433 research outputs found
On Vector Bundles of Finite Order
We study growth of holomorphic vector bundles E over smooth affine manifolds.
We define Finsler metrics of finite order on E by estimates on the holomorphic
bisectional curvature. These estimates are very similar to the ones used by
Griffiths and Cornalba to define Hermitian metrics of finite order. We then
generalize the Vanishing Theorem of Griffiths and Cornalba to the Finsler
context. We develop a value distribution theory for holomorphic maps from the
projectivization of E to projective space. We show that the projectivization of
E can be immersed into a projective space of sufficiently large dimension via a
map of finite order.Comment: version 2 has some typos corrected; to appear in Manuscripta
Mathematic
Can radiosensitivity associated with defects in DNA repair be overcome by mitochondrial-targeted antioxidant radioprotectors
Radiation oncologists have observed variation in normal tissue responses between patients in many instances with no apparent explanation. The association of clinical tissue radiosensitivity with specific genetic repair defects (Wegner's syndrome, Ataxia telangiectasia, Bloom's syndrome, and Fanconi anemia) has been well established, but there are unexplained differences between patients in the general population with respect to the intensity and rapidity of appearance of normal tissue toxicity including radiation dermatitis, oral cavity mucositis, esophagitis, as well as differences in response of normal tissues to standard analgesic or other palliative measures. Strategies for the use of clinical radioprotectors have included modalities designed to either prevent and/or palliate the consequences of radiosensitivity. Most prominently, modification of total dose, fraction size, or total time of treatment delivery has been necessary in many patients, but such modifications may reduce the likelihood of local control and/or radiocurability. As a model system in which to study potential radioprotection by mitochondrial-targeted antioxidant small molecules, we have studied cell lines and tissues from Fanconi anemia (Fancd2-/-) mice of two background strains (C57BL/6NHsd and FVB/N). Both were shown to be radiosensitive with respect to clonogenic survival curves of bone marrow stromal cells in culture and severity of oral cavity mucositis during single fraction or fractionated radiotherapy. Oral administration of the antioxidant GS-nitroxide, JP4-039, provided significant radioprotection, and also ameliorated distant bone marrow suppression (abscopal effect of irradiation) in Fancd2-/- mice. These data suggest that radiation protection by targeting the mitochondria may be of therapeutic benefit even in the setting of defects in the DNA repair process for irradiation-induced DNA double strand breaks. © 2014 Greenberger, Berhane, Shinde, Han Rhieu, Bernard, Wipf, Skoda and Epperly
Hyperholomorpic connections on coherent sheaves and stability
Let be a hyperkaehler manifold, and a torsion-free and reflexive
coherent sheaf on . Assume that (outside of its singularities) admits a
connection with a curvature which is invariant under the standard SU(2)-action
on 2-forms. If the curvature is square-integrable, then is stable and its
singularities are hyperkaehler subvarieties in . Such sheaves (called
hyperholomorphic sheaves) are well understood. In the present paper, we study
sheaves admitting a connection with SU(2)-invariant curvature which is not
necessarily square-integrable. This situation arises often, for instance, when
one deals with higher direct images of holomorphic bundles. We show that such
sheaves are stable.Comment: 37 pages, version 11, reference updated, corrected many minor errors
and typos found by the refere
Analysis of radiation-induced cell death in head and neck squamous cell carcinoma and rat liver maintained in microfluidic devices
Objective The aim of this study was to investigate how head and neck squamous cell carcinoma (HNSCC) tissue biopsies maintained in a pseudo in vivo environment within a bespoke microfluidic device respond to radiation treatment. Study Design Feasibility study. Setting Tertiary referral center. Subjects and Methods Thirty-five patients with HNSCC were recruited, and liver tissue from 5 Wistar rats was obtained. A microfluidic device was used to maintain the tissue biopsy samples in a viable state. Rat liver was used to optimize the methodology. HNSCC was obtained from patients with T1-T3 laryngeal or oropharyngeal SCC; N1-N2 metastatic cervical lymph nodes were also obtained. Irradiation consisted of single doses of between 2 Gy and 40 Gy and a fractionated course of 5Ă—2 Gy. Cell death was assessed in the tissue effluent using the soluble markers lactate dehydrogenase (LDH) and cytochrome c and in the tissue by immunohistochemical detection of cleaved cytokeratin18 (M30 antibody). Results A significant surge in LDH release was demonstrated in the rat liver after a single dose of 20 Gy; in HNSCC, it was seen after 40 Gy compared with the control. There was no significant difference in cytochrome c release after 5 Gy or 10 Gy. M30 demonstrated a dose-dependent increase in apoptotic index for a given increase in single-dose radiotherapy. There was a significant increase in apoptotic index between 1Ă—2 Gy and 5Ă—2 Gy. Conclusion M30 is a superior method compared with soluble markers in detecting low-dose radiation-induced cell death. This microfluidic technique can be used to assess radiation-induced cell death in HNSCC and therefore has the potential to be used to predict radiation response
On the cohomology of pseudoeffective line bundles
The goal of this survey is to present various results concerning the
cohomology of pseudoeffective line bundles on compact K{\"a}hler manifolds, and
related properties of their multiplier ideal sheaves. In case the curvature is
strictly positive, the prototype is the well known Nadel vanishing theorem,
which is itself a generalized analytic version of the fundamental
Kawamata-Viehweg vanishing theorem of algebraic geometry. We are interested
here in the case where the curvature is merely semipositive in the sense of
currents, and the base manifold is not necessarily projective. In this
situation, one can still obtain interesting information on cohomology, e.g. a
Hard Lefschetz theorem with pseudoeffective coefficients, in the form of a
surjectivity statement for the Lefschetz map. More recently, Junyan Cao, in his
PhD thesis defended in Grenoble, obtained a general K{\"a}hler vanishing
theorem that depends on the concept of numerical dimension of a given
pseudoeffective line bundle. The proof of these results depends in a crucial
way on a general approximation result for closed (1,1)-currents, based on the
use of Bergman kernels, and the related intersection theory of currents.
Another important ingredient is the recent proof by Guan and Zhou of the strong
openness conjecture. As an application, we discuss a structure theorem for
compact K{\"a}hler threefolds without nontrivial subvarieties, following a
joint work with F.Campana and M.Verbitsky. We hope that these notes will serve
as a useful guide to the more detailed and more technical papers in the
literature; in some cases, we provide here substantially simplified proofs and
unifying viewpoints.Comment: 39 pages. This survey is a written account of a lecture given at the
Abel Symposium, Trondheim, July 201
Enhanced Structural Control of Soft-Templated Mesoporous Inorganic Thin Films by Inert Processing Conditions
Mesoporous thin films are widely used for applications in need of high surface area and efficient mass and charge transport properties. A well-established fabrication process involves the supramolecular assembly of organic molecules (e.g., block copolymers and surfactants) with inorganic materials obtained by sol-gel chemistry. Typically, subsequent calcination in air removes the organic template and reveals the porous inorganic network. A significant challenge for such coatings is the anisotropic shrinkage due to the volume contraction related to solvent evaporation, inorganic condensation, and template removal, affecting the final porosity as well as pore shape, size, arrangement, and accessibility. Here, we show that a two-step calcination process, composed of high-temperature treatment in argon followed by air calcination, is an effective fabrication strategy to reduce film contraction and enhance structural control of mesoporous thin films. Crucially, the formation of a transient carbonaceous scaffold enables the inorganic matrix to fully condense before template removal. The resulting mesoporous films retain a higher porosity as well as bigger pores with extended porous order. Such films present favorable characteristics for mass transport of large molecules. This is demonstrated for lysozyme adsorption into the mesoporous thin films as an example of enzyme storage
A remark on the dimension of the Bergman space of some Hartogs domains
Let D be a Hartogs domain of the form D={(z,w) \in CxC^N : |w| < e^{-u(z)}}
where u is a subharmonic function on C. We prove that the Bergman space of
holomorphic and square integrable functions on D is either trivial or infinite
dimensional.Comment: 12 page
Talin is required for integrin-mediated platelet function in hemostasis and thrombosis
Integrins are critical for hemostasis and thrombosis because they mediate both platelet adhesion and aggregation. Talin is an integrin-binding cytoplasmic adaptor that is a central organizer of focal adhesions, and loss of talin phenocopies integrin deletion in Drosophila. Here, we have examined the role of talin in mammalian integrin function in vivo by selectively disrupting the talin1 gene in mouse platelet precursor megakaryocytes. Talin null megakaryocytes produced circulating platelets that exhibited normal morphology yet manifested profoundly impaired hemostatic function. Specifically, platelet-specific deletion of talin1 led to spontaneous hemorrhage and pathological bleeding. Ex vivo and in vitro studies revealed that loss of talin1 resulted in dramatically impaired integrin αIIbβ3-mediated platelet aggregation and β1 integrin–mediated platelet adhesion. Furthermore, loss of talin1 strongly inhibited the activation of platelet β1 and β3 integrins in response to platelet agonists. These data establish that platelet talin plays a crucial role in hemostasis and provide the first proof that talin is required for the activation and function of mammalian α2β1 and αIIbβ3 integrins in vivo
Lipoprotein ability to exchange and remove lipids from model membranes as a function of fatty acid saturation and presence of cholesterol
Lipoproteins play a central role in the development of atherosclerosis. High and low-density lipoproteins (HDL and LDL), known as 'good' and 'bad' cholesterol, respectively, remove and/or deposit lipids into the artery wall. Hence, insight into lipid exchange processes between lipoproteins and cell membranes is of particular importance in understanding the onset and development of cardiovascular disease. In order to elucidate the impact of phospholipid tail saturation and the presence of cholesterol in cell membranes on these processes, neutron reflection was employed in the present investigation to follow lipid exchange with both HDL and LDL against model membranes. Mirroring clinical risk factors for the development of atherosclerosis, lower exchange was observed in the presence of cholesterol, as well as for an unsaturated phospholipid, compared to faster exchange when using a fully saturated phospholipid. These results highlight the importance of membrane composition on the interaction with lipoproteins, chiefly the saturation level of the lipids and presence of cholesterol, and provide novel insight into factors of importance for build-up and reversibility of atherosclerotic plaque. In addition, the correlation between the results and well-established clinical risk factors suggests that the approach taken can be employed also for understanding a broader set of risk factors including, e.g., effects of triglycerides and oxidative stress, as well as local effects of drugs on atherosclerotic plaque formation
Loss of Ezh2 synergizes with JAK2-V617F in initiating myeloproliferative neoplasms and promoting myelofibrosis
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