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Vigor, C.

Publications and source records attributed to Vigor, C..

2 recordsLinked to original sources

Pigment and isoprostanoid responses to cold atmospheric plasma-induced oxidative conditions in a natural epipelic diatom assemblage

Intertidal mudflats hosting diatom-dominated microphytobenthic communities experience strong variability in environmental conditions, which can lead to cellular oxidative stress. These constraints can, in some cases, affect diatom metabolism and photosynthetic performance in the short term, potentially compromising their survival and even leading to cell death. This study investigates pigment, isoprostanoid, and photophysiological changes in a diatom assemblage originating from a natural microphytobenthic biofilm under different durations of helium-oxygen bubbling cold atmospheric plasma experimental treatments, mimicking complex oxidative conditions of the environment. To this end, 2-min and 5-min treatments were applied to the diatom assemblage, and metabolic parameters were monitored over time up to +180 min after plasma treatment cessation. Despite physicochemical changes and slight perturbations in metabolite profiles induced by plasma treatments, photosynthetic capacities of the diatoms remained largely preserved. The duration-dependent effects of plasma treatments induced selective and mostly reversible changes, primarily characterized by an increase in the relative proportions of pheopigments and a decrease in the relative proportions of {beta}-carotenes following the 5-min treatment. A transient decrease in the relative proportions of the isoprostanoids 10-F4t-neuroP and 5-F2t-IsoP was also observed. By exposing natural diatom assemblage to plasma-generated oxidative conditions, this study provides novel insights into how marine microbiome respond to oxidative perturbations, contributing to our understanding of diatom success in fluctuating intertidal environments.

biophysics↗

Activation of hTREK-1 by polyunsaturated fatty acids does not only involve membrane tension

TREK-1 is a mechanosensitive channel also activated by polyunsaturated fatty acids (PUFAs). In this study, we compared the effect of multiple fatty acids and ML402. First, we showed a variable TREK-1 activation by PUFAs related to the variable constitutive activity of TREK-1. Then, we observed no correlation between TREK-1 activation and acyl chain length or number of double bonds suggesting that the bilayer-couple hypothesis cannot explain by itself the activation of TREK-1 by PUFAs. The membrane fluidity measurement is not modified by PUFAs at 10 {micro}M. The spectral shift analysis in TREK-1-enriched microsomes indicates a KD,TREK1 at 44 {micro}M of C22:6 n-3. PUFAs display the same activation and reversible kinetics than the direct activator ML402 and activate TREK-1 in both whole-cell and inside-out configurations of patch-clamp suggesting that the binding site of PUFAs is accessible from both sides of the membrane, as for ML402. Finally, we proposed a two steps mechanism for TREK-1 activation by PUFAs: first, insertion into the membrane, without fluidity or curvature modifications, and then interaction with TREK-1 channel to open it.

biophysics↗