作者
Eduardo A Albornoz, Alberto A Amarilla, Naphak Modhiran, Sandra Parker, Xaria X Li, Danushka K Wijesundara, Julio Aguado, Adriana Pliego Zamora, Christopher LD McMillan, Benjamin Liang, Nias YG Peng, Julian DJ Sng, Fatema Tuj Saima, Jenny N Fung, John D Lee, Devina Paramitha, Rhys Parry, Michael S Avumegah, Ariel Isaacs, Martin W Lo, Zaray Miranda-Chacon, Daniella Bradshaw, Constanza Salinas-Rebolledo, Niwanthi W Rajapakse, Ernst J Wolvetang, Trent P Munro, Alejandro Rojas-Fernandez, Paul R Young, Katryn J Stacey, Alexander A Khromykh, Keith J Chappell, Daniel Watterson, Trent M Woodruff
发表日期
2023/7
期刊
Molecular psychiatry
卷号
28
期号
7
页码范围
2878-2893
出版商
Nature Publishing Group UK
简介
Coronavirus disease-2019 (COVID-19) is primarily a respiratory disease, however, an increasing number of reports indicate that SARS-CoV-2 infection can also cause severe neurological manifestations, including precipitating cases of probable Parkinson’s disease. As microglial NLRP3 inflammasome activation is a major driver of neurodegeneration, here we interrogated whether SARS-CoV-2 can promote microglial NLRP3 inflammasome activation. Using SARS-CoV-2 infection of transgenic mice expressing human angiotensin-converting enzyme 2 (hACE2) as a COVID-19 pre-clinical model, we established the presence of virus in the brain together with microglial activation and NLRP3 inflammasome upregulation in comparison to uninfected mice. Next, utilising a model of human monocyte-derived microglia, we identified that SARS-CoV-2 isolates can bind and enter human microglia in the absence of viral …
引用总数