tetano
Editor, Senior Moderator
Sci Rep
. 2022 Mar 31;12(1):5496.
doi: 10.1038/s41598-022-09410-7.
SARS-CoV-2 spike protein induces cognitive deficit and anxiety-like behavior in mouse via non-cell autonomous hippocampal neuronal death
Junyoung Oh[SUP] #[/SUP][SUP] 1 [/SUP], Woo-Hyun Cho[SUP] #[/SUP][SUP] 1 [/SUP], Ellane Barcelon[SUP] 1 [/SUP], Kwang Hwan Kim[SUP] 2 [/SUP], Jinpyo Hong[SUP] 3 [/SUP], Sung Joong Lee[SUP] 4 [/SUP]
Affiliations
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is accompanied by chronic neurological sequelae such as cognitive decline and mood disorder, but the underlying mechanisms have not yet been elucidated. We explored the possibility that the brain-infiltrating SARS-CoV-2 spike protein contributes to the development of neurological symptoms observed in COVID-19 patients in this study. Our behavioral study showed that administration of SARS-CoV-2 spike protein S1 subunit (S1 protein) to mouse hippocampus induced cognitive deficit and anxiety-like behavior in vivo. These neurological symptoms were accompanied by neuronal cell death in the dorsal and ventral hippocampus as well as glial cell activation. Interestingly, the S1 protein did not directly induce hippocampal cell death in vitro. Rather, it exerted neurotoxicity via glial cell activation, partially through interleukin-1β induction. In conclusion, our data suggest a novel pathogenic mechanism for the COVID-19-associated neurological symptoms that involves glia activation and non-cell autonomous hippocampal neuronal death by the brain-infiltrating S1 protein.
. 2022 Mar 31;12(1):5496.
doi: 10.1038/s41598-022-09410-7.
SARS-CoV-2 spike protein induces cognitive deficit and anxiety-like behavior in mouse via non-cell autonomous hippocampal neuronal death
Junyoung Oh[SUP] #[/SUP][SUP] 1 [/SUP], Woo-Hyun Cho[SUP] #[/SUP][SUP] 1 [/SUP], Ellane Barcelon[SUP] 1 [/SUP], Kwang Hwan Kim[SUP] 2 [/SUP], Jinpyo Hong[SUP] 3 [/SUP], Sung Joong Lee[SUP] 4 [/SUP]
Affiliations
- PMID: 35361832
- DOI: 10.1038/s41598-022-09410-7
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is accompanied by chronic neurological sequelae such as cognitive decline and mood disorder, but the underlying mechanisms have not yet been elucidated. We explored the possibility that the brain-infiltrating SARS-CoV-2 spike protein contributes to the development of neurological symptoms observed in COVID-19 patients in this study. Our behavioral study showed that administration of SARS-CoV-2 spike protein S1 subunit (S1 protein) to mouse hippocampus induced cognitive deficit and anxiety-like behavior in vivo. These neurological symptoms were accompanied by neuronal cell death in the dorsal and ventral hippocampus as well as glial cell activation. Interestingly, the S1 protein did not directly induce hippocampal cell death in vitro. Rather, it exerted neurotoxicity via glial cell activation, partially through interleukin-1β induction. In conclusion, our data suggest a novel pathogenic mechanism for the COVID-19-associated neurological symptoms that involves glia activation and non-cell autonomous hippocampal neuronal death by the brain-infiltrating S1 protein.