Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, Brisbane, QLD 4072, Australia.
Dementia Research Centre, Macquarie Medical School, Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, NSW 2109, Australia.
Sci Adv. 2023 Jun 9;9(23):eadg2248. doi: 10.1126/sciadv.adg2248. Epub 2023 Jun 7.
Numerous viruses use specialized surface molecules called fusogens to enter host cells. Many of these viruses, including the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), can infect the brain and are associated with severe neurological symptoms through poorly understood mechanisms. We show that SARS-CoV-2 infection induces fusion between neurons and between neurons and glia in mouse and human brain organoids. We reveal that this is caused by the viral fusogen, as it is fully mimicked by the expression of the SARS-CoV-2 spike (S) protein or the unrelated fusogen p15 from the baboon orthoreovirus. We demonstrate that neuronal fusion is a progressive event, leads to the formation of multicellular syncytia, and causes the spread of large molecules and organelles. Last, using Ca imaging, we show that fusion severely compromises neuronal activity. These results provide mechanistic insights into how SARS-CoV-2 and other viruses affect the nervous system, alter its function, and cause neuropathology.
许多病毒利用称为融合蛋白的专门表面分子进入宿主细胞。许多此类病毒,包括严重急性呼吸综合征冠状病毒 2(SARS-CoV-2),可以感染大脑,并通过尚未完全了解的机制与严重的神经症状相关联。我们表明,SARS-CoV-2 感染可诱导小鼠和人脑类器官中的神经元之间以及神经元与神经胶质细胞之间的融合。我们揭示,这是由病毒融合蛋白引起的,因为它完全可以通过表达 SARS-CoV-2 刺突(S)蛋白或来自狒狒正呼肠孤病毒的不相关融合蛋白 p15 来模拟。我们证明神经元融合是一个渐进的事件,导致多细胞合胞体的形成,并导致大分子和细胞器的扩散。最后,通过钙成像,我们表明融合严重损害了神经元活动。这些结果为 SARS-CoV-2 和其他病毒如何影响神经系统、改变其功能以及导致神经病理学提供了机制见解。