2,648 research outputs found
Dynamical Synapses Enhance Neural Information Processing: Gracefulness, Accuracy and Mobility
Experimental data have revealed that neuronal connection efficacy exhibits
two forms of short-term plasticity, namely, short-term depression (STD) and
short-term facilitation (STF). They have time constants residing between fast
neural signaling and rapid learning, and may serve as substrates for neural
systems manipulating temporal information on relevant time scales. The present
study investigates the impact of STD and STF on the dynamics of continuous
attractor neural networks (CANNs) and their potential roles in neural
information processing. We find that STD endows the network with slow-decaying
plateau behaviors-the network that is initially being stimulated to an active
state decays to a silent state very slowly on the time scale of STD rather than
on the time scale of neural signaling. This provides a mechanism for neural
systems to hold sensory memory easily and shut off persistent activities
gracefully. With STF, we find that the network can hold a memory trace of
external inputs in the facilitated neuronal interactions, which provides a way
to stabilize the network response to noisy inputs, leading to improved accuracy
in population decoding. Furthermore, we find that STD increases the mobility of
the network states. The increased mobility enhances the tracking performance of
the network in response to time-varying stimuli, leading to anticipative neural
responses. In general, we find that STD and STP tend to have opposite effects
on network dynamics and complementary computational advantages, suggesting that
the brain may employ a strategy of weighting them differentially depending on
the computational purpose.Comment: 40 pages, 17 figure
Electrical transport in amorphous semiconducting AlMgB14 films
The electrical transport properties of semiconducting AlMgB14films deposited at room temperature and 573K are reported in this letter. The as-deposited films are amorphous, and they exhibit high n-type electrical conductivity, which is believed to stem from the conduction electrons donated by Al, Mg, and/or Fe impurities in these films. The film deposited at 573K is less conductive than the room-temperature-deposited film. This is attributed to the nature of donor or trap states in the band gap related to the different deposition temperatures
Epigenomic differences in the human and chimpanzee genomes are associated with structural variation
Structural variation (SV), including insertions and deletions (indels), is a primary mechanism of genome evolution. However, the mechanism by which SV contributes to epigenome evolution is poorly understood. In this study, we characterized the association between lineage-specific indels and epigenome differences between human and chimpanzee to investigate how SVs might have shaped the epigenetic landscape. By intersecting medium-to-large human-chimpanzee indels (20bp-50kb) with putative promoters and enhancers in cranial neural crest cells (CNCC) and repressed regions in induced pluripotent cells (iPSC), we found that ~12% indels overlap putative regulatory and repressed regions (RRRs), and 15% of these indels are associated with lineage-biased RRRs. Indel-associated putative enhancer and repressive regions are ~1.3 and ~3 times as likely to be lineage-biased, respectively, as those not associated with indels. We found a 2-fold enrichment of medium-sized indels (20bp to 50bp) in CpG island (CGI)-containing promoters than expected by chance. Lastly, from human-specific transposable element insertions, we identified putative regulatory elements, including NR2F1-bound putative CNCC enhancers derived from SVAs and putative iPSC promoters derived from LTR5s. Our results demonstrate that different types of indels are associated with specific epigenomic diversity between human and chimpanzee
Numerical Models of Binary Neutron Star System Mergers. I.: Numerical Methods and Equilibrium Data for Newtonian Models
The numerical modeling of binary neutron star mergers has become a subject of
much interest in recent years. While a full and accurate model of this
phenomenon would require the evolution of the equations of relativistic
hydrodynamics along with the Einstein field equations, a qualitative study of
the early stages on inspiral can be accomplished by either Newtonian or
post-Newtonian models, which are more tractable. In this paper we offer a
comparison of results from both rotating and non-rotating (inertial) frame
Newtonian calculations. We find that the rotating frame calculations offer
significantly improved accuracy as compared with the inertial frame models.
Furthermore, we show that inertial frame models exhibit significant and
erroneous angular momentum loss during the simulations that leads to an
unphysical inspiral of the two neutron stars. We also examine the dependence of
the models on initial conditions by considering initial configurations that
consist of spherical neutron stars as well as stars that are in equilibrium and
which are tidally distorted. We compare our models those of Rasio & Shapiro
(1992,1994a) and New & Tohline (1997). Finally, we investigate the use of the
isolated star approximation for the construction of initial data.Comment: 32 pages, 19 gif figures, manuscript with postscript figures
available at http://www.astro.sunysb.edu/dswesty/docs/nspap1.p
Gonad differentiation in zebrafish is regulated by the canonical Wnt signalling pathway
Zebrafish males undergo a ‘‘juvenile ovary-to-testis’’ gonadal transformation process. Several genes, including nuclear receptor subfamily 5, group A (nr5a) and anti-Mu¨ llerian hormone (amh), and pathways such as Tp53-mediated germ-cell apoptosis have been implicated in zebrafish testis formation. However, our knowledge of the regulation of this complex process is incomplete, and much remains to be investigated about the molecular pathways and network of genes that control it. Using a microarray-based analysis of transforming zebrafish male
gonads, we demonstrated that their transcriptomes undergo transition from an ovary-like pattern to an ovotestis to a testislike profile. Microarray results also validated the previous histological and immunohistochemical observation that there
is high variation in the duration and extent of commitment to the juvenile ovary phase among individuals. Interestingly, global gene expression profiling of diverging zebrafish juvenile ovaries and transforming ovotestes revealed that some members of the canonical Wnt/beta-catenin signaling pathway were differentially expressed between these two phases. To investigate whether Wnt/beta-catenin signaling plays a role in zebrafish gonad differentiation, we used the Tg (hsp70l:dkk1b-GFP)w32 line to inhibit Wnt/beta-catenin signaling during gonad differentiation. Activation of dkk1b-GFP expression by heat shock resulted in an increased proportion of males and corresponding decrease in gonadal aromatase gene (cyp19a1a) expression. The Wnt target gene, lymphocyte enhancer binding factor 1 (lef1), was also down-regulated in the process. Together, these results provide the first functional evidence that, similarly to mammals,
Wnt/beta-catenin signaling is a ‘‘pro-female’’ pathway that regulates gonad differentiation in zebrafish.Web of Scienc
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GPER-induced signaling is essential for the survival of breast cancer stem cells.
G protein-coupled estrogen receptor-1 (GPER), a member of the G protein-coupled receptor (GPCR) superfamily, mediates estrogen-induced proliferation of normal and malignant breast epithelial cells. However, its role in breast cancer stem cells (BCSCs) remains unclear. Here we showed greater expression of GPER in BCSCs than non-BCSCs of three patient-derived xenografts of ER- /PR+ breast cancers. GPER silencing reduced stemness features of BCSCs as reflected by reduced mammosphere forming capacity in vitro, and tumor growth in vivo with decreased BCSC populations. Comparative phosphoproteomics revealed greater GPER-mediated PKA/BAD signaling in BCSCs. Activation of GPER by its ligands, including tamoxifen (TMX), induced phosphorylation of PKA and BAD-Ser118 to sustain BCSC characteristics. Transfection with a dominant-negative mutant BAD (Ser118Ala) led to reduced cell survival. Taken together, GPER and its downstream signaling play a key role in maintaining the stemness of BCSCs, suggesting that GPER is a potential therapeutic target for eradicating BCSCs
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