523 research outputs found
Hyperon polarization along the beam direction relative to the second and third harmonic event planes in isobar collisions at = 200 GeV
The polarization of and hyperons along the beam
direction has been measured relative to the second and third harmonic event
planes in isobar Ru+Ru and Zr+Zr collisions at = 200 GeV. This
is the first experimental evidence of the hyperon polarization by the
triangular flow originating from the initial density fluctuations. The
amplitudes of the sine modulation for the second and third harmonic results are
comparable in magnitude, increase from central to peripheral collisions, and
show a mild dependence. The azimuthal angle dependence of the
polarization follows the vorticity pattern expected due to elliptic and
triangular anisotropic flow, and qualitatively disagree with most hydrodynamic
model calculations based on thermal vorticity and shear induced contributions.
The model results based on one of existing implementations of the shear
contribution lead to a correct azimuthal angle dependence, but predict
centrality and dependence that still disagree with experimental
measurements. Thus, our results provide stringent constraints on the thermal
vorticity and shear-induced contributions to hyperon polarization. Comparison
to previous measurements at RHIC and the LHC for the second-order harmonic
results shows little dependence on the collision system size and collision
energy.Comment: 6 pages, 5 figures, Published in Physical Review Letter
Observation of the electromagnetic field effect via charge-dependent directed flow in heavy-ion collisions at the Relativistic Heavy Ion Collider
The deconfined quark-gluon plasma (QGP) created in relativistic heavy-ion
collisions enables the exploration of the fundamental properties of matter
under extreme conditions. Non-central collisions can produce strong magnetic
fields on the order of Gauss, which offers a probe into the
electrical conductivity of the QGP. In particular, quarks and anti-quarks carry
opposite charges and receive contrary electromagnetic forces that alter their
momenta. This phenomenon can be manifested in the collective motion of
final-state particles, specifically in the rapidity-odd directed flow, denoted
as . Here we present the charge-dependent measurements of
near midrapidities for , , and
in Au+Au and isobar (Ru+Ru and
Zr+Zr) collisions at 200 GeV, and
in Au+Au collisions at 27 GeV, recorded by the STAR detector at the
Relativistic Heavy Ion Collider. The combined dependence of the signal on
collision system, particle species, and collision centrality can be
qualitatively and semi-quantitatively understood as several effects on
constituent quarks. While the results in central events can be explained by the
and quarks transported from initial-state nuclei, those in peripheral
events reveal the impacts of the electromagnetic field on the QGP. Our data put
valuable constraints on the electrical conductivity of the QGP in theoretical
calculations
Event-by-event correlations between () hyperon global polarization and handedness with charged hadron azimuthal separation in Au+Au collisions at from STAR
Global polarizations () of () hyperons have been
observed in non-central heavy-ion collisions. The strong magnetic field
primarily created by the spectator protons in such collisions would split the
and global polarizations (). Additionally, quantum chromodynamics (QCD) predicts
topological charge fluctuations in vacuum, resulting in a chirality imbalance
or parity violation in a local domain. This would give rise to an imbalance
() between left- and right-handed
() as well as a charge separation along the magnetic field,
referred to as the chiral magnetic effect (CME). This charge separation can be
characterized by the parity-even azimuthal correlator () and
parity-odd azimuthal harmonic observable (). Measurements of
, , and have not led to definitive
conclusions concerning the CME or the magnetic field, and has not
been measured previously. Correlations among these observables may reveal new
insights. This paper reports measurements of correlation between and
, which is sensitive to chirality fluctuations, and correlation
between and sensitive to magnetic field in Au+Au
collisions at 27 GeV. For both measurements, no correlations have been observed
beyond statistical fluctuations.Comment: 10 pages, 10 figures; paper from the STAR Collaboratio
Measurement of electrons from open heavy-flavor hadron decays in Au+Au collisions at GeV with the STAR detector
We report a new measurement of the production of electrons from open
heavy-flavor hadron decays (HFEs) at mid-rapidity ( 0.7) in Au+Au
collisions at GeV. Invariant yields of HFEs are
measured for the transverse momentum range of GeV/ in
various configurations of the collision geometry. The HFE yields in head-on
Au+Au collisions are suppressed by approximately a factor of 2 compared to that
in + collisions scaled by the average number of binary collisions,
indicating strong interactions between heavy quarks and the hot and dense
medium created in heavy-ion collisions. Comparison of these results with models
provides additional tests of theoretical calculations of heavy quark energy
loss in the quark-gluon plasma
Elliptic Flow of Heavy-Flavor Decay Electrons in Au+Au Collisions at = 27 and 54.4 GeV at RHIC
We report on new measurements of elliptic flow () of electrons from
heavy-flavor hadron decays at mid-rapidity () in Au+Au collisions at
= 27 and 54.4 GeV from the STAR experiment. Heavy-flavor
decay electrons () in Au+Au collisions at =
54.4 GeV exhibit a non-zero in the transverse momentum ()
region of 2 GeV/ with the magnitude comparable to that at
GeV. The measured at 54.4 GeV is
also consistent with the expectation of their parent charm hadron
following number-of-constituent-quark scaling as other light and strange flavor
hadrons at this energy. These suggest that charm quarks gain significant
collectivity through the evolution of the QCD medium and may reach local
thermal equilibrium in Au+Au collisions at GeV. The
measured in Au+Au collisions at 27
GeV is consistent with zero within large uncertainties. The energy dependence
of for different flavor particles () shows an
indication of quark mass hierarchy in reaching thermalization in high-energy
nuclear collisions.Comment: 12 pages, 7 figures, 1 tabl
Search for the Chiral Magnetic Effect in Au+Au collisions at GeV with the STAR forward Event Plane Detectors
A decisive experimental test of the Chiral Magnetic Effect (CME) is
considered one of the major scientific goals at the Relativistic Heavy-Ion
Collider (RHIC) towards understanding the nontrivial topological fluctuations
of the Quantum Chromodynamics vacuum. In heavy-ion collisions, the CME is
expected to result in a charge separation phenomenon across the reaction plane,
whose strength could be strongly energy dependent. The previous CME searches
have been focused on top RHIC energy collisions. In this Letter, we present a
low energy search for the CME in Au+Au collisions at
GeV. We measure elliptic flow scaled charge-dependent correlators relative to
the event planes that are defined at both mid-rapidity and at
forward rapidity . We compare the results based on the
directed flow plane () at forward rapidity and the elliptic flow plane
() at both central and forward rapidity. The CME scenario is expected
to result in a larger correlation relative to than to , while
a flow driven background scenario would lead to a consistent result for both
event planes[1,2]. In 10-50\% centrality, results using three different event
planes are found to be consistent within experimental uncertainties, suggesting
a flow driven background scenario dominating the measurement. We obtain an
upper limit on the deviation from a flow driven background scenario at the 95\%
confidence level. This work opens up a possible road map towards future CME
search with the high statistics data from the RHIC Beam Energy Scan Phase-II.Comment: main: 8 pages, 5 figures; supplementary material: 2 pages, 1 figur
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An integrated omics analysis reveals molecular mechanisms that are associated with differences in seed oil content between Glycine max and Brassica napus
Abstract
Background: Rapeseed (Brassica napus L.) and soybean (Glycine max L.) seeds are rich in both protein and oil, which
are major sources of biofuels and nutrition. Although the difference in seed oil content between soybean (~ 20%) and
rapeseed (~ 40%) exists, little is known about its underlying molecular mechanism.
Results: An integrated omics analysis was performed in soybean, rapeseed, Arabidopsis (Arabidopsis thaliana L. Heynh),
and sesame (Sesamum indicum L.), based on Arabidopsis acyl-lipid metabolism- and carbon metabolism-related genes.
As a result, candidate genes and their transcription factors and microRNAs, along with phylogenetic analysis and
co-expression network analysis of the PEPC gene family, were found to be largely associated with the difference
between the two species. First, three soybean genes (Glyma.13G148600, Glyma.13G207900 and Glyma.12G122900)
co-expressed with GmPEPC1 are specifically enriched during seed storage protein accumulation stages, while the
expression of BnPEPC1 is putatively inhibited by bna-miR169, and two genes BnSTKA and BnCKII are co-expressed
with BnPEPC1 and are specifically associated with plant circadian rhythm, which are related to seed oil biosynthesis. Then,
in de novo fatty acid synthesis there are rapeseed-specific genes encoding subunits β-CT (BnaC05g37990D) and BCCP1
(BnaA03g06000D) of heterogeneous ACCase, which could interfere with synthesis rate, and β-CT is positively regulated by
four transcription factors (BnaA01g37250D, BnaA02g26190D, BnaC01g01040D and BnaC07g21470D). In triglyceride synthesis,
GmLPAAT2 is putatively inhibited by three miRNAs (gma-miR171, gma-miR1516 and gma-miR5775). Finally, in rapeseed
there was evidence for the expansion of gene families, CALO, OBO and STERO, related to lipid storage, and
the contraction of gene families, LOX, LAH and HSI2, related to oil degradation.
Conclusions: The molecular mechanisms associated with differences in seed oil content provide the basis for
future breeding efforts to improve seed oil content
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
In 2008 we published the first set of guidelines for standardizing research in autophagy. Since then, research on this topic has continued to accelerate, and many new scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Accordingly, it is important to update these guidelines for monitoring autophagy in different organisms. Various reviews have described the range of assays that have been used for this purpose. Nevertheless, there continues to be confusion regarding acceptable methods to measure autophagy, especially in multicellular eukaryotes. For example, a key point that needs to be emphasized is that there is a difference between measurements that monitor the numbers or volume of autophagic elements (e.g., autophagosomes or autolysosomes) at any stage of the autophagic process versus those that measure fl ux through the autophagy pathway (i.e., the complete process including the amount and rate of cargo sequestered and degraded). In particular, a block in macroautophagy that results in autophagosome accumulation must be differentiated from stimuli that increase autophagic activity, defi ned as increased autophagy induction coupled with increased delivery to, and degradation within, lysosomes (inmost higher eukaryotes and some protists such as Dictyostelium ) or the vacuole (in plants and fungi). In other words, it is especially important that investigators new to the fi eld understand that the appearance of more autophagosomes does not necessarily equate with more autophagy. In fact, in many cases, autophagosomes accumulate because of a block in trafficking to lysosomes without a concomitant change in autophagosome biogenesis, whereas an increase in autolysosomes may reflect a reduction in degradative activity. It is worth emphasizing here that lysosomal digestion is a stage of autophagy and evaluating its competence is a crucial part of the evaluation of autophagic flux, or complete autophagy. Here, we present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes. These guidelines are not meant to be a formulaic set of rules, because the appropriate assays depend in part on the question being asked and the system being used. In addition, we emphasize that no individual assay is guaranteed to be the most appropriate one in every situation, and we strongly recommend the use of multiple assays to monitor autophagy. Along these lines, because of the potential for pleiotropic effects due to blocking autophagy through genetic manipulation it is imperative to delete or knock down more than one autophagy-related gene. In addition, some individual Atg proteins, or groups of proteins, are involved in other cellular pathways so not all Atg proteins can be used as a specific marker for an autophagic process. In these guidelines, we consider these various methods of assessing autophagy and what information can, or cannot, be obtained from them. Finally, by discussing the merits and limits of particular autophagy assays, we hope to encourage technical innovation in the field
Receptor Tyrosine Kinases in Osteosarcoma: 2019 Update
The primary conclusions of our 2014 contribution to this series were as follows:
Multiple receptor tyrosine kinases (RTKs) likely contribute to aggressive phenotypes in osteosarcoma and, therefore, inhibition of multiple RTKs is likely necessary for successful clinical outcomes.
Inhibition of multiple RTKs may also be useful to overcome resistance to inhibitors of individual RTKs as well as resistance to conventional chemotherapies.
Different combinations of RTKs are likely important in individual patients.
AXL, EPHB2, FGFR2, IGF1R, and RET were identified as promising therapeutic targets by our in vitro phosphoproteomic/siRNA screen of 42 RTKs in the highly metastatic LM7 and 143B human osteosarcoma cell lines.
This chapter is intended to provide an update on these topics as well as the large number of osteosarcoma clinical studies of inhibitors of multiple tyrosine kinases (multi-TKIs) that were recently published
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