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Filipkowski, R. K.

Publications and source records attributed to Filipkowski, R. K..

3 recordsLinked to original sources

Spatial learning-specific remodeling of the hippocampal palmitoylome

Protein S-palmitoylation is a reversible lipid modification that regulates protein trafficking, membrane association, and synaptic signaling, yet its role in learning-induced neuronal plasticity remains incompletely understood. Here, we investigated how spatial learning remodels the hippocampal palmitoylome in rats trained in the Morris water maze using short-term (STT; one session, 15 trials; probe at 1 h) or long-term (LTT; four sessions over four days; probe at 24 h) paradigms. Palmitoylated proteins were profiled by acyl-biotin exchange coupled with tandem mass tag labeling and LC-MS/MS. We identified 5,260 proteins, including 763 palmitoylated species. Spatial learning induced extensive remodeling of protein S-palmitoylation, with markedly greater changes after STT than LTT. Using yoked controls, we distinguished palmitoylation changes associated with learning the hidden platform location from those induced by general behavioral experience. Comparison of trained and yoked animals identified 186 and 62 differentially palmitoylated proteins after STT and LTT, respectively, whereas yoked animals also exhibited extensive changes relative to naive controls, demonstrating that behavioral experience alone substantially reshapes the hippocampal palmitoylome. Functional enrichment revealed that STT preferentially engaged pathways related to synaptic transmission, cytoskeletal remodeling, GTPase signaling, and cellular metabolism, whereas LTT was associated with protein translation and synaptic organization. Site-specific analysis identified numerous previously unreported palmitoylation sites. Hierarchical analysis further identified diacylglycerol lipase- (DAGLA) as the only protein whose palmitoylation consistently reflected both general Morris water maze experience and learning the hidden platform location across both paradigms. Together, these findings establish S-palmitoylation as a dynamic regulator of experience-dependent hippocampal plasticity.

neuroscience↗

Rats emit aversive 44-kHz ultrasonic vocalizations during prolonged Pavlovian fear conditioning

Rats are believed to communicate their emotional state by emitting two distinct types of ultrasonic vocalizations. The first is long "22-kHz" vocalizations (>300 ms, <32 kHz) with constant frequency, signaling aversive states and the second, is short "50-kHz" calls (<150 ms, >32 kHz), often frequency-modulated, in appetitive situations. Here we describe aversive vocalizations emitted at a higher pitch by male Wistar and spontaneously hypertensive rats (SHR) in an intensified aversive state - prolonged fear conditioning. These calls, which we named "44-kHz" vocalizations, are long (>150 ms), generally at a constant frequency (usually within 35-50 kHz range) and have an overall spectrographic image similar to 22-kHz calls. Some 44-kHz vocalizations are comprised of both 22-kHz-like and 44-kHz-like elements. Furthermore, two separate clustering methods confirmed that these 44-kHz calls can be separated from other vocalizations. We observed 44-kHz calls to be associated with freezing behavior during fear conditioning training, during which they constituted up to 19.4% of all calls and most of them appeared next to each other forming uniform groups of vocalizations (bouts). We also show that some of rats responses to the playback of 44-kHz calls were more akin to that of aversive calls, e.g., heart rate changes, whereas other responses were at an intermediate level between aversive and appetitive calls. Our results suggest that rats have a wider vocal repertoire than previously believed, and current definitions of major call types may require reevaluation. We hope that future investigations of 44-kHz calls in rat models of human diseases will contribute to expanding our understanding and therapeutic strategies related to human psychiatric conditions.

neuroscience↗

The molecular fingerprint of stress resilience

Stress resilience is the ability of neuronal networks to maintain their function despite the stress exposure. Using a mouse model we here investigate stress resilience phenomenon. To assess the resilient and anhedonic behavioral phenotypes developed after the induction of chronic unpredictable stress, we quantitatively characterized the structural and functional plasticity of excitatory synapses in the hippocampus using a combination of proteomic, electrophysiological, and imaging methods. Our results indicate that stress resilience is an active and multifactorial process manifested by structural, functional, and molecular changes in synapses. We reveal that chronic stress influences palmitoylation of synaptic proteins, whose profiles differ between resilient and anhedonic animals. The changes in palmitoylation are predominantly related with the glutamate receptor signaling thus affects synaptic transmission and associated structures of dendritic spines. We show that stress resilience is associated with structural compensatory plasticity of the postsynaptic parts of synapses in CA1 subfield of the hippocampus. One Sentence SummaryCompensatory remodeling of dendritic spines at the structural and molecular levels underlies stress resilience.

neuroscience↗