دورية أكاديمية

Crosstalk between hepatitis B virus X and high‐mobility group box 1 facilitates autophagy in hepatocytes

التفاصيل البيبلوغرافية
العنوان: Crosstalk between hepatitis B virus X and high‐mobility group box 1 facilitates autophagy in hepatocytes
المؤلفون: Sha Fu, Juan Wang, Xingwang Hu, Rong‐rong Zhou, Yongming Fu, Daolin Tang, Rui Kang, Yan Huang, Lunquan Sun, Ning Li, Xue‐Gong Fan
المصدر: Molecular Oncology, Vol 12, Iss 3, Pp 322-338 (2018)
بيانات النشر: Wiley, 2018.
سنة النشر: 2018
المجموعة: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
مصطلحات موضوعية: acetylation, autophagy, hepatitis B virus, high‐mobility group box 1, histone deacetylases, protein protein interaction, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: Hepatitis B virus (HBV) X (HBx) protein is a pivotal regulator of HBV‐triggered autophagy. However, the role of HBx‐induced epigenetic changes in autophagy remains largely unknown. The cytoplasmic (Cyt) high‐mobility group box 1 (HMGB1) has been identified as a positive regulator of autophagy, and its Cyt translocation is closely associated with its acetylation status. Here, we evaluated the function of HMGB1 in HBx‐mediated autophagy and its association with histone deacetylase (HDAC). Using cell lines with enforced expression of HBx, we demonstrated that HBx upregulated the expression of HMGB1 and promoted its Cyt translocation by acetylation to facilitate autophagy. We further identified the underlying mechanism by which decreased nuclear HDAC activity and expression levels contribute to the HBx‐promoted hyperacetylation and subsequent translocation of HMGB1. We also identified the HDAC1 isoform as a critical factor in regulating this phenomenon. In addition, HBx bound to HMGB1 in the cytoplasm, which triggered autophagy in hepatocytes. Pharmacological inhibition of HMGB1 Cyt translocation with ethyl pyruvate prevented HBx‐induced autophagy. These results demonstrate a novel function of acetylated HMGB1 in HBx‐mediated autophagy in hepatocytes.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1878-0261
1574-7891
Relation: https://doaj.org/toc/1574-7891; https://doaj.org/toc/1878-0261
DOI: 10.1002/1878-0261.12165
URL الوصول: https://doaj.org/article/b3c88aac8d474df284e0592b822094ec
رقم الأكسشن: edsdoj.b3c88aac8d474df284e0592b822094ec
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:18780261
15747891
DOI:10.1002/1878-0261.12165