Neuropilin-1 Mediates SARS-CoV-2 Infection of Astrocytes in Brain Organoids, Inducing Inflammation Leading to Dysfunction and Death of Neurons

Weili Kong(Gladstone Institutes), Mauricio Montaño(Gladstone Institutes), Michael J. Corley(Cornell University), Ekram Helmy(Gladstone Institutes), Hirofumi Kobayashi(Chan Zuckerberg Biohub San Francisco), Martin Kinisu(Gladstone Institutes), Rahul K. Suryawanshi(Gladstone Institutes), Xiaoyu Luo(Gladstone Institutes), Löıc A. Royer(Chan Zuckerberg Biohub San Francisco), Nadia R. Roan(Gladstone Institutes), Mélanie Ott(Gladstone Institutes), Lishomwa C. Ndhlovu(Cornell University), Warner C. Greene(Gladstone Institutes)
mBio
October 31, 2022
Cited by 127Open Access
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Abstract

SARS-CoV-2 infection primarily targets the lung but may also damage other organs, including the brain, heart, kidney, and intestine. Central nervous system (CNS) pathologies include loss of smell and taste, headache, delirium, acute psychosis, seizures, and stroke. Pathological loss of gray matter occurs in SARS-CoV-2 infection, but it is unclear whether this is due to direct viral infection, indirect effects associated with systemic inflammation, or both. Here, we used induced pluripotent stem cell (iPSC)-derived brain organoids and primary human astrocytes from the cerebral cortex to study direct SARS-CoV-2 infection. Our findings support a model where SARS-CoV-2 infection of astrocytes produces a panoply of changes in the expression of genes regulating innate immune signaling and inflammatory responses. The deregulation of these genes in astrocytes produces a microenvironment within the CNS that ultimately disrupts normal neuron function, promoting neuronal cell death and CNS deficits.


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