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Frankiv, N.

Publications and source records attributed to Frankiv, N..

3 recordsLinked to original sources

Inhaled black carbon induces depressive-like behavior and enhances stress-related blood-brain molecular vulnerability in mice

Black carbon (BC), a combustion-derived component of fine particulate matter, has been linked to depressive symptoms, but controlled experimental evidence remains limited. We established a controlled BC inhalation model combined with chronic restraint stress (CRS) to determine whether inhaled BC alone induces depressive-like behavior and whether concurrent stress enhances behavioral and molecular vulnerability. Male C57BL/6J mice were assigned to Control, CRS, BC, or BC+CRS groups and exposed for 21 consecutive days, followed by behavioral testing and molecular analyses of plasma-depleted whole blood and stress-related brain regions. BC exposure alone induced depressive-like behavior, and the combined BC+CRS condition showed the most pronounced phenotype. These findings indicate that inhaled BC is sufficient to influence stress-relevant behavior and may heighten vulnerability under chronic stress. At the molecular level, BC shifted peripheral responses toward a stress- and inflammation-associated state with reduced plasticity-related signaling, whereas CRS preferentially engaged glucocorticoid-responsive regulation. Combined BC+CRS exposure further altered plasticity- and transcription-related regulatory programs in blood and stress-related brain regions, with prominent changes in the nucleus accumbens. These condition-dependent molecular patterns suggest that BC engages blood-brain stress-related pathways in a context- and region-specific manner. Together, these findings identify inhaled BC as a neurobehaviorally relevant environmental hazard.

neuroscience↗

Turning the Fluorescent Protein Barrel into a Programmable Electrostatic Device Reveals Differential Bleaching States of the Chromophore

Genetically encoded voltage indicators (GEVIs) based on fluorescent proteins (FPs) report membrane potential changes through voltage-driven conformational rearrangements of a voltage-sensing domain that perturb the electrostatic and hydrogen-bonding environment of a fused FP chromophore. While the chromophore is largely protected from the external environment by the FP {beta}-can, previous results suggest that this structure can also act as a programmable electrostatic grid that influences chromophore flexibility and fluorescence transition states. Here, we show that varying the external polar offset of {beta}-sheet residues flanking a chromophore-proximal position systematically reshapes fluorescence transitions, altering response polarity and kinetics. Importantly, the influence of these external residues depends strongly on the internal sidechain chemistry, revealing reciprocal coupling between {beta}-sheet electrostatics and chromophore-proximal residues. We further show that the functional effects of glutamine and asparagine substitutions at this position are strongly context-dependent and can be tuned by appropriate external polar offsets, consistent with electrostatic control of internal sidechain orientation and expanding the molecular switch repertoire. Disrupting steady-state fluorescence further revealed that the secondary component of the voltage-dependent fluorescence transition is preferentially light-sensitive and can be selectively diminished by repeated stimulation, indicating that it arises from a photophysically distinct process separable from the primary response. In addition, altering the chromophore protonation equilibrium (e.g., T65S) substantially changes response kinetics, indicating that chromophore state influences how {beta}-can electrostatics couple to fluorescence transitions. Together, these results define general programming rules by which the electrostatic grid of the FP {beta}-barrel can be tuned to control chromophore optical properties both at rest and during perturbation of the steady state.

biophysics↗

MeCP2 regulates cell type-specific functions of depressive-like symptoms in the nucleus accumbens

MeCP2 (methyl CpG binding protein 2) is a transcriptional regulator that modulates gene expression in response to environmental stimuli. Although recent studies have implicated MeCP2 in stress responses and depression, its precise role is not completely understood. In this study, we identify a cell type-specific function of MeCP2 in the regulation of depression-like symptoms within the nucleus accumbens (NAc), a key brain region for emotional and stress processing. We observed differential MeCP2 expression in distinct cell populations of the NAc following chronic restraint stress (CRS) and investigated the behavioral and electrophysiological consequences of cell type-specific MeCP2 manipulation. We also explored the molecular mechanisms by which MeCP2 alleviates depression-like symptoms in the NAc and associated neural circuit regions through cell type-specific profiling of the spatial transcriptome. Our findings demonstrate that MeCP2 contributes to synaptic and circuit-level regulation in a cell type-specific manner within the NAc and ultimately mitigates CRS-induced depression-like behaviors. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=147 SRC="FIGDIR/small/666523v1_ufig1.gif" ALT="Figure 1"> View larger version (26K): org.highwire.dtl.DTLVardef@1ae5875org.highwire.dtl.DTLVardef@1319231org.highwire.dtl.DTLVardef@174ef60org.highwire.dtl.DTLVardef@fb061_HPS_FORMAT_FIGEXP M_FIG Graphical abstract.Schematic Summary of the functional role of accumbal MeCP2 C_FIG

neuroscience↗