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Biomedical subjects

D Arnold

Publications and source records attributed to D Arnold.

At least 145 records · Page 8Linked to original sources
PubMed1976

Cell surface mannosyl transferase activity in the liver of embryonic chick. A mannose containing glycolipid as intermediate in glycoprotein synthesis.

Trypsin dissociated intact cells of embryonic chick liver catalyze the transfer of mannose from exogenous GDP-mannose to glycoprotein in vitro. In cells of 8 day old embryos a surface bound mannosyltransferase-system forms several mannose containing isoprenoid-lipids in a primary step. One of these compounds serves as a substrate in the highly specific second step of the overall reaction, the transfer of mannose to glycoprotein. The isoprenoic intermediate has been isolated and its effectivity as substrate for the incorporation of mannose into glycoprotein has been examined.

Animals↗
PubMed1976

Cell surface glycosyl transferase activities in liver cells of developing chicken embryos.

The cell surface of embryonic chick liver cells contains transferases for mannose, fucose, galactose, N-acetyl-glucosamine and N-acetyl-neuraminic acid. Liver cells obtained by trypsin-dissociation of the tissue use the corresponding exogenous sugar nucleotides as substrates. The activities of the enzymes tested do not depend neither no the dissociation procedure nor on de novo protein synthesis. They vary considerably during development of the embryos, reaching maximal values at the 8th+/-1 day and at the 12th+/-1 day. Glycoproteins are the final stable endogenous acceptors for all sugars. Mannose transfer proceeds via a two or multistep reaction sequence. In a first step labile lipophilic intermediates are formed. Mannose can be liberated by treating the intermediates with 0.1 N HCl at 100 degrees C. In a second reaction step mannose becomes attached to glycoproteins. From embryonic chick liver cells a glycopeptide fraction has been obtained by pronase digestion followed by several purification steps. The purified glycopeptides inhibit all transferase systems and act as exogenous acceptors for mannose transfered from exogenous GDP-mannose.

Animals↗
PubMedDate not supplied

Autoschizis of human ovarian carcinoma cells: scanning electron and light microscopy of a new cell death induced by sodium ascorbate: menadione treatment.

Human ovarian carcinoma (MDAH 2774) cells were treated with sodium ascorbate (VC), menadione (VK3), or a combination of both in a ratio 100:1 for 1h and then examined with scanning electron microscopy (SEM) and light microscopy (LM). Light microscopy data corroborated SEM observations, which demonstrated that death of VC+VK3-treated tumor cells occurred primarily by autoschizis. This type of cell death is characterized by a decrease in cell size, cytoplasmic self-excisions, and nuclear and nucleolar morphologic degradations without the formation of apoptotic bodies. Ultimately, cell death results from karyorrhexis and karyolysis. This study illustrates that plasma membrane damage (branching filopodia, blisters, blebs) results from VC treatment; cytoskeletal damage and self-morsellation are caused by VC, VK3 and VC+VK, treatments. The VC treatment results in a 23% decrease in cell diameter while VK3-treated cells decrease cell diameter by 66%. After 1h of VC+VK3 treatment, a heterogenous cell population is found. This population can be resolved into one population whose diameters are 23% smaller than those of sham-treated cells, and a second population whose diameters are approximately twice those of sham-treated cells. This second population is indicative of doublet formation in which the cells appear to be dividing (an early stage of autoschizic cell death). One half of the doublet contains the cell nucleus while the other half consists of cytoplasm and membrane only. The enucleate portion of this doublet will then be excised. When the types of cell death are enumerated following VC+VK3 treatment, 43% of the cells die by autoschizis, 3% by apoptosis, and 1.9% by oncosis. These results confirm that autoschizis is the principal form of cell death that results from the in vitro treatment of human ovarian carcinoma cells with the vitamin combination.

Adenocarcinoma↗
PubMedDate not supplied

Efficiency calibration of high volume samples using the GESPECOR software.

In this paper the Monte Carlo simulation program GESPECOR is applied for the computation of the efficiency of an HPGe gamma-spectrometry system used for the measurement of high volume samples. The detector characterization required for Monte Carlo simulation is achieved by a trial and error procedure using the efficiency values measured with point sources placed in several positions. After detector characterization, the efficiency values appropriate for the assessment of 220l waste drums are computed and compared with experimental values.

Journal Article↗
PubMedDate not supplied

Underground measurements of radioactivity.

The exceptional sensitivity of gamma-ray spectrometry in underground laboratories has increasing application because of the important science and technology that it allows to be studied. Early work focused on rare fundamental phenomena, e.g. double beta decay, but a growing number of underground measurements is being performed in fields such as environmental monitoring, surveillance of nuclear activities, benchmarking of other physical techniques and materials selection for equipment which require materials with extremely low levels of radioactivity. This report describes the state of the art in underground gamma-ray spectrometry. Backgrounds of HPGe-detectors at various underground laboratories are presented and compared. Improved techniques and detectors are described and needs of deep underground facilities for higher sensitivity measurements are discussed.

Journal Article↗
PubMedDate not supplied

Reference measurements of low levels of 60Co in steel.

Analysis of 60Co traces in the matrix steel has recently gained in importance. This paper deals with the low-level gamma-ray spectrometry measurements that were part of a recent German survey aiming at determining the present levels of artificial radionuclides in commercial steel. Specific 60Co activities in the order of 10(-5) Bq g(-1) were measured. To show equivalence in these measurements, a comparison exercise of European underground laboratories has been carried out, additionally.

Journal Article↗
PubMedDate not supplied

Transfer of the efficiency calibration of Germanium gamma-ray detectors using the GESPECOR software.

The GESPECOR software was extended to incorporate procedures for the computation of the efficiency transfer factor for cases of practical interest: (a) sources with identical geometry, but different matrices, (b) sources with similar (but not identical) geometry; and (c) transfer from a point source to a volume source. Fast and accurate algorithms. based on correlated sampling, were implemented for solving the first two cases. A procedure to take into account the imperfect charge collection in the detector was implemented.

Journal Article↗
PubMedDate not supplied

Development of the NIST bone ash standard reference material for environmental radioactivity measurement.

The bone ash standard reference material (SRM), a blend of 4% contaminated human bone and 96% diluent bovine bone, has been developed for radiochemical method validation and quality control for radio-bone analysis. The massic activities of 90Sr, 226Ra, 230Th, 232Th, 234U, 235U, 238U, 238Pu, (239 + 240)Pu and (243 + 244)Cm were certified using a variety of radiochemical procedures and detection methods. Measurements confirmed undetectable radionuclide heterogeneity down to a sample size of 5 g. thereby implying adequate blending of particulate materials with dilution factors of up to 17,900. The results among most of the intercomparison laboratories and their methods were consistent. Disequilibrium was observed for decay chains: 234U(0.67 mBq/g)-230Th(0.47 mBq/g)-226Ra(15.1 mBq/g)-210Pb(23 mBq/g)-210Po(13 mBq/g) and 232Th(0.99 mBq/g)-228 Ra(6.1 mBq/g)-228Th(7.1 mBq/g). The disequilibria were the results of mixing occupationally contaminated human bone with natural bovine bone and the fractionation during internal biological processes. The massic activity of 210Pb, 228Th and 241Am were not certified because of insufficient 228Ra and 241Pu data and lack of knowledge in how 222Rn and its daughters will be fractionated in the SRM bottle over time.

Animals↗