Concerning the classical molecular and cellular neuroscience approach, we follow the molecular and functional study of memory. In this approach, we promote the concept of dynamic protein-protein interaction network domains assembled around the key regulator proteins, which predetermine the fate of molecular mechanisms of memory formation and their disorders. We consider that factors leading to memory impairment, e.g. aging, should affect the signaling interaction networks of these key molecules. Our endeavor to identify these dynamic signaling networks and associated key regulator proteins led us to several important network domains responsible in memory formation at its different stages. Currently, we are investigating the role of these domains and their key regulator proteins, which include different protein kinases and synaptic proteins. We expect the further outcome of our research will create a robust systemic platform of the key regulator-based framework, which will serve as a reference for the study of disorders involving memory deterioration. Hence, using our platform, we intend to study the role of the key regulators in pathogenesis of memory impairment and as possible therapeutic targets. Concepts of the key regulators demonstrated its robustness in the study of potential shared mechanisms of pathogenesis of early cognitive impairments and depressive-like behavior. This study is in progress and conducted in close collaboration with Prof. A. Pinhasov’s laboratory.
Principal Investigator: Prof. Izhak Michaelevski
Molecular & Functional Neurobiology Lab
Based on the research, we approached to the important field of investigation of alteration in molecular and functional mechanisms of memory formation upon normal and diseased aging processes.In regard of the second approach, which implicates artificial NNs for understanding information processing and encoding in the neural system, we introduce fundamentally a new concept, which ditch the classical simplified model of the neurons and the principal processing units. Instead, we hypothesize a non-deterministic, quantum-like behavior of the neural system with subsequent implications on the information processing and encoding. This novel concept is so far on the stage of theoretical modeling. Methodologies necessary for experimental implementation of the concept is not available yet, although the technology exists. Hence, currently, we are working to design and assemble the concept device, which would be capable to conduct experimental test of the proposed idea.In addition to the fundamental research, our laboratory is interested in the applicative and clinical aspects of neuroscience. Our laboratory is investigating the role of non-ionizing electromagnetic radiation on protein misfolding as a part of potential ways to affect protein aggregation issues occurring in neurodegenerative diseases, such Alzheimer’s disease, Huntington disease, prion disease etc.
This research was published in a scientific journals (recent publications):
Maryia Bairachnaya, Alexey Shnyder , Albert Pinhasov, Izhak Michaelevski, Distinct brain electrical activity patterns in dominant and submissive mice: Implications for Cognitive Impairments, Eur J Neuroscience, 2025 Jul;62(2):e70184.
https://pubmed.ncbi.nlm.nih.gov/40699122/
M Kabirova, M Reichenstein, N Borovok, A Sheinin, D Gorobets, I Michaelevski, Abl2 Kinase Differentially Regulates iGluRs Current Activity and Synaptic Localization, Cell Mol Neurobiol., 2023 Aug;43(6):2785-2799.
https://pubmed.ncbi.nlm.nih.gov/36689065/
M Reichenstein, N Borovok, A Sheinin, T Brider, I Michaelevski, Abelson Kinases Mediate the Depression of Spontaneous Synaptic Activity Induced by Amyloid Beta 1-42 Peptides, Cell Mol Neurobiol., 2021 Apr;41(3):431-448.
https://pubmed.ncbi.nlm.nih.gov/32399753/