Type I astrocytes and microglia induce a cytokine response in an encephalitic murine coronavirus infection

The pathogenesis of viral infections involves an immune response by cytokines, causing a deleterious effect on organ function, in addition to tissue destruction due to viral replication. Clinical symptoms and laboratory findings of the human coronavirus disease COVID-19, caused by the novel coronavi...

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Veröffentlicht in:Experimental and molecular pathology 2020-08, Vol.115, p.104474-104474, Article 104474
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description The pathogenesis of viral infections involves an immune response by cytokines, causing a deleterious effect on organ function, in addition to tissue destruction due to viral replication. Clinical symptoms and laboratory findings of the human coronavirus disease COVID-19, caused by the novel coronavirus SARS CoV-2, indicate cytokine involvement. Our laboratory showed that an experimental murine coronavirus (MHV-A59) can be transmitted into the brain by intranasal or intracerebral exposure and that neurovirulence is mediated by cytokine secretion. In this study we investigated which cells in the brain produce cytokines, thus functioning as the brain's innate immune system. Using tissue cultures of microglia, and clonal populations of astrocytes, we found that microglia and type I astrocytes (but not types II and III), produced pro-inflammatory cytokines in response to MHV-A59 infection. A molecularly closely related, non-encephalitic strain of the virus (MHV-2) caused in vitro infection, but without cytokine induction. Furthermore, immunofluorescence and immunohistochemistry revealed that type I astrocytes and microglia have perivascular foot processes necessary for the formation of the perivascular glymphatic system, the anatomical site of the brain's innate immune system. Cytokine secretion by type I astrocytes and microglia, as part of the brain's glymphatic and innate immune system, contributes to the pathogenesis of an encephalitic coronavirus infection, and indicates the rationale for anti-cytokine therapies for COVID-19. •Cytokine induction mediates the neurologic pathogenesis of coronavirus infection.•Type I astrocytes and microglia send foot-processes around blood vessels in the brain, forming the glymphatic system.•The glymphatic system is the site of the brain’s innate immune system.•The brain’s innate immune system functions during coronavirus infection by the induction of pro-inflammatory cytokines.•This experimental coronavirus model system sheds light on the neurologic manifestations of the human disease COVID-19.
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Clinical symptoms and laboratory findings of the human coronavirus disease COVID-19, caused by the novel coronavirus SARS CoV-2, indicate cytokine involvement. Our laboratory showed that an experimental murine coronavirus (MHV-A59) can be transmitted into the brain by intranasal or intracerebral exposure and that neurovirulence is mediated by cytokine secretion. In this study we investigated which cells in the brain produce cytokines, thus functioning as the brain's innate immune system. Using tissue cultures of microglia, and clonal populations of astrocytes, we found that microglia and type I astrocytes (but not types II and III), produced pro-inflammatory cytokines in response to MHV-A59 infection. A molecularly closely related, non-encephalitic strain of the virus (MHV-2) caused in vitro infection, but without cytokine induction. 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Cytokine secretion by type I astrocytes and microglia, as part of the brain's glymphatic and innate immune system, contributes to the pathogenesis of an encephalitic coronavirus infection, and indicates the rationale for anti-cytokine therapies for COVID-19. •Cytokine induction mediates the neurologic pathogenesis of coronavirus infection.•Type I astrocytes and microglia send foot-processes around blood vessels in the brain, forming the glymphatic system.•The glymphatic system is the site of the brain’s innate immune system.•The brain’s innate immune system functions during coronavirus infection by the induction of pro-inflammatory cytokines.•This experimental coronavirus model system sheds light on the neurologic manifestations of the human disease COVID-19.</description><identifier>ISSN: 0014-4800</identifier><identifier>EISSN: 1096-0945</identifier><identifier>DOI: 10.1016/j.yexmp.2020.104474</identifier><identifier>PMID: 32454103</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Animals ; Astrocytes ; Astrocytes - immunology ; Betacoronavirus ; Brain - immunology ; Brain - pathology ; Cell Line ; Cells, Cultured ; Coronavirus ; Coronavirus - metabolism ; Coronavirus Infections - immunology ; Coronavirus Infections - transmission ; Coronavirus Infections - virology ; COVID-19 ; Cytokines ; Cytokines - immunology ; Humans ; Mice ; Microglia ; Microglia - immunology ; Mouse hepatitis virus ; Murine hepatitis virus - immunology ; Murine hepatitis virus - metabolism ; Murine hepatitis virus - pathogenicity ; Pandemics ; Pneumonia, Viral ; SARS-CoV-2 ; Virus Replication - immunology ; Virus Replication - physiology</subject><ispartof>Experimental and molecular pathology, 2020-08, Vol.115, p.104474-104474, Article 104474</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. 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subjects Animals
Astrocytes
Astrocytes - immunology
Betacoronavirus
Brain - immunology
Brain - pathology
Cell Line
Cells, Cultured
Coronavirus
Coronavirus - metabolism
Coronavirus Infections - immunology
Coronavirus Infections - transmission
Coronavirus Infections - virology
COVID-19
Cytokines
Cytokines - immunology
Humans
Mice
Microglia
Microglia - immunology
Mouse hepatitis virus
Murine hepatitis virus - immunology
Murine hepatitis virus - metabolism
Murine hepatitis virus - pathogenicity
Pandemics
Pneumonia, Viral
SARS-CoV-2
Virus Replication - immunology
Virus Replication - physiology
title Type I astrocytes and microglia induce a cytokine response in an encephalitic murine coronavirus infection
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