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Life Events and Psychopathology: The Explanatory Role of Affect and Emotion Regulation
Most studies on significant life events have examined deleterious mental health outcomes resulting from stressful or negative events. Recent work examining both negative and positive aspects of life events has found that positive aspects of significant life events protect against psychopathology. However, mechanisms by which positive aspects of events confer their beneficial effects are unclear. Clarifying mechanisms of protection may aid in the identification of novel intervention targets. The current studies examined affective states and cognitive reappraisal, an emotion regulation strategy, as possible explanatory factors. Study 1 tested longitudinal relationships between positive and negative aspects of life events, affective states, cognitive reappraisal, and transdiagnostic symptoms. Study 2 assessed whether experimental manipulation of affective states alters cognitive appraisals, represented by interpretive bias. Study 3 explored the role of positive affect and cognitive reappraisal as predictors of treatment response within a novel treatment aimed at promoting positive affect, compared to a treatment targeting reductions in negative affect. Study 1 found that positivity of interpersonal, but not non-interpersonal events promoted positive affect, and offered preliminary support for positive affect as a mediator of the relationship between positivity of events and symptomatology. Study 2 found that a positive mood induction produced more positive interpretive bias to non-social situations than a negative induction condition, whereas a negative induction condition demonstrated greater negative response bias for social scenarios and a greater positive response bias for non-social scenarios. Study 3 demonstrated that positive affect, but not cognitive reappraisal, predicted symptom reduction across treatment conditions, and higher average positive affect predicted higher average cognitive reappraisal and vice versa. The current studies examined affective states and emotion regulation as possible mechanisms of protection against psychopathology originating from positive aspects of life events. Findings suggest that interventions which seek to upregulate positive emotional states may facilitate emotion regulation and reduce risk for psychopathology
Serine Phosphorylation of HIV-1 Vpu and Its Binding to Tetherin Regulates Interaction with Clathrin Adaptors
HIV-1 Vpu prevents incorporation of tetherin (BST2/ CD317) into budding virions and targets it for ESCRT-dependent endosomal degradation via a clathrin-dependent process. This requires a variant acidic dileucine-sorting motif (ExxxLV) in Vpu. Structural studies demonstrate that recombinant Vpu/tetherin fusions can form a ternary complex with the clathrin adaptor AP-1. However, open questions still exist about Vpu's mechanism of action. Particularly, whether endosomal degradation and the recruitment of the E3 ubiquitin ligase SCFβTRCP1/2 to a conserved phosphorylated binding site, DSGNES, are required for antagonism. Re-evaluation of the phenotype of Vpu phosphorylation mutants and naturally occurring allelic variants reveals that the requirement for the Vpu phosphoserine motif in tetherin antagonism is dissociable from SCFβTRCP1/2 and ESCRT-dependent tetherin degradation. Vpu phospho-mutants phenocopy ExxxLV mutants, and can be rescued by direct clathrin interaction in the absence of SCFβTRCP1/2 recruitment. Moreover, we demonstrate physical interaction between Vpu and AP-1 or AP-2 in cells. This requires Vpu/tetherin transmembrane domain interactions as well as the ExxxLV motif. Importantly, it also requires the Vpu phosphoserine motif and adjacent acidic residues. Taken together these data explain the discordance between the role of SCFβTRCP1/2 and Vpu phosphorylation in tetherin antagonism, and indicate that phosphorylation of Vpu in Vpu/tetherin complexes regulates promiscuous recruitment of adaptors, implicating clathrin-dependent sorting as an essential first step in tetherin antagonism
Infection by a foliar endophyte elicits novel arabidopside-based plant defence reactions in its host, Cirsium arvense
Endophytic fungi live asymptomatically within plants. They are usually regarded as non-pathogenic or even mutualistic, but whether plants respond antagonistically to their presence remains unclear, particularly in the little-studied associations between endophytes and nong-raminoid herbaceous plants.
We investigated the effects of the endophyte Chaetomium cochlioides on leaf chemistry in Cirsium arvense. Plants were sprayed with spores; leaf material from both subsequent new growth and the sprayed leaves was analysed 2 wk later. Infection frequency was 91% and63% for sprayed and new growth, respectively, indicating that C. cochlioides rapidly infects new foliage.
Metabolomic analyses revealed marked changes in leaf chemistry with infection, especially in new growth. Changes in several novel oxylipin metabolites were detected, including arabi-dopsides reported here for the first time in a plant species other than Arabidopsis thaliana,and a jasmonate-containing galactolipid.
The production of these metabolites in response to endophyte presence, particularly in newly infected foliage, suggests that endophytes elicit similar chemical responses in plants to those usually produced following wounding, herbivory and pathogen invasion. Whether en-dophytes benefit their hosts may depend on a complex series of chemically mediated interactions between the plant, the endophyte, other microbial colonists and natural enemies
Automated Speckle Interferometry of Known Binaries
Astronomers have been measuring the separations and position angles between
the two components of binary stars since William Herschel began his
observations in 1781. In 1970, Anton Labeyrie pioneered a method, speckle
interferometry, that overcomes the usual resolution limits induced by
atmospheric turbulence by taking hundreds or thousands of short exposures and
reducing them in Fourier space. Our 2022 automation of speckle interferometry
allowed us to use a fully robotic 1.0-meter PlaneWave Instruments telescope,
located at the El Sauce Observatory in the Atacama Desert of Chile, to obtain
observations of many known binaries with established orbits. The long-term
objective of these observations is to establish the precision, accuracy, and
limitations of this telescope's automated speckle interferometry measurements.
This paper provides an early overview of the Known Binaries Project and provide
example results on a small-separation (0.27") binary, WDS 12274-2843 B 228
A central component of the N1 event-related brain potential could index the early and automatic inhibition of the actions systematically activated by objects
Stimuli of the environment, like objects, systematically activate the actions they are associated to. These activations occur extremely fast. Nevertheless, behavioural data reveal that, in most cases, these activations are then automatically inhibited, around 100 ms after the occurrence of the stimulus. We thus tested whether this early inhibition could be indexed by a central component of the N1 event-related brain potential (ERP). To achieve that goal, we looked at whether this ERP component is greater in tasks that could increase the inhibition and in trials where reaction times happen to be long. The illumination of a real space bar of a keyboard out of the dark was used as a stimulus. To maximize the modulation of the inhibition, the task participants had to perform was manipulated across blocks. A look-only task and a count task were used to increase inhibition and an immediate press task was used to decrease it. ERPs of the two block-conditions where presses had to be prevented and where the largest central N1s were predicted were compared to those elicited in the press task, differentiating the ERPs to the third of the trials where presses were the slowest from the ERPs to the third of the trials with the fastest presses. Despite larger negativities due to motor potentials and despite greater attention likely in immediate press-trials, central N1s were found to be minimal for the fastest presses, intermediate for the slowest ones and maximal for the two no-press conditions. These results thus provide a strong support for the idea that the central N1 indexes an early and short lasting automatic inhibition of the actions systematically activated by objects. They also confirm that the strength of this automatic inhibition spontaneously fluctuates across trials and tasks. On the other hand, just before N1s, parietal P1s were found greater for fastest presses. They might thus index the initial activation of these actions. Finally, consistent with the idea that N300s index late inhibition processes, that occur preferentially when the task requires them, these ERPs were quasi absent for fast presses trials and much larger in the three other conditions
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