182 research outputs found
Transverse Magnetic Anisotropy in Mn12-acetate: Direct Determination by Inelastic Neutron Scattering
A high resolution inelastic neutron scattering (INS) study of fully
deuterated Mn-acetate provides the most accurate spin Hamiltonian
parameters for this prototype single molecule magnet so far. The
Mn-clusters deviate from axial symmetry, a non-zero rhombic term in the
model Hamiltonian leading to excellent agreement with observed positions and
intensities of the INS peaks. The following parameter set provides the best
agreement with the experimental data: meV,
meV, meV and
\textit{E} meV. Crystal dislocations are not
the likely cause of the symmetry lowering. Rather, this study lends strong
support to a recently proposed model, which is based on the presence of several
molecular isomers with distinct spin Hamiltonian parameters.Comment: 4 pages, 4 figure
Pressure Dependence of the Magnetic Anisotropy in the "Single-Molecule Magnet" [Mn4O3Br(OAc)3(dbm)3]
The anisotropy splitting in the ground state of the single-molecule magnet
[Mn4O3Br(OAc)3(dbm)3] is studied by inelastic neutron scattering as a function
of hydrostatic pressure. This allows a tuning of the anisotropy and thus the
energy barrier for slow magnetisation relaxation at low temperatures. The value
of the negative axial anisotropy parameter changes from
-0.0627(1) meV at ambient to -0.0603(3) meV at 12 kbar pressure, and in the
same pressure range the height of the energy barrier between up and down spins
is reduced from 1.260(5) meV to 1.213(9) meV. Since the bond is
significantly softer and thus more compressible than the bonds,
pressure induces a tilt of the single ion Mn anisotropy axes, resulting
in the net reduction of the axial cluster anisotropy.Comment: 4 pages, 3 figure
Narcolepsy-Cataplexy Today
peer reviewedDiagnostic criteria and pathophysiology of narcolepsy-
cataplexy have evolved considerably over the last 10 years.
The main cause, already mentioned in a previous paper, in the
Revue Médicale de Liège, in 2002, is based, in human beings,
on a destruction of specific cells located in the lateral and
posterior part of the hypothalamus (the perifornical nuclei,
containing some 70,000 neurons), producing peptides which
stimulate the central nervous system; they are called hypocretins
or orexins. The role of autoimmunity in their disappearance
becomes more evident. The treatment is simplified but
remains symptomatic. It is mainly based on Sodium Oxybate
or Gamma-Hydroxybutyrate, syrup, prescribed for the night.
The authors report on their own experience in this regard and
on future therapeutics more targeted towards the cause of the
disease
Nestin-positive mesenchymal stem cells favour the astroglial lineage in neural progenitors and stem cells by releasing active BMP4
BACKGROUND: Spontaneous repair is limited after CNS injury or degeneration because neurogenesis and axonal regrowth rarely occur in the adult brain. As a result, cell transplantation has raised much interest as potential treatment for patients with CNS lesions. Several types of cells have been considered as candidates for such cell transplantation and replacement therapies. Foetal brain tissue has already been shown to have significant effects in patients with Parkinson's disease. Clinical use of the foetal brain tissue is, however, limited by ethical and technical problems as it requires high numbers of grafted foetal cells and immunosuppression. Alternatively, several reports suggested that mesenchymal stem cells, isolated from adult bone marrow, are multipotent cells and could be used in autograft approach for replacement therapies. RESULTS: In this study, we addressed the question of the possible influence of mesenchymal stem cells on neural stem cell fate. We have previously reported that adult rat mesenchymal stem cells are able to express nestin in defined culture conditions (in the absence of serum and after 25 cell population doublings) and we report here that nestin-positive (but not nestin-negative) mesenchymal stem cells are able to favour the astroglial lineage in neural progenitors and stem cells cultivated from embryonic striatum. The increase of the number of GFAP-positive cells is associated with a significant decrease of the number of Tuj1- and O4-positive cells. Using quantitative RT-PCR, we demonstrate that mesenchymal stem cells express LIF, CNTF, BMP2 and BMP4 mRNAs, four cytokines known to play a role in astroglial fate decision. In this model, BMP4 is responsible for the astroglial stimulation and oligodendroglial inhibition, as 1) this cytokine is present in a biologically-active form only in nestin-positive mesenchymal stem cells conditioned medium and 2) anti-BMP4 antibodies inhibit the nestin-positive mesenchymal stem cells conditioned medium inducing effect on astrogliogenesis. CONCLUSIONS: When thinking carefully about mesenchymal stem cells as candidates for cellular therapy in neurological diseases, their effects on resident neural cell fate have to be considered
Dynamic Phase Transitions in Cell Spreading
We monitored isotropic spreading of mouse embryonic fibroblasts on
fibronectin-coated substrates. Cell adhesion area versus time was measured via
total internal reflection fluorescence microscopy. Spreading proceeds in
well-defined phases. We found a power-law area growth with distinct exponents
a_i in three sequential phases, which we denote basal (a_1=0.4+-0.2), continous
(a_2=1.6+-0.9) and contractile (a_3=0.3+-0.2) spreading. High resolution
differential interference contrast microscopy was used to characterize local
membrane dynamics at the spreading front. Fourier power spectra of membrane
velocity reveal the sudden development of periodic membrane retractions at the
transition from continous to contractile spreading. We propose that the
classification of cell spreading into phases with distinct functional
characteristics and protein activity patterns serves as a paradigm for a
general program of a phase classification of cellular phenotype. Biological
variability is drastically reduced when only the corresponding phases are used
for comparison across species/different cell lines.Comment: 4 pages, 5 figure
Periodic Lamellipodial Contractions Correlate with Rearward Actin Waves
AbstractCellular lamellipodia bind to the matrix and probe its rigidity through forces generated by rearward F-actin transport. Cells respond to matrix rigidity by moving toward more rigid matrices using an unknown mechanism. In spreading and migrating cells we find local periodic contractions of lamellipodia that depend on matrix rigidity, fibronectin binding and myosin light chain kinase (MLCK). These contractions leave periodic rows of matrix bound β3-integrin and paxillin while generating waves of rearward moving actin bound α-actinin and MLCK. The period between contractions corresponds to the time for F-actin to move across the lamellipodia. Shortening lamellipodial width by activating cofilin decreased this period proportionally. Increasing lamellipodial width by Rac signaling activation increased this period. We propose that an actin bound, contraction-activated signaling complex is transported locally from the tip to the base of the lamellipodium, activating the next contraction/extension cycle
Butterfly Hysteresis and Slow Relaxation of the Magnetization in (Et4N)3Fe2F9: Manifestations of a Single-Molecule Magnet
(Et4N)3Fe2F9 exhibits a butterfly--shaped hysteresis below 5 K when the
magnetic field is parallel to the threefold axis, in accordance with a very
slow magnetization relaxation in the timescale of minutes. This is attributed
to an energy barrier Delta=2.40 K resulting from the S=5 dimer ground state of
[Fe2F9]^{3-} and a negative axial anisotropy. The relaxation partly occurs via
thermally assisted quantum tunneling. These features of a single-molecule
magnet are observable at temperatures comparable to the barrier height, due to
an extremely inefficient energy exchange between the spin system and the
phonons. The butterfly shape of the hysteresis arises from a phonon avalanche
effect.Comment: 18 pages, 5 eps figures, latex (elsart
Caseous calcification of the mitral annulus: an uncommon cause of acute mitral regurgitation.
peer reviewe
Use of percutaneous ventricular assist device as bridge to high risk combined heart valve surgery.
peer reviewe
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