RESUMO
Carbon burning is a key step in the evolution of massive stars, Type 1a supernovae and superbursts in x-ray binary systems. Determining the ^{12}C+^{12}C fusion cross section at relevant energies by extrapolation of direct measurements is challenging due to resonances at and below the Coulomb barrier. A study of the ^{24}Mg(α,α^{'})^{24}Mg reaction has identified several 0^{+} states in ^{24}Mg, close to the ^{12}C+^{12}C threshold, which predominantly decay to ^{20}Ne(ground state)+α. These states were not observed in ^{20}Ne(α,α_{0})^{20}Ne resonance scattering suggesting that they may have a dominant ^{12}C+^{12}C cluster structure. Given the very low angular momentum associated with sub-barrier fusion, these states may play a decisive role in ^{12}C+^{12}C fusion in analogy to the Hoyle state in helium burning. We present estimates of updated ^{12}C+^{12}C fusion reaction rates.
RESUMO
Several radionuclide production facilities based on a new generation of high-current, 70 MeV H- cyclotrons have been established in recent years and a number of new facilities are either under construction or being planned. In this study, the feasibility to produce 225Ac/213Bi and 230U/226Th generators via Th + p reactions at such a facility has been investigated. From the perspective of production yields, it has been found useful to compare the relevant reactions on thorium with those on other targets regularly employed in this energy region, in particular the natMg(p,x)22Na, natGa(p,x)68Ge, and natRb(p,x)82Sr reactions that have been exploited with 66 MeV proton beams at iThemba LABS for many years. Therefore, various tandem configurations of thorium with magnesium, gallium and rubidium are discussed based on the relevant nuclear data. In a few cases, the available data were judged to be insufficient in this energy region. New experimental cross sections are presented for 225Ac, 225Ra, and 230Pa in Th + p reactions as well as 22,24Na in natMg + p reactions. Integral yields have been derived for those radionuclides of main interest. Production yields expected from extended 70 MeV proton bombardments, on selected tandem-target configurations, are presented for 22Na, 68Ge, 82Sr, 225Ac, and 230Pa. It is concluded that 225Ac/213Bi generators can, in principle, be added to a production programme based at a 70 MeV H- cyclotron facility as the production rate is of similar magnitude to those of other well-established radionuclides in this energy region. Also, radio-contaminant levels for 225Ac are similar to those found in higher proton-energy windows. The scope for 230U/226Th generators, via bulk production of the precursor 230Pa, seems to be more limited due to a lower yield but can nevertheless be produced in clinically relevant quantities.
RESUMO
The large-scale production of 88Y with proton-induced reactions has been investigated from the perspective of new generation 70 MeV H- cyclotrons. Tandem target configurations are presented for both the direct production of 88Y as well as for producing 88Zr/88Y generators. Based on the relevant excitation functions, physical yields have been derived for 88Y production with Y2O3/SrCO3 tandem targets and 88Zr production with Zr/Y2O3 tandem targets. Yields are presented for optimized targets (i.e. optimum yield) as well as for balanced thermal loads on the individual targets. Liquid 88Zr/88Y generators have been produced using both natural Zr and Nb target materials, the former for dedicated productions and the latter as a byproduct by processing spent irradiated Nb capsules which normally would constitute radioactive waste. These stock solutions, which contain both the target material and 88Zr precursor, are retained virtually unchanged after processing except for the removal of 88Y on AG MP-50 macroporous cation-exchange resin. Methods are presented for the preparation of Nb stock solutions in hydrofluoric acid and Zr stock solutions in sulphuric acid. It is shown that multi-Ci productions of 88Y are feasible at a 70 MeV cyclotron facility, suitable for the needs of fracking applications. In addition, 88Zr/88Y generators can provide 88Y with very high specific activity, suitable for labelling of biomolecules. LA-UR-20-24305.
RESUMO
Absorption spectra (77 and 298 K), luminescence spectra (5-80 K), and luminescence lifetimes (5-80 K) for the title complexes have been correlated to increasing diphosphine basicity (R = 4-CF(3)-Ph < 4-H-Ph < 4-CH(3)O-Ph < Et). As a consequence, spectral peaks have been assigned to (1,3)MLCT (B(1u), W --> phosphorus) and (1,3)LF (B(2g)) terms. As the ligand basicity increases, the (3)MLCT bands observed in absorption blue-shift nearly 8000 cm(-1) and the vibrationally structured (3)LF bands observed in emission red-shift approximately 1300 cm(-1). (3)LF terms lie lowest in energy in the 4-H-Ph, 4-CH(3)O-Ph, and Et compounds, and temperature-dependent lifetime data suggest emission from each be assigned to the equilibrated, spin-orbit split levels of the (3)LF term. The (3)LF and (3)MLCT excited-state terms lie close in energy in the 4-CF(3)-Ph compound, resulting in an emission band shape that is temperature-dependent. At 77 K, the emission band is broad and structureless and is assigned to arise primarily from the (3)MLCT term. As the temperature is lowered toward 5 K, the (3)MLCT emission diminishes in intensity accompanied by the development of a vibrational structure that is characteristic of emission from the (3)LF term. These excited-state terms satisfy the requirements (different orbital origins, near-degeneracy) for separation by a Franck-Condon energy barrier, resulting in simultaneous emission from both terms between 5 and 77 K.
RESUMO
Survival and growth characteristics of two montane riparian willow species, Geyer willow (Salix geyeriana Andersson) and mountain willow (Salix monticola Bebb), grown in amended fluvial mine tailing were investigated in a greenhouse study. Willow stem cuttings were planted in lysimeters that simulated a 60-cm amended tailing profile with three static water depths (20, 40, and 60 cm) and a fluctuating water table for a total of four water table treatments. Species and water table treatments affected plant biomass and chemical composition of the soil and plant tissue. Mountain willow leaf, stem, and root biomass were 62, 95, and 164% greater, respectively, than for Geyer willow. Averaging across species, the fluctuating water table negatively affected leaf and stem biomass compared with the 20- and 60-cm water table treatments. Manganese was the only metal in plant tissue to strongly respond to water table treatments. Manganese concentrations in mountain willow leaf tissue were approximately twofold higher in the two most saturated water table treatments (20 cm and fluctuating) than in the least saturated water table treatment (60 cm). This trend was consistent with chemical analyses of the growth media, which reflected higher bioavailable Mn in the saturated tailing profile compared with the unsaturated profile. Results from this study indicate that mountain willow is a more vigorous and possibly more metal-tolerant species than Geyer willow when grown in amended mine tailing and that a fluctuating water table negatively affects willow growth.
Assuntos
Manganês/farmacocinética , Mineração , Salix/crescimento & desenvolvimento , Abastecimento de Água , Adaptação Fisiológica , Resíduos Industriais , Salix/fisiologia , Água/química , Poluentes da ÁguaRESUMO
Engulfment of foreign pathogens is an evolutionary ancient host cell endocytic response. Signaling pathways effecting phagocytosis are divergent and largely depend on the structural features of the cell surface receptor utilized. CEACAM3, a member of the CD66 complex on human neutrophils, has been implicated as a cellular receptor promoting phagocytosis of microorganisms. The cytoplasmic domain of CEACAM3 (CEACAM3(cyt)) contains an immunoreceptor tyrosine-based activation motif. In this study we demonstrate that CEACAM3(cyt) is phosphorylated by protein kinase C, casein kinase I, and Src-kinase in vitro. To identify molecules binding to CEACAM3(cyt) in vivo, we used differentially phosphorylated recombinant expressed CEACAM cytoplasmic domains to isolate CEACAM3(cyt)-associated proteins from granulocyte extracts. Calprotectin, which modulates neutrophil integrin-mediated adhesion and leukocyte trafficking and displays antimicrobial activity, interacts specifically with CEACAM3(cyt). This interaction is calcium-modulated but independent of phosphorylation of CEACAM3(cyt). Although tyrosine-phosphorylated CEACAM3(cyt) binds and stimulates Src-kinases in vitro, no CEACAM3(cyt)-associated phosphokinase activity was copurified.
Assuntos
Antígeno Carcinoembrionário/metabolismo , Granulócitos/microbiologia , Granulócitos/fisiologia , Glicoproteínas de Membrana/metabolismo , Moléculas de Adesão de Célula Nervosa/metabolismo , Sinalização do Cálcio , Antígeno Carcinoembrionário/química , Antígeno Carcinoembrionário/genética , Caseína Quinases , Humanos , Técnicas In Vitro , Complexo Antígeno L1 Leucocitário , Glicoproteínas de Membrana/química , Glicoproteínas de Membrana/genética , Moléculas de Adesão de Célula Nervosa/química , Moléculas de Adesão de Célula Nervosa/genética , Fagocitose , Fosforilação , Proteína Quinase C/metabolismo , Proteínas Quinases/metabolismo , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Especificidade por Substrato , Quinases da Família src/metabolismoRESUMO
CEACAM1 is a cell adhesion molecule that has been implicated in a number of physiological processes (eg, tumor suppressor in epithelial tissues, potent angiogenic factor in microvessel formation, microbial receptor in human granulocytes and epithelial cells). The mechanism of CEACAM1 action is still largely unresolved but recent findings demonstrated that the cytoplasmic CEACAM1 domain is linked indirectly to the actin-based cytoskeleton. We have isolated integrin beta(3) as an associated protein using CEACAM1 tail affinity purification. This association depends on phosphorylation of Tyr-488 in the CEACAM1 cytoplasmic domain. Confocal laser scanning microscopy confirmed in vivo colocalization of both molecules in human granulocytes and epithelial cells. Furthermore, the concentrated colocalization at the tumor-stroma interface of invading melanoma masses suggests a functional role of CEACAM1-integrin beta(3) interaction in melanoma invasion. Moreover, colocalization of the two adhesion molecules is also found at the apical surface of glandular cells of pregnancy endometrium. Colocalization of CEACAM1 and integrin beta(3) at the transitional zone from proliferative to invasive extravillous trophoblast of the maternal-fetal interface supports a role for CEACAM1/integrin beta(3) complexes in cell invasion.
Assuntos
Antígenos CD/metabolismo , Antígenos de Diferenciação/metabolismo , Neoplasias do Colo/patologia , Melanoma/patologia , Glicoproteínas da Membrana de Plaquetas/metabolismo , Antígenos CD/química , Antígenos CD/isolamento & purificação , Antígenos de Diferenciação/química , Antígenos de Diferenciação/isolamento & purificação , Sítios de Ligação , Moléculas de Adesão Celular/química , Moléculas de Adesão Celular/isolamento & purificação , Moléculas de Adesão Celular/metabolismo , Cromatografia de Afinidade , Endométrio/citologia , Feminino , Granulócitos/fisiologia , Humanos , Integrina beta3 , Microscopia Confocal , Fosforilação , Glicoproteínas da Membrana de Plaquetas/química , Glicoproteínas da Membrana de Plaquetas/isolamento & purificação , Gravidez , Primeiro Trimestre da Gravidez , Células Tumorais Cultivadas , TirosinaRESUMO
CEACAM1 functions as an epithelial tumor suppressor and as an angiogenic growth factor. In the present study, utilizing differentially (serine/threonine or tyrosine) phosphorylated cytoplasmic domains of CEACAM1 and CEACAM3 as bait to isolate associated proteins from granulocyte extracts, we have identified human paxillin as a binding partner of the tyrosine-phosphorylated cytoplasmic CEACAM1 domain. CEACAM1-paxillin complexes were coimmunoprecipitated from extracts of granulocytes, the colonic cell line HT29, and HUVECs. We identified phosphorylated Tyr-488-a residue in the cytoplasmic CEACAM1 domain known to be essential for the tumor suppressive effect-to be necessary for this association. The CEACAM1-paxillin interaction was confirmed using laser scanning confocal microscopy analyses in granulocytes and HT29 cells, where CEACAM1 colocalizes with paxillin at the plasma membrane. In HUVECs a highly polarized expression pattern and colocalization of paxillin and CEACAM1 was observed. These findings support the findings that CEACAM1 is linked to the actin-based cytoskeleton.
Assuntos
Adenosina Trifosfatases/metabolismo , Antígenos CD/metabolismo , Antígenos de Diferenciação/metabolismo , Moléculas de Adesão Celular/metabolismo , Proteínas do Citoesqueleto/metabolismo , Granulócitos/metabolismo , Fosfoproteínas/metabolismo , Animais , Sítios de Ligação , Antígeno Carcinoembrionário , Extratos Celulares , Citoplasma/metabolismo , Endotélio Vascular/citologia , Células Epiteliais/citologia , Células Epiteliais/metabolismo , Glicoproteínas , Granulócitos/citologia , Células HT29 , Humanos , Camundongos , Paxilina , Fosforilação , Testes de Precipitina , Tirosina/metabolismoRESUMO
A 28-year-old patient with a 5-year history of bipolar disorder developed signs of encephalopathy 2 weeks after the addition of valproic acid to his treatment regimen of doxepine, risperidone, and biperidene. The clinical signs were drowsiness, ataxic gait, asterixis, and a generalized epileptic seizure. Discontinuation of valproic acid gradually resulted in complete remission of these symptoms. Valproate encephalopathy has been described mainly in patients receiving anticonvulsant polytherapy. This complication might become more prevalent in psychiatric pharmacotherapy due to the increasing use of valproic acid.
Assuntos
Antimaníacos/efeitos adversos , Transtorno Bipolar/tratamento farmacológico , Encefalopatias Metabólicas/induzido quimicamente , Ácido Valproico/efeitos adversos , Adulto , Ataxia/etiologia , Encefalopatias Metabólicas/complicações , Discinesias/etiologia , Epilepsia Generalizada/etiologia , Humanos , Masculino , Indução de Remissão , Fases do Sono , Resultado do TratamentoAssuntos
Síndrome da Imunodeficiência Adquirida/complicações , Sobreviventes de Longo Prazo ao HIV , Hemocromatose/sangue , Síndrome da Imunodeficiência Adquirida/imunologia , Síndrome da Imunodeficiência Adquirida/patologia , Adulto , Contagem de Linfócito CD4 , Ferritinas/sangue , Hemocromatose/complicações , Hemocromatose/genética , Homossexualidade Masculina , Humanos , Ferro/sangue , Masculino , FlebotomiaRESUMO
CD66a (BGP, C-CAM) is an adhesion molecule of the carcinoembryonic antigen family that has been shown to be down-regulated in colorectal, prostate, and breast cancers. The purpose of the present study was to determine its expression pattern in the normal human endometrium and in endometrial neoplasia. For this purpose, we performed immunohistochemistry using the 4D1/C2 monoclonal antibody on a series of 24 normal endometrial samples and 47 endometrial carcinomas. Strong CD66a expression was observed in glandular and luminal epithelial cells of the normal endometrium with a consistent localization at the apical poles of these cells throughout the cycle. In late secretory (premenstrual) phase, loss of cellular polarity resulted in a membranous expression pattern in some glandular cells. In the analyzed tumor samples increasing areas with a complete loss of expression were observed with increasing malignancy grade. The apical expression pattern of the normal epithelium was changed to a membranous all-around pattern in 55% of the tumors, mostly in solid areas. This change correlated with malignancy grade and could be observed in 3 of 15 G1 tumors, 4 of 12 G2 tumors, 11 of 12 G3 tumors, and 8 of 8 serous-papillary carcinomas. Areas with membranous expression pattern could be observed along with areas with a normal apical expression pattern in lower grade carcinomas and with areas with complete loss of expression in high grade tumors. Northern blot analysis showed a loss of mRNA expression in tumor samples and HEC-1B endometrial adenocarcinoma cells. Loss of protein expression in the tumor samples was also observed by Western blot. In conclusion, CD66a protein expression is dysregulated in endometrial carcinomas, showing reduction or loss of expression with increasing malignancy grade and a change from the apical to a membranous localization.
Assuntos
Antígenos CD/metabolismo , Antígenos de Diferenciação/metabolismo , Neoplasias do Endométrio/metabolismo , Regulação Neoplásica da Expressão Gênica , Northern Blotting , Western Blotting , Carcinoma/metabolismo , Moléculas de Adesão Celular/metabolismo , Neoplasias do Colo/metabolismo , Endométrio/metabolismo , Feminino , Humanos , Imuno-Histoquímica , RNA Mensageiro/análise , Células Tumorais CultivadasRESUMO
CD66a, also known as 'biliary glycoprotein (BGP)', is the human homologue of a cell adhesion molecule (CAM) of the rat (Cell-CAM). CD66a, which belongs to the carcinoembryonic antigen family and the immunoglobulin superfamily, is expressed in cells of myeloid and epithelial origin. The cytoplasmic domain of the major isoform of CD66a (CD66acyt) contains two tyrosine residues in amino acid motifs potentially interacting with protein tyrosine kinases of the Src family. Here we provide evidence that CD66a is associated with pp60c-src. From membrane fractions of granulocytes and the colonic cell line HT29, phosphokinase activity was co-immunoprecipitated with CD66a when monoclonal CD66 antibodies or an antiserum against the recombinant cytoplasmic domain of CD66a were used. From the dissociated immunecomplexes, a phosphokinase of M(r) 60,000 was reprecipitated using antibodies against pp60c-src. In vitro, the recombinant cytoplasmic domain was a substrate and binding partner of pp60c-src. Phosphopeptides corresponding to the tyrosine containing amino acid sequences of CD66acyt activated the kinase activity of pp60c-src to a greater extent than a phosphopeptide containing Tyr527 from the SH2-binding regulatory domain of pp60c-src. The down-regulation of CD66a in about 80% of colorectal carcinomas may contribute to a dysregulation of pp60c-src in colorectal cancer.
Assuntos
Antígenos CD/metabolismo , Antígenos de Diferenciação/metabolismo , Moléculas de Adesão Celular/metabolismo , Glicoproteínas/metabolismo , Proteínas Proto-Oncogênicas pp60(c-src)/metabolismo , Sequência de Aminoácidos , Antígeno Carcinoembrionário/genética , Carcinoma/metabolismo , Células Cultivadas , Neoplasias Colorretais/metabolismo , Regulação para Baixo , Ativação Enzimática , Granulócitos/citologia , Humanos , Dados de Sequência Molecular , Família Multigênica , Fosfopeptídeos/química , Fosfopeptídeos/metabolismo , Fosforilação , Fosfotirosina/metabolismo , Testes de Precipitina , Transdução de Sinais , Domínios de Homologia de srcRESUMO
The inhibitory effect of pure alpha and beta hordothionins on protein synthesis directed by pea mRNA has been studied in the wheat-germ translation system. It is demonstrated that a component of the wheat germ counteracts the thionin effect. Formation of polysomes in vitro in the presence of thionin was inhibited to the same extent as the total translation system while run-off translation of isolated polysomes from pea plants was not affected by thionin. These data are consistent with an effect of thionin on the initiation reaction. Analyses of the formation of initiation complexes in the presence and absence of mRNA support this view and show that thionin interferes with the formation of the 43S complex. In accordance with this observation and in contrast to earlier studies no evidence has been obtained for a direct interaction between mRNAs and thionins. The analysis of the translation products also gave no indication for preferential translation of individual mRNAs by the thionin-inhibited translation system. Compared to translation in vitro, exposure of barley protoplasts to thionins showed a less dramatic effect on protein synthesis as measured by incorporation of [35S]methionine into proteins. These data are discussed with respect to the effects of thionins on the plasma membranes as shown previously with animal cell cultures. It is concluded that at least in barley such effects would need higher concentrations of thionins than are required for the inhibition of protein synthesis.
Assuntos
Fabaceae/metabolismo , Proteínas de Choque Térmico/biossíntese , Iniciação Traducional da Cadeia Peptídica/efeitos dos fármacos , Proteínas de Plantas/farmacologia , Plantas Medicinais , Biossíntese de Proteínas/efeitos dos fármacos , Inibidores da Síntese de Proteínas/farmacologia , RNA Mensageiro/metabolismo , Triticum/metabolismo , Peptídeos Catiônicos Antimicrobianos , Proteínas de Choque Térmico/isolamento & purificação , Hordeum/efeitos dos fármacos , Hordeum/metabolismo , Temperatura Alta , Cinética , Poli A/isolamento & purificação , Poli A/metabolismo , Polirribossomos/efeitos dos fármacos , Polirribossomos/metabolismo , Protoplastos/efeitos dos fármacos , Protoplastos/metabolismo , RNA/isolamento & purificação , RNA/metabolismo , Sementes/efeitos dos fármacos , Sementes/metabolismo , Triticum/efeitos dos fármacosRESUMO
This paper describes data collection during open chest cardiovascular research based on an IBM compatible personal computer. Data from eight analogue data channels are collected at a rate of 500 Hz per channel for a period of more than 40 sec per run. General analysis functions include the integration of the data obtained from any channel as well as an exponential curve fitting routine. Special functions are available for the calculation of cardiac parameters. This includes the automatic determination of end-diastole and end-systole, as well as maximum and minimum values of all curves for both the systolic and diastolic phases of contraction.