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Unichenko, P.

Publications and source records attributed to Unichenko, P..

3 recordsLinked to original sources

Local differences in baseline sodium shape astrocytic potassium uptake by the NKA

Astrocytes are vital for the maintenance of ion and transmitter homeostasis in the extracellular space, with the inward Na gradient playing a pivotal role in these processes. Earlier studies not only reported a low baseline Na+ concentration ([Na+]) in astrocytes, but also suggested an equilibration of [Na+] within the gap-junction-coupled syncytium. This is consistent with the view that the basic homeostatic properties of astrocytes are largely identical due to their critical role in brain function. Here, we used multi-photon fluorescence lifetime imaging for a quantitative determination of astrocytic [Na+] in mouse forebrain tissue slices and in vivo. Contrary to the prevailing notion of a rather uniform Na distribution, we detected a previously unobserved subcellular and cellular heterogeneity in astrocytic [Na+], accompanied by differences in the capacity for Na+/K+-ATPase (NKA)-mediated uptake of extracellular K+. Biophysical modelling showed that this heterogeneity can be replicated by the reported differential expression of NKA isoforms in astrocytes together with a different strength of Na+ influx over the plasma membranes. Altogether, our results thus suggest the existence of functionally distinct astrocytes and astrocyte subdomains in which Na+ homeostasis is locally adapted to the specific requirements of surrounding neural networks.

neuroscience↗

A marker chromosome in psychosis identifies glycine decarboxylase (GLDC) as a novel regulator of neuronal and synaptic function in the hippocampus

The biological significance of a small supernumerary marker chromosome that results in dosage alterations to chromosome 9p24.1, including triplication of the GLDC gene encoding glycine decarboxylase, in two patients with psychosis is unclear. In an allelic series of copy number variant mouse models, we identify that triplication of Gldc reduces extracellular glycine levels as determined by optical fluorescence resonance energy transfer (FRET) in dentate gyrus (DG) but not in CA1, suppresses long-term potentiation (LTP) in mPP-DG synapses but not in CA3-CA1 synapses, reduces the activity of biochemical pathways implicated in schizophrenia and mitochondrial bioenergetics, and displays deficits in prepulse inhibition, startle habituation, latent inhibition, working memory, sociability and social preference. Our results thus provide a link between a genomic copy number variation, biochemical, cellular and behavioral phenotypes, and further demonstrate that GLDC negatively regulates long-term synaptic plasticity at specific hippocampal synapses, possibly contributing to the development of neuropsychiatric disorders.

neuroscience↗

A computationally designed fluorescent biosensor for D-serine

Solute-binding proteins (SBPs) have evolved to balance the demands of ligand affinity, thermostability and conformational change to accomplish diverse functions in small molecule transport, sensing and chemotaxis. Although the ligand-induced conformational changes that occur in SBPs make them useful components in biosensors, they are challenging targets for protein engineering and design. Here we have engineered a D-alanine-specific SBP into a fluorescent biosensor with specificity for the signaling molecule D-serine (D-serFS). This was achieved through binding site and remote mutations that improved affinity (KD = 6.7 {+/-} 0.5 M), specificity (40-fold increase vs. glycine), thermostability (Tm = 79 {degrees}C) and dynamic range (~14%). This sensor allowed measurement of physiologically relevant changes in D-serine concentration using two-photon excitation fluorescence microscopy in rat brain hippocampal slices. This work illustrates the functional trade-offs between protein dynamics, ligand affinity and thermostability, and how these must be balanced to achieve desirable activities in the engineering of complex, dynamic proteins.

biochemistry↗