3,712 research outputs found
The new English A Levels 2015: a guide to the specs
Ian Cushing, Marcello Giovanelli and Gary Snapper summarise the changes at A Level from September 2015 and explore the features of each of the new specs in all three A Level English subjects
Rational parametrization of conchoids to algebraic curves
We study the rationality of each of the components of the conchoid to an irreducible algebraic affine plane curve, excluding the trivial cases of the lines through the focus and the circle centered at the focus and radius the distance involved in the conchoid. We prove that conchoids having all their components rational can only be generated by rational curves. Moreover, we show that reducible conchoids to rational curves have always their two components rational. In addition, we prove that the rationality of the conchoid component, to a rational curve, does depend on the base curve and on the focus but not on the distance. As a consequence, we provide an algorithm that analyzes the rationality of all the components of the conchoid and, in the affirmative case, parametrizes them. The algorithm only uses a proper parametrization of the base curve and the focus and, hence, does not require the previous computation of the conchoid. As a corollary, we show that the conchoid to the irreducible conics, with conchoid-focus on the conic, are rational and we give parametrizations. In particular we parametrize the Limaçons of Pascal. We also parametrize the conchoids of Nicomedes. Finally, we show how to find the foci from where the conchoid is rational or with two rational components
Total Degree Formula for the Generic Offset to a Parametric Surface
We provide a resultant-based formula for the total degree w.r.t. the spatial
variables of the generic offset to a parametric surface. The parametrization of
the surface is not assumed to be proper.Comment: Preprint of an article to be published at the International Journal
of Algebra and Computation, World Scientific Publishing,
DOI:10.1142/S021819671100680
Cortactin regulates cell migration via activation of N-WASP
Cortactin is an actin-associated scaffolding protein that regulates cell migration. Amplification of the human gene, EMS1, has been detected in breast, head and neck tumors, where it correlates with increased invasiveness. Cortactin can regulate actin dynamics directly via its N-terminal half, which can bind and activate the Arp2/3 complex. The C-terminal portion of cortactin, however, is thought to have limited function in its regulation of the actin polymerization machinery. In this report, we identify a role for the cortactin C-terminus in regulating cell migration and, more specifically, actin dynamics. Overexpression of either full-length cortactin or cortactin C-terminus is sufficient to enhance migration of mammary epithelial cells. In vitro, cortactin binds to and activates, via its SH3 domain, a regulator of the Arp2/3 complex, neural Wiskott Aldrich Syndrome protein (N-WASP). This in vitro activation of N-WASP is likely to be important in vivo, as cortactin-enhanced migration is dependent upon N-WASP. Thus, our results suggest that cortactin has multiple mechanisms by which it can recruit and modulate the actin machinery and ultimately regulate cell migration
Evaluation of DNA primase DnaG as a potential target for antibiotics
Mycobacteria contain genes for several DNA-dependent RNA primases, including dnaG, which encodes an essential replication enzyme that has been proposed as a target for antituberculosis compounds. An in silico analysis revealed that mycobacteria also possess archaeo-eukaryotic superfamily primases (AEPs) of unknown function. Using a homologous recombination system, we obtained direct evidence that wild-type dnaG cannot be deleted from the chromosome of Mycobacterium smegmatis without disrupting viability, even in backgrounds in which mycobacterial AEPs are overexpressed. In contrast, single-deletion AEP mutants or mutants defective for all four identified M. smegmatis AEP genes did not exhibit growth defects under standard laboratory conditions. Deletion of native dnaG in M. smegmatis was tolerated only after the integration of an extra intact copy of the M. smegmatis or Mycobacterium tuberculosis dnaG gene, under the control of chemically inducible promoters, into the attB site of the chromosome. M. tuberculosis and M. smegmatis DnaG proteins were overproduced and purified, and their primase activities were confirmed using radioactive RNA synthesis assays. The enzymes appeared to be sensitive to known inhibitors (suramin and doxorubicin) of DnaG. Notably, M. smegmatis bacilli appeared to be sensitive to doxorubicin and resistant to suramin. The growth and survival of conditional mutant mycobacterial strains in which DnaG was significantly depleted were only slightly affected under standard laboratory conditions. Thus, although DnaG is essential for mycobacterial viability, only low levels of protein are required for growth. This suggests that very efficient inhibition of enzyme activity would be required for mycobacterial DnaG to be useful as an antibiotic target
WIP and WASP play complementary roles in T cell homing and chemotaxis to SDF-1a
Producción CientíficaHoming of lymphocytes to tissues is a biologically important multistep process that involves selectindependent
rolling, integrin-dependent adhesion and chemokine-directed chemotaxis. The actin
cytoskeleton plays a central role in lymphocyte adhesion and motility. Wiskott–Aldrich syndrome
protein (WASP), the product of the gene mutated in Wiskott–Aldrich syndrome, and its partner,
the Wiskott–Aldrich syndrome protein-interacting protein (WIP), play important roles in actin
re-organization in T lymphocytes. We used mice with disruption of the WASP and WIP genes to
examine the role of WASP and WIP in T cell homing. T cell homing to spleen and lymph nodes in vivo
was deficient in WASP / and WIP / mice and severely impaired in WASP / WIP / double knockout
(DKO) mice. Deficiency of WASP, WIP or both did not interfere with selectin-dependent rolling or
integrin-dependent adhesion of T cells in vitro. Chemotaxis to stromal cell-derived factor-1a (SDF-1a)
in vitro was mildly reduced in T cells from WASP / mice. In contrast, it was significantly impaired in
T cells from WIP / mice and severely reduced in T cells from DKO mice. Cellular F-actin increase
following SDF-1a stimulation was normal in WASP / and WIP / T cells, but severely reduced in
T cells from DKO mice. Actin re-organization and polarization in response to SDF-1a was abnormal in
T cells from all knockout mice. Early biochemical events following SDF-1a stimulation that are
important for chemotaxis and that included phosphorylation of Lck, cofilin, PAK1 and extracellular
regulated kinase (Erk) and GTP loading of Rac-1 were examined in T cells from DKO mice and found to
be normal. These results suggest that WASP and WIP are not essential for T lymphocyte rolling and
adhesion, but play important and partially redundant roles in T cell chemotaxis in vitro and homing
in vivo and function downstream of small GTPases
N-wasp Is Required For Structural Integrity Of The Blood-testis Barrier.
published_or_final_versio
Wiskott-Aldrich syndrome protein deficiency in innate immune cells leads to mucosal immune dysregulation and colitis in mice
BACKGROUND & AIMS: Immunodeficiency and autoimmune sequelae, including colitis, develop in patients and mice deficient in Wiskott-Aldrich Syndrome protein (WASP), a hematopoietic-specific intracellular signaling molecule that regulates the actin cytoskeleton. Development of colitis in WASP-deficient mice requires lymphocytes; transfer of T cells is sufficient to induce colitis in immunodeficient mice. We investigated the interactions between innate and adaptive immune cells in mucosal regulation during development of T-cell-mediated colitis in mice with WASP-deficient cells of the innate immune system. METHODS: Naïve and/or regulatory CD4(+) T cells were transferred from 129 SvEv mice into RAG-2 deficient (RAG-2 KO) mice or mice lacking WASP and RAG-2 (WRDKO). Animals were observed for the development of colitis; effector and regulatory functions of innate immune and T cells were analyzed with in vivo and in vitro assays. RESULTS: Transfer of unfractionated CD4(+) T cells induced severe colitis in WRDKO, but not RAG-2 KO, mice. Naïve wild-type T cells had higher levels of effector activity and regulatory T cells had reduced suppressive function when transferred into WRDKO mice compared to RAG-2 KO mice. Regulatory T-cell proliferation, generation, and maintenance of FoxP3 expression were reduced in WRDKO recipients, and associated with reduced numbers of CD103(+) tolerogenic dendritic cells and levels of interleukin (IL)-10. Administration of IL-10 prevented induction of colitis following transfer of T cells into WRDKO mice. CONCLUSIONS: Defective interactions between WASP-deficient innate immune cells and normal T cells disrupt mucosal regulation, potentially by altering the functions of tolerogenic dendritic cells, production of IL-10, and homeostasis of regulatory T cells
Characterization of Adherent Bacteroidales from Intestinal Biopsies of Children and Young Adults with Inflammatory Bowel Disease
There is extensive evidence implicating the intestinal microbiota in inflammatory bowel disease [IBD], but no microbial agent has been identified as a sole causative agent. Bacteroidales are numerically dominant intestinal organisms that associate with the mucosal surface and have properties that both positively and negatively affect the host. To determine precise numbers and species of Bacteroidales adherent to the mucosal surface in IBD patients, we performed a comprehensive culture based analysis of intestinal biopsies from pediatric Crohn's disease [CD], ulcerative colitis [UC], and control subjects. We obtained biopsies from 94 patients and used multiplex PCR or 16S rDNA sequencing of Bacteroidales isolates for species identification. Eighteen different Bacteroidales species were identified in the study group, with up to ten different species per biopsy, a number higher than demonstrated using 16S rRNA gene sequencing methods. Species diversity was decreased in IBD compared to controls and with increasingly inflamed tissue. There were significant differences in predominant Bacteroidales species between biopsies from the three groups and from inflamed and uninflamed sites. Parabacteroides distasonis significantly decreased in inflamed tissue. All 373 Bacteroidales isolates collected in this study grew with mucin as the only utilizable carbon source suggesting this is a non-pathogenic feature of this bacterial order. Bacteroides fragilis isolates with the enterotoxin gene [bft], previously associated with flares of colitis, were not found more often at inflamed colonic sites or within IBD subjects. B. fragilis isolates with the ability to synthesize the immunomodulatory polysaccharide A [PSA], previously shown to be protective in murine models of colitis, were not detected more often from healthy versus inflamed tissue
An Algebraic Analysis of Conchoids to Algebraic Curves
We study the conchoid to an algebraic affine plane curve C from the perspective of algebraic geometry, analyzing their main algebraic properties. Beside C, the notion of conchoid involves a point A in the affine plane (the focus) and a nonzero field element d (the distance).We introduce the formal definition of conchoid by means of incidence diagrams.We prove that the conchoid is a 1-dimensional algebraic set having atmost two irreducible components. Moreover, with the exception of circles centered at the focus A and taking d as its radius, all components of the corresponding conchoid have dimension 1. In addition, we introduce the notions of special and simple components of a conchoid. Furthermore we state that, with the exception of lines passing through A, the conchoid always has at least one simple component and that, for almost every distance, all the components of the conchoid are simple. We state that, in the reducible case, simple conchoid components are birationally equivalent to C, and we show how special components can be used to decide whether a given algebraic curve is the conchoid of another curve
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