16 research outputs found

    Differential Effects of Early- and Late-Life Access to Carotenoids on Adult Immune Function and Ornamentation in Mallard Ducks (Anas platyrhynchos)

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    Environmental conditions early in life can affect an organism’s phenotype at adulthood, which may be tuned to perform optimally in conditions that mimic those experienced during development (Environmental Matching hypothesis), or may be generally superior when conditions during development were of higher quality (Silver Spoon hypothesis). Here, we tested these hypotheses by examining how diet during development interacted with diet during adulthood to affect adult sexually selected ornamentation and immune function in male mallard ducks (Anas platyrhynchos). Mallards have yellow, carotenoid-pigmented beaks that are used in mate choice, and the degree of beak coloration has been linked to adult immune function. Using a 2×2 factorial experimental design, we reared mallards on diets containing either low or high levels of carotenoids (nutrients that cannot be synthesized de novo) throughout the period of growth, and then provided adults with one of these two diets while simultaneously quantifying beak coloration and response to a variety of immune challenges. We found that both developmental and adult carotenoid supplementation increased circulating carotenoid levels during dietary treatment, but that birds that received low-carotenoid diets during development maintained relatively higher circulating carotenoid levels during an adult immune challenge. Individuals that received low levels of carotenoids during development had larger phytohemagglutinin (PHA)-induced cutaneous immune responses at adulthood; however, dietary treatment during development and adulthood did not affect antibody response to a novel antigen, nitric oxide production, natural antibody levels, hemolytic capacity of the plasma, or beak coloration. However, beak coloration prior to immune challenges positively predicted PHA response, and strong PHA responses were correlated with losses in carotenoid-pigmented coloration. In sum, we did not find consistent support for either the Environmental Matching or Silver Spoon hypotheses. We then describe a new hypothesis that should be tested in future studies examining developmental plasticity

    Analysis of Familial Hemophagocytic Lymphohistiocytosis type 4 (FHL-4) mutant proteins reveals that S-acylation is required for the function of syntaxin 11 in natural killer cells

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    Natural killer (NK) cell secretory lysosome exocytosis and cytotoxicity are impaired in familial hemophagocytic lymphohistiocytosis type 4 (FHL-4), a disorder caused by mutations in the gene encoding the SNARE protein syntaxin 11. We show that syntaxin 11 binds to SNAP23 in NK cells and that this interaction is reduced by FHL-4 truncation and frameshift mutation proteins that delete all or part of the SNARE domain of syntaxin 11. In contrast the FHL-4 mutant proteins bound to the Sec-1/Munc18-like (SM) protein Munc18-2. We demonstrate that the C-terminal cysteine rich region of syntaxin 11, which is deleted in the FHL-4 mutants, is S-acylated. This posttranslational modification is required for the membrane association of syntaxin 11 and for its polarization to the immunological synapse in NK cells conjugated to target cells. Moreover, we show that Munc18-2 is recruited by syntaxin 11 to intracellular membranes in resting NK cells and to the immunological synapse in activated NK cells. This recruitment of Munc18-2 is abolished by deletion of the C-terminal cysteine rich region of syntaxin 11. These results suggest a pivotal role for S-acylation in the function of syntaxin 11 in NK cells

    Low-Frequency hybrid earthquakes near a magma chamber in Afar: quantifying path effects

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    Areas of active volcanism contain elaborate velocity structures that complicate interpretations of earthquake source mechanisms. We examine the spectral characteristics of 805 earthquakes that immediately followed a large volume basaltic dike intrusion and associated silicic flank eruption of Dabbahu volcano in the Afar Depression as recorded on near-source seismometers. We use these results to quantify the contribution of scattering and attenuation to the observed spectra of low-frequency hybrid and volcano-tectonic earthquake clusters from beneath Dabbahu volcano and around the dike zone. We find strong variations in the signal amplitude and frequency content of earthquakes recorded at stations separated by as little as 2 km, caused by preferential attenuation of high frequencies depending on the vantage point. These observations imply that there are large impedance contrasts near the cooling, solidifying, and recently intruded dike. We estimate the intrinsic absorption attenuation coefficient, QI, and inverse scattering length, g0, averaged over a 300-sq-km area beneath Dabbahu. Our results are consistent with the highest attenuation coefficients from studies of volcanic provinces in Italy (QI-1 ? 0.02, g0?0.1 km-1 for a signal at 2 Hz). The magnitude of these two parameters indicates there are large impedance contrasts present in the area due to the recent intrusion of magma and associated fracturing

    Protein tyrosine phosphatase function: the substrate perspective

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    It is now well established that the members of the PTP (protein tyrosine phosphatase) superfamily play critical roles in fundamental biological processes. Although there has been much progress in defining the function of PTPs, the task of identifying substrates for these enzymes still presents a challenge. Many PTPs have yet to have their physiological substrates identified. The focus of this review will be on the current state of knowledge of PTP substrates and the approaches used to identify them. We propose experimental criteria that should be satisfied in order to rigorously assign PTP substrates as bona fide. Finally, the progress that has been made in defining the biological roles of PTPs through the identification of their substrates will be discussed

    Molecular mechanisms and functional implications of polarized actin remodeling at the T cell immunological synapse

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    Is signal transduction modulated by an interaction between heterotrimeric G-proteins and tubulin?

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    Microtubules in the Nervous System

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    Immunological Synapse Formation: Cell Polarity During T Cell–APC Interaction

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