1,536 research outputs found

    The Ages and Abundances of the M87 Globular Clusters

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    A subset of 150 globular clusters in M87 has been selected on the basis of S/N ratio for abundance and age determinations from the sample of Paper I. Indices measuring the strength of the strongest spectral features were determined for the M87 GCs and from new data for twelve galactic GCs. Combining the new and existing data for the galactic GCs and comparing the (U−R)(U-R) colors and the line indices gives qualitative indications for the ages and abundances of the GCs. Quantitative results are obtained by applying the Worthey (1994) models for the integrated light of stellar systems of a single age, calibrated by observations of galactic GCs, to deduce abundances and ages for the objects in our sample. We find that the M87 GCs span a wide range in metallicity, from very metal poor to somewhat above solar metallicity. The mean [Fe/H] of -0.95 dex is higher than that of the galactic GC system, and there is a metal rich tail that reaches to higher [Fe/H] than one finds among the galactic GCs. The mean metallicity of the M87 GC system is about a factor of four lower than that of the M87 stellar halo at a fixed projected radius RR. The metallicity inferred from the X-ray studies is similar to that of the M87 stellar halo, not to that of GCs. We infer the relative abundances of Na, Mg, and Fe in the M87 GCs from the strength of their spectral features. The behavior of these elements between the metal rich and metal poor M87 GCs is similar to that shown by the galactic GCs and by halo stars in the Galaxy. The pattern of chemical evolution in these disparate old stellar systems is indistinguishable. We obtain a median age for the M87 GC system of 13 Gyr, similar to that of the galactic GCs, with a small dispersion about this value.Comment: 56 pages with included postscript figures; added derived M87 GC metallicities to Table 2, a statistical analysis of possible bimodality, an appendix on the metallicity calibration of U-R and the Washington system, and other smaller changes. Accepted for publication in ApJ. (See paper for complete version of the Abstract.

    Human Papillomavirus 16 E5 Induces Bi-Nucleated Cell Formation By Cell-Cell Fusion

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    Human Papillomaviruses (HPV) 16 is a DNA virus encoding three oncogenes – E5, E6, and E7. The E6 and E7 proteins have well-established roles as inhibitors of tumor suppression, but the contribution of E5 to malignant transformation is controversial. Using spontaneously immortalized human keratinocytes (HaCaT cells), we demonstrate that expression of HPV16 E5 is necessary and sufficient for the formation of bi-nucleated cells, a common characteristic of precancerous cervical lesions. Expression of E5 from non-carcinogenic HPV6b does not produce bi-nucleate cells. Video microscopy and biochemical analyses reveal that bi-nucleates arise through cell-cell fusion. Although most E5-induced bi-nucleates fail to propagate, co-expression of HPV16 E6/E7 enhances the proliferation of these cells. Expression of HPV16 E6/E7 also increases bi-nucleated cell colony formation. These findings identify a new role for HPV16 E5 and support a model in which complementary roles of the HPV16 oncogenes lead to the induction of carcinogenesis

    Arene–Ruthenium(II) Acylpyrazolonato Complexes: Apoptosis-Promoting Effects on Human Cancer Cells

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    A series of ruthenium(II) arene complexes with the 4-(biphenyl-4-carbonyl)-3-methyl-1-phenyl-5-pyrazolonate ligand, and related 1,3,5-triaza-7-phosphaadamantane (PTA) derivatives, has been synthesized. The compounds have been characterized by NMR and IR spectroscopy, ESI mass spectrometry, elemental analysis, and X-ray crystallography. Antiproliferative activity in four human cancer cell lines was determined by MTT assay, yielding dose- and cancer cell line-dependent IC50 values of 9-34 ÎŒM for three hexamethylbenzene-ruthenium complexes, whereas the other metal complexes were much less active. Apoptosis was the mechanism involved in the anticancer activity of such compounds. In fact, the hexamethylbenzene-ruthenium complexes activated caspase activity, with consequent DNA fragmentation, accumulation of pro-apoptotic proteins (p27, p53, p89 PARP fragments), and the concomitant down-regulation of antiapoptotic protein Bcl-2. Biosensor-based binding studies indicated that the ancillary ligands were critical in determining the DNA binding affinities, and competition binding experiments further characterized the nature of the interaction

    Star Clusters

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    This review concentrates almost entirely on globular star clusters. It emphasises the increasing realisation that few of the traditional problems of star cluster astronomy can be studied in isolation: the influence of the Galaxy affects dynamical evolution deep in the core, and the spectrum of stellar masses; in turn the evolution of the core determines the highest stellar densities, and the rate of encounters. In this way external tidal effects indirectly influence the formation and evolution of blue stragglers, binary pulsars, X-ray sources, etc. More controversially, the stellar density appears to influence the relative distribution of normal stars. In the opposite sense, the evolution of individual stars governs much of the early dynamics of a globular cluster, and the existence of large numbers of primordial binary stars has changed important details of our picture of the dynamical evolution. New computational tools which will become available in the next few years will help dynamical theorists to address these questions.Comment: 10 pages, 3 figures, Te

    Expression of vascular endothelial growth factor mRNA in non-small-cell lung carcinomas

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    The vascular endothelial growth factor (VEGF) has been shown to be strictly related to vascular permeability and endothelial cell growth under physiological and pathological conditions. In tumour development and progression, VEGF plays a pivotal role in the development of the tumoral vascular network, and useful information in the progression of human cancer can be obtained by analysing the vascular endothelial growth factor expression of the tumours. In this study, we investigated the vascular endothelial growth factor transcript expression in non-small-cell lung carcinomas to evaluate the significance of this factor in a group of cancers in which the vascular pattern has been shown to significantly affect progression. Surgical samples of 42 patients with NSCLC were studied using reverse transcription polymerase chain reaction (PCR) analysis and in situ hybridization. Thirty-three out of 42 cases (78.6%) showed VEGF transcript expression predominantly as transcripts for the secretory forms of VEGF (isoforms 121 and 165). In situ hybridization, performed on 24 out of 42 samples, showed that the VEGF transcript expression was in several cases present in the cytoplasm both of neoplastic and normal cells, even if the VEGF mRNA was less expressed in the corresponding non-tumoral part. The VEGF 121 expression was associated with hilar and/or mediastinal nodal involvement (P = 0.02), and, taken together, the VEGF isoforms were shown to significantly influence overall (P = 0.02) and disease-free survival (P = 0.03). As a regulator of tumour angiogenesis, VEGF may represent a useful indicator of progression and poor prognosis in non-small-cell lung carcinomas. © 1999 Cancer Research Campaig
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