278 research outputs found

    The Planet, 2001, Winter

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    https://cedar.wwu.edu/planet/1032/thumbnail.jp

    The Planet, 2000, Fall

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    https://cedar.wwu.edu/planet/1028/thumbnail.jp

    The Planet, 2001, Spring

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    https://cedar.wwu.edu/planet/1031/thumbnail.jp

    In Tribute: M. Katherine B. Darmer

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    The editors of the Chapman Law Review respectfully dedicate this issue to Professor M. Katherine B. Darmer

    Functional paralysis of human natural killer cells by alphaherpesviruses

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    Natural killer (NK) cells are implicated as important anti-viral immune effectors in varicella zoster virus (VZV) infection. VZV can productively infect human NK cells, yet it is unknown how, or if, VZV can directly affect NK cell function. Here we demonstrate that VZV potently impairs the ability of NK cells to respond to target cell stimulation in vitro, leading to a loss of both cytotoxic and cytokine responses. Remarkably, not only were VZV infected NK cells affected, but VZV antigen negative NK cells that were exposed to virus in culture were also inhibited. This powerful impairment of function was dependent on direct contact between NK cells and VZV infected inoculum cells. Profiling of the NK cell surface receptor phenotype by multiparameter flow cytometry revealed that functional receptor expression is predominantly stable. Furthermore, inhibited NK cells were still capable of releasing cytotoxic granules when the stimulation signal bypassed receptor/ligand interactions and early signalling, suggesting that VZV paralyses NK cells from responding. Phosflow examination of key components in the degranulation signalling cascade also demonstrated perturbation following culture with VZV. In addition to inhibiting degranulation, IFN-γ and TNF production were also repressed by VZV co-culture, which was most strongly regulated in VZV infected NK cells. Interestingly, the closely related virus, herpes simplex virus type 1 (HSV-1), was also capable of efficiently infecting NK cells in a cell-associated manner, and demonstrated a similar capacity to render NK cells unresponsive to target cell stimulation–however HSV-1 differentially targeted cytokine production compared to VZV. Our findings progress a growing understanding of pathogen inhibition of NK cell function, and reveal a previously unreported strategy for VZV to manipulate the immune response.This work was funded by NHMRC project grant APP1088005 awarded to AA, BS and BM. and NHMRC project grant APP1126599 awarded to DT and AA. DT was funded by NHMRC fellowship APP110432

    EARLY RESULTS OF ECOPOESIS EXPERIMENTS IN THE SHOT MARTIAN ENVIRONMENT SIMULATOR

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    ABSTRACT Humanity is on the verge of having the capability of constructively directing environmental changes on a planetary scale. One could argue that we are making these changes on Earth today, but in a negative manner. Within the foreseeable future, we will have the technology to modify Mars' environment, and make it a habitable planet. However, we do not have enough information to determine the course of such an event. SHOT has designed and built a test-bed apparatus that can replicate most of Mars' environment conditions (with the notable exceptions of gravity and cosmic radiation) within a 5.6 liter chamber. Here, we present the results of initial experiments to determine the suitability of specific microorganisms as pioneering life-forms for Mars. Included among the potential pioneers were five genera of cyanobacteria (Anabaena, Chroococcidiopsis, Plectonema, Synechococcus and Syenechocystis), and three partially-characterized eubacterial strains that were isolated from Chile's Atacama Desert (two species of Bacillus and Klebsiella oxytoca). During these initial trials, we used a present-day mix of martian atmsospheric gases, but at a pressure of 100 mbar (10 times Mars's current atmospheric pressure). Organisms were inoculated into samples of JSC Mars-1 soil stimulant and exposed to full-spectrum simulated martian sunlight. Day/night temperature cycled from 26°C to -80°C and back. Experiments included a 24-hour, brief-exposure trial, a 7-day trial, a14-day trial and a 5-week trial to determine the survival and growth of our potential martian pioneers

    Respondent-Driven Sampling in Participatory Research Contexts: Participant-Driven Recruitment

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    This article reports on the use of respondent-driven sampling (RDS) in participatory and community-based research. Participant-driven recruitment (PDR) retains all of the analytic capabilities of RDS while enhancing the role of respondents in framing research questions, instrument development, data interpretation, and other aspects of the research process. Merging the capabilities of RDS with participatory research methods, PDR creates new opportunities for engaging community members in research addressing social issues and in utilizing research findings within community contexts. This article outlines PDR’s synthesis of RDS and participatory research approaches, describes how PDR is implemented in community contexts, and provides two examples of the use of PDR, illustrating its process, potentials, and challenges

    Considering the Definition of Addiction

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    The definition of addiction is explored. Elements of addiction derived from a literature search that uncovered 52 studies include: (a) engagement in the behavior to achieve appetitive effects, (b) preoccupation with the behavior, (c) temporary satiation, (d) loss of control, and (e) suffering negative consequences. Differences from compulsions are suggested. While there is some debate on what is intended by the elements of addictive behavior, we conclude that these five constituents provide a reasonable understanding of what is intended by the concept. Conceptual challenges for future research are mentioned
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