3,023 research outputs found

    Synergistic interaction between the Arp2/3 complex and cofilin drives stimulated lamellipod extension

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    Both the Arp2/3 complex and cofilin are believed to be important for the generation of protrusive force at the leading edge; however, their relative contributions have not been explored in vivo. Our results with living cells show that cofilin enters the leading edge immediately before the start of lamellipod extension, slightly earlier than Arp2/3, which begins to be recruited slightly later as the lamellipod is extended. Blocking either the Arp2/3 complex or cofilin function in cells results in failure to extend broad lamellipods and inhibits free barbed ends, suggesting that neither factor on its own can support actin polymerization-mediated protrusion in response to growth factor stimulation. High-resolution analysis of the actin network at the leading edge supports the idea that both the severing activity of cofilin and the specific branching activity of the Arp2/3 complex are essential for lamellipod protrusion. These results are the first to document the relative contributions of cofilin and Arp2/3 complex in vivo and indicate that cofilin begins to initiate the generation of free barbed ends that act in synergy with the Arp2/3 complex to create a large burst in nucleation activity

    B\,^1\Sigma^{+}_{u} and EF\,^{1}\Sigma^{+}_{g} level energies of D2_{2}

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    Accurate absolute level energies of the B\,^1\Sigma^{+}_{u}, v=08,Nv=0-8, N and EF\,^{1}\Sigma^{+}_{g}, v=021,Nv=0-21, N rovibrational quantum states of molecular deuterium are derived by combining results from a Doppler-free two-photon laser excitation study on several lines in the EF1Σg+X1Σg+EF\,{}^{1}\Sigma_{g}^{+}-X\,{}^{1}\Sigma_{g}^{+} (0,0) band, with results from a Fourier-transform spectroscopic emission study on a low-pressure hydrogen discharge. Level energy uncertainties as low as 0.0005 cm1^{-1} are obtained for some low-lying E\,^{1}\Sigma^{+}_{g} inner-well rovibrational levels, while uncertainties for higher-lying rovibrational levels and those of the F\,^{1}\Sigma^{+}_{g} outer-well states are nominally 0.005 cm1^{-1}. Level energies of B\,^1\Sigma^{+}_{u} rovibrational levels, for v8v \leq 8 and N10N \leq 10 are determined at an accuracy of 0.001 cm1^{-1}. Computed wavelengths of D2_2 Lyman transitions in the B\,^1\Sigma^{+}_{u}-X\,^{1}\Sigma^{+}_{g} (v,0v,0) bands are also tabulated for future applications.Comment: appears in Journal of Molecular Spectroscopy (2014

    Actin at cell-cell junctions is composed of two dynamic and functional populations

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    The ability of epithelial cells to polarize requires cell-cell adhesion mediated by cadherin receptors. During cell-cell contact, the mechanism via which a flat, spread cell shape is changed into a tall, cuboidal epithelial morphology is not known. We found that cadherin-dependent adhesion modulates actin dynamics by triggering changes in actin organization both locally at junctions and within the rest of the cell. Upon induction of cell-cell contacts, two spatial actin populations are distinguishable: junctional actin and peripheral thin bundles. With time, the relative position of these two populations changes and becomes indistinguishable to form a cortical actin ring that is characteristic of mature, fully polarized epithelial cells. Junctional actin and thin actin bundles differ in their actin dynamics and mechanism of formation, and interestingly, have distinct roles during epithelial polarization. Whereas junctional actin stabilizes clustered cadherin receptors at cell-cell contacts, contraction of peripheral actin bundle is essential for an increase in the maximum height at the lateral domain during polarization (cuboidal morphology). Thus, both junctional actin and thin bundles are necessary, and cooperate with each other to generate a polarized epithelial morphology

    Reduced dimension modeling of leading edge turbulent interaction noise

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    A computational aeroacoustics approach is used to model the effects of real airfoil geometry on leading edge turbulent interaction noise for symmetric airfoils at zero angle of attack. For the first time, one-component (transverse), two-component (transverse and streamwise), and three-component (transverse, streamwise, and spanwise) synthesized turbulent disturbances are modeled instead of single frequency transverse gusts, which previous computational studies of leading edge noise have been confined to. The effects of the inclusion of streamwise and spanwise disturbances on the noise are assessed, and it is shown that accurate noise predictions for symmetric airfoils can be made by modeling only the transverse disturbances, which reduces the computational expense of simulations. Additionally, the two-component turbulent synthesis method is used to model the effects of airfoil thickness on the noise for thicknesses ranging from 2% to 12%. By using sufficient airfoil thicknesses to show trends, it is found that airfoil thickness will reduce the noise at high frequency, and that the sound power P will reduce linearly with increasing airfoil thickness

    The BMV project: Search for photon oscillations into massive particles

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    In this contribution to PSAS08 we report on the research activities developed in our Toulouse group, in the framework of the BMV project, concerning the search for photon oscillations into massive particles, such as axion-like particles in the presence of a strong transverse magnetic field. We recall our main result obtained in collaboration with LULI at \'Ecole Polytechnique (Palaiseau, France). We also present the very preliminary results obtained with the BMV experiment which is set up at LNCMP (Toulouse, France).Comment: Proceedings of PSAS'08, to be published in Can. J. Phy

    Numerical Modeling of the Propagation of Infrasonic Acoustic Waves Through the Turbulent Field Generated by the Breaking of Mountain Gravity Waves

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    The nonlinear propagation of low-frequency acoustic waves through the turbulent fluctuations induced by breaking mountain gravity waves is investigated via 2-D numerical simulations of the Navier-Stokes equations, to understand the effects of atmospheric dynamics on ground-based infrasound measurements. Emphasis is placed on acoustic signals of frequency around 0.1 Hz, traveling through tens-of-kilometers-scale gravity waves and subkilometer-scale turbulence. The sensitivity of the infrasonic phases to small-scale fluctuations is found to depend on the altitudes through which they are refracted toward the Earth. For the considered cases, the dynamics in the stratosphere impact the refracting acoustic waves to a greater extent than those in the thermosphere. This work clearly demonstrates the need for accurate descriptions of the effects of atmospheric dynamics on acoustic propagation, such as here captured by the full set of fluid dynamic equations, as well as of the subsequent effects on measured signals

    Thrombospondin modulates melanoma--platelet interactions and melanoma tumour cell growth in vivo.

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    In this study we have investigated the role of thrombospondin (TSP) as a possible ligand playing a key role in human M3Da. melanoma cell interaction with platelets and in tumour growth. TSP is secreted (80 +/- 6 ng TSP 10(-6) cells) and bound to the surface of M3Da. cells via receptors different from CD36, as shown by biosynthetic labelling and immunofluorescence studies. The levels of TSP binding to M3Da. cells evaluated by binding studies, using an anti-TSP monoclonal antibody (MAb) (LYP8), shows 367,000 +/- 58,000 (mean +/- s.d.) LYP8 binding sites per cell with a dissociation constant (Kd) of 67 nM. TSP binding to M3Da. cells shows 400,000 +/- 50,000 TSP binding sites per cell with a Kd of 10 nM. The capacity of anti-TSP MAb (LYP8) to inhibit M3Da.-platelet interactions was followed on an aggregometer and evaluated by electron microscopy studies. The biological role of TSP binding to M3Da. cells was investigated by implanting subcutaneously the M3Da. cell line in nude mice and following the size and time of in vivo tumour growth. Reducing the availability or the functional level of TSP by using an anti-TSP MAb (LYP8) resulted in a significant decrease in platelet aggregates interacting with M3Da. melanoma cells. Using an enzyme-linked immunosorbent assay, purified alpha nu beta 3 was shown to bind TSP. Moreover, LYP8-coated M3Da. cells showed a reduced capacity to form tumours in vivo. M3Da. cells were observed to attach and spread on human platelet TSP-coated plastic wells. This attachment by M3Da. cells was inhibited in a similar way by LYP8 and an anti-alpha nu beta 3 MAb (LYP18). The results obtained in this study show that TSP secreted and bound to the surface of a human melanoma cell line (M3Da.) acts as a link between aggregated platelets and the M3Da. cell surface. Moreover, these results shows that TSP can modulate tumour growth in vivo. Reagents such as MAbs directed against TSP and peptides derived from TSP could not only be used as a new therapeutic approach in the control of tumour metastasis of melanoma, but may also contribute to elucidation of the role of TSP in cancer biology
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