6,189 research outputs found
Fear Conditioning Potentiates Synaptic Transmission onto Long-Range Projection Neurons in the Lateral Subdivision of Central Amygdala
Recent studies indicate that the lateral subdivision of the central amygdala (CeL) is essential for fear learning. Specifically, fear conditioning induces cell-type-specific synaptic plasticity in CeL neurons that is required for the storage of fear memories. The CeL also controls fear expression by gating the activity of the medial subdivision of the central amygdala (CeM), the canonical amygdala output to areas that mediate defensive responses. In addition to the connection with CeM, the CeL sends long-range projections to innervate extra-amygdala areas. However, the long-range projection CeL neurons have not been well characterized, and their role in fear regulation is unknown. Here we show in mice that a subset of CeL neurons directly project to the midbrain periaqueductal gray (PAG) and the paraventricular nucleus of the thalamus, two brain areas implicated in defensive behavior. These long-range projection CeL neurons are predominantly somatostatin-positive (SOM(+)) neurons, which can directly inhibit PAG neurons, and some of which innervate both the PAG and paraventricular nucleus of the thalamus. Notably, fear conditioning potentiates excitatory synaptic transmission onto these long-range projection CeL neurons. Thus, our study identifies a subpopulation of SOM(+) CeL neurons that may contribute to fear learning and regulate fear expression independent of CeM
Long-Range Exciton Diffusion in Two-Dimensional Assemblies of Cesium Lead Bromide Perovskite Nanocrystals
F\"orster Resonant Energy Transfer (FRET)-mediated exciton diffusion through
artificial nanoscale building block assemblies could be used as a new
optoelectronic design element to transport energy. However, so far nanocrystal
(NC) systems supported only diffusion length of 30 nm, which are too small to
be useful in devices. Here, we demonstrate a FRET-mediated exciton diffusion
length of 200 nm with 0.5 cm2/s diffusivity through an ordered, two-dimensional
assembly of cesium lead bromide perovskite nanocrystals (PNC). Exciton
diffusion was directly measured via steady-state and time-resolved
photoluminescence (PL) microscopy, with physical modeling providing deeper
insight into the transport process. This exceptionally efficient exciton
transport is facilitated by PNCs high PL quantum yield, large absorption
cross-section, and high polarizability, together with minimal energetic and
geometric disorder of the assembly. This FRET-mediated exciton diffusion length
matches perovskites optical absorption depth, opening the possibility to design
new optoelectronic device architectures with improved performances, and
providing insight into the high conversion efficiencies of PNC-based
optoelectronic devices
A New Scintillator Tile/Fiber Preshower Detector for the CDF Central Calorimeter
A detector designed to measure early particle showers has been installed in
front of the central CDF calorimeter at the Tevatron. This new preshower
detector is based on scintillator tiles coupled to wavelength-shifting fibers
read out by multi-anode photomultipliers and has a total of 3,072 readout
channels. The replacement of the old gas detector was required due to an
expected increase in instantaneous luminosity of the Tevatron collider in the
next few years. Calorimeter coverage, jet energy resolution, and electron and
photon identification are among the expected improvements. The final detector
design, together with the R&D studies that led to the choice of scintillator
and fiber, mechanical assembly, and quality control are presented. The detector
was installed in the fall 2004 Tevatron shutdown and started collecting
colliding beam data by the end of the same year. First measurements indicate a
light yield of 12 photoelectrons/MIP, a more than two-fold increase over the
design goals.Comment: 5 pages, 10 figures (changes are minor; this is the final version
published in IEEE-Trans.Nucl.Sci.
Cyclic nucleotide signalling in malaria parasites.
The cyclic nucleotides 3', 5'-cyclic adenosine monophosphate (cAMP) and 3', 5'-cyclic guanosine monophosphate (cGMP) are intracellular messengers found in most animal cell types. They usually mediate an extracellular stimulus to drive a change in cell function through activation of their respective cyclic nucleotide-dependent protein kinases, PKA and PKG. The enzymatic components of the malaria parasite cyclic nucleotide signalling pathways have been identified, and the genetic and biochemical studies of these enzymes carried out to date are reviewed herein. What has become very clear is that cyclic nucleotides play vital roles in controlling every stage of the complex malaria parasite life cycle. Our understanding of the involvement of cyclic nucleotide signalling in orchestrating the complex biology of malaria parasites is still in its infancy, but the recent advances in our genetic tools and the increasing interest in signalling will deliver more rapid progress in the coming years
Design and construction of new central and forward muon counters for CDF II
New scintillation counters have been designed and constructed for the CDF
upgrade in order to complete the muon coverage of the central CDF detector, and
to extend this coverage to larger pseudorapidity. A novel light collection
technique using wavelength shifting fibers, together with high quality
polystyrene-based scintillator resulted in compact counters with good and
stable light collection efficiency over lengths extending up to 320 cm. Their
design and construction is described and results of their initial performance
are reported.Comment: 20 pages, 15 figure
Human dyskerin binds to cytoplasmic H/ACA-box-containing transcripts affecting nuclear hormone receptor dependence
Background Dyskerin is a nuclear protein involved in H/ACA box snoRNA-guided uridine modification of RNA. In humans, its defective function is associated with cancer development and induces specific post-transcriptional alterations of gene expression. In this study, we seek to unbiasedly identify mRNAs regulated by dyskerin in human breast cancer-derived cells. Results We find that dyskerin depletion affects the expression and the association with polysomes of selected mRNA isoforms characterized by the retention of H/ACA box snoRNA-containing introns. These snoRNA retaining transcripts (snoRTs) are bound by dyskerin in the cytoplasm in the form of shorter 3 ' snoRT fragments. We then characterize the whole cytoplasmic dyskerin RNA interactome and find both H/ACA box snoRTs and protein-coding transcripts which may be targeted by the snoRTs' guide properties. Since a fraction of these protein-coding transcripts is involved in the nuclear hormone receptor binding, we test to see if this specific activity is affected by dyskerin. Obtained results indicate that dyskerin dysregulation may alter the dependence on nuclear hormone receptor ligands in breast cancer cells. These results are paralleled by consistent observations on the outcome of primary breast cancer patients stratified according to their tumor hormonal status. Accordingly, experiments in nude mice show that the reduction of dyskerin levels in estrogen-dependent cells favors xenograft development in the absence of estrogen supplementation. Conclusions Our work suggests a cytoplasmic function for dyskerin which could affect mRNA post-transcriptional networks relevant for nuclear hormone receptor functions
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