Junction conditions in General Relativity with spin sources

The junction conditions for General Relativity in the presence of domain walls with intrinsic spin are derived in three and higher dimensions. A stress tensor and a spin current can be defined just by requiring the existence of a well defined volume element instead of an induced metric, so as to allow for generic torsion sources. In general, when the torsion is localized on the domain wall, it is necessary to relax the continuity of the tangential components of the vielbein. In fact it is found that the spin current is proportional to the jump in the vielbein and the stress-energy tensor is proportional to the jump in the spin connection. The consistency of the junction conditions implies a constraint between the direction of flow of energy and the orientation of the spin. As an application, we derive the circularly symmetric solutions for both the rotating string with tension and the spinning dust string in three dimensions. The rotating string with tension generates a rotating truncated cone outside and a flat space-time with inevitable frame dragging inside. In the case of a string made of spinning dust, in opposition to the previous case no frame dragging is present inside, so that in this sense, the dragging effect can be "shielded" by considering spinning instead of rotating sources. Both solutions are consistently lifted as cylinders in the four-dimensional case.Comment: 24 pages, no figures, CECS style. References added and misprints corrected. Published Versio

The Universe as a topological defect

Four-dimensional Einstein's General Relativity is shown to arise from a gauge theory for the conformal group, SO(4,2). The theory is constructed from a topological dimensional reduction of the six-dimensional Euler density integrated over a manifold with a four-dimensional topological defect. The resulting action is a four-dimensional theory defined by a gauged Wess-Zumino-Witten term. An ansatz is found which reduces the full set of field equations to those of Einstein's General Relativity. When the same ansatz is replaced in the action, the gauged WZW term reduces to the Einstein-Hilbert action. Furthermore, the unique coupling constant in the action can be shown to take integer values if the fields are allowed to be analytically continued to complex values.Comment: 18 pages, LaTex, 4 figures. Title of the published version changed to "Universe as a Topological defect" by the journa

Gauged WZW models for space-time groups and gravitational actions

In this paper we investigate gauged Wess-Zumino-Witten models for space-time groups as gravitational theories, following the trend of recent work by Anabalon, Willison and Zanelli. We discuss the field equations in any dimension and study in detail the simplest case of two space-time dimensions and gauge group SO(2,1). For this model we study black hole solutions and we calculate their mass and entropy which resulted in a null value for both.Comment: 26 pages, no figure

Evaluating Unpaid Time Contributions by Seniors: A Conceptual Framework

In the past, considerable research in gerontology has focused on services provided to seniors. Recently, however, there has a been a growing recognition of the contributions made by seniors to their families, communities and to society. Empirical estimates have been provided by researchers to show how much these contributions are worth in terms of savings in dollar amounts. A critical review of the literature identifies unresolved issues concerning which contributions to count and how to measure and value these contributions. As yet, no clear criteria exist that readily identify the distinction between volunteer activities and unpaid work, what specifically should be counted as an unpaid time contribution, how it should be quantified, and how this unit of contribution should be monetarily valued. The market replacement approach and the opportunity cost approach that are used to assign value to unpaid work often use very different wage rates or levels of income loss. This paper reviews the relevant literature and identifies important issues in evaluating unpaid time contribution of seniors. The authors propose a framework which addresses some of the methodological shortcomings identified in previous research and which provides a guide for future research in this area.seniors; valuing unpaid work

Identification moléculaire des souches de mycobactéries

L’identification moléculaire des souches de mycobactéries disponibles dans notre laboratoire a été réalisée. L’amplification par PCR des gènes de hsp, ARNr16S, espaceurs intergéniques ARNr16S-23S suivie de l’électrophorèse sur gel d’agarose des fragments obtenus avec les oligonucléotides Tb11 et Tb12, 248 et 42, Int16S et Int23S, révèle la constance dans la taille des fragments pour toutes les souches et par paire d’oligonucléotides. Ces résultats sont confirmés par la RFLP qui ne montre pas de différences significatives entre les différentes souches. Dans ce cas la discrimination des souches est difficile, on peut penser qu’il s’agit d’un seul genre. Par contre la taille des fragments obtenus avec les oligonucléotides H49 et H50, GyrAF et GyrAR permet de distinguer trois groupes de souches, les souches 6PY, C-8, C-18, et C-19 forment un premier groupe, les souches BHF004, C-20 et SPYR forment un deuxième groupe, et enfin la souche PYR-1 forme un troisième groupe.Le séquençage et l’alignement multiple avec Clustal des séquences en comparaison d’une part avec Mycobacterium gilvum pour le premier groupe et d’autre part avec Mycobacterium vanbaalenii et Mycobacterium austroafricanum pour le deuxième groupe, confirment par le taux de similarité élevé (99- 100%) cette classification. Un arbre phylogénétique basée sur les séquences partielles du gène hsp65, permet de situer les nouvelles par rapport aux autres mycobactéries .Cela corrobore bien avec nos résultats, tout en confirmant la cohérence de ces trois espèces dans le genre monophylétique Mycobacterium.Mots-clés : mycobactéries, oligonucléotides, amplification par PCR, séquençage, alignement multiple

Differential binding patterns of anti-sulfatide antibodies to glial membranes

Sulfatide is a major glycosphingolipid in myelin and a target for autoantibodies in autoimmune neuropathies. However neuropathy disease models have not been widely established, in part because currently available monoclonal antibodies to sulfatide may not represent the diversity of anti-sulfatide antibody binding patterns found in neuropathy patients. We sought to address this issue by generating and characterising a panel of new anti-sulfatide monoclonal antibodies. These antibodies have sulfatide reactivity distinct from existing antibodies in assays and in binding to peripheral nerve tissues and can be used to provide insights into the pathophysiological roles of anti-sulfatide antibodies in demyelinating neuropathies

Tetanus toxin is internalized by a sequential clathrin-dependent mechanism initiated within lipid microdomains and independent of epsin1

Ligand–receptor complexes are internalized by a variety of endocytic mechanisms. Some are initiated within clathrin-coated membranes, whereas others involve lipid microdomains of the plasma membrane. In neurons, where alternative targeting to short- or long-range trafficking routes underpins the differential processing of synaptic vesicle components and neurotrophin receptors, the mechanism giving access to the axonal retrograde pathway remains unknown. To investigate this sorting process, we examined the internalization of a tetanus neurotoxin fragment (TeNT HC), which shares axonal carriers with neurotrophins and their receptors. Previous studies have shown that the TeNT HC receptor, which comprises polysialogangliosides, resides in lipid microdomains. We demonstrate that TeNT HC internalization also relies on a specialized clathrin-mediated pathway, which is independent of synaptic vesicle recycling. Moreover, unlike transferrin uptake, this AP-2–dependent process is independent of epsin1. These findings identify a pathway for TeNT, beginning with the binding to a lipid raft component (GD1b) and followed by dissociation from GD1b as the toxin internalizes via a clathrin-mediated mechanism using a specific subset of adaptor proteins

Multigene expression of protein complexes by iterative modification of genomic Bacmid DNA

<p>Abstract</p> <p>Background</p> <p>Many cellular multi-protein complexes are naturally present in cells at low abundance. Baculovirus expression offers one approach to produce milligram quantities of correctly folded and processed eukaryotic protein complexes. However, current strategies suffer from the need to produce large transfer vectors, and the use of repeated promoter sequences in baculovirus, which itself produces proteins that promote homologous recombination. One possible solution to these problems is to construct baculovirus genomes that express each protein in a complex from a separate locus within the viral DNA. However current methods for selecting such recombinant genomes are too inefficient to routinely modify the virus in this way.</p> <p>Results</p> <p>This paper reports a method which combines the lambda red and bacteriophage P1 Cre-recombinase systems to efficiently generate baculoviruses in which protein complexes are expressed from multiple, single-locus insertions of foreign genes. This method is based on an 88 fold improvement in the selection of recombinant viruses generated by red recombination techniques through use of a bipartite selection cassette. Using this system, seven new genetic loci were identified in the AcMNPV genome suitable for the high level expression of recombinant proteins. These loci were used to allow the recovery two recombinant virus-like particles with potential biotechnological applications (influenza A virus HA/M1 particles and bluetongue virus VP2/VP3/VP5/VP7 particles) and the mammalian chaperone and cancer drug target CCT (16 subunits formed from 8 proteins).</p> <p>Conclusion</p> <p><b>1</b>. Use of bipartite selections can significantly improve selection of modified bacterial artificial chromosomes carrying baculovirus DNA. Furthermore this approach is sufficiently robust to allow routine modification of the virus genome. <b>2</b>. In addition to the commonly used <it>p10 </it>and polyhedrin loci, the <it>ctx, egt, 39k, orf51, gp37, iap2 </it>and <it>odv-e56 </it>loci in AcMNPV are all suitable for the high level expression of heterologous genes. <b>3</b>. Two protein, four protein and eight protein complexes including virus-like particles and cellular chaperone complexes can be produced using the new approach.</p