Search bioRxiv⌕ Search

Biology subjects

Im, H.-I.

Publications and source records attributed to Im, H.-I..

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↗

Spatial transcriptomics reveals D2-associated synaptic transcriptional attenuation in the chronically stressed dorsal striatum

Chronic stress alters striatal functions involved in motivation, action selection, and behavioral adaptation, yet cell-type-associated transcriptional organization in the dorsal striatum remains unclear. We used RNAscope-guided GeoMx spatial transcriptomics to compare D1 and D2 neuronal compartments in matched dorsal striatal regions after chronic restraint stress (CRS). CRS engaged both populations and produced comparable numbers of differentially expressed genes. Gene set enrichment analysis revealed partially overlapping CRS-associated pathway attenuation in D1 and D2 neurons, indicating stress-responsive transcriptional organization in both populations. However, D2 responses showed more coherent convergence around receptor-trafficking and synaptic signaling programs, including AMPA receptor trafficking and EPHB-mediated signaling. Moreover, under the same threshold-defined DEG criteria, CRS-downregulated D2 genes resolved into synapse-centered functional annotation categories, including glutamatergic synapse, postsynaptic organization, and dendritic spine, whereas D1 gene sets did not show a comparable pattern. These findings provide a framework for comparing stress-associated D1/D2 transcriptional organization in the dorsal striatum. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=179 SRC="FIGDIR/small/737112v1_ufig1.gif" ALT="Figure 1"> View larger version (50K): org.highwire.dtl.DTLVardef@a57a73org.highwire.dtl.DTLVardef@a2cf8org.highwire.dtl.DTLVardef@e6ea0org.highwire.dtl.DTLVardef@180f997_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗

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↗