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Published on: September 25, 2019
Circulating hepatitis B surface antigen particles carry hepatocellular microRNAs
Luisa Novellino1, Riccardo L Rossi, Ferruccio Bonino
1Hepatology Unit and Liver Physiopathology Laboratory, University Hospital of Pisa, Pisa, Italy.
Hepatitis B surface antigen particles carry specific liver and immune-regulating microRNAs. This discovery offers a new non-invasive method to study liver epigenetics and host-pathogen interactions in Hepatitis B virus infection.
Area of Science:
- Virology
- Molecular Biology
- Epigenetics
Background:
- Hepatitis B virus (HBV) produces abundant subviral surface antigen particles (HBsAg) in the blood.
- These HBsAg particles can encapsulate other molecules, as seen with Hepatitis Delta virus (HDV) components.
- Cellular microRNAs (miRNAs) are released into circulation within extracellular vesicles.
Purpose of the Study:
- To investigate whether HBsAg particles can carry cellular miRNAs.
- To identify specific miRNAs associated with circulating HBsAg.
- To explore the potential of HBsAg-associated miRNAs as biomarkers for liver epigenetics.
Main Methods:
- Isolation of circulating HBsAg particles from HBV carriers' sera using immunoprecipitation.
- Extraction of total RNA from isolated HBsAg particles.
- Screening of human miRNAs using TaqMan real-time quantitative PCR Arrays and statistical analysis.
- Detection of Ago2 protein within HBsAg particles.
Main Results:
- Thirty-nine human miRNAs were significantly associated with immunoprecipitated HBsAg particles.
- HBsAg-associated miRNAs included liver-specific (e.g., miR-122) and immune-regulatory (e.g., miR-223) types.
- Ago2 protein was detected within HBsAg particles, suggesting a potential role in miRNA packaging.
Conclusions:
- HBsAg particles selectively package hepatocellular miRNAs.
- This finding provides a novel non-invasive tool for studying liver epigenetics in HBV infection.
- Understanding HBsAg-miRNA interactions can elucidate host-pathogen dynamics in HBV.
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