65 research outputs found
The in-medium isovector pi N amplitude from low energy pion scattering
Differential cross sections for elastic scattering of 21.5 MeV positive and
negative pions by Si, Ca, Ni and Zr have been measured as part of a study of
the pion-nucleus potential across threshold. The `anomalous' repulsion in the
s-wave term was observed, as is the case with pionic atoms. The extra repulsion
can be accounted for by a chiral-motivated model where the pion decay constant
is modified in the medium. Unlike in pionic atoms, the anomaly cannot be
removed by merely introducing an empirical on-shell energy dependence.Comment: 9 pages, 2 figures. Minor changes, to appear in PR
Elastic scattering of low energy pions by nuclei and the in-medium isovector pi N amplitude
Measurements of elastic scattering of 21.5 MeV pi+ and pi- by Si, Ca, Ni and
Zr were made using a single arm magnetic spectrometer. Absolute calibration was
made by parallel measurements of Coulomb scattering of muons. Parameters of a
pion-nucleus optical potential were obtained from fits to all eight angular
distributions put together. The `anomalous' s-wave repulsion known from pionic
atoms is clearly observed and could be removed by introducing a
chiral-motivated density dependence of the isovector scattering amplitude,
which also greatly improved the fits to the data. The empirical energy
dependence of the isoscalar amplitude also improves the fits to the data but,
contrary to what is found with pionic atoms, on its own is incapable of
removing the anomaly.Comment: 20 pages, 5 figures, 5 tables. V2 added details on
uncertainties,extended discussion. To appear in PR
Pionic charge exchange on the proton from 40 to 250 MeV
The total cross sections for pionic charge exchange on hydrogen were measured
using a transmission technique on thin CH2 and C targets. Data were taken for
pi- lab energies from 39 to 247 MeV with total errors of typically 2% over the
Delta-resonance and up to 10% at the lowest energies. Deviations from the
predictions of the SAID phase shift analysis in the 60 to 80 MeV region are
interpreted as evidence for isospin-symmetry breaking in the s-wave amplitudes.
The charge dependence of the Delta-resonance properties appears to be smaller
than previously reported
Low Energy Analyzing Powers in Pion-Proton Elastic Scattering
Analyzing powers of pion-proton elastic scattering have been measured at PSI
with the Low Energy Pion Spectrometer LEPS as well as a novel polarized
scintillator target. Angular distributions between 40 and 120 deg (c.m.) were
taken at 45.2, 51.2, 57.2, 68.5, 77.2, and 87.2 MeV incoming pion kinetic
energy for pi+ p scattering, and at 67.3 and 87.2 MeV for pi- p scattering.
These new measurements constitute a substantial extension of the polarization
data base at low energies. Predictions from phase shift analyses are compared
with the experimental results, and deviations are observed at low energies.Comment: 15 pages, 4 figure
Phase-shift analysis of low-energy elastic-scattering data
Using electromagnetic corrections previously calculated by means of a
potential model, we have made a phase-shift analysis of the
elastic-scattering data up to a pion laboratory kinetic energy of 100 MeV. The
hadronic interaction was assumed to be isospin invariant. We found that it was
possible to obtain self-consistent databases by removing very few measurements.
A pion-nucleon model was fitted to the elastic-scattering database obtained
after the removal of the outliers. The model-parameter values showed an
impressive stability when the database was subjected to different criteria for
the rejection of experiments. Our result for the pseudovector
coupling constant (in the standard form) is . The six
hadronic phase shifts up to 100 MeV are given in tabulated form. We also give
the values of the s-wave scattering lengths and the p-wave scattering volumes.
Big differences in the s-wave part of the interaction were observed when
comparing our hadronic phase shifts with those of the current GWU solution. We
demonstrate that the hadronic phase shifts obtained from the analysis of the
elastic-scattering data cannot reproduce the measurements of the
charge-exchange reaction, thus corroborating past evidence that the hadronic
interaction violates isospin invariance. Assuming the validity of the result
obtained within the framework of chiral perturbation theory, that the mass
difference between the - and the -quark has only a very small effect on
the isospin invariance of the purely hadronic interaction, the
isospin-invariance violation revealed by the data must arise from the fact that
we are dealing with a hadronic interaction which still contains residual
effects of electromagnetic origin.Comment: 43 pages, 6 figure
pi+- p differential cross sections at low energies
Differential cross sections for pi- p and pi+ p elastic scattering were
measured at five energies between 19.9 and 43.3 MeV. The use of the CHAOS
magnetic spectrometer at TRIUMF, supplemented by a range telescope for muon
background suppression, provided simultaneous coverage of a large part of the
full angular range, thus allowing very precise relative cross section
measurements. The absolute normalisation was determined with a typical accuracy
of 5 %. This was verified in a simultaneous measurement of muon proton elastic
scattering. The measured cross sections show some deviations from phase shift
analysis predictions, in particular at large angles and low energies. From the
new data we determine the real part of the isospin forward scattering
amplitude.Comment: 13 pages, 5 figures. To appear in PL
Cyclic Expression of Lhx2 Regulates Hair Formation
Hair is important for thermoregulation, physical protection, sensory activity, seasonal camouflage, and social interactions. Hair is generated in hair follicles (HFs) and, following morphogenesis, HFs undergo cyclic phases of active growth (anagen), regression (catagen), and inactivity (telogen) throughout life. The transcriptional regulation of this process is not well understood. We show that the transcription factor Lhx2 is expressed in cells of the outer root sheath and a subpopulation of matrix cells during both morphogenesis and anagen. As the HFs enter telogen, expression becomes undetectable and reappears prior to initiation of anagen in the secondary hair germ. In contrast to previously published results, we find that Lhx2 is primarily expressed by precursor cells outside of the bulge region where the HF stem cells are located. This developmental, stage- and cell-specific expression suggests that Lhx2 regulates the generation and regeneration of hair. In support of this hypothesis, we show that Lhx2 is required for anagen progression and HF morphogenesis. Moreover, transgenic expression of Lhx2 in postnatal HFs is sufficient to induce anagen. Thus, our results reveal an alternative interpretation of Lhx2 function in HFs compared to previously published results, since Lhx2 is periodically expressed, primarily in precursor cells distinct from those in the bulge region, and is an essential positive regulator of hair formation
Urochordate Histoincompatible Interactions Activate Vertebrate-Like Coagulation System Components
The colonial ascidian Botryllus schlosseri expresses a unique allorecognition system. When two histoincompatible Botryllus colonies come into direct contact, they develop an inflammatory-like rejection response. A surprising high number of vertebrates' coagulation genes and coagulation-related domains were disclosed in a cDNA library of differentially expressed sequence tags (ESTs), prepared for this allorejection process. Serine proteases, especially from the trypsin family, were highly represented among Botryllus library ortholgues and its “molecular function” gene ontology analysis. These, together with the built-up clot-like lesions in the interaction area, led us to further test whether a vertebrate-like clotting system participates in Botryllus innate immunity. Three morphologically distinct clot types (points of rejection; POR) were followed. We demonstrated the specific expression of nine coagulation orthologue transcripts in Botryllus rejection processes and effects of the anti-coagulant heparin on POR formation and heartbeats. In situ hybridization of fibrinogen and von Willebrand factor orthologues elucidated enhanced expression patterns specific to histoincompatible reactions as well as common expressions not augmented by innate immunity. Immunohistochemistry for fibrinogen revealed, in naïve and immune challenged colonies alike, specific antibody binding to a small population of Botryllus compartment cells. Altogether, molecular, physiological and morphological outcomes suggest the involvement of vertebrates-like coagulation elements in urochordate immunity, not assigned with vasculature injury
Atg5-Independent Sequestration of Ubiquitinated Mycobacteria
Like several other intracellular pathogens, Mycobacterium marinum (Mm) escapes from phagosomes into the host cytosol where it can polymerize actin, leading to motility that promotes spread to neighboring cells. However, only ∼25% of internalized Mm form actin tails, and the fate of the remaining bacteria has been unknown. Here we show that cytosolic access results in a new and intricate host pathogen interaction: host macrophages ubiquitinate Mm, while Mm shed their ubiquitinated cell walls. Phagosomal escape and ubiquitination of Mm occured rapidly, prior to 3.5 hours post infection; at the same time, ubiquitinated Mm cell wall material mixed with host-derived dense membrane networks appeared in close proximity to cytosolic bacteria, suggesting cell wall shedding and association with remnants of the lysed phagosome. At 24 hours post-infection, Mm that polymerized actin were not ubiquitinated, whereas ubiquitinated Mm were found within LAMP-1–positive vacuoles resembling lysosomes. Though double membranes were observed which sequestered Mm away from the cytosol, targeting of Mm to the LAMP-1–positive vacuoles was independent of classical autophagy, as demonstrated by absence of LC3 association and by Atg5-independence of their formation. Further, ubiquitination and LAMP-1 association did not occur with mutant avirulent Mm lacking ESX-1 (type VII) secretion, which fail to escape the primary phagosome; apart from its function in phagosome escape, ESX-1 was not directly required for Mm ubiquitination in macrophages or in vitro. These data suggest that virulent Mm follow two distinct paths in the cytosol of infected host cells: bacterial ubiquitination is followed by sequestration into lysosome-like organelles via an autophagy-independent pathway, while cell wall shedding may allow escape from this fate to permit continued residence in the cytosol and formation of actin tails
Expression of the proapoptotic protein Bid is an adverse prognostic factor for radiotherapy outcome in carcinoma of the cervix
The Bcl-2 family of apoptotic regulators is thought to play an essential role in cancer development and influence the sensitivity of tumour cells to radiotherapy. Bid is an abundantly expressed Bcl-2 family protein playing a central role in various pathways of apoptosis by integrating and converging signals at the mitochondria. The relevance of apoptotic modulation by Bcl-2 and related proteins in tumour development and radiation response for human tumours remains undefined. Therefore, a study was made regarding the expression of Bid in patients with locally advanced cervix carcinoma who received radiotherapy. Bid expression was assessed using immunohistochemistry in pretreatment archival biopsies from 98 patients. The data were correlated with clinicopathologic characteristics and treatment outcome. Pretreatment tumour radiosensitivity data were available for 60 patients. Strong Bid expression was associated with a patient age less than the median of 52 years (P=0.034) and poor metastasis-free survival. In multivariate analysis, after allowing for stage, Bid expression was a significant prognostic factor for both disease-specific and metastasis-free survival (P=0.026). It is concluded that strong tumour Bid expression is associated with poor outcome following radiotherapy regardless of intrinsic tumour cell radiosensitivity, and is adverse prognostic for disease-specific and metastasis-free survival in younger patients
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