363 research outputs found
The Endosymbiont Wolbachia pipientis Induces the Expression of Host Antioxidant Proteins in an Aedes albopictus Cell Line
Wolbachia are obligate intracellular bacteria which commonly infect arthropods. They are maternally inherited and capable of altering host development, sex determination, and reproduction. Reproductive manipulations include feminization, male-killing, parthenogenesis, and cytoplasmic incompatibility. The mechanism by which Wolbachia avoid destruction by the host immune response is unknown. Generation of antimicrobial peptides (AMPs) and reactive oxygen species (ROS) by the host are among the first lines of traditional antimicrobial defense. Previous work shows no link between a Wolbachia infection and the induction of AMPs. Here we compare the expression of protein in a cell line naturally infected with Wolbachia and an identical cell line cured of the infection through the use of antibiotics. Protein extracts of each cell line were analyzed by two dimensional gel electrophoresis and LC/MS/MS. Our results show the upregulation of host antioxidant proteins, which are active against ROS generated by aerobic cell metabolism and during an immune response. Furthermore, flow cytometric and microscopic analysis demonstrates that ROS production is significantly greater in Wolbachia-infected mosquito cells and is associated with endosymbiont-containing vacuoles located in the host cell cytoplasm. This is the first empirical data supporting an association between Wolbachia and the insect antioxidant system
Efficacy and Safety of Microsurgery in Interdisciplinary Treatment of Sarcoma Affecting the Bone
Background: Sarcomas are tumors of mesenchymal origin with high variation in anatomical localization. Sarcomas affecting the bone often require an interdisciplinary resection and reconstruction approach. However, it is critical that microsurgical reconstruction strategies do not negatively impact tumor safety and overall survival, as limb salvage is only the secondary goal of tumor surgery. Here, we analyzed the efficacy and safety of microsurgery in interdisciplinary treatment of sarcoma affecting the bone.
Patients and Methods: We performed a retrospective chart review of all patients treated for soft-tissue and bone sarcoma at the senior author's institution with a focus on bone affection and microsurgical reconstruction between 2000 and 2019. This particular subgroup was further investigated for tumor resection status, 5-year survival rate, length of hospital stay, as well as overall complication and amputation rates.
Results: Between 2000 and 2019, 803 patients were operated for sarcoma resection and reconstruction by the Department of Plastic and Hand Surgery. Of these, 212 patients presented with sarcoma of the extremity affecting the bone. Within this subgroup, 40 patients required microsurgical reconstruction for limb salvage, which was possible in 38 cases. R0 resection was achieved in 93.8%. The 5-year survival was 96.7%, and the overall complication rate was 25%, of which 40% were microsurgery associated complications.
Conclusion: Safe and function-preserving treatment of soft-tissue and bone sarcoma is challenging. Primary reconstruction with microsurgical techniques of sarcoma-related defects enables limb-sparing and adequate oncosurgical cancer treatment without increasing the risk for local recurrence or prolonged hospital stay. The treatment of sarcoma patients should be reserved to high-volume centers with experienced plastic surgeon embedded in a comprehensive treatment concept
A transitional fossil mite (Astigmata: Levantoglyphidae fam. n.) from the early Cretaceous suggests gradual evolution of phoresy-related metamorphosis
Abstract Metamorphosis is a key innovation allowing the same species to inhabit different environments and accomplish different functions, leading to evolutionary success in many animal groups. Astigmata is a megadiverse lineage of mites that expanded into a great number of habitats via associations with invertebrate and vertebrate hosts (human associates include stored food mites, house dust mites, and scabies). The evolutionary success of Astigmata is linked to phoresy-related metamorphosis, namely the origin of the heteromorphic deutonymph, which is highly specialized for phoresy (dispersal on hosts). The origin of this instar is enigmatic since it is morphologically divergent and no intermediate forms are known. Here we describe the heteromorphic deutonymph of Levantoglyphus sidorchukae n. gen. and sp. (Levantoglyphidae fam. n.) from early Cretaceous amber of Lebanon (129 Ma), which displays a transitional morphology. It is similar to extant phoretic deutonymphs in its modifications for phoresy but has the masticatory system and other parts of the gnathosoma well-developed. These aspects point to a gradual evolution of the astigmatid heteromorphic morphology and metamorphosis. The presence of well-developed presumably host-seeking sensory elements on the gnathosoma suggests that the deutonymph was not feeding either during phoretic or pre- or postphoretic periods
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BCL6 enables Ph+ acute lymphoblastic leukaemia cells to survive BCR-ABL1 kinase inhibition.
Tyrosine kinase inhibitors (TKIs) are widely used to treat patients with leukaemia driven by BCR-ABL1 (ref. 1) and other oncogenic tyrosine kinases. Recent efforts have focused on developing more potent TKIs that also inhibit mutant tyrosine kinases. However, even effective TKIs typically fail to eradicate leukaemia-initiating cells (LICs), which often cause recurrence of leukaemia after initially successful treatment. Here we report the discovery of a novel mechanism of drug resistance, which is based on protective feedback signalling of leukaemia cells in response to treatment with TKI. We identify BCL6 as a central component of this drug-resistance pathway and demonstrate that targeted inhibition of BCL6 leads to eradication of drug-resistant and leukaemia-initiating subclones
Radiosensitization of HNSCC cells by EGFR inhibition depends on the induction of cell cycle arrests
The increase in cellular radiosensitivity by EGF receptor (EGFR) inhibition has been shown to be attributable to the induction of a G1-arrest in p53-proficient cells. Because EGFR targeting in combination with radiotherapy is used to treat head and neck squamous cell carcinomas (HNSCC) which are predominantly p53 mutated, we tested the effects of EGFR targeting on cellular radiosensitivity, proliferation, apoptosis, DNA repair and cell cycle control using a large panel of HNSCC cell lines. In these experiments EGFR targeting inhibited signal transduction, blocked proliferation and induced radiosensitization but only in some cell lines and only under normal (pre-plating) conditions. This sensitization was not associated with impaired DNA repair (53BP1 foci) or induction of apoptosis. However, it was associated with the induction of a lasting G2-arrest. Both, the radiosensitization and the G2-arrest were abrogated if the cells were re-stimulated (delayed plating) with actually no radiosensitization being detectable in any of the 14 tested cell lines. Therefore we conclude that EGFR targeting can induce a reversible G2 arrest in p53 deficient HNSCC cells, which does not consequently result in a robust cellular radiosensitization. Together with recent animal and clinical studies our data indicate that EGFR inhibition is no effective strategy to increase the radiosensitivity of HNSCC cells.</p
Spin states of the first four holes in a silicon nanowire quantum dot
We report measurements on a silicon nanowire quantum dot with a clarity that
allows for a complete understanding of the spin states of the first four holes.
First, we show control of the hole number down to one. Detailed measurements at
perpendicular magnetic fields reveal the Zeeman splitting of a single hole in
silicon. We are able to determine the ground-state spin configuration for one
to four holes occupying the quantum dot and find a spin filling with
alternating spin-down and spin-up holes, which is confirmed by
magnetospectroscopy up to 9T. Additionally, a so far inexplicable feature in
single-charge quantum dots in many materials systems is analyzed in detail. We
observe excitations of the zero-hole ground-state energy of the quantum dot,
which cannot correspond to electronic or Zeeman states. We show that the most
likely explanation is acoustic phonon emission to a cavity between the two
contacts to the nanowire.Comment: 24 pages, 8 figures, both including supporting informatio
Theory of Vibrationally Inelastic Electron Transport through Molecular Bridges
Vibrationally inelastic electron transport through a molecular bridge that is
connected to two leads is investigated. The study is based on a generic model
of vibrational excitation in resonant transmission of electrons through a
molecular junction. Employing methods from electron-molecule scattering theory,
the transmittance through the molecular bridge can be evaluated numerically
exactly. The current through the junction is obtained approximately using a
Landauer-type formula. Considering different parameter regimes, which include
both the case of a molecular bridge that is weakly coupled to the leads,
resulting in narrow resonance structures, and the opposite case of a broad
resonance caused by strong interaction with the leads, we investigate the
characteristic effects of coherent and dissipative vibrational motion on the
electron transport. Furthermore, the validity of widely used approximations
such as the wide-band approximation and the restriction to elastic transport
mechanisms is investigated in some detail.Comment: Submited to PRB, revised version according to comments of referees
(minor text changes and new citations
Vibrational Excitations in Weakly Coupled Single-Molecule Junctions: A Computational Analysis
In bulk systems, molecules are routinely identified by their vibrational
spectrum using Raman or infrared spectroscopy. In recent years, vibrational
excitation lines have been observed in low-temperature conductance measurements
on single molecule junctions and they can provide a similar means of
identification. We present a method to efficiently calculate these excitation
lines in weakly coupled, gateable single-molecule junctions, using a
combination of ab initio density functional theory and rate equations. Our
method takes transitions from excited to excited vibrational state into account
by evaluating the Franck-Condon factors for an arbitrary number of vibrational
quanta, and is therefore able to predict qualitatively different behaviour from
calculations limited to transitions from ground state to excited vibrational
state. We find that the vibrational spectrum is sensitive to the molecular
contact geometry and the charge state, and that it is generally necessary to
take more than one vibrational quantum into account. Quantitative comparison to
previously reported measurements on pi-conjugated molecules reveals that our
method is able to characterize the vibrational excitations and can be used to
identify single molecules in a junction. The method is computationally feasible
on commodity hardware.Comment: 9 pages, 7 figure
MultiFit: a web server for fitting multiple protein structures into their electron microscopy density map
Advances in electron microscopy (EM) allow for structure determination of large biological assemblies at increasingly higher resolutions. A key step in this process is fitting multiple component structures into an EM-derived density map of their assembly. Here, we describe a web server for this task. The server takes as input a set of protein structures in the PDB format and an EM density map in the MRC format. The output is an ensemble of models ranked by their quality of fit to the density map. The models can be viewed online or downloaded from the website. The service is available at; http://salilab.org/multifit/ and http://bioinfo3d.cs.tau.ac.il/
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