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Compartmentalized protein expression in rat hippocampal neurons undergoing homeostatic plasticity

ABSTRACT: Synaptic scaling is a form of homeostatic plasticity which allows neurons to adjust their action potential firing rate in response to chronic alterations in neural activity. Synaptic scaling requires profound changes in gene expression, but the relative contribution of local and cell-wide mechanisms is controversial. Here we performed a comprehensive multi-omics characterization of the somatic and process compartments of primary rat hippocampal neurons during synaptic scaling. Thereby, we uncovered highly compartment-specific and correlated changes in the neuronal transcriptome and proteome. Specifically, we identified highly compartment-specific downregulation of crucial regulators of neuronal excitability and excitatory synapse structure. Motif analysis further suggests an important role for trans-acting post-transcriptional regulators, including RNA-binding proteins and microRNAs, in the local regulation of the corresponding mRNAs. Altogether, our study indicates that compartmentalized gene expression changes are widespread in synaptic scaling and might co-exist with neuron-wide mechanisms to allow synaptic computation and homeostasis

INSTRUMENT(S): Q Exactive HF

ORGANISM(S): Rattus Norvegicus (rat)

TISSUE(S): Neuron, Cell Culture

SUBMITTER: Lukas von Ziegler

LAB HEAD: Gerhard Schratt

PROVIDER: PXD020745 | Pride | 2021-07-09

REPOSITORIES: Pride

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			Action	DRS
	20191111_002_S207924_Insertproteomics_4_CD1.raw	Raw
	20191111_003_S207925_Insertproteomics_1_PC1.raw	Raw
	20191111_005_S207926_Insertproteomics_2_PD1.raw	Raw
	20191111_006_S207927_Insertproteomics_3_CC1.raw	Raw
	20191111_008_S207928_Insertproteomics_5_PC2.raw	Raw

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