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Guranda, M.

Publications and source records attributed to Guranda, M..

2 recordsLinked to original sources

More running causes more ocular dominance plasticity in mouse primary visual cortex: new gated running wheel setup allows to quantify individual running behaviour of group-housed mice

Environmental enrichment boosts neuronal plasticity of standard-cage raised (SC) mice. Since it becomes increasingly more important to track individual mouse behaviours and its influence on brain plasticity, we designed a gated running wheel (gRW) setup allowing to correlate wheel running with neuronal plasticity, using the established paradigm of ocular dominance (OD)-plasticity after monocular deprivation (MD). After SC-rearing until adulthood (>P110), group-housed mice were transferred to gRW cages, that provided an additional running wheel compartment for tracking individual wheel activity via implanted RFID chips. Notably, individual running parameters varied enormously: mice ran from close to 0 to [~]20 km across the 7 days of gRW experience, with on average running 0-3.96 km in 0-3.85 h/d and running bouts lasting from <1 up to 10 min, while running at a speed of 6-26 cm/s. OD-plasticity in V1 after 7 days of MD in the gRW was visualized using intrinsic signal optical imaging, and compared to control gRW-mice without MD via calculation of an OD-index. Most, notably - while wheel running enabled OD-plasticity -individual running parameters correlated with individual OD-indices after MD: Mice running longer distances, for longer time, at higher speeds and with longer and more frequent bouts displayed more experience-dependent V1-plasticity. In turn, a composite measure of overall running wheel activity derived from principal component analysis of running parameters accounted for 65% of inter-individual variability of OD-index following MD. Together our study demonstrates that interindividual variability of running behaviour is high, and mice intrinsically motivated to run more show enhanced V1-plasticity, underscoring the huge importance of analysing individual behavioural parameters together with any measure of brain plasticity. End Graphical abstract With our newly developed gated running wheel setup, we observed a striking correlation between individual running activity, and a measure of experience dependent plasticity in mouse primary visual cortex. More running caused more plasticity: running speed, running distance, total running time, number of running bouts and bout duration all correlated with a measure of visual cortical plasticity, the ocular dominance index. Thus, our observations add to the growing body of evidence that individual behavioural choices strongly affect individual brain plasticity. O_FIG O_LINKSMALLFIG WIDTH=149 HEIGHT=200 SRC="FIGDIR/small/647197v2_ufig1.gif" ALT="Figure 1"> View larger version (21K): org.highwire.dtl.DTLVardef@e1045dorg.highwire.dtl.DTLVardef@e5af90org.highwire.dtl.DTLVardef@1693a46org.highwire.dtl.DTLVardef@170ec3d_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗

Comparative profiling of N-respirasomes predicts aberrant mitochondrial bioenergetics at single-cell resolution

AO_SCPLOWBSTRACTC_SCPLOWMitochondria sustain the energy demand of the cell. The composition and functional state of the mitochondrial oxidative phosphorylation system are informative indicators of organelle homeostasis and bioenergetic capacity. Here we describe a highly sensitive and reproducible method for single-cell visualization and quantification of mitochondrial respiratory supercomplexes as a novel means of measuring mitochondrial respiratory chain integrity. We apply a proximity ligation assay (PLA) and perform comparative studies of mitochondrial CI, CIII and CIV-containing supercomplexes (or N-respirasomes) in fixed human and mouse brain tissues, tumorigenic cells, iPSCs and iPSC-derived NPCs and neurons. Our optimized approach enables a quantitative in-situ assessment of even subtle mitochondrial lesions associated with aberrant respiration. By combining quantitative proteomics with single cell imaging analysis, we also report the mechanistic contribution of the MICOS complex subunit CHCHD3 in regulating N-respirasomes. Overall, our PLA-based profiling of N-respirasomes establishes a sensitive and complementary technique for detecting cell-type specific mitochondrial perturbations in fixed materials.

cell biology↗