PMC:7455777 / 6088-7703 JSONTXT 11 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T37 0-145 Sentence denotes Cases have emerged in which patients had clinical manifestations of encephalitis and positive results of SARS-CoV-2 in cerebrospinal fluid (CSF).
T38 146-314 Sentence denotes However, these findings cannot prove the neurotropism of SARS-CoV-2 directly, since the CSF may also contain the virus from the meninges and cerebral microvasculatures.
T39 315-500 Sentence denotes In fact, based on the HPA and Genotype Tissue Expression (GTEx) databases, the CNS cells express rather low levels of TMPRSS2, which are required by SARS-CoV-2 for host cell entry [12].
T40 501-661 Sentence denotes Lately, Bullen et al. reported the potential neurotropism of SARS-CoV-2 by employing a human induced pluripotent stem cell (iPSC)-derived BrainSphere mode [13].
T41 662-828 Sentence denotes Virus infection and replication can be observed in BrainSphere despite the TMPRSS2 gene expression being below the detection limit, suggesting alternative processing.
T42 829-900 Sentence denotes In fact, a few proteins are found to act as co-factors for viral entry.
T43 901-1126 Sentence denotes A Disintegrin and Metalloproteases 17 (ADAM17) is a co-factor that can compete with TMPRSS2 or work independently for ACE2 shedding, and down regulation of ADAM17 by siRNA may result in a decreased in SARS-CoV infection [14].
T44 1127-1228 Sentence denotes According to HPA database, ADAM17 is more widely distributed than TMPRSS2 in human brain tissue [12].
T45 1229-1317 Sentence denotes Nevertheless, it should be emphasized that the current information is far from complete.
T46 1318-1615 Sentence denotes Several aspects still remain to be elucidated before drawing a final conclusion about the neurotropism of SARS-CoV-2, such as the potential host receptors and infection co-factors, the susceptibility of CNS resident cells, as well as possible host–pathogen interactions on ACE2/TMPRSS2 expression.