3,826 research outputs found
Microglial K(+) channel expression in young adult and aged mice.
The K(+) channel expression pattern of microglia strongly depends on the cells' microenvironment and has been recognized as a sensitive marker of the cells' functional state. While numerous studies have been performed on microglia in vitro, our knowledge about microglial K(+) channels and their regulation in vivo is limited. Here, we have investigated K(+) currents of microglia in striatum, neocortex and entorhinal cortex of young adult and aged mice. Although almost all microglial cells exhibited inward rectifier K(+) currents upon membrane hyperpolarization, their mean current density was significantly enhanced in aged mice compared with that determined in young adult mice. Some microglial cells additionally exhibited outward rectifier K(+) currents in response to depolarizing voltage pulses. In aged mice, microglial outward rectifier K(+) current density was significantly larger than in young adult mice due to the increased number of aged microglial cells expressing these channels. Aged dystrophic microglia exhibited outward rectifier K(+) currents more frequently than aged ramified microglia. The majority of microglial cells expressed functional BK-type, but not IK- or SK-type, Ca(2+) -activated K(+) channels, while no differences were found in their expression levels between microglia of young adult and aged mice. Neither microglial K(+) channel pattern nor K(+) channel expression levels differed markedly between the three brain regions investigated. It is concluded that age-related changes in microglial phenotype are accompanied by changes in the expression of microglial voltage-activated, but not Ca(2+) -activated, K(+) channels
The Long and Viscous Road: Uncovering Nuclear Diffusion Barriers in Closed Mitosis
During Saccharomyces cerevisiae closed mitosis, parental identity is
sustained by the asymmetric segregation of ageing factors. Such asymmetry has
been hypothesized to occur via diffusion barriers, constraining protein lateral
exchange in cellular membranes. Diffusion barriers have been extensively
studied in the plasma membrane, but their identity and organization within the
nucleus remain unknown. Here, we propose how sphingolipid domains, protein
rings, and morphological changes of the nucleus may coordinate to restrict
protein exchange between nuclear lobes. Our spatial stochastic model is based
on several lines of experimental evidence and predicts that, while a
sphingolipid domain and a protein ring could constitute the barrier during
early anaphase; a sphingolipid domain spanning the bridge between lobes during
late anaphase would be entirely sufficient. Additionally, we explore the
structural organization of plausible diffusion barriers. Our work shows how
nuclear diffusion barriers in closed mitosis may be emergent properties of
simple nanoscale biophysical interactions.Comment: 21 pages, 6 figures and supplementary material (including 8
additional figures and a Table
Anomalous Spin and Charge Dynamics of the 2D t-J Model at low doping
We present an exact diagonalization study of the dynamical spin and density
correlation function of the 2D t-J model for hole doping < 25%. Both
correlation functions show a remarkably regular, but completely different
scaling behaviour with both hole concentration and parameter values: the
density correlation function is consistent with that of bosons corresponding to
the doped holes and condensed into the lowest state of the noninteracting band
of width 8t, the spin correlation function is consistent with Fermions in a
band of width J. We show that the spin bag picture gives a natural explanation
for this unusual behaviour.Comment: Revtex-file, 4 PRB pages + 5 figures attached as uu-encoded ps-files
Hardcopies of figures (or the entire manuscript) can also be obtained by
e-mailing to: [email protected]
Validity of the rigid band picture for the t-J model
We present an exact diagonalization study of the doping dependence of the
single particle Green's function in 16, 18 and 20 site clusters of t-J model.
We find evidence for rigid-band behaviour starting from the half-filled case:
upon doping, the topmost states of the quasiparticle band observed in the
photoemisson spectrum at half-filling cross the chemical potential and reappear
as the lowermost states of the inverse photoemission spectrum. Features in the
inverse photoemission spectra which are inconsistent with rigid-band behaviour
are shown to originate from the nontrivial point group symmetry of the ground
state with two holes, which enforces different selection rules than at
half-filling. Deviations from rigid band behaviour which lead to the formation
of the `large Fermi surface' in the momentum distribution occur only at
energies far from the chemical potential. A Luttinger Fermi surface and a
nearest neighbor hopping band do not exist.Comment: Remarks: Revtex file + 7 figures attached as compressed postscript
files Figures can also be obtained by ordinary mail on reques
Entwicklung von Populationen bei Mais (Zea mays L.) Selektionseffizienz und Leistungsfähigkeit
Maize is one of the most important crops around the world. Global players in seed production offer more than hundreds of different varieties. All of them are hybrids whereas open pollinated varieties (OPVs) are rare or extinct. In Germany (and many other European countries) no new OPVs are registered; efforts to do so failed in the past. The main advantage of OPVs is their phenotypic and genetic heterogeneity and thus their ability to adapt to different environmental conditions. This could be of utmost
interest facing the complex challenge of climate change. Populations based on new breeding material were developed and tested in comparison to actual hybrids and
landraces. While the new populations achieved about 80 % of the hybrid yield, landraces failed with only 65 %. The efficiency of selection methods needs to be improved
Direct current arc-plasma synthesis of B-C powder product
Measurement of blood oxygen saturation in biological tissue is of great interest for medical applications as it allows the detection of pathological alterations. Fibre based re-emission spectroscopy enables this parameter to be determined minimally-invasively in organ tissue inside the human body. In this report a measurement system for the contactless determination of blood oxygenation, as well as simulations regarding light diffusion in tissue are presented
In situ observation of shrinking and swelling of normal and compression Chinese fir wood at the tissue, cell and cell wall level
The shrinking and swelling of wood due to moisture changes are intrinsic material properties that control and limit the use of wood in many applications. Herein, hygroscopic deformations of normal and compression wood of Chinese fir (Cunninghamia lanceolata [Lamb.] Hook.) were measured during desorption and absorption processes. The dimensional changes were observed in situ by an environmental scanning electron microscope and analyzed at different hierarchical levels (tissue, cell and cell wall). The relationship between moisture variation and hygroscopic deformation was measured. During initial desorption periods from 95 to 90 or 75% RH, an expansion of the lumen and a shrinkage of the cell wall were observed, revealing a non-uniform and directional deformation of single wood cells. The variation of shrinking or swelling at different hierarchical levels (tissue, cell and cell wall) indicates that the hygroscopic middle lamella plays a role in the deformation at the tissue level. Higher microfibril angles and helical cavities on the cell wall in compression wood correlate with a lower shrinking/swelling ratio. Normal wood showed a more pronounced swelling hysteresis than compression wood, while the sorption hysteresis was almost the same for both wood types. This finding is helpful to elucidate effects of micro- and ultrastructure on sorption. The present findings suggest that the sophisticated system of wood has the abilities to adjust the hygroscopic deformations by fine-tuning its hierarchical structures
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