133 research outputs found
Fundamentals of the oxidation protection of tantalum Final report
Fundamentals of oxidation protection of tantalum by silicide
Fundamentals of the oxidation protection of columbium and tantalum Semiannual report, Apr. 1 - Oct. 1, 1967
Oxidation protection of niobium and tantalum by their silicide
Fundamentals of the oxidation protection of columbium and tantalum Semiannual report, 1 Apr. - 1 Oct. 1969
Oxidation protection by silicides of niobium and tantalum, and thermochemical dat
The role of the cytoskeleton in volume regulation and beading transitions in PC12 neurites
We present investigations on volume regulation and beading shape transitions
in PC12 neurites conducted using a flow-chamber technique. By disrupting the
cell cytoskeleton with specific drugs we investigate the role of its individual
components in the volume regulation response. We find that microtubule
disruption increases both swelling rate and maximum volume attained, but does
not affect the ability of the neurite to recover its initial volume. In
addition, investigation of axonal beading --also known as pearling
instability-- provides additional clues on the mechanical state of the neurite.
We conclude that the initial swelling phase is mechanically slowed down by
microtubules, while the volume recovery is driven by passive diffusion of
osmolites. Our experiments provide a framework to investigate the role of
cytoskeletal mechanics in volume homeostasis
Cell–Matrix De-Adhesion Dynamics Reflect Contractile Mechanics
Measurement of the mechanical properties of single cells is of increasing interest both from a fundamental cell biological perspective and in the context of disease diagnostics. In this study, we show that tracking cell shape dynamics during trypsin-induced de-adhesion can serve as a simple but extremely useful tool for probing the contractility of adherent cells. When treated with trypsin, both SW13−/− epithelial cells and U373 MG glioma cells exhibit a brief lag period followed by a concerted retraction to a rounded shape. The time–response of the normalized cell area can be fit to a sigmoidal curve with two characteristic time constants that rise and fall when cells are treated with blebbistatin and nocodazole, respectively. These differences can be attributed to actomyosin-based cytoskeletal remodeling, as evidenced by the prominent buildup of stress fibers in nocodazole-treated SW13−/− cells, which are also two-fold stiffer than untreated cells. Similar results observed in U373 MG cells highlights the direct association between cell stiffness and the de-adhesion response. Faster de-adhesion is obtained with higher trypsin concentration, with nocodazole treatment further expediting the process and blebbistatin treatment blunting the response. A simple finite element model confirms that faster contraction is achieved with increased stiffness
C60: the first one-component gel?
Until now, gels have been formed of multicomponent soft matter systems,
consisting of a solvent and one or more macromolecular or colloidal species.
Here we show that, for sufficient quench rates, the Girifalco model of C60 can
form gels which we identify by their slow dynamics and long-lived network
structure. These gels are stable at room temperature, at least on the
simulation timescale up to 100 ns. At moderate temperatures around 1000 K,
below the bulk glass transition temperature, C60 exhibits crystallisation and
phase separation proceeds without the dynamical arrest associated with
gelation, in contrast to many colloidal systems.Comment: Accepted by J. Phys. Chem. C. special issue 'Clusters in complex
fluids
Vasodilator Phosphostimulated Protein (VASP) Protects Endothelial Barrier Function During Hypoxia
The endothelial barrier controls the passage of solutes from the vascular space. This is achieved through active reorganization of the actin cytoskeleton. A central cytoskeletal protein involved into this is vasodilator-stimulated phosphoprotein (VASP). However, the functional role of endothelial VASP during hypoxia has not been thoroughly elucidated. We determined endothelial VASP expression through real-time PCR (Rt-PCR), immunhistochemistry, and Western blot analysis during hypoxia. VASP promoter studies were performed using a PGL3 firefly luciferase containing plasmid. Following approval by the local authorities, VASP−/− mice and littermate controls were subjected to normobaric hypoxia (8% O2, 92% N2) after intravenous injection of Evans blue dye. In in vitro studies, we found significant VASP repression in human microvascular and human umbilical vein endothelial cells through Rt-PCR, immunhistochemistry, and Western blot analysis. The VASP promoter construct demonstrated significant repression in response to hypoxia, which was abolished when the binding of hypoxia-inducible factor 1 alpha was excluded. Exposure of wild-type (WT) and VASP−/− animals to normobaric hypoxia for 4 h resulted in an increase in Evans blue tissue extravasation that was significantly increased in VASP−/− animals compared to WT controls. In summary, we demonstrate here that endothelial VASP holds significant importance for endothelial barrier properties during hypoxia
Expression of Calmodulin and Myosin Light Chain Kinase during Larval Settlement of the Barnacle Balanus amphitrite
Barnacles are one of the most common organisms in intertidal areas. Their life cycle includes seven free-swimming larval stages and sessile juvenile and adult stages. The transition from the swimming to the sessile stages, referred to as larval settlement, is crucial for their survivor success and subsequent population distribution. In this study, we focused on the involvement of calmodulin (CaM) and its binding proteins in the larval settlement of the barnacle, Balanus ( = Amphibalanus) amphitrite. The full length of CaM gene was cloned from stage II nauplii of B. amphitrite (referred to as Ba-CaM), encoding 149 amino acid residues that share a high similarity with published CaMs in other organisms. Quantitative real-time PCR showed that Ba-CaM was highly expressed in cyprids, the stage at which swimming larvae are competent to attach and undergo metamorphosis. In situ hybridization revealed that the expressed Ba-CaM gene was localized in compound eyes, posterior ganglion and cement glands, all of which may have essential functions during larval settlement. Larval settlement assays showed that both the CaM inhibitor compound 48/80 and the CaM-dependent myosin light chain kinase (MLCK) inhibitor ML-7 effectively blocked barnacle larval settlement, whereas Ca2+/CaM-dependent kinase II (CaMKII) inhibitors did not show any clear effects. The subsequent real-time PCR assay showed a higher expression level of Ba-MLCK gene in larval stages than in adults, suggesting an important role of Ba-MLCK gene in larval development and competency. Overall, the results suggest that CaM and CaM-dependent MLCK function during larval settlement of B. amphitrite
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