed the local glacier flow direction to be determined. The relative movements of the individual surveying points indicated longitudinal compressive stresses parallel to the glacier flow. Finally, numerical modelling of the ice flow permitted estimation of the local stress distribution. An integrated analysis of all the data sets provided indications and suggestions for the development of the four-maxima patterns. The centroid of the four-maxima patterns of the individual core samples and the coinciding maximum eigenvector approximately align with the compressive stress directions obtained from numerical modelling with an exception for the deepest sample. The clustering of the c axes in four maxima surrounding the predominant compressive stress direction is most likely the result of a fast migration recrystallisation. This interpretation is supported by air bubble analysis of large-area scanning macroscope (LASM) images. Our results indicate that COF studies, which have so far predominantly been performed on cold ice samples from the polar regions, can also provide valuable insights into the stress and strain rate distribution within temperate glaciers

    Regulatory and coding sequences of TRNP1 co-evolve with brain size and cortical folding in mammals

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    Brain size and cortical folding have increased and decreased recurrently during mammalian evolution. Identifying genetic elements whose sequence or functional properties co-evolve with these traits can provide unique information on evolutionary and developmental mechanisms. A good candidate for such a comparative approach is TRNP1, as it controls proliferation of neural progenitors in mice and ferrets. Here, we investigate the contribution of both regulatory and coding sequences of TRNP1 to brain size and cortical folding in over 30 mammals. We find that the rate of TRNP1 protein evolution (omega) significantly correlates with brain size, slightly less with cortical folding and much less with body size. This brain correlation is stronger than for >95% of random control proteins. This co-evolution is likely affecting TRNP1 activity, as we find that TRNP1 from species with larger brains and more cortical folding induce higher proliferation rates in neural stem cells. Furthermore, we compare the activity of putative cis-regulatory elements (CREs) of TRNP1 in a massively parallel reporter assay and identify one CRE that likely co-evolves with cortical folding in Old World monkeys and apes. Our analyses indicate that coding and regulatory changes that increased TRNP1 activity were positively selected either as a cause or a consequence of increases in brain size and cortical folding. They also provide an example how phylogenetic approaches can inform biological mechanisms, especially when combined with molecular phenotypes across several species

    Sensitive and powerful single-cell RNA sequencing using mcSCRB-seq

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    Single-cell RNA sequencing (scRNA-seq) has emerged as a central genome-wide method to characterize cellular identities and processes. Consequently, improving its sensitivity, flexibility, and cost-efficiency can advance many research questions. Among the flexible platebased methods, single-cell RNA barcoding and sequencing (SCRB-seq) is highly sensitive and efficient. Here, we systematically evaluate experimental conditions of this protocol and find that adding polyethylene glycol considerably increases sensitivity by enhancing cDNA synthesis. Furthermore, using Terra polymerase increases efficiency due to a more even cDNA amplification that requires less sequencing of libraries. We combined these and other improvements to develop a scRNA-seq library protocol we call molecular crowding SCRB-seq (mcSCRB-seq), which we show to be one of the most sensitive, efficient, and flexible scRNA-seq methods to date

    "Eigentlich hätte ich nach drei Monaten tot sein müssen, aber ich lebe immer noch!" – die Grenzen des lebenslangen Lernens aus der Perspektive von Biographie und Lebenslauf

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    All jene Erziehungswissenschaftler*innen, für die das lebenslange Lernen eine pädagogische Leitkategorie darstellt, sind sich sehr wohl darüber bewusst, dass der Begriff bei nahen und fernen akademischen Nachbarn – also bei anderen erziehungswissenschaftlichen Subdisziplinen (z. B. Schulpädagogik) und in der Psychologie, vor allem aber in der Soziologie – u. a. aufgrund seines Charakters als absolute Metapher (de Haan 1991; Dellori 2016) nicht selten auf Vorbehalte, ja sogar auf eine massive Reserviertheit stößt. Das hat zum einen mit der großen Nähe dieser Kategorie zur Sinnwelt der Alltagswelt zu tun. Zum anderen hängt dies aber auch mit der Neigung der Bildungspolitik zusammen, diesbezügliche Konzepte im Sinne einer Pädagogisierung sozialer Probleme einseitig zu instrumentalisieren. ..
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