| Literature DB >> 36098656 |
Youssef Hamway1,2, Kaspar Zimmermann3, Marcel J J Blommers3, Mariana V Sousa1,2, Cécile Häberli4,5, Shashank Kulkarni6, Susanna Skalicky7, Matthias Hackl7, Marjo Götte3, Jennifer Keiser4,5, Clarissa Prazeres da Costa1,2, Thomas Spangenberg8, Kamal Azzaoui3.
Abstract
Parasites use different strategies of communication with their hosts. One communication channel that has been studied in recent years is the use of vesicle microRNAs to influence the host immune system by trematodes. sma-microRNA-10, secreted from Schistosoma mansoni, has been shown to influence the fate of host T-cells through manipulation of the NF-κB pathway. We have identified low molecular weight tool compounds that can interfere with this microRNA-mediated manipulation of the host immune system. We used a fragment-based screening approach by means of nuclear magnetic resonance (NMR) to identify binders to the precursor of the parasite sma-microRNA-10 present in their extracellular vesicles. The small fragments identified were used to select larger molecules. These molecules were shown to counteract the inhibition of NF-κB activity by sma-microRNA-10 in cell-based assays.Entities:
Keywords: FBS; NMR; host−parasite; microRNA; schistosome
Mesh:
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Year: 2022 PMID: 36098656 PMCID: PMC9578036 DOI: 10.1021/acsinfecdis.2c00360
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.578