Evidence map›Paper›PMID 41949543›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2026

The Roles of Alix and VPS4A in Autophagy and Endosomal Pathways and Their Relation to HBV Replication.

Jia Li, Thekla Kemper, Shuping Tong, Xueyue Wang, Yong Lin, Mengji Lu

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jia LiInstitute for Virology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Thekla KemperInstitute for Virology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Shuping TongLiver Research Center, Rhode Island Hospital, the Warren Alpert School of Medicine, Brown University, Providence, Rhode Island, USA.
Xueyue WangState Key Laboratory for Diagnostic and Treatment of Infectious Diseases, the First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Yong LinThe Key Laboratory of Molecular Biology of Infectious Diseases Designated by the Chinese Ministry of Education, Chongqing Medical University, Chongqing, China.ORCID https://orcid.org/0000-0001-9171-0195
Mengji LuInstitute for Virology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Funding

Deutsche Forschungsgemeinschaft (DFG) Lu 669/12-1Deutsche Forschungsgemeinschaft (DFG) Lu 669/13-1
6 · The paper itself

Abstract

Autophagic and endosomal pathways coordinately contribute to hepatitis B virus (HBV) production, with the endosomal sorting complex required for transport (ESCRT) components ALG-2-interacting protein X (Alix) and the vacuolar protein sorting 4A (VPS4A) playing important but mechanistically elusive roles. This study investigates the roles of Alix and VPS4A in HBV biogenesis within the context of endosomal trafficking and autophagy. Using gene silencing and overexpression of wild-type (WT) or dominant-negative (DN) mutants of Alix and VPS4A in HBV replication cell models, we found that Alix silencing increased intracellular HBV DNA and HBV surface antigen (HBsAg), extracellular HBsAg, and virions, while decreasing secreted naked capsids. It promoted HBsAg secretion along the early endosomes but reduced its transport to late endosomes and autophagosomes. Furthermore, Alix silencing impaired autophagosome formation by activating the AKT/MTOR pathway. In contrast, VPS4A silencing had minimal effects, whereas DN VPS4A significantly blocked HBV secretion by disrupting endosomal trafficking, promoting autophagosome formation and lysosome activity, ultimately leading to HBV degradation. Our findings demonstrate that the endosomal pathway is critical for HBV secretion when lysosomal activity is suppressed. Conversely, increased lysosomal function drives HBV degradation through the autophagosome-lysosome pathway.

Indexed as

ATPases Associated with Diverse Cellular ActivitiesAutophagyCalcium-Binding ProteinsCell Cycle ProteinsEndosomal Sorting Complexes Required for TransportEndosomesHepatitis B virusVacuolar Proton-Translocating ATPasesVirus ReplicationAutophagosomesHepatitis B Surface AntigensHep G2 CellsHumansATPases Associated with Diverse Cellular ActivitiesCalcium-Binding ProteinsCell Cycle ProteinsEndosomal Sorting Complexes Required for TransportHepatitis B Surface AntigensPDCD6IP protein, humanVacuolar Proton-Translocating ATPasesVPS4A protein, humanAlixautophagosomedegradationendosomal traffickingHBVVPS4A

Identifiers

PMID41949543
PMCPMC13060583

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.