Acetylcholine-induced production of platelet-activating factor by human fetal brain cells in culture

1990 ◽  
Vol 27 (4) ◽  
pp. 706-711 ◽  
Author(s):  
V. Sogos ◽  
F. Bussolino ◽  
E. Pilia ◽  
S. Torelli ◽  
F. Gremo
2016 ◽  
Vol 37 ◽  
pp. 88-96 ◽  
Author(s):  
Delyan P. Ivanov ◽  
Abdal-jabbar Al-Rubai ◽  
Anna M. Grabowska ◽  
Margaret K. Pratten

Endocrinology ◽  
1991 ◽  
Vol 129 (2) ◽  
pp. 931-938 ◽  
Author(s):  
AYALLA BARNEA ◽  
GLORIA CHO ◽  
ASGHAR HAJIBEIGI ◽  
M. CECILIA AGUILA ◽  
PAOLO MAGNI

1984 ◽  
Vol 5 (12) ◽  
pp. 1657-1661 ◽  
Author(s):  
Steven M. D'Ambrosio ◽  
Gulzar Wani ◽  
Mervyn Samuel ◽  
Ruth E. Gibson-D'Ambrosio

2020 ◽  
Author(s):  
Daniel Limonta ◽  
Lovely Dyna-Dagman ◽  
William Branton ◽  
Tadashi Makio ◽  
Richard W. Wozniak ◽  
...  

ABSTRACTIn the present report, we describe two small molecules with broad-spectrum antiviral activity. These drugs block formation of the nodosome. The studies were prompted by the observation that infection of human fetal brain cells with Zika virus (ZIKV) induces expression of nucleotide-binding oligomerization domain-containing protein 2 (NOD2), a host factor that was found to promote ZIKV replication and spread. A drug that targets NOD2 was shown to have potent broad-spectrum antiviral activity against other flaviviruses, alphaviruses and SARS-CoV-2, the causative agent of COVID-19. Another drug that inhibits the receptor-interacting serine/threonine-protein kinase 2 (RIPK2) which functions downstream of NOD2, also decreased replication of these pathogenic RNA viruses. The broad-spectrum action of nodosome targeting drugs is mediated, at least in part, by enhancement of the interferon response. Together, these results suggest that further preclinical investigation of nodosome inhibitors as potential broad-spectrum antivirals is warranted.


Sign in / Sign up

Export Citation Format

Share Document