ANGELOVSKI, Andrijana, Barbora LIŠČÁKOVÁ, Olga ŠVECOVÁ, Hana HŘÍBKOVÁ, Jiří SEDMÍK, Dáša BOHAČIAKOVÁ, Petr KLIMEŠ, Martina KOLAJOVÁ, Milan BRÁZDIL and Markéta BÉBAROVÁ. The impact of neurodegeneration on the electrical activity of brain tissue: multielectrode array analysis. In FENS Forum 2024. 2024.
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Basic information
Original name The impact of neurodegeneration on the electrical activity of brain tissue: multielectrode array analysis
Authors ANGELOVSKI, Andrijana (688 Serbia, belonging to the institution), Barbora LIŠČÁKOVÁ (703 Slovakia, belonging to the institution), Olga ŠVECOVÁ (203 Czech Republic, belonging to the institution), Hana HŘÍBKOVÁ (203 Czech Republic, belonging to the institution), Jiří SEDMÍK (203 Czech Republic, belonging to the institution), Dáša BOHAČIAKOVÁ (703 Slovakia, belonging to the institution), Petr KLIMEŠ (203 Czech Republic), Martina KOLAJOVÁ, Milan BRÁZDIL (203 Czech Republic) and Markéta BÉBAROVÁ (203 Czech Republic, guarantor, belonging to the institution).
Edition FENS Forum 2024, 2024.
Other information
Original language English
Type of outcome Conference abstract
Field of Study 30210 Clinical neurology
Country of publisher Austria
Confidentiality degree is not subject to a state or trade secret
Organization unit Faculty of Medicine
Keywords in English cerebral organoids; Alzheimer disease; electrical activity; multielectrode array analysis
Tags International impact
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 19/8/2024 14:19.
Abstract
Alzheimer's disease (AD) is characterized by neurodegeneration due to an accumulation of abnormal amounts of neurodegenerative proteins (NP). Elevated levels of NP have also been observed in patients suffering from temporal lobe epilepsy (TLE) which brings neurodegeneration into association with an increased risk of epileptic seizures. This study aimed to provide pilot data on the possible relationship between excitability and neurodegeneration. Electrical activity was recorded at 37°C using the multielectrode array (MEA) technique in cerebral organoids prepared from induced pluripotent stem cells (iPSCs) derived from a patient with the familial form of AD (nAD = 6) and an unrelated healthy subject (nWT = 5). The study found a significantly increased number of active electrodes, showing both spikes and bursts, in AD organoids compared to healthy controls (e.g. differentiation day D105: WT 3.39 vs. AD 20.34% in the case of spikes, P < 0.01, and WT 1.7 vs. AD 17.0 % in the case of bursts, P < 0.05). On some days, a significant increase was also observed in the case of burst duration (D118; P < 0.05), burst count (D105; P < 0.05), or intraburst spike number (D114; P < 0.05). These pilot data indicate that neurodegenerative cerebral organoids show signs of heightened neural tissue excitability compared to healthy ones. Our ongoing analysis aims to validate these pilot results further and incorporate data describing the content of NP in these cerebral organoids for establishing an association between neurodegeneration and increased neuronal excitability.
Links
GA24-12028S, research and development projectName: Atlas Alzheimerovy choroby: Mapování vývoje demence u cerebrálních organoidů pomocí single-cell transkriptomiky
Investor: Czech Science Foundation, Constructing the Developmental Atlas of Alzheimer’s Disease using Cerebral Organoids and Single-Cell Transcriptomics
LX22NPO5107, research and development projectName: Národní ústav pro neurologický výzkum
Investor: Ministry of Education, Youth and Sports of the CR, 5.1 EXCELES
MUNI/A/1547/2023, interní kód MUName: Analýza (dys)funkce: od molekul k živému organismu
Investor: Masaryk University, Analysis of (dys)function: from molecules to the living organism
NU22-04-00366, research and development projectName: Role neurodegenerace v patogenezi, manifestaci a prognóze MTLE/HS - in vivo, ex vivo a in vitro perspektiva
Investor: Ministry of Health of the CR, The role of neurodegeneration in pathogenesis, manifestations and prognosis of MTLE/HS - in vivo, ex vivo and in vitro perspective, Subprogram 1 - standard
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