Intracellular Injection of Brain Extracts from Alzheimer’s Disease Patients Triggers Unregulated Ca2+ Release from Intracellular Stores That Hinders Cellular Bioenergetics

• Published in: Cells (Basel, Switzerland) Vol. 11; no. 22; p. 3630
• Main Authors: Pensalfini, Anna, Umar, Abdul Rahim, Glabe, Charles, Parker, Ian, Ullah, Ghanim, Demuro, Angelo
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 16-11-2022; MDPI
• Subjects: Alzheimer's disease; Alzheimer’s; amyloid beta (Aβ); Animal cognition; Antibodies; Bioenergetics; Brain research; Caffeine; Calcium (intracellular); Calcium (reticular); Calcium homeostasis; cellular bioenergetics; Computational neuroscience; Conformation; Endoplasmic reticulum; Experiments; Homeostasis; inositol 1,4,5-trisphospahte receptors; Intracellular; Neurodegenerative diseases; Oligomers; Oocytes; Pathology; Toxicity; upregulated calcium signaling; United States > US
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells11223630

Strong evidence indicates that amyloid beta (Aβ) inflicts its toxicity in Alzheimer’s disease (AD) by promoting uncontrolled elevation of cytosolic Ca2+ in neurons. We have previously shown that synthetic Aβ42 oligomers stimulate abnormal intracellular Ca2+ release from the endoplasmic reticulum stores, suggesting that a similar mechanism of Ca2+ toxicity may be common to the endogenous Aβs oligomers. Here, we use human postmortem brain extracts from AD-affected patients and test their ability to trigger Ca2+ fluxes when injected intracellularly into Xenopus oocytes. Immunological characterization of the samples revealed the elevated content of soluble Aβ oligomers only in samples from AD patients. Intracellular injection of brain extracts from control patients failed to trigger detectable changes in intracellular Ca2+. Conversely, brain extracts from AD patients triggered Ca2+ events consisting of local and global Ca2+ fluorescent transients. Pre-incubation with either the conformation-specific OC antiserum or caffeine completely suppressed the brain extract’s ability to trigger cytosolic Ca2+ events. Computational modeling suggests that these Ca2+ fluxes may impair cells bioenergetic by affecting ATP and ROS production. These results support the hypothesis that Aβ oligomers contained in neurons of AD-affected brains may represent the toxic agents responsible for neuronal malfunctioning and death associated with the disruption of Ca2+ homeostasis.