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Biology subjects

George, V.

Publications and source records attributed to George, V..

3 recordsLinked to original sources

Conceptualising and quantifying phenological plasticity through latent responses to seasonal environmental progression

Quantifying how individuals adjust the seasonal timings of life-history events (i.e. their phenology) in response to seasonal environmental conditions is fundamental to predicting impacts of changing seasonality. However, the current standard approach of inferring phenological responses by directly analysing observed event dates relies on foundational assumptions that could be invalidated by changing seasonality, and excludes individuals that do not express focal events, potentially generating misleading inferences. To overcome these limitations, we devised a Phenological Threshold Model (PTM) that conceptualizes phenological events as switches between discrete life-history states and primarily estimates variation in underlying latent dynamic responses to seasonal progression, from which event dates secondarily arise. We demonstrate that the PTM can accurately retrieve simulated parameter values, including given incomplete seasonal field observations. Application to multi-year data on annual breeding in black-legged kittiwakes (Rissa tridactyla) demonstrated substantial among-individual variation in latent responses to seasonally varying environmental drivers, and associated daily probabilities that individuals will initiate breeding, revealing how annual distributions of breeding dates and proportions of non-breeders jointly arise. We thereby formalise a new conceptual and statistical framework for quantifying the potential for, and constraints on, rapid plastic and micro-evolutionary changes in phenology in changing seasonal climatic and environmental regimes.

ecology↗

Visualization of Retroplacental Clear Space Disruption in a Mouse Model of Placental Accreta

IntroductionPrior preclinical studies established the utility of liposomal nanoparticle blood-pool contrast agents in visualizing the retroplacental clear space (RPCS), a marker of normal placentation, while sparing fetuses from exposure because the agent does not cross the placental barrier. In this work we characterized RPCS disruption in a mouse model of placenta accreta spectrum (PAS) using these agents. MethodsContrast-enhanced MRI (CE-MRI) and computed tomography (CE-CT) using liposomal nanoparticles bearing gadolinium (liposomal-Gd) and iodine were performed in pregnant Gab3-/- and wild type (WT) mice at day 16 of gestation. CE-MRI was performed on a 1T scanner using a 2D T1-weighted sequence (100x100x600 {micro}m3 voxels) and CE-CT was performed at a higher resolution (70x70x70 {micro}m3 voxels). Animals were euthanized post-imaging and feto-placental units (FPUs) were harvested for histological examination. RPCS conspicuity was scored through blinded assessment of images. ResultsPregnant Gab3-/- mice show elevated rates of complicated pregnancy. Contrast-enhanced imaging demonstrated frank infiltration of the RPCS of Gab3-/- FPUs. RPCS in Gab3-/- FPUs was smaller in volume, demonstrated a heterogeneous signal profile, and received lower conspicuity scores than WT FPUs. Histology confirmed in vivo findings and demonstrated staining consistent with a thinner RPCS in Gab3-/- FPUs. DiscussionImaging of the Gab3-/- mouse model at late gestation with liposomal contrast agents enabled in vivo characterization of morphological differences in the RPCS that could cause the observed pregnancy complications. An MRI-based method for visualizing the RPCS would be valuable for early detection of invasive placentation.

developmental biology↗

Cholesterol is a strong promoter of an α-Synuclein membrane binding mode that accelerates oligomerization

Dysregulation of the biosynthesis of cholesterol and other lipids has been implicated in neurological diseases, including Parkinson's disease, where the misfolding of membraneassociated -Synuclein is a key molecular event. Recent research also suggests that -Synuclein aggregation is influenced by the lipid environment. The exact molecular mechanisms responsible for cholesterols effect on -Synuclein binding to lipids and how this binding may affect -Synuclein oligomerization and fibrillation remain elusive, as does the relative importance of cholesterol versus other lipid factors. We probed the interactions and fibrillation behaviour of -Synuclein using SMA nanodiscs, containing zwitterionic and anionic lipid model systems with and without cholesterol. SPR and ThT fluorescence assays were then employed to monitor -Synuclein binding, as well as fibrillation in the absence and presence of membrane models. 1H-15N correlated NMR was used to monitor the fold of -Synuclein in response to nanodisc binding, and we determined individual residue apparent affinities for the nanodisc-contained bilayers. Cholesterol inhibited -Synuclein interaction with lipid bilayers. We also find that cholesterol significantly promotes -Synuclein fibrillation, with a more than 20-fold reduction of lag-times before fibrillation onset. When -Synuclein-bilayer interactions were analysed for individual residues by solution-state NMR, we observed two different effects of cholesterol. In nanodiscs made of DOPC, cholesterol modulated the NAC part of -Synuclein, leading to stronger interaction of this region with the lipid bilayer. In contrast, in the nanodiscs comprising DOPC, DOPE and DOPG, the NAC part was mostly unaffected by cholesterol, while the binding of the N-terminal and the C-terminal were both inhibited.\n\n\n\nO_FIG O_LINKSMALLFIG WIDTH=194 HEIGHT=200 SRC=\"FIGDIR/small/725762v3_ufig1.gif\" ALT=\"Figure 1\">\nView larger version (54K):\norg.highwire.dtl.DTLVardef@1c9c126org.highwire.dtl.DTLVardef@a7e026org.highwire.dtl.DTLVardef@16d1a9forg.highwire.dtl.DTLVardef@1eeda2d_HPS_FORMAT_FIGEXP M_FIG C_FIG

molecular biology↗