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miR-466 is putative negative regulator of Coxsackie virus and Adenovirus Receptor.
Lam, W Y; Cheung, Ariel C Y; Tung, Christine K C; Yeung, Apple C M; Ngai, Karry L K; Lui, Vivian W Y; Chan, Paul K S; Tsui, Stephen K W.
Affiliation
  • Lam WY; School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong.
  • Cheung AC; School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong.
  • Tung CK; School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong.
  • Yeung AC; Department of Microbiology, The Chinese University of Hong Kong, Hong Kong.
  • Ngai KL; Department of Microbiology, The Chinese University of Hong Kong, Hong Kong.
  • Lui VW; Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong.
  • Chan PK; Department of Microbiology, The Chinese University of Hong Kong, Hong Kong; Stanley Ho Centre for Emerging Infectious Diseases, The Chinese University of Hong Kong, Hong Kong.
  • Tsui SK; School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong. Electronic address: kwtsui@cuhk.edu.hk.
FEBS Lett ; 589(2): 246-54, 2015 Jan 16.
Article de En | MEDLINE | ID: mdl-25497012
ABSTRACT
This study aimed at elucidating how Coxsackie B virus (CVB) perturbs the host's microRNA (miRNA) regulatory pathways that lead to antiviral events. The results of miRNA profiling in rat pancreatic cells infection models revealed that rat rno-miR-466d was up-regulated in CVB infection. Furthermore, in silico studies showed that Coxsackie virus and Adenovirus Receptor (CAR), a cellular receptor, was one of the rno-miR-466d targets involved in viral entry. Subsequent experiments also proved that both the rno-miR-466d and the human hsa-miR-466, which are orthologs of the miR-467 gene family, could effectively down-regulate the levels of rat and human CAR protein expression, respectively.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Entérovirus humain B / MicroARN / Protéine membranaire apparentée au récepteur des coxsackievirus et adénovirus Limites: Animals / Humans Langue: En Journal: FEBS Lett Année: 2015 Type de document: Article Pays d'affiliation: Hong Kong

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Entérovirus humain B / MicroARN / Protéine membranaire apparentée au récepteur des coxsackievirus et adénovirus Limites: Animals / Humans Langue: En Journal: FEBS Lett Année: 2015 Type de document: Article Pays d'affiliation: Hong Kong
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