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Infection of Brain Organoids and 2D Cortical Neurons with SARS-CoV-2 Pseudovirus.
Yi, Sang Ah; Nam, Ki Hong; Yun, Jihye; Gim, Dongmin; Joe, Daeho; Kim, Yong Ho; Kim, Han-Joo; Han, Jeung-Whan; Lee, Jaecheol.
  • Yi SA; Epigenome Dynamics Control Research Center, School of Pharmacy, Sungkyunkwan University, Suwon 16419, Korea.
  • Nam KH; Epigenome Dynamics Control Research Center, School of Pharmacy, Sungkyunkwan University, Suwon 16419, Korea.
  • Yun J; Epigenome Dynamics Control Research Center, School of Pharmacy, Sungkyunkwan University, Suwon 16419, Korea.
  • Gim D; Epigenome Dynamics Control Research Center, School of Pharmacy, Sungkyunkwan University, Suwon 16419, Korea.
  • Joe D; Epigenome Dynamics Control Research Center, School of Pharmacy, Sungkyunkwan University, Suwon 16419, Korea.
  • Kim YH; SKKU Advanced Institute of Nanotechnology (SAINT), Sungkyunkwan University, Suwon 16419, Korea.
  • Kim HJ; Department of Biomedical Engineering, Sungkyunkwan University, Suwon 16419, Korea.
  • Han JW; Department of Nano Engineering, Sungkyunkwan University, Suwon 16419, Korea.
  • Lee J; Biomedical Institute for Convergence at SKKU (BICS), Sungkyunkwan University, Suwon 16419, Korea.
Viruses ; 12(9)2020 09 08.
Article in English | MEDLINE | ID: covidwho-760952
ABSTRACT
Since the global outbreak of SARS-CoV-2 (COVID-19), infections of diverse human organs along with multiple symptoms continue to be reported. However, the susceptibility of the brain to SARS-CoV-2, and the mechanisms underlying neurological infection are still elusive. Here, we utilized human embryonic stem cell-derived brain organoids and monolayer cortical neurons to investigate infection of brain with pseudotyped SARS-CoV-2 viral particles. Spike-containing SARS-CoV-2 pseudovirus infected neural layers within brain organoids. The expression of ACE2, a host cell receptor for SARS-CoV-2, was sustained during the development of brain organoids, especially in the somas of mature neurons, while remaining rare in neural stem cells. However, pseudotyped SARS-CoV-2 was observed in the axon of neurons, which lack ACE2. Neural infectivity of SARS-CoV-2 pseudovirus did not increase in proportion to viral load, but only 10% of neurons were infected. Our findings demonstrate that brain organoids provide a useful model for investigating SARS-CoV-2 entry into the human brain and elucidating the susceptibility of the brain to SARS-CoV-2.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Organoids / Prosencephalon / Spike Glycoprotein, Coronavirus / Betacoronavirus / Neurons Limits: Humans Language: English Year: 2020 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Organoids / Prosencephalon / Spike Glycoprotein, Coronavirus / Betacoronavirus / Neurons Limits: Humans Language: English Year: 2020 Document Type: Article