547 research outputs found

    On a notion of maps between orbifolds, I. function spaces

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    This is the first of a series of papers which are devoted to a comprehensive theory of maps between orbifolds. In this paper, we define the maps in the more general context of orbispaces, and establish several basic results concerning the topological structure of the space of such maps. In particular, we show that the space of such maps of C^r-class between smooth orbifolds has a natural Banach orbifold structure if the domain of the map is compact, generalizing the corresponding result in the manifold case. Motivations and applications of the theory come from string theory and the theory of pseudoholomorphic curves in symplectic orbifolds.Comment: Final version, 46 pages. Accepted for publication in Communications in Contemporary Mathematics. A preliminary version of this work is under a different title "A homotopy theory of orbispaces", arXiv: math. AT/010202

    Genital Chlamydia trachomatis: understanding the roles of innate and adaptive immunity in vaccine research.

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    Chlamydia trachomatis is the leading cause of bacterial sexually transmitted disease worldwide, and despite significant advances in chlamydial research, a prophylactic vaccine has yet to be developed. This Gram-negative obligate intracellular bacterium, which often causes asymptomatic infection, may cause pelvic inflammatory disease (PID), ectopic pregnancies, scarring of the fallopian tubes, miscarriage, and infertility when left untreated. In the genital tract, Chlamydia trachomatis infects primarily epithelial cells and requires Th1 immunity for optimal clearance. This review first focuses on the immune cells important in a chlamydial infection. Second, we summarize the research and challenges associated with developing a chlamydial vaccine that elicits a protective Th1-mediated immune response without inducing adverse immunopathologies

    Targeting endothelial connexin40 inhibits tumor growth by reducing angiogenesis and improving vessel perfusion.

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    Endothelial connexin40 (Cx40) contributes to regulate the structure and function of vessels. We have examined whether the protein also modulates the altered growth of vessels in tumor models established in control mice (WT), mice lacking Cx40 (Cx40-/-), and mice expressing the protein solely in endothelial cells (Tie2-Cx40). Tumoral angiogenesis and growth were reduced, whereas vessel perfusion, smooth muscle cell (SMC) coverage and animal survival were increased in Cx40-/- but not Tie2-Cx40 mice, revealing a critical involvement of endothelial Cx40 in transformed tissues independently of the hypertensive status of Cx40-/- mice. As a result, Cx40-/- mice bearing tumors survived significantly longer than corresponding controls, including after a cytotoxic administration. Comparable observations were made in WT mice injected with a peptide targeting Cx40, supporting the Cx40 involvement. This involvement was further confirmed in the absence of Cx40 or by peptide-inhibition of this connexin in aorta-sprouting, matrigel plug and SMC migration assays, and associated with a decreased expression of the phosphorylated form of endothelial nitric oxide synthase. The data identify Cx40 as a potential novel target in cancer treatment
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