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Plataki, M.

Publications and source records attributed to Plataki, M..

2 recordsLinked to original sources

Effects of working memory training on cognitive flexibility, dendritic spine density and long-term potentiation in female mice

Working memory (WM) is a cognitive function that refers to the ability of short-term storage and manipulation of information necessary for the accomplishment of a task. Two brain regions involved in WM are the prefrontal cortex (PFC) and the hippocampus (HPC). Several studies have suggested that training in WM (WMT) can improve performance in other cognitive tasks. However, our understanding of the neurobiological changes induced by WMT is very limited. Previous work from our lab has shown that WMT enhances synaptic and structural plasticity in the PFC and HPC in male mice. In this study, we investigate the effect of WMT on cognitive flexibility and synaptic properties in PFC and HPC in adult female mice. To this end, female adult mice were split into 3 groups: a) naive which remained in their home cage, b) non-adaptive which learned to alternate the arms in the T-maze but without any delays and c) adaptive which were trained in the delayed alternation task for 9 days. The delayed alternation task was used for WMT. In one cohort, following the delayed alternation task, all mice were tested in the attention set-shifting (AST) task in order to measure cognitive flexibility, and then, the brains were harvested for Golgi-Cox staining to study dendritic spine density. Our results showed that in female mice, there were no differences in performance in the AST among the three groups tested, however, the latency to make a choice was reduced. With regards to dendritic spine density, no significant differences were identified in PFC while increased dendritic spine density was found in the hippocampus of the adaptive group, compared to the naive group. In a second cohort, acute brain slices were prepared following the delayed alternation task to investigate the synaptic properties in the PFC and the HPC. Evoked field excitatory post-synaptic potential (fEPSP) recordings were performed in either PFC or HPC brain slices. Our results show that tetanic-induced long-term potentiation (LTP) in the PFC was not different among the three training groups. In the HPC, theta-burst induced LTP was significantly increased in the adaptive group also compared to the other two groups. These results reveal both similarities and differences of WMT on cognitive flexibility, dendritic spine density and LTP in females, compared to males.

neuroscience↗

Long-term synaptic depression triggers local biogenesis of autophagic vesicles in dendrites and requires autophagic degradation

In neurons, biogenesis of autophagic vesicles (AVs) is spatially confined to the axon tip under baseline conditions. However, it remains unknown whether their biogenesis can be induced in other neuronal compartments following synaptic activity in order to serve local functions. Here, we show that both major types of long-term synaptic depression (LTD), a form of plasticity expressed by the shrinkage and elimination of dendritic spines, trigger the rapid and local biogenesis of AVs in post-synaptic dendrites. In return, autophagy is indispensable for LTD, as either genetic ablation of atg5 in pyramidal neurons or acute pharmacological inhibition of AV biogenesis totally prevents LTD induction. Using quantitative proteomic profiling of purified AVs, we reveal that upon LTD the autophagic cargo is significantly enriched for synaptic proteins, as well as modulators of the actin cytoskeleton and autism-implicated proteins. In line with these findings, a mild autophagy deficit is sufficient to impair behavioral flexibility, a cognitive function that requires efficient LTD. Therefore, local synthesis and assembly of the autophagic machinery in dendrites ensure the elimination of synaptic structures via degradation of their components, facilitating plasticity and associated behaviors. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=165 HEIGHT=200 SRC="FIGDIR/small/983965v1_ufig1.gif" ALT="Figure 1"> View larger version (43K): org.highwire.dtl.DTLVardef@1a7bc14org.highwire.dtl.DTLVardef@12cece0org.highwire.dtl.DTLVardef@738687org.highwire.dtl.DTLVardef@8518af_HPS_FORMAT_FIGEXP M_FIG C_FIG In briefKallergi, Daskalaki and colleagues demonstrate that autophagy is cell autonomously required in pyramidal excitatory neurons for the induction of long-term synaptic depression (LTD). They uncover the novel and local biogenesis of autophagic vesicles (AVs) in dendrites upon LTD, by which post-synaptic components are rapidly accessible on-site for autophagic degradation. Using quantitative proteomics on purified AVs, they reveal that upon LTD the autophagic cargo is enriched in synaptic, cytoskeletal and autism-implicated proteins. HighlightsO_LIAutophagy is required cell-autonomously in pyramidal neurons for LTD. C_LIO_LINMDAR- and mGluR-mediated LTD trigger the local biogenesis of autophagic vesicles in dendrites. C_LIO_LIAutophagic vesicles sequester primarily synaptic and cytoskeletal cargo upon LTD. C_LIO_LIMild impairment in autophagy leads to deficits in cognitive flexibility. C_LI

neuroscience↗