N-methyl-d-aspartate receptor-mediated preconditioning mitigates excitotoxicity in human induced pluripotent stem cell-derived brain organoids

• Verfasst von: Bauersachs, Hanke [VerfasserIn]
• Verfasst von: Bengtson, C. Peter [VerfasserIn]
• Verfasst von: Weiss, Ursula [VerfasserIn]
• Verfasst von: Hellwig, Andrea [VerfasserIn]
• Verfasst von: García-Vilela, Celia [VerfasserIn]
• Verfasst von: Zaremba, Bastienne [VerfasserIn]
• Verfasst von: Kaessmann, Henrik [VerfasserIn]
• Verfasst von: Pruunsild, Priit [VerfasserIn]
• Verfasst von: Bading, Hilmar [VerfasserIn]
• Titel: N-methyl-d-aspartate receptor-mediated preconditioning mitigates excitotoxicity in human induced pluripotent stem cell-derived brain organoids
• Verf.angabe: Hanke Gwendolyn Bauersachs, C. Peter Bengtson, Ursula Weiss, Andrea Hellwig, Celia García-Vilela, Bastienne Zaremba, Henrik Kaessmann, Priit Pruunsild and Hilmar Bading
• E-Jahr: 2022
• Jahr: 21 February 2022
• Umfang: 15 S.
• Fussnoten: Gesehen am 07.06.2022
• Titel Quelle: Enthalten in: Neuroscience
• Ort Quelle: Amsterdam [u.a.] : Elsevier Science, 1976
• Jahr Quelle: 2022
• Band/Heft Quelle: 484(2022), Seite 83-97
• ISSN Quelle: 1873-7544
• DOI: doi:10.1016/j.neuroscience.2021.12.026
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: glutamate
• Sach-SW: human neuron
• Sach-SW: neurodegeneration
• Sach-SW: neuroprotection
• Sach-SW: pro-survival signaling
• Sach-SW: synaptic activity
• K10plus-PPN: 1806275333

Abstract

Studies in rodent models of acute and chronic neurodegenerative disorders have uncovered that glutamate-induced excitotoxic cell death is mediated primarily by extrasynaptic N-methyl-d-aspartate receptors (NMDARs). Rodent neurons can also build up in an activity-dependent manner a protective shield against excitotoxicity. This form of acquired neuroprotection is induced by preconditioning with low doses of NMDA or by activation of synaptic NMDARs triggered by bursts of action potentials. Whether NMDARs in human neurons have similar dichotomous actions in cell death and survival is unknown. To investigate this, we established an induced pluripotent stem cell (iPSC)-derived forebrain organoid model for excitotoxic cell death and explored conditions of NMDAR activation that promote neuronal survival when applied prior to a toxic insult. We found that glutamate-induced excitotoxicity in human iPSC-derived neurons is mediated by NMDARs. Treatment of organoids with high concentrations of glutamate or NMDA caused the typical excitotoxicity pathology, comprising structural disintegration, neurite blebbing, shut-off of the transcription factor CRE binding protein (CREB), and cell death. In contrast, bath-applied low doses of NMDA elicited synaptic activity, a robust and sustained increase in CREB phosphorylation as well as function, and upregulation of immediate-early genes, including neuroprotective genes. Moreover, we found that conditions of enhanced synaptic activity increased survival of human iPSC-derived neurons if applied as pre-treatment before toxic NMDA application. These results revealed that both toxic and protective actions of NMDARs are preserved in human neurons. The experimental platform described in this study may prove useful for the validation of neuroprotective gene products and drugs in human neurons.