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Viruses ; 13(11)2021 11 12.
Article in English | MEDLINE | ID: mdl-34835072

ABSTRACT

TGF-ß has been shown to play a differential role in either restricting or aiding HIV infection in different cell types, however its role in the cervical cells is hitherto undefined. Among females, more than 80% of infections occur through heterosexual contact where cervicovaginal mucosa plays a critical role, however the early events during the establishment of infection at female genital mucosa are poorly understood. We earlier showed that increased TGF-ß level has been associated with cervical viral shedding in the HIV infected women, however a causal relationship could not be examined. Therefore, here we first established an in vitro cell-associated model of HIV infection in the cervical epithelial cells (ME-180) and demonstrated that TGF-ß plays an important role as a negative regulator of HIV release in the infected cervical epithelial cells. Inhibition of miR-155 upregulated TGF-ß signaling and mRNA expression of host restriction factors such as APOBEC-3G, IFI-16 and IFITM-3, while decreased the HIV release in ME-180 cells. To conclude, this is the first study to decipher the complex interplay between TGF-ß, miR-155 and HIV release in the cervical epithelial cells. Collectively, our data suggest the plausible role of TGF-ß in promoting HIV latency in cervical epithelial cells which needs further investigations.


Subject(s)
Cervix Uteri/virology , Epithelial Cells/virology , HIV-1/physiology , MicroRNAs/antagonists & inhibitors , Transforming Growth Factor beta/metabolism , Virus Shedding , Antiviral Restriction Factors/genetics , Cell Line , Cervix Uteri/cytology , Cervix Uteri/metabolism , Epithelial Cells/metabolism , Female , Humans , MicroRNAs/genetics , Signal Transduction/genetics , Transforming Growth Factor beta/antagonists & inhibitors
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