On "the authentic damping mechanism" of the phonon damping model

Some general features of the phonon damping model are presented. It is concluded that the fits performed within this model have no physical content

Many-body effects in nuclear structure

We calculate, for the first time, the state-dependent pairing gap of a finite nucleus (120Sn) diagonalizing the bare nucleon-nucleon potential (Argonne v14) in a Hartree-Fock basis (with effective k-mass m_k eqult to 0.7 m), within the framework of the BCS approximation including scattering states up to 800 MeV above the Fermi energy to achieve convergence. The resulting gap accounts for about half of the experimental gap. We find that a consistent description of the low-energy nuclear spectrum requires, aside from the bare nucleon-nucleon interaction, not only the dressing of single-particle motion through the coupling to the nuclear surface, to give the right density of levels close to the Fermi energy (and thus an effective mass m* approximately equal to m), but also the renormalization of collective vibrational modes through vertex and self-energy processes, processes which are also found to play an essential role in the pairing channel, leading to a long range, state dependent component of the pairing interaction. The combined effect of the bare nucleon-nucleon potential and of the induced pairing interaction arising from the exchange of low-lying surface vibrations between nucleons moving in time reversal states close to the Fermi energy accounts for the experimental gap.Comment: 5 pages, 4 figures; author list correcte

Beta decay of r-process waiting-point nuclei in a self-consistent approach

Beta-decay rates for spherical neutron-rich r-process waiting-point nuclei are calculated within a fully self-consistent Quasiparticle Random-Phase Approximation, formulated in the Hartree-Fock-Bogolyubov canonical single-particle basis. The same Skyrme force is used everywhere in the calculation except in the proton-neutron particle-particle channel, where a finite-range force is consistently employed. In all but the heaviest nuclei, the resulting half-lives are usually shorter by factors of 2 to 5 than those of calculations that ignore the proton-neutron particle-particle interaction. The shorter half-lives alter predictions for the abundance distribution of r-process elements and for the time it takes to synthesize them.Comment: 14 pages RevTex, 10 eps figures, submitted to Phys. Rev.

Search for particle–vibration coupling in 65Cu

The lifetime of the 9/2 + state of 65 Cu, at 2534 keV, has been measured by fast timing techniques, in order to establish wether such state arises from a weak coupling between a p3=2 proton and the 3 octupole vibration at 3.56 MeV in the 64 Ni core. The 65 Cu nucleus was populated by the reaction 7 Li + 64 Ni at 32 MeV, at the Horia Hu- lubei National Institute of Physics and Nuclear Engineering (NIPNE) in Bucharest, and its -decay was detected by the ROSPHERE array. The measured lifetime coresponds to a B(E3) reduced transition probability to the ground state equal to 8.89 W.u., in agreement with theoretical predictions in the weak coupling limit

Influence of GB virus C on IFN-γ and IL-2 production and CD38 expression in T lymphocytes from chronically HIV-infected and HIV-HCV-co-infected patients

This study was designed to assess the effect of GB virus (GBV)-C on the immune response to human immunodeficiency virus (HIV) in chronically HIV-infected and HIV- hepatitis C virus (HCV)-co-infected patients undergoing antiretroviral therapy. A cohort of 159 HIV-seropositive patients, of whom 52 were HCV-co-infected, was included. Epidemiological data were collected and virological and immunological markers, including the production of interferon gamma (IFN-γ) and interleukin (IL)-2 by CD4, CD8 and Tγδ cells and the expression of the activation marker, CD38, were assessed. A total of 65 patients (40.8%) presented markers of GBV-C infection. The presence of GBV-C did not influence HIV and HCV replication or TCD4 and TCD8 cell counts. Immune responses, defined by IFN-γ and IL-2 production and CD38 expression did not differ among the groups. Our results suggest that neither GBV-C viremia nor the presence of E2 antibodies influence HIV and HCV viral replication or CD4 T cell counts in chronically infected patients. Furthermore, GBV-C did not influence cytokine production or CD38-driven immune activation among these patients. Although our results do not exclude a protective effect of GBV-C in early HIV disease, they demonstrate that this effect may not be present in chronically infected patients, who represent the majority of patients in outpatient clinics.Universidade Federal de São Paulo (UNIFESP) Laboratório de Virologia e Imunologia Disciplina de InfectologiaFleury Medicina DiagnósticaUNIFESP, Laboratório de Virologia e Imunologia Disciplina de InfectologiaSciEL

Probing the nature of particle–core couplings in 49Ca with γ spectroscopy and heavy-ion transfer reactions

This work was supported by the Italian Istituto Nazionale di Fisica Nucleare and partially by the Spanish MICINN (ACI2009-1070 bilateral action) and Generalitat Valenciana (Grant Nos. BEST/2009/073 and PROMETEO/2010/101). The work has also been partially supported by the Polish Ministry of Science and Higher Education (Grant No. N N202 309135)

High-resolution study of Gamow-Teller excitations in the Ca42(He3,t)Sc42 reaction and the observation of a “low-energy super-Gamow-Teller state”

Y. Fujita et al.; 15 pags.; 6 figs.; 7 tabs.; PACS number(s): 21.10.Hw, 25.55.Kr, 27.40.+z, 25.40.Ep© 2015 American Physical Society. To study the Gamow-Teller (GT) transitions from the Tz=+1 nucleus Ca42 to the Tz=0 nucleus Sc42, where Tz is the z component of isospin T, we performed a (p,n)-type (He3,t) charge-exchange reaction at 140 MeV/nucleon and scattering angles around 0. With an energy resolution of 29 keV, states excited by GT transitions (GT states) could be studied accurately. The reduced GT transition strengths B(GT) were derived up to the excitation energy of 13 MeV, assuming the proportionality between the cross sections at 0 and B(GT) values. The main part of the observed GT transition strength is concentrated in the lowest 0.611-MeV, Jπ=1+ GT state. All the other states at higher energies are weakly excited. Shell-model calculations could reproduce the gross feature of the experimental B(GT) distribution, and random-phase-approximation calculations including an attractive isoscalar interaction showed that the 0.611-MeV state has a collective nature. It was found that this state has all of the properties of a >low-energy super-Gamow-Teller state.> It is expected that low-lying Jπ=1+ GT states have T=0 in the Tz=0 nucleus Sc42. However, T=1 states are situated in a higher energy region. Assuming an isospin-analogous structure in A=42 isobars, analogous T=1, 1+ states are also expected in Ca42. Comparing the Ca42(He3,t)Sc42 and Ca42(p,p′) spectra measured at 0, candidates for T=1 GT states could be found in the 10-12-MeV region of Sc42. They were all weakly excited. The mass dependence of the GT strength distributions in Sc isotopes is also discussed.Y.F. also acknowledges the support of MEXT, Japan under Grants No. 18540270, No. 22540310, and No. 15K05104. Y.F. and B.R. are grateful for the support of the Japan-Spain collaboration program by JSPS and CSIC; A.A., E.E.A., and B.R. are thankful for the support of Spanish Ministry under Grants No. FPA2005-03993, No. FPA2008-06419-C02-01, and No. FPA2011-24553. G.S. acknowledges the support of TUBITAK, Turkey under Research Scholarship No. BIDEB 2214. J.M.D., C.J.G., R.M., G.P., and R.G.T.Z. are grateful for the support of the US NSF under Grants No. PHY-0606007 and No. PHY-0822648 (JINA). M.C., J.G., and A.K. acknowledge the support of the OTKA Foundation, Hungary, under Grant No. K106035. This work was in part supported by the RIKENCNS joint research project on large-scale nuclear-structure calculations.Peer Reviewe

Hemoxygenase-1 Promotes Head and Neck Cancer Cell Viability

Head and neck squamous cell carcinoma (HNSCC) is a remarkably heterogeneous disease with around 50% mortality, a fact that has prompted researchers to try new approaches to improve patient survival. Hemoxygenase-1 (HO-1) is the rate-limiting step for heme degradation into carbon monoxide, free iron and biliverdin. We have previously reported that HO-1 protein is upregulated in human HNSCC samples and that it is localized in the cytoplasmic and nuclear compartments; additionally, we have demonstrated that HO-1 nuclear localization is associated with malignant progression. In this work, by using pharmacological and genetic experimental approaches, we begin to elucidate the mechanisms through which HO-1 plays a role in HNSCC. We found that high HO-1 mRNA was associated with decreased patient survival in early stages of HNSCC. In vitro experiments have shown that full-length HO-1 localizes in the cytoplasm, and that, depending on its enzymatic activity, it increases cell viability and promotes cell cycle progression. Instead, HO-1 does not alter migration capacity. Furthermore, we show that C-terminal truncated HO-1 localizes into the nucleus, increases cell viability and promotes cell cycle progression. In conclusion, we herein demonstrate that HO-1 displays protumor activities in HNSCC that depend, at least in part, on the nuclear localization of HO-1.Centro de Investigaciones Inmunológicas Básicas y Aplicada

Functional microarray analysis suggests repressed cell-cell signaling and cell survival-related modules inhibit progression of head and neck squamous cell carcinoma

<p>Abstract</p> <p>Background</p> <p>Cancer shows a great diversity in its clinical behavior which cannot be easily predicted using the currently available clinical or pathological markers. The identification of pathways associated with lymph node metastasis (N+) and recurrent head and neck squamous cell carcinoma (HNSCC) may increase our understanding of the complex biology of this disease.</p> <p>Methods</p> <p>Tumor samples were obtained from untreated HNSCC patients undergoing surgery. Patients were classified according to pathologic lymph node status (positive or negative) or tumor recurrence (recurrent or non-recurrent tumor) after treatment (surgery with neck dissection followed by radiotherapy). Using microarray gene expression, we screened tumor samples according to modules comprised by genes in the same pathway or functional category.</p> <p>Results</p> <p>The most frequent alterations were the repression of modules in negative lymph node (N0) and in non-recurrent tumors rather than induction of modules in N+ or in recurrent tumors. N0 tumors showed repression of modules that contain cell survival genes and in non-recurrent tumors cell-cell signaling and extracellular region modules were repressed.</p> <p>Conclusions</p> <p>The repression of modules that contain cell survival genes in N0 tumors reinforces the important role that apoptosis plays in the regulation of metastasis. In addition, because tumor samples used here were not microdissected, tumor gene expression data are represented together with the stroma, which may reveal signaling between the microenvironment and tumor cells. For instance, in non-recurrent tumors, extracellular region module was repressed, indicating that the stroma and tumor cells may have fewer interactions, which disable metastasis development. Finally, the genes highlighted in our analysis can be implicated in more than one pathway or characteristic, suggesting that therapeutic approaches to prevent tumor progression should target more than one gene or pathway, specially apoptosis and interactions between tumor cells and the stroma.</p